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 ~  Abstract
 ~  Historical Persp...
 ~  Taxonomy
 ~  Causative Agents...
 ~  Antigenic Components
 ~  Genome
 ~  Virulence Factor...
 ~  Epidemiology
 ~  Spectrum of Disease
 ~  Laboratory Diagnosis
 ~  Treatment and Pr...
 ~  Acknowledgements
 ~  References
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Year : 2007  |  Volume : 25  |  Issue : 3  |  Page : 188-202

Review of clinical and laboratory features of human Brucellosis

1 Department of Microbiology, Belgaum Institute of Medical Sciences, District Hospital Campus, Belgaum - 590 001, India
2 Department of Microbiology, Manipal Hospital, Bangalore - 590 017, Medical Director, Manipal Cure and Care, Manipal Towers, 14 Air Port Road, Bangalore - 560 008, Karnataka, India

Date of Submission01-Mar-2007
Date of Acceptance25-Apr-2007

Correspondence Address:
B G Mantur
Department of Microbiology, Belgaum Institute of Medical Sciences, District Hospital Campus, Belgaum - 590 001
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0255-0857.34758

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 ~ Abstract 

Infection with Brucella spp. continues to pose a human health risk globally despite strides in eradicating the disease from domestic animals. Brucellosis has been an emerging disease since the discovery of Brucella melitensis by Sir David Bruce in 1887. Although many countries have eradicated B. abortus from cattle, in some areas B. melitensis and B. suis have emerged as causes of this infection in cattle, leading to human infections. Currently B. melitensis remains the principal cause of human brucellosis worldwide including India. The recent isolation of distinct strains of Brucella from marine mammals as well as humans is an indicator of an emerging zoonotic disease. Brucellosis in endemic and non-endemic regions remains a diagnostic puzzle due to misleading non-specific manifestations and increasing unusual presentations. Fewer than 10% of human cases of brucellosis may be clinically recognized and treated or reported. Routine serological surveillance is not practiced even in Brucella - endemic countries and we suggest that this should be a part of laboratory testing coupled with a high index of clinical suspicion to improve the level of case detection. The screening of family members of index cases of acute brucellosis in an endemic area should be undertaken to pick up additional unrecognised cases. Rapid and reliable, sensitive and specific, easy to perform and automated detection systems for Brucella spp. are urgently needed to allow early diagnosis and adequate antibiotic therapy in time to decrease morbidity / mortality. The history of travel to endemic countries along with exposure to animals and exotic foods are usually critical to making the clinical diagnosis. Laboratory testing is indispensable for diagnosis. Therefore alertness of clinician and close collaboration with microbiologist are essential even in endemic areas to correctly diagnose and treat this protean human infection. Existing treatment options, largely based on experience gained > 30 years ago, are adequate but not optimal. In our experience, an initial combination therapy with a three drug-regimen followed by a two-drug regimen for at least six weeks and a combination of two drugs with a minimum of six weeks seems warranted to improve outcome in children and adult patients respectively with laboratory monitoring. A safe and effective vaccine in humans is not yet available. Prevention is dependent upon the control of the disease in animal hosts, effective heat treatment of dairy produce and hygienic precautions to prevent occupational exposure. This review compiles the experiences and diagnostic and treatment paradigms currently employed in fighting this disease.

Keywords: Brucella spp, combined and prolonged therapy, epidemiology, protean manifestations, serological surveillance

How to cite this article:
Mantur B G, Amarnath S K, Shinde R S. Review of clinical and laboratory features of human Brucellosis. Indian J Med Microbiol 2007;25:188-202

How to cite this URL:
Mantur B G, Amarnath S K, Shinde R S. Review of clinical and laboratory features of human Brucellosis. Indian J Med Microbiol [serial online] 2007 [cited 2021 Jan 22];25:188-202. Available from:

 ~ Historical Perspective Top

 Brucellosis More Details is a zoonosis transmitted to humans from infected animals. A type of fever characterized by fairly regular remissions or intermissions has been recognized along the Mediterranean littoral since the time of Hippocrates in 450 B.C. Much later in the 19 th century, the disease was found to affect British armed forces and the local population of Malta. J. A. Marston, an assistant surgeon of the British Medical Department working in the Mediterranean in 1861, first described the symptoms of brucellosis in himself as" gastric remittent fever." [1] Brucellosis has many synonyms derived from the geographical regions in which disease occurs e.g.,  Mediterranean fever More Details,  Malta fever More Details,  Gibraltar fever More Details,  Cyprus fever More Details; from the remittent character of the fever e.g., undulant fever; or from its resemblance to malaria and typhoid e.g., typhomalarial fever, intermittent typhoid. The cause of this disease was obscure until 1887 when Sir David Bruce - a Scottish physician reported numerous small coccal organisms in stained sections of spleen from a fatally infected soldier and isolated and identified organism in culture from spleen tissue of four other British soldiers stationed at Malta. [2] This organism, which he designated Micrococcus melitensis, produced a remittent fever in inoculated monkeys. One animal died from the infection and the organism was recovered in pure culture from the liver and spleen. The organism derived its species name from Melita (honey), the Roman name for the Isle of Malta. Hughes ML, in a monograph in 1897, portrayed the findings in people in greater detail, emphasizing "undulant fever" and suggested the name undulant fever. [3] Wright and Smith in 1897 detected antibodies to M. melitensis in human and animal sera through agglutination test, which unravelled the zoonotic potential of the disease. [4] Later, Zammit an young Maltese physician working with Mediterranean Fever Commission in 1905 confirmed it by isolating the organism from the milk and urine of goats. [5] Thus he concluded that the goat was the reservoir of M. melitensis and the consumption of the raw milk and cheese infects man.

In the same year that Hughes monograph appeared, Bang in Denmark isolated a gram-negative rod from cattle, which had aborted. The third member of the group, which also is bacillary in shape was recovered from the foetus of aborted swine by Traum in 1914 in the United States of America and implicated as an agent of brucellosis in man by Huddleson in 1943. In 1918, Alice Evans an American bacteriologist published reports which contained convincing evidence that M. melitensis from goats and a gram-negative rod from cows could not be differentiated morphologically or by their cultural and biochemical reactions but there were antigenic differences which could be shown by agglutination absorption test. She also showed in 1920 that M. melitensis was also a bacillus. She showed that M. melitensis , isolates of cows and pigs belonged to one genus. Meyer and Shaw [6] further confirmed Evan's observations and suggested the generic name  Brucella More Details in honour of Sir David Bruce. The possible pathogenicity of B. abortus to man was suggested by Evan in 1918 and confirmed by others.

In 1956, Buddle and Boyce discovered B. ovis , the cause of epididymitis in rams. In 1957, Stoenner and Lackman isolated B. neotomae from desert wood rat in Utah in USA. In 1968, Carmicheal and Bruner discovered B. canis as the cause of an epidemic of abortions in beagles. Human infections due to B. canis have been reported. [7] Two new Brucella species, provisionally called B. pinnipediae and B.cetaceae ,have been isolated from marine hosts within the past few years. [8],[9] There are three reports in the literature of humans infected with marine mammal strains of Brucella ; one infection occurred in a research laboratory worker after occupational exposure, [10] and the other two were community- acquired infections [11],[12] including the recent report in a patient of New Zealand with spinal osteomyelitis.

 ~ Taxonomy Top

The taxonomy of Brucella species is still unclear and unresolved. Based on 16S rRNA gene sequences, Brucellae are categorised as α-2 proteobacteria and have close phylogenetic relationships with Agrobacterium, Rickettsia, Rhizobium and Rhodobacter . [13] Brucellae have been classified according to differences in pathogenicity and host preference, into six species: B. melitensis, B. abortus, B. suis, B. ovis, B. canis and B. neotomae . In fact Verger and colleagues used DNA-DNA hybridization studies to investigate 51 Brucella strains of all species and found them to be identical. [14] With these results, they proposed that all species should be considered as biovars of B. melitensis . However, because of the differences in the animal reservoirs and in the severity of clinical disease associated with the different species, this proposal has not been widely accepted. [Table - 1] summarizes the taxonomic characteristics of Brucella species. [15]

 ~ Causative Agents, Sources and Modes of Transmission Top

Brucellae are facultative intracellular, gram-negative, partially acidfast coccobacilli that lack capsules, flagellae, endospores or native plasmids. The bacterium is of 0.5-0.7µ in diameter and 0.6-1.5µ in length. They are oxidase, catalase and urease positive. Brucella species considered as important agents of human disease are B. melitensis, B. abortus and B. suis . [16] The transmission of Brucella infection and its prevalence in a region depends upon several factors like food habits, methods of processing milk and milk products, social customs, husbandry practices, climatic conditions, socio-economic status and environment hygiene. Environmental sanitation is particularly important in the context of air borne transmission. [17] Brucellosis is almost invariably transmitted to man from infected domestic animals. However, the possibility of human to human transmission of Brucella infection has also been reported in the literature. [18],[19],[20],[21],[22],[23] Human brucellosis was once thought to be predominantly transmitted through animal contact. However, it is now being realized increasingly that animal products such as milk and meat products also play important role in the disease transmission. Dairy products prepared from unpasteurized milk such as soft cheese, yoghurts and ice-creams may contain high concentration of the bacteria and consumption of these is an important cause of brucellosis. [24] It is the commonest mode of transmission in case of B. melitensis and B. abortus infections in general population. Camel milk is also considered to be the important source of infection in Middle East countries and Mongolia. Bacterial load in animal muscle tissues is low, but consumption of undercooked traditional delicacies such as liver has been implicated in human infection. [25] Other means of infection include skin abrasions [26] or inhalation of airborne animal manure particles. [27] In addition, laboratory acquired Brucella infection due to accidental ingestion, inhalation and mucosal or skin contact is a major health hazard for the laboratory workers handling the cultures of the virulent or attenuated Brucella strains. The disease has been recognized as one of the common laboratory- transmitted infections and has been reported to occur in clinical, research, and production laboratories. [10],[28],[29],[30],[31] Increased business and leisure travel to endemic countries have led to diagnostic challenge in areas where brucellosis is uncommon.

 ~ Antigenic Components Top

A substantial number of antigenic components of Brucella have been characterized. However, the antigen that dominates the antibody response is the lipopolysaccharide (LPS). LPS of non-smooth strains (R-LPS) is similar to LPS of smooth strains (S-LPS) except that the O-chain is either absent or reduced to a few residues. Strong cross-reactions in both the agglutination and complement fixation tests have been reported between smooth species of Brucella and  Yersinia More Details enterocolitica O:9,  Escherichia More Details hermanni, Escherichia coli O:157,  Salmonella More Details O:30, Stenotrophomonas maltophila and Vibrio cholerae O:1. [32] These have been attributed to similarities on the O-specific side chains of the lipopolysaccharide molecule of the organisms. Numerous outer and inner membrane, cytoplasmic and periplasmic protein antigens have also been characterized. Some are recognized by the immune system during infection and are potentially useful in diagnostic tests. [33] Omp25 is an outer membrane structural protein that is highly conserved in all Brucellae . It is associated with both lipopolysaccharide and peptidoglycan. Recently, ribosomal proteins have emerged as immunologically important components since they confer protection against challenge with Brucella on account of both antibody and cell mediated responses. [34] One such example is L7/L12. This elicits delayed hypersensitivity response as component of brucellins [35] and as fusion proteins, which has been shown to stimulate protective response. [36] Hence this appears to have potential as candidate vaccine component.

 ~ Genome Top

In the initial years of this decade, the complete genomic sequence of B. melitensis, B. abortus and B. suis has been achieved. [37],[38],[39] The average size of the genome is 2.37 x 10 9 daltons, with a DNA G + C content of 58-59mol%. [40] All types show > 95% homology in DNA-DNA pairing studies, justifying the nomination of Brucella as a monospecific genus. Restriction fragment patterns produced by infrequently cutting endonucleases support the differentiation of the nomen species. [41] Restriction endonuclease analysis has generally been unsuccessful for strain differentiation, but polymerase chain amplification of selected sequences followed by restriction analysis has provided evidence of polymorphism in a number of genes including omp 2, dnaK, htr and ery (the erythrulose-1-phosphate dehydrogenase gene). [42],[43],[44] The omp 2 gene is believed to determine dye sensitivity, one of the traditional typing methods for biotype differentiation. Its polymorphism and the capacity for post-translational modification of its product may explain the tendency for variation in dye sensitivity patterns even within species and have been used as the basis for a genetic classification of Brucella . [45],[46] A 7.2 kbp deletion in the ery gene in B. abortus strain 19 [44] may explain the erythritol sensitivity of this strain which is a major factor in its attenuation. The genome of Brucella contains two circular chromosomes of 2.1 and 1.5 Mb, respectively. Both replicons encode essential metabolic and replicative functions and therefore are chromosomes, not plasmids. [47],[48] Natural plasmids have not been detected in Brucella , although transformation has been effected by wide host range plasmids following conjugative transfer or electroporation. [49]

 ~ Virulence Factors, Pathogenic Mechanisms and Immune response Top

The pathogenicity in human brucellosis is related to various factors. The S-LPS is a major determinant of virulence and dominates the antibody response. It is the main component responsible for conferring incomplete and short-term protection against infection in passive transfer experiments with monoclonal and polyclonal antibodies. [50] The elimination of virulent Brucellae depends upon activated macrophages and hence requires development of Th1 type cell-mediated immunity. Brucella LPS is a relatively poor inducer of gamma-interferon and tumour necrosis factor-α, both of which are essential for the elimination of the organism. [51],[52] Unusually, it is an effective inducer of interleukin 12, which stimulates Th1 type response and is closely correlated with gamma interferon production. Other important virulence factors include: production of inhibitors of phagolysosome fusion such as adenine and guanine monophosphate levels; [53] outer membrane protein 25 which has been identified as the down regulator of TNF alpha [54] especially in an early stage of infection. This leads to impaired activation and cytotoxic function of natural killer cells. The phenotypic difference and host preference of Brucella spp. can be attributed to various specific outer membrane protein markers. [55] Survival within macrophages is also associated with the synthesis of stress induced proteins of different molecular weight, notably 24 kDa which induces acid environment of pH< 4. This acid environment is also responsible for limiting antibiotic action and explains the discrepancy between in vitro studies and in vivo events. [56] Recently urease enzyme has been identified as an important determinant of virulence. [57] Urease has the role to protect Brucellae in their passage through the stomach when acquired by the oral route, which is the major way of infection in human brucellosis. All these factors probably play a substantial role in the intracellular survival of at least 15 to 30% of Brucellae ingested and these Brucellae start replicating in the endoplasmic reticulum. After entering the human body and being taken up by local tissue lymphocytes, Brucellae are transferred through regional lymphnodes into the circulation and are subsequently seeded throughout the body, with tropism for the reticuloendothelial system.

 ~ Epidemiology Top

The epidemiology of brucellosis is complex and it changes from time to time. Wide host range and resistance of Brucellae to environment and host immune system facilitate its survival in the populations.

Global scenario

Worldwide, brucellosis remains a major source of disease in humans and domesticated animals. The disease is endemic especially in countries of the Mediterranean basin, the Arabian gulf, the Indian subcontinent and parts of Mexico and Central and South America. Human brucellosis is found to have significant presence in rural/nomadic communities where people live in close association with animals. Worldwide, reported incidence of human brucellosis in endemic disease areas varies widely, from <0.01 to >200 per 100,000 population. [58] The true incidence of human brucellosis however, is unknown for most countries including India. It has been estimated that the true incidence may be 25 times higher than the reported incidence due to misdiagnosis and underreporting. It has been shown that the incidence of human brucellosis is significantly high where ovine/caprine brucellosis caused by B. melitensis is endemic. [59] Recent re-emergence in Malta and Oman indicates the difficulty of eradicating this infection. [60] Sheep and goats and their products remain the main source of infection, but B. melitensis in cattle has emerged as an important problem in some southern European countries, Israel, Kuwait and Saudi Arabia. B. melitensis infection is particularly problematic because B. abortus vaccines do not protect effectively against B. melitensis infection; the B. melitensis Rev.1 vaccine has not been fully evaluated for use in cattle. Despite vaccine campaigns with Rev.1 strain, B. melitensis remains the principal cause of human brucellosis worldwide. In some South American countries, particularly Brazil and Colombia B. suis biovar 1 has become established in cattle. [61] In some areas, cattle are now more important than pigs as a source of human infection. Screening of household members of an index case is important epidemiological step since this picks up additional unrecognised cases. [62],[63] This must be taken into account by the family clinicians caring for these patients, so that timely diagnosis and provision of therapy occur, resulting in lower morbidity. The recent isolation of distinctive strains of Brucella from marine mammals [8],[9] as well as humans [10],[11],[12] has extended the ecological range of human brucellosis. Because new strains may emerge and existing types adapt to changing social and agricultural practices, the picture remains incomplete.

It is a well-characterized occupational disease in shepherds, abattoir workers, veterinarians, dairy industry professionals and personnel in microbiologic laboratories. Males are affected more commonly than females, [63] which may be due to risk of occupational exposure. Human brucellosis affects all age groups.

Indian scenario

The occurrence of brucellosis in India was first established early in the previous century and since then has been reported from almost all states. [64],[65] Several publications indicate that human brucellosis can be a fairly common disease in India. Mathur reported 8.5% seroprevalence of brucellosis among dairy personnel in contact with infected animals with the isolation of Brucella strains from seven cases of human brucellosis. [66] As many as 4.2% aborted women were seropositive for the disease. [67] In Gujarat, 8.5% prevalence of Brucella agglutinins was recorded in human cases. [68] In Haryana, 34% prevalence of human brucellosis was recorded among veterinarians, attendants and compounders in contact with animals. [69] The study conducted by Thakur et al . [70] revealed a prevalence rate of 4.97% in samples obtained from persons exposed to animals with the markedly higher prevalence of 17.39% among field veterinarians. In a study conducted by Hemashettar et al . [71] 24(8.2%) veterinary workers showed Brucella specific antibodies in significant titres. High seroprevalence rate has been also noted in specific risk groups such as abattoir workers. [72],[73] These observations support the occupational risk factors for brucellosis.

Since uncharacterised fever is the only manifestation in a large number of patients some workers screen pyrexia of unknown origin (PUO) cases for evidence of brucellosis. Handa and coworkers identified four (3.3%) cases with acute brucellosis in a group of 121 patients with PUO. [74] Sen and co-workers identified 28 (6.8%) seropositive cases in a group of 414 patients with PUO and Kadri and co-workers identified 28 (0.8%) seropositive cases in a group of 3,532 patients with PUO. [75],[76]

A prevalence of 3% was observed among patients attending Karnataka Medical College, Hubli. [77] A study by Mantur and colleagues [78] reported 93 children with brucellosis identified from 5726 children in Bijapur during a period of 13 years. The seroprevalence was 1.6% by standard tube agglutination test (≥ 1:160) and the diagnosis was confirmed in 43 of these paediatric patients by the isolation of B. melitensis . A recent publication by Mantur and colleagues [63] reported 495 adults with brucellosis with the prevalence of 1.8% who were identified by testing blood samples from 26,948 adults in Bijapur during a period of 16 years from 1988 to 2004 and isolated B. melitensis from 191 cases. Subsequent continuation of the study after publications in Bijapur till 8 th April 2006, diagnosed additional 111 cases of brucellosis from testing 6765 blood samples (Mantur BG, unpublished work). A separate study by Mantur and colleagues identified 11(0.62%) patients by SAT (≥ 1:160) and isolated two Brucella strains, one from blood and the other from testicular fluid by testing blood samples from 1750 patients seen at Belgaum Institute of Medical Sciences in Belgaum during the period June 2006 to January 2007 (Mantur BG and colleagues, unpublished work).

 ~ Spectrum of Disease Top

Brucellosis is a systemic disease that can involve any organ or system of the body. Four species are responsible for most human cases: B. melitensis (found in sheep and goats), B. abortus (found in cattle), B. suis (found in swine) and B. canis (found in dogs). Disease from marine species has also emerged. [10],[11],[12] B. melitensis remains the principal cause of human brucellosis worldwide. A recent study did not report any clinical difference between cases caused by B. melitensis and B. abortus . [79] Sufficient data on virulence and clinical presentation of biotypes of B. melitensis are lacking, although separate biotypes that predominate in various regions such as type 1 in India [63],[78] and Spain, [80] type 2 in northwestern Greece and type 3 in Turkey [81] may account for variations in clinical presentation. The infective dose of Brucella , especially that of B. melitensis is very low (10 organisms). The incubation period is usually between seven days and three months, although as long as 10 months have been reported. [82]

Human brucellosis is known for presenting with protean manifestations [63],[78] [Table - 2]. However, the most common presenting symptom is fever. Some authors [83] consider malodorous perspiration as almost pathognomonic. Pityriasis alba was found to be the consistent physical finding, with fever in the majority of patients suffering from childhood brucellosis. [78] Human brucellosis usually manifests as an acute (< 2 months) or subacute (2-12 months) febrile illness, which may persist and progress to a chronically (> 1 year) incapacitating disease with severe complications. Some authors [83] have considered this classical categorization to be of limited clinical interest. Persons infected with Brucella spp. usually have signs and symptoms consistent with an influenza like or septicaemic illness, often with insidious onset. The symptoms and clinical signs most commonly reported are fever, fatigue, malaise, chills, sweats, headaches, myalgia, arthralgia and weight loss. [63],[78],[84],[85],[86],[87] Some cases have presented with only joint pain, [63],[78] low back ache, [63] involuntary movements of limbs, [78] burning feet, [78] or ischemic heart attacks. [88] Medical literature [63],[78] [Table - 3] under reports brucellosis cases because of misleading clinical pictures. [89],[90],[91] Typically, no or few objective signs are apparent that specifically point to brucellosis. Enlargement of the liver, spleen and/or lymph nodes may occur as may other signs referable to almost any other organ system. These febrile patients may be referred to as patients with pyrexia of unknown origin or the symptoms and signs are confused with those of other diseases such as enteric fever, malaria, rheumatic fever, tuberculosis, cholecystitis, thrombophlebitis, fungal infection, autoimmune disease and tumours. [63],[78],[84],[92],[93],[94] Thus to an unaware physician, the clinical diagnosis becomes a challenging one.

B. melitensis is associated with acute infection whereas the infections with other species are usually subacute and prolonged. The acute form of human brucellosis is characterised by an undulating fever, in addition to the signs and symptoms mentioned. The temperature remains normal during the early part of the day and rises during the evening. Lack of appropriate therapy during the acute phase may result in localization of bacteria in various tissues and lead to subacute or chronic disease that can have serious clinical manifestations. [16],[91] Brucellosis in humans occurs in all age groups. [25],[63],[78],[95] Brucellosis in children can be very common particularly with B. melitensis . [78],[96],[97] The clinical presentation, epidemiology, diagnosis and treatment outcome were similar to those seen in non human immunodeficiency virus (HIV) infected patients emphasizing a casual relationship of brucellosis and HIV infection in both endemic and non-endemic areas. [63],[98],[99],[100]

Human brucellosis is known for complications. Complications can be very diverse depending on the specific site of infection. [101] Osteoarticular, genitourinary, gastrointestinal, nervous, cardiovascular, skin and mucous membranes and respiratory complications are observed. Bone and joint involvement is the most frequent complication of brucellosis and occurs in up to 40% of cases in some series. [102] Three distinct forms exist; peripheral arthritis, sacroilitis and spondylitis. Peripheral arthritis is the most common and is non-erosive, since it usually involves the knees, hips, ankles and wrists in the context of acute infection. [63],[78],[95],[103] Epididymoorchitis [63],[104] is the most frequent genitourinary complication in men and may be confused with testicular cancer or tuberculosis. [105],[106] Brucellosis during pregnancy poses a substantial risk of spontaneous abortion or intrauterine transmission of infection to the infant. [107],[108] As the largest organ of the reticuloendothelial system, the liver is probably involved in the majority of cases of brucellosis even though liver function tests are normal or values are usually only mildly abnormal. Invasion of central nervous system (CNS) occurs in about 5-7% of the cases of B. melitensis infection. Meningitis, encephalitis, meningoencephalitis, meningovascular disease, brain abscesses and demyelinating syndromes have all been reported. [63],[78],[95],[109] Brucellae are rarely isolated from cerebrospinal fluid (CSF), but antibodies to Brucella species are present in the serum and CSF in the majority of cases. [63],[78],[95] Brucella endocarditis occurs in less than 2% of cases but accounts for the majority of Brucella -related deaths. Early recognition, adequate antibiotic treatment and the absence of signs of heart failure can guide the practitioner toward prolonged, conservative treatment. [110] Complications involving the skin, although rare, are reported in the literature. [63],[78] Respiratory tract complications may be seen in abattoir workers and are thought to be caused by the inhalation of Brucellae . [111] A multinational review of cases by Pappas et al . [112] and a recent publication by Mantur and coworkers [63] indicate that the pulmonary involvement is not rare.

The reports of unusual manifestations with atypical lesions in brucellosis are on the rise due to availability of diagnostic facilities and awareness. Tsolia and colleagues [95] have noted unusual complications in two children; one developed acute left facial nerve palsy and the other thrombocytopenic purpura. We reported complications (arthritis excluded) in 9.7% [Table - 4], most part published) of patients with unusual manifestations like chorea, [78] hydrocele, [63]  Stevens-Johnson syndrome More Details, [63] and urinary tract infection. [63]

Neurobrucellosis has been reported as an exceptional cause of transient ischemic attacks. [88] Very recently, we have identified in Belgaum, two patients with atypical lesions, one was with hemorrhagic epididymoorchitis and the other with cellulitis. In conclusion, it should be noted that brucellosis may affect essentially any organ - a fact that reinforces the importance of including brucellosis in the differential diagnosis even if clinical features are not entirely compatible, especially in endemic areas. [83]

 ~ Laboratory Diagnosis Top

Clinician must develop a high degree of clinical suspicion based on epidemiological information. A thorough travel history as well as history of exposure to animals and exotic foods are usually critical to making the clinical diagnosis. [16] In all cases a blood sample should be collected from the patient and laboratory testing should be requested as the definite diagnosis of brucellosis is impossible without laboratory confirmation. [16] A proper and prompt diagnosis is important, as the treatment requires specific and prolonged antibiotics. [113]

Laboratory tools include isolation and identification of Brucellae from clinical samples, detection of antigen, demonstration of genome and demonstration of Brucella specific antibodies. Blood culture provides definite proof of brucellosis but may not provide a positive result for all patients even under ideal conditions. [80] Brucellae are relatively slow growing and the culture result may not become available for several days or weeks. In particular for patients with chronic disease, the sensitivity of culture can be low. Recently, higher rates of positive blood cultures (91% in acute brucellosis and 74% in chronic brucellosis) along with the rapid confirmation of clinical diagnosis have been reported by lysis centrifugation technique. [114] The modern automated blood culture systems have somewhat improved the speed of detection but are still too slow to make a rapid diagnosis. [115] Although bone marrow culture has been considered the gold standard for the diagnosis of brucellosis in some studies, [63],[95],[116],[117] results have not been universally reproducible, [86],[118],[119] suggesting that the bacteraemia is as unpredictable as clinical manifestations in human brucellosis. Identification of Brucella strains is done using standard classification tests, including Gram stain, a modified Ziehl-Neelsen (ZN) stain, growth characteristics, oxidase activity, urease activity, H 2 S production (four days), dye tolerance such as basic fuchsin (1: 50000 and 1: 100000) and thionin (1:25000, 1:50000 and 1:100000) and seroagglutination. Mantur and colleagues [63] have recommended Gram stain morphology and modified ZN staining, coupled with the urease test, for rapid identification of Brucella to the level of genus where facilities for further identification are not available. To the best of our knowledge, there is only one report [120] suggesting antigen detection by enzyme-linked immunosorbent assay (ELISA) as an acceptable alternative to blood culture for the diagnosis of brucellosis since sensitivity and specificity were 100% and 99.2% respectively. Antigen detection methods are potentially useful but have not been validated. Though co-agglutination has been reported as a technique for antigen detection, there seems to be paucity of published literature. Laboratory detection of Brucella and species identification is based largely on culture isolation and phenotypic characterization. This process is lengthy and labour-intensive and has been associated with a heightened risk of laboratory-acquired infections. To surmount these problems, nucleic acid amplification has been explored for the rapid detection and confirmation of Brucella .

Polymerase chain reaction (PCR) is fast and can be performed on any clinical specimen. [121] A number of nucleic acid sequences have been targeted for the development of Brucella genus-specific PCR assays, including 16S rRNA, the 16S-23S intergenic spacer region, omp2 and bcsp31 . [122],[123],[124],[125] Recently, Redkar et al . [126] described real-time PCR assays for the detection of B. abortus, B. melitensis and B. suis biovar1. These PCR assays target the specific integration of IS711 elements within the genome of the respective Brucella species or biovar. Currently, a real-time multiplex PCR assay has been developed for rapid confirmatory identification of Brucella with speciation. The genus, B. abortus and B. melitensis specific primers confirm the organism from isolates. [127],[128] One case of neurobrucellosis was confirmed in our laboratory with the CSF being positive by PCR but undetectable from the blood. The agglutinins were positive in CSF and blood. However, culture of blood and CSF was negative showing the utility of molecular methods in tertiary care centres. Molecular characterisation techniques described in the literature are very useful tools for differentiating Brucella spp. especially follow-up testing of unusual phenotypic results of Brucella isolates. Although PCR is very promising, standardization of extraction methods, infrastructure, equipment and expertise are lacking and a better understanding of the clinical significance of the results is still needed. [129] The use of molecular methods in Brucella endemic areas needs to be explored before they can be applied in these areas to diagnose brucellosis.

Unequivocal diagnosis of brucellosis requires isolation of the causal agent. Blood culture is the method of choice, but specimens need to be obtained early prior to antibiotic administration and need prolonged periods of incubation. In addition, failure to detect the pathogen is a frequent occurrence. Although in the last few years PCR-based laboratory tests have been proposed, they cannot be considered a routine diagnostic method yet. These limitations make serology for antibody detection the most useful tool for the laboratory diagnosis of brucellosis. Antibodies usually begin to appear in the blood at the end of the first week of the disease, IgM appearing first followed by IgG. The serological tests like Rose Bengal Plate Agglutination Test (RBPT), standard tube agglutination test (SAT), Coombs test, immunocapture agglutination test, [130] latex agglutination, complement fixation test, ELISA, lateral flow assay-a simplified version of ELISA, dipstick assay, fluorescence polarization assay (FPA), [131] have all been applied in the diagnosis of human brucellosis. The RBPT is often used as a rapid screening test. [132] The sensitivity is very high (>99%) but the specificity is disappointingly low. [63],[133],[134] However, this is of value as a screening test in high risk rural areas where it is not always possible to perform the tube agglutination titration test. To increase the specificity and the positive predictive value of the RBPT, the test may be applied to a serial dilution (1:2 through 1:64) of the serum sample. The specificity of the test increases when higher dilutions agglutinate and titres of 1:8 or 1:16 and above may be regarded as positive. [135] This approach may result in a lower sensitivity. Whenever possible, a serum that gives a positive result should be confirmed by a more specific test. The RBPT is also of value in the rapid confirmation of neurobrucellosis, arthritis, epididymoorchitis, hydrocele due to Brucella if the neat is positive in CSF, synovial fluid, testicular fluid /semen and hydrocele fluid respectively. [63],[78]

SAT developed by Wright and colleagues [4] remains the most popular and yet used worldwide diagnostic tool for the diagnosis of brucellosis because it is easy to perform, does not need expensive equipments and training. SAT measures the total quantity of agglutinating antibodies (IgM and IgG), [136] the quantity of specific IgG is determined by treatment of the serum with 0.05M 2-mercaptoethanol (2ME), which inactivates the agglutinability of IgM. SAT titres above 1:160 are considered diagnostic in conjunction with a compatible clinical presentation. However, in areas of endemic disease, using a titre of 1:320 as cutoff may make the test more specific. The differentiation in the type of antibody is also important, as IgG antibodies are considered a better indicator of active infection than IgM and the rapid fall in the level of IgG antibodies is said to be prognostic of successful therapy. [137] A survey conducted by Almuneef and coworkers [138] in 2002 in Saudi Arabia found various levels of SAT antibodies in many clinically cured patients. Recently, Mantur and colleagues [63] followed-up 79 patients diagnosed as having active brucellosis for different lengths of time and monitored for Brucella antibodies by SAT and 2ME agglutination. In most cases, Brucella SAT titres remained measurable, in spite of falling to low levels [Figure - 1] ranging from 1:160 to 1:640 (diagnostic titres), despite an effective therapy and clinical cure. A remarkable finding of the study was that there was a sustained drop in 2ME titres in 97.5% of cases [Figure - 1], reflecting the importance of the 2ME test for diagnosis of brucellosis in conjunction with the SAT, as well as for follow up brucellosis in Brucella -endemic countries. Gazapo et al . [139] claimed that ELISA was an excellent method for follow up of brucellosis; however, the results of our study [63] clearly indicate that the 2ME agglutination test is a useful assay, as it is inexpensive and technologically simple with stable reagents. Coombs test that detects incomplete antibodies and immunocapture-agglutination tests have shown similar performance with higher sensitivity and specificity in the diagnosis of human brucellosis, both in the first stage of the disease and in cases with long evolution as well as in relapses and reinfections. [130] Indirect enzyme-linked immunosorbent assay typically uses cytoplasmic proteins as antigens. ELISA measures IgM, IgG and IgA, which allows for a better interpretation of the clinical situation. A comparison with the SAT, ELISA yields higher sensitivity and specificity. [140] ELISA is also reported to be the most sensitive test for the diagnosis of CNS brucellosis. [95],[141],[142] Among the newer serologic tests, the ELISA appears to be the most sensitive; however, more experience is needed before it replaces the SAT as the test of choice for brucellosis. A dipstick assay [143] offers a rapid and reliable diagnostic alternative in acute brucellosis. The rapid and simple assays like Brucella IgM and IgG lateral flow [144] and latex agglutination [145] have been developed recently. The sensitivity and specificity of lateral flow assay for culture confirmed brucellosis is >95%. The sensitivity of the latex agglutination assay was determined to be 89.1% for the initial serum samples collected for the patients with culture confirmed brucellosis and the specificity was 98.2%. Both these tests are ideal for use as field tests in remote areas and as point of care tests in hospitals and health care centres that lack the expertise and facilities to perform the more demanding classic serologic tests. Routine serological surveillance is not practiced even in Brucella -endemic areas and we suggest that this should be a part of laboratory testing coupled with a high index of clinical suspicion to improve the level of case detection. It is important to realize that household members of index cases of acute brucellosis may have been exposed to the pathogen as well and have become infected and ill. [62],[63] Therefore, we also recommend for the routine screening of family members of index cases of acute brucellosis in an endemic area.

 ~ Treatment and Prevention Top

The prerequisites for an effective therapy are: treatment should start on time, should consist of combination of drugs along with at least one drug having a good penetration into cells and should be prolonged. It seems advisable to follow-up the cases to assess the response to therapy as a guide for treatment with the help of either 2-ME or ELISA tests. The treatment of human brucellosis is a controversial area because of the spectrum of disease, the possibility of chronic infection and the development of complications. [146] Many antimicrobial agents are active against Brucella species; however, clinical efficacy does not always correlate with in vitro susceptibility. [147] In all cases it is important that the patient completes the full course of therapy because the risk of incomplete recovery and relapse is otherwise increased considerably. [148] The treatment recommended by the World Health Organization for acute brucellosis in adults is rifampicin 600 to 900 mg and doxycycline100 mg twice daily for a minimum of six weeks. [17] Some still claim that the long- established combination of intramuscular streptomycin (1 g/day for two-three weeks) with an oral tetracycline (2 g/day for six weeks) gives fewer relapses. [63],[149] Trimethoprim-sulfamethoxazole is a popular compound in many areas, usually used in triple regimens. Quinolones are an alternative. Various combinations that incorporate ciprofloxacin and ofloxacin have been tried clinically, yielding similar efficacy to that of the classic regimens. [150] Although the results are encouraging, additional experience is needed in order to determine the role of fluoroquinolones in the treatment of brucellosis. [151] Childhood brucellosis can be successfully treated with a combination of two drugs; doxycycline 4 mg / kg / day and rifampicin 10 mg/kg /day orally for six weeks. [78] Some authors advise that gentamicin (5 mg/kg/day intramuscularly) be administered concomitantly for the initial five to seven days of therapy in order to prevent relapse. [78],[147] Co-trimoxazole (TMP/SMX) 8 mg / 40 mg/kg/day can be used for children < 6 years of age. Rifampicin with or without a combination of cotrimoxazole has proved safe to treat brucellosis during pregnancy. [83],[152] Relapses occur at a rate of about 10% and are often milder in severity than the initial disease and can be treated with a repeated course of the usual antibiotic regimens. [83] Most complications of brucellosis can be adequately treated with standard regimens. Treatment of some complications like spondylitis, osteomyelitis, neurobrucellosis and endocarditis also require combination therapy but longer courses. For neurobrucellosis, combination therapy with two or three drugs - that is doxycycline, rifampicin and trimethoprim-sulfamethoxazole that penetrate CNS and are active against the infecting isolate is recommended. [141] The combination of doxycycline with rifampicin and trimethoprim-sulfamethoxazole has been used successfully in the treatment of brucellar endocarditis. [141] Although cases of endocarditis caused by Brucellae have been cured with antimicrobial chemotherapy alone, [63],[78],[153],[154] it is generally believed that surgical intervention (valve replacement) combined with antibiotic therapy is the best approach. [16]

Prevention of human brucellosis is dependent on control of the disease in domestic livestock mainly by mass vaccination. [155] In many countries, the use of B. abortus strain vaccine in cattle and B. melitensis strain Rev-1 vaccine in goats and sheep has resulted in the elimination or near-elimination of brucellosis in these animals. Studies are ongoing to develop an effective vaccine against B. suis . Since the treatment of animal brucellosis is very expensive, one should encourage the mass vaccination of livestock. Animal owners should be taught about the importance of vaccination of their animals. In spite of the clinical efficacy and cost effectiveness of vaccination, the limited availability of vaccines and lack of awareness has led to the persistence of brucellosis in most areas including India. The lack of human vaccines and effective control measures make it necessary for the doctors and other health care workers to take protective measures. Protective clothing / barriers while handling still births / products of conception and cultures can reduce occupation-related brucellosis. [16],[93] The avoidance of unpasteurised dairy products will prevent infection in the general population. [156]

 ~ Acknowledgements Top

We are grateful to Dr. S. S. Tallur, Professor and Head, Department of Microbiology, S. Nijalingappa Medical college, Bagalkot for the inspiration for this work and thank Journal of Tropical Paediatrics and Journal of Medical Microbiology for allowing us to use the tables and figure published in the articles of the journals.

 ~ References Top

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Indian Journal of Medical Research. 2012; 136(4): 680
33 Serological trail of Brucella infection in an urban slum population in Brazil
Angel, M.O. and Ristow, P. and Ko, A.I. and Di-Lorenzo, C.
Journal of Infection in Developing Countries. 2012; 6(9): 675-679
34 Genotypic variation in the Brucella melitensis hemagglutinin gene in vaccine strains and field isolates in palestine
Awwad, E. and Farraj, M.A. and Adwan, K. and Essawi, T.A.
Turkish Journal of Veterinary and Animal Sciences. 2012; 36(4): 395-399
35 Chaperone-dependent mechanisms for acid resistance in enteric bacteria
Hong, W. and Wu, Y.E. and Fu, X. and Chang, Z.
Trends in Microbiology. 2012; 20(7): 328-335
36 Pedro ponsæ sign in forensic anthropology [Signo de pedro pons en antropología forense]
Armentano, N. and Nociarová, D. and Subirana, M.
Cuadernos de Medicina Forense. 2012; 18(3-4): 135-138
37 Brucellosis induced ascites, cholestasis and elevated serum CA 125 level: Case report [Brusellaya baǧli{dotless
Kaya, M. and Beştaş, R. and Cangül, M.S. and Kaya, B.
Turkiye Klinikleri Journal of Medical Sciences. 2012; 32(4): 1187-1190
38 Sero-prevalence of brucellosis in Egypt with emphasis on potential risk factors
Hassanain, N.A. and Ahmed, W.M.
World Journal of Medical Sciences. 2012; 7(2): 81-86
39 In vitro activities of antimicrobials against Brucella abortus isolates from cattle in Korea during 1998-2006
Heo, E.-J. and Kang, S.-I. and Kim, J.-W. and Her, M. and Cho, D. and Cho, Y.-S. and Hwang, I.-Y. and Moon, J.-S. and Wee, S.-H. and Jung, S.-C. and Nam, H.-M.
Journal of Microbiology and Biotechnology. 2012; 22(4): 567-570
40 Pulmonary involvement in brucellosis
Uluǧ, M. and Can-Uluǧ, N.
Canadian Journal of Infectious Diseases and Medical Microbiology. 2012; 23(1): e13-e15
41 Detection and segregation of Brucella abortus and Brucella melitensis in aborted bovine, ovine, caprine, buffaloes and camelid fetuses by application of conventional and real-time polymerase chain reaction
Dehkordi, F.S. and Saberian, S. and Momtaz, H.
Thai Journal of Veterinary Medicine. 2012; 42(1): 13-20
42 Dementia, peripheral neuropathy, and chronic meningitis in Neurobrucellosis
Nalini, A. and Nagarathna, S. and Rajeshwari, S. and Rose, D. and Veena Kumari, H.B. and Nagalingam, M.
Indian Journal of Pathology and Microbiology. 2012; 55(1): 128-130
43 Application of polymerase chain reaction to detect Burkholderia pseudomallei and Brucella species in buffy coat from patients with febrile illness among rural and peri-urban population
Nandagopal, B. and Sankar, S. and Lingesan, K. and Appu, K.C. and Sridharan, G. and Gopinathan, A.
Journal of Global Infectious Diseases. 2012; 4(1): 31-37
44 The efficacy of multipex PCR in comparioson with agglutination and ELISA in human Brucellosis diagnostic
Lari, R.A. and Fallah, F. and Karimi, A. and Gachkar, L. and Angoti, G. and Sanaei, A. and Azimi, L.
Iranian Journal of Clinical Infectious Diseases. 2011; 6(3 SUPPL.): 143-146
45 Isolation, cloning and expression of the Brucella melitensis Omp31 gene
Vahedi, F. and Talebi, A.F. and Ghorbani, E. and Behroozikhah, A.M. and Shahriari Ahmadi, F. and Mahmoudi, M.
Iranian Journal of Veterinary Research. 2011; 12(2): 156-162
46 Isolation and identification of Brucella species from blood samples of the patients with brucellosis by biochemical, PCR and serological methods in Kurdistan province
Rahmani, M.R. and Motaharinia, Y. and Rezaie, M.A. and Asadzadeh, N. and Hoseini, V. and Pour, B.M. and Bahmani, N. and Hakhamaneshi, M.S. and Rashidi, K.
Scientific Journal of Kurdistan University of Medical Sciences. 2011; 16(3)
47 Molecular detection of brucella spp. DNA in patients with manifestations compatible with emotional disorders
Kechagia, M. and Mitka, S. and Papadogiannakis, E. and Kontos, V. and Koutis, C.
Open Infectious Diseases Journal. 2011; 5(1): 8-12
48 Systems biology approach predicts antibody signature associated with Brucella melitensis infection in humans
Liang, L. and Tan, X. and Juarez, S. and Villaverde, H. and Pablo, J. and Nakajima-Sasaki, R. and Gotuzzo, E. and Saito, M. and Hermanson, G. and Molina, D. and Felgner, S. and Morrow, W.J.W. and Liang, X. and Gilman, R.H. and Davies, D.H. and Tsolis, R.M. and Vinetz, J.M. and Felgner, P.L.
Journal of Proteome Research. 2011; 10(10): 4813-4824
49 Erythrocyte sedimentation rate, serum amyloid A and C-reactive protein levels in patients with acute brucellosis
Kenan Celik, V. and Sari, I. and Bakir, S. and Engin, A. and Bakir, D. and Sari, M. and Poyraz, O. and Yildiz, G.
Pakistan Journal of Medical Sciences. 2011; 27(4): 823-826
50 A review of the english and Russian language literature on the osteoarticular manifestations of brucellosis infection
Akhvlediani, T. and Ellis, M.W. and Rivard, R. and Zenaishvili, O. and Battafarano, D.J. and Hepburn, M.J.
Current Rheumatology Reviews. 2011; 7(3): 263-271
51 Direct detection of the brucellosis-causing pathogen - A case report [Přímý průkaz původce maltské horečky - Kazuistika]
Bardoň, J. and Kohnová, I. and Prokeš, Z. and Skalka, P. and Bzdil, J.
Klinicka Mikrobiologie a Infekcni Lekarstvi. 2011; 17(2): 50-54
52 Isolation, identification and molecular characterization of Brucella strains isolated from small ruminants in the West Bank, Palestine
Awwad, E. and Farraj, M.A. and Adwan, K. and Essawi, T.A.
Revue de Medecine Veterinaire. 2011; 162(5): 236-239
53 Chronic meningitis: Differential diagnosis [Diagnostic des méningites chroniques]
de Broucker, T. and Martinez-Almoyna, L.
Revue de Medecine Interne. 2011; 32(3): 159-172
54 The first prevalence report of direct identification and differentiation of B. abortus and B. melitensis using real time PCR in house mouse of Iran
Doosti, A. and Moshkelani, S.
World Academy of Science, Engineering and Technology. 2011; 74: 84-87
55 Pedro Ponsæ sign as a Brucellosis complication
Tuna, N. and Ogutlu, A. and Gozdas, H.T. and Karabay, O.
Indian Journal of Pathology and Microbiology. 2011; 54(1): 183-184
56 One health national programme across species on zoonoses: a call to the developing world
G. V. Asokan, Vanitha Asokan, Prathap Tharyan
Infection Ecology & Epidemiology. 2011; 1(0)
[VIEW] | [DOI]
57 Comparison of conventional and non-conventional techniques for the diagnosis of bovine brucellosis in Sudan
Amel Abdalla, Mohamed E. Hamid
Tropical Animal Health and Production. 2011;
[VIEW] | [DOI]
58 Direct detection of the brucellosis-causing pathogen - A case report | [Přímý průkaz původce maltské horečky - Kazuistika]
Bardoň, J., Kohnová, I., Prokeš, Z., Skalka, P., Bzdil, J.
Klinicka Mikrobiologie a Infekcni Lekarstvi. 2011; 17(2): 50-54
59 Chronic meningitis: Differential diagnosis | [Diagnostic des méningites chroniques]
de Broucker, T., Martinez-Almoyna, L.
Revue de Medecine Interne. 2011; 32(3): 159-172
60 Experimental infection of rabbits (Cuniculus orictolagus) with Brucella suis biovar 1 isolated from wild hares (Lepus europaeus)
Marcelo Fort, Valeria Baldone, Lumila Fuchs, Hugo Giménez, María Rojas, Javier D. Breccia, Jorge Oyhenart
Veterinary Microbiology. 2011;
[VIEW] | [DOI]
61 Experimental infection of rabbits (Oryctolagus cuniculus) with Brucella suis biovar 1 isolated from wild hares (Lepus europaeus)
Marcelo Fort, Valeria Baldone, Lumila Fuchs, Hugo Giménez, María Rojas, Javier D. Breccia, Jorge Oyhenart
Veterinary Microbiology. 2011;
[VIEW] | [DOI]
62 Brucellosis: a rare cause of febrile neutropenia in acute myeloblastic leukemia
Demircan Ozbalci, Ulku Ergene, Cigdem Banu Cetin
Medical Oncology. 2011; 28(1): 255
[VIEW] | [DOI]
63 Diagnostic des méningites chroniques
T. de Broucker,L. Martinez-Almoyna
La Revue de Médecine Interne. 2011; 32(3): 159
[Pubmed] | [DOI]
64 Systems Biology Approach Predicts Antibody Signature Associated with <i>Brucella melitensis</i> Infection in Humans
Journal of Proteome Research. 2011; 10(10): 4813
[VIEW] | [DOI]
65 Brucellosis presenting as septal panniculitis with vasculitis : Brucellosis presenting as septal panniculitis with vasculitis
Mohammed Al Jasser, Waleed Al Ajroush
International Journal of Dermatology. 2011; : no
[VIEW] | [DOI]
66 Acute Postinfectious Glomerulonephritis with Native Aorta Valve Endocarditis and Myopericarditis Due to Brucellosis
Ismail Kocyigit, Ahmet Celik, Bülent Tokgoz, Ibrahim Ozdogru, Hulya Akgun, Mehmet Doganay, Oktay Oymak, Cengiz Utas
Renal Failure. 2011; 33(3): 367
[VIEW] | [DOI]
67 Brucellosis: A re-emerging zoonosis
Mohamed N. Seleem,Stephen M. Boyle,Nammalwar Sriranganathan
Veterinary Microbiology. 2010; 140(3-4): 392
[Pubmed] | [DOI]
68 Coexistence of pancreatic tuberculosis with systemic brucellosis: a case report
İlker Sücüllü, Orhan Baylan, Ali İlker Filiz, Hüsrev Diktaş, Mert Kıvanc, Oral Öncül, Levent Görenek, Ali Acar
Central European Journal of Medicine. 2010; 5(5): 573
[VIEW] | [DOI]
69 Brucellosis serology in HIV-infected patients
Alireza Abdollahi, Afsaneh Morteza, Omid Khalilzadeh, Mehrnaz Rasoulinejad
International Journal of Infectious Diseases. 2010; 14(10): e904
[VIEW] | [DOI]
70 Acute brucellosis complicated by fatal myocarditis
Vinay Ramakrishna Pandit,Shubha Seshadri,Rohit Valsalan,Shibu Bahuleyan,K.E. Vandana,Prakash Kori
International Journal of Infectious Diseases. 2010; 14(4): e358
[Pubmed] | [DOI]
71 Bovine Brucellosis
Steven Olsen,Fred Tatum
Veterinary Clinics of North America: Food Animal Practice. 2010; 26(1): 15
[Pubmed] | [DOI]
72 Coexistence of pancreatic tuberculosis with systemic brucellosis: A case report
Acar, A., Sücüllü, I., Baylan, O., Filiz, A.I., Diktaş, H., KIvanc, M., Öncül, O., Görenek, L.
Central European Journal of Medicine. 2010; 5(5): 573-576
73 Novel antimicrobial peptides that exhibit activity against select agents and other drug resistant bacteria
Divakaramenon Venugopal, David Klapper, Antoine H. Srouji, Jayendra B. Bhonsle, Richard Borschel, Allen Mueller, Amanda L. Russell, Brittany C. Williams, Rickey P. Hicks
Bioorganic & Medicinal Chemistry. 2010; 18(14): 5137
[VIEW] | [DOI]
74 New aspects in the diagnosis and treatment of Brucella infection
Apostolou, F., Liberopoulos, E., Elisaf, M.
Archives of Hellenic Medicine. 2010; 27(1): 37-47
75 Brucellosis infection presenting with cholestasis
M.A. Fernández Fernández, M. García de Paso Mora, R. Mateos Checa, B. Croche, A. Porras Gonzalez, I. Obando Santaella
International Journal of Infectious Diseases. 2010; 14: e322
[VIEW] | [DOI]
76 Acute brucellosis complicated by fatal myocarditis
Pandit, V.R., Seshadri, S., Valsalan, R., Bahuleyan, S., Vandana, K.E., Kori, P.
International Journal of Infectious Diseases. 2010; 14(4): e358-e360
77 Does brucellosis in human pregnancy increase abortion risk? Presentation of two cases and review of literature
Karcaaltincaba, D., Sencan, I., Kandemir, O., Guvendag-Guven, E.S., Yalvac, S.
Journal of Obstetrics and Gynaecology Research. 2010; 36(2): 418-423
78 Update on laboratory diagnosis of human brucellosis
George F. Araj
International Journal of Antimicrobial Agents. 2010; 36: S12
[VIEW] | [DOI]
79 Ophthalmoparesis, papillitis and premacular hemorrhage in a case with endocarditis: A rare presentation of Brucellosis
Sahin, O.G., Pelit, A., Turunc, T., Akova, Y.
Indian Journal of Ophthalmology. 2010; 58(2): 164-166
80 Acute brucellosis complicated by fatal myocarditis
Pandit, V.R., Seshadri, S., Valsalan, R., Bahuleyan, S., Vandana, K.E., Kori, P.
International Journal of Infectious Diseases. 2010; 14(4): e358-e360
81 Bovine Brucellosis
Olsen, S., Tatum, F.
Veterinary Clinics of North America - Food Animal Practice. 2010; 26(1): 15-27
82 Brucellosis: A re-emerging zoonosis
Seleem, M.N., Boyle, S.M., Sriranganathan, N.
Veterinary Microbiology. 2010; 140((3-4)): 392-398
83 Update on laboratory diagnosis of human brucellosis
Araj, G.F.
International Journal of Antimicrobial Agents. 2010; 36(sup 1): s 12-s 17
84 Brucellosis serology in HIV-infected patients
Abdollahi, A., Morteza, A., Khalilzadeh, O., Rasoulinejad, M.
International Journal of Infectious Diseases. 2010; 14(10): e904-e906
85 Brucellosis infection presenting with cholestasis
Fernández, M.A.F., Mora, M.G.D.P., Checa, R.M., Croche, B., Gonzalez, A.P., Santaella, I.O.
International Journal of Infectious Diseases. 2010; 14(sup 3): e322-e324
86 Diagnostic challenges of human brucellosis in Hong Kong: A case series in two regional hospitals
Luk, S., To, W.K.
Hong Kong Medical Journal. 2010; 16(4): 299-303
87 Brucellosis - Regionally emerging zoonotic disease?
Gwida, M., Al Dahouk, S., Melzer, F., Rösler, U., Neubauer, H., Tomaso, H.
Croatian Medical Journal. 2010; 51(4): 289-295
88 Human brucellosis in Macedonia - 10 years of clinical experience in endemic region
Bosilkovski, M., Krteva, L., Dimzova, M., Vidinic, I., Sopova, Z., Spasovska, K.
Croatian Medical Journal. 2010; 51(4): 327-336
89 Brucella endocarditis, a report of 14 cases (1991-2009)
Keshtkar-Jahromi, M., Boroumand, M., Razavi, S.-M., Gholamin, S., Haghighat, B., Hashemi, M.-J., Khani, M., (...), Naghili, B.
Journal of Infection. 2010; 61(1): 89-92
90 Novel antimicrobial peptides that exhibit activity against select agents and other drug resistant bacteria
Venugopal, D., Klapper, D., Srouji, A.H., Bhonsle, J.B., Borschel, R., Mueller, A., Russell, A.L., (...), Hicks, R.P.
Bioorganic and Medicinal Chemistry. 2010; 18(14): 5137-5147
91 Brucellosis in children: Report of 6 cases and literature review
Ji, L.-L., Wang, W., Hu, M.-Y.
Chinese Journal of Contemporary Pediatrics. 2010; 12(6): 494-495
92 Brucellosis-regionally emerging zoonotic disease?
Gwida, M., Dahouk, S.A., Melzer, F., Rösler, U., Neubauer, H., Tomaso, H.
Croatian Medical Journal. 2010; 51(3): 289-295
93 Human brucellosis in Macedonia-10 years of clinical experience in endemic region
Bosilkovski, M., Krteva, L., Dimzova, M., Vidinic, I., Sopova, Z., Spasovska, K.
Croatian Medical Journal. 2010; 51(3): 327-336
94 Ophthalmoparesis, papillitis and premacular hemorrhage in a case with endocarditis: A rare presentation of Brucellosis
Sahin, O.G., Pelit, A., Turunc, T., Akova, Y.
Indian Journal of Ophthalmology. 2010; 58(2): 164-166
95 Bovine Brucellosis
Olsen, S., Tatum, F.
Veterinary Clinics of North America - Food Animal Practice. 2010; 26(1): 15-27
96 Does brucellosis in human pregnancy increase abortion risk? Presentation of two cases and review of literature
Deniz Karcaaltincaba, Irfan Sencan, Omer Kandemir, Emine Seda Guvendag-Guven, Serdar Yalvac
Journal of Obstetrics and Gynaecology Research. 2010; 36(2): 418-423
[Pubmed] | [DOI]
97 Brucella endocarditis, a report of 14 cases (1991–2009)
Maryam Keshtkar-Jahromi, Mohammadali Boroumand, Seyed-Mostafa Razavi, Sharareh Gholamin, Babak Haghighat, Mohammad-Jafar Hashemi, Mohammad Khani, Marzieh Keshtkar-Jahromi, Behrooz Naghili
Journal of Infection. 2010; 61(1): 89
[VIEW] | [DOI]
98 Diagnostic challenges of human brucellosis in Hong Kong: A case series in two regional hospitals
Luk, S. and To, W.K.
Hong Kong Medical Journal. 2010; 16(4): 299-303
99 Brucellosis - Regionally emerging zoonotic disease?
Gwida, M. and Al Dahouk, S. and Melzer, F. and Rösler, U. and Neubauer, H. and Tomaso, H.
Croatian Medical Journal. 2010; 51(4): 289-295
100 Brucella endocarditis, a report of 14 cases (1991-2009)
Keshtkar-Jahromi, M. and Boroumand, M. and Razavi, S.-M. and Gholamin, S. and Haghighat, B. and Hashemi, M.-J. and Khani, M. and Keshtkar-Jahromi, M. and Naghili, B.
Journal of Infection. 2010; 61(1): 89-92
101 Brucellosis in children: Report of 6 cases and literature review
Ji, L.-L. and Wang, W. and Hu, M.-Y.
Chinese Journal of Contemporary Pediatrics. 2010; 12(6): 494-495
102 Human brucellosis in Macedonia-10 years of clinical experience in endemic region
Bosilkovski, M. and Krteva, L. and Dimzova, M. and Vidinic, I. and Sopova, Z. and Spasovska, K.
Croatian Medical Journal. 2010; 51(3): 327-336
103 Brucellosis-regionally emerging zoonotic disease?
Gwida, M. and Dahouk, S.A. and Melzer, F. and Rösler, U. and Neubauer, H. and Tomaso, H.
Croatian Medical Journal. 2010; 51(3): 289-295
104 Peritoneal dialysis-related peritonitis caused by Brucella melitensis
Unal, A. and Sipahioglu, M.H. and Kavuncuoglu, F. and Tokgoz, B. and Oymak, O. and Sumerkan, B. and Utas, C.
Dialysis and Transplantation. 2009; 38(12): 515-516
105 A rare manifestation of brucellosis: Cervical lymphadenitis
Özhan, B. and Kamit, F. and Akduman, I. and Ay, Y. and Helvaci, M.
Cocuk Enfeksiyon Dergisi. 2009; 3(4): 190-191
106 Serological findings in chronic and recurrent brucellosis
Poulopoulou, Ch. and Lazaridou, A. and Sotiropoulou, H. and Zarkotou, O. and Gianneli, D. and Themeli-Digalaki, K.
Acta Microbiologica Hellenica. 2009; 54(6): 369-374
107 Brucella: An elusive microbe
Vassalos, C.M. and Vrioni, G.
Acta Microbiologica Hellenica. 2009; 54(6): 361-368
108 Epidemiological, clinical, diagnostic and treatment aspects of hospitalized Brucellosis patients in Hamadan
Hajia, M. and Rahbar, M. and Keramat, F.
Annals of Tropical Medicine and Public Health. 2009; 2(2): 42-45
109 Seroprevalence and risk factors of brucellosis among slaughterhouse workers in Korea
Yoo, S.-J. and Choi, Y.-S. and Lim, H.-S. and Lee, K. and Mi, Y.P. and Chu, C. and Kang, Y.-A.
Journal of Preventive Medicine and Public Health. 2009; 42(4): 237-242
110 Peritoneal dialysis-related peritonitis caused by Brucella melitensis
Aydin Unal, Murat Hayri Sipahioglu, Feridun Kavuncuoglu, Bulent Tokgoz, Oktay Oymak, Bulent Sumerkan, Cengiz Utas
Dialysis & Transplantation. 2009; 38(12): 515-516
[Pubmed] | [DOI]
111 Epidemiological, clinical, diagnostic and treatment aspects of hospitalized Brucellosis patients in Hamadan
Hajia, M., Rahbar, M., Keramat, F.
Annals of Tropical Medicine and Public Health. 2009; 2(2): 42-45
112 Evaluation of Brucella indirect enzyme linked immunosorbent assay in comparison with conventional serological tests in pyrexia of unknown origin cases
Agasthya, A.S., Isloor, S., Prabhudas, K.
Asian Journal of Microbiology, Biotechnology and Environmental Sciences. 2009; 11(3): 671-675
113 Brucellosis in humans: Why is it so elusive?
Vassalos, C.M., Economou, V., Vassalou, E., Papadopoulou, C.
Reviews in Medical Microbiology. 2009; 20(4): 63-73
114 Post vaccination follow-up of Brucella melitensis in blood stream of sheep by PCR assay
Kojouri, G.A., Gholami, M.
Comparative Clinical Pathology. 2009; 18(4): 439-442
115 Presumptive diagnosis of brucella epididymoorchitis by modified cold ZN staining of testicular pus sample
Kulkarni, R.D., Chunchanur, S.K., Ajantha, G.S., Shubhada, C., Jain, P.
Indian Journal of Medical Research. 2009; 130(4): 484-486
116 Status and strategies for control of brucellosis - A review
Boral, R., Singh, M., Singh, D.K.
Indian Journal of Animal Sciences. 2009; 79(12): 1191-1199
117 Brucellosis in humans: why is it so elusive? :
Constantine M Vassalos, Vangelis Economou, Evdokia Vassalou, Chryssanthy Papadopoulou
Reviews in Medical Microbiology. 2009; 20(4): 63
[VIEW] | [DOI]
118 A Rare Complication of Brucella Infection: Myocarditis and Heart Failure
Cumali Efe, Tuba Can, Münevver Ince, Hasan Tunca, Fatih Yildiz, Engin Sennaroglu
Internal Medicine. 2009; 48(19): 1773-1774
[Pubmed] | [DOI]
119 A case of Brucella endocarditis in association with superficial femoral artery thrombus
A case of Brucella endocarditis in association with superficial femoral artery thrombus
Tropical Doctor. 2009; 39(4): 251-252
120 Establishment of systemic Brucella melitensis infection through the digestive tract requires urease, the type IV secretion system, and lipopolysaccharide O antigen
Paixão, T.A., Roux, C.M., Den Hartigh, A.B., Sankaran-Walters, S., Dandekar, S., Santos, R.L., Tsolis, R.M.
Infection and Immunity. 2009; 77(10): 4197-4208
121 Seroprevalence of Brucella agglutinins: A pilot study
Nagarathna, S., Sharmada, S., Veena Kumari, H.B., Arvind, N., Sundar, P., Sangeetha, S.
Indian Journal of Pathology and Microbiology. 2009; 52(3): 457-458
122 Seroprevalence and Risk Factors of Brucellosis among Slaughterhouse Workers in Korea
Seok-Ju Yoo,Young-Sill Choi,Hyun-Sul Lim,Kwan Lee,Mi Yeoun Park,Chaeshin Chu,Young-A Kang
Journal of Preventive Medicine and Public Health. 2009; 42(4): 237
[Pubmed] | [DOI]
123 Epididymo-orchitis due to brucellosis: Not only to be considered in endemic areas
Moens, A.A., Vlaspolder, F., Verlind, J., Sepers, J.M., Stam, F.
Urologia Internationalis. 2009; 82(4): 481-483
124 Comparison of a flow assay for brucellosis antibodies with the reference cELISA test in West African Bos indicus
de C. Bronsvoort, B.M., Koterwas, B., Land, F., Handel, I.G., Tucker, J., Morgan, K.L., Tanya, V.N., (...), Smits, H.L.
PLoS ONE. 2009; 4(4): e5221
125 Serodiagnosis of brucellosis in cattle and humans in Egypt
Samaha, H., Mohamed, T.R., Khoudair, R.M., Ashour, H.M.
Immunobiology. 2009; 214(3): 223-226
126 Cytokine response and clinicopathological findings in Brucella infected camels (Camelus dromedarius)
El-Boshy, M., Abbas, H., El-Khodery, S., Osman, S.
Veterinarni Medicina. 2009; 54(1): 25-32
127 The Relationship between Cerebrovascular Mortality and Community Health Indicators in Gangwon-do
Jeoung-Ha Sim,Mi-A Son
Journal of agricultural medicine and community health. 2009; 34(1): 1
[Pubmed] | [DOI]
128 Awareness of Zoonoses among Cattle Slaughterhouse Workers in Korea
Hyun-Sul Lim,Seok-Ju Yoo,Kwan Lee
Journal of agricultural medicine and community health. 2009; 34(1): 101
[Pubmed] | [DOI]
129 Post vaccination follow-up of Brucella melitensis in blood stream of sheep by PCR assay
Gholam Ali Kojouri,Masood Gholami
Comparative Clinical Pathology. 2009; 18(4): 439
[Pubmed] | [DOI]
130 Emerging and re-emerging bacterial diseases in India
T. D. Chugh
Journal of Biosciences. 2008; 33(4): 549
[Pubmed] | [DOI]
131 Brucella sacroiliitis and osteomyelitis of the humeral bone in an adolescent | [Sacro-iléite et ostéo-myélite de læhumérus dues à Brucella melitensis chez une adolescente]
Mamalis, I.P., Panagopoulos, M.I., Papanastasiou, D.A., Bricteux, G.
Revue Medicale de Liege. 2008; 63(12): 742-745
132 Detection of Brucella by peripheral blood PCR and comparison with culture and serological methods in suspected cases
Kazemi, B., Yousefi Namin, S.A., Dowlatshahi, M., Bandepour, M., Kafilzadeh, F., Gachkar, L., Mahmoudinejad, F., (...), Mardani, M.
Iranian Journal of Public Health. 2008; 37(4): 96-102
133 Emerging and re-emerging bacterial diseases in India
Chugh, T.D.
Journal of Biosciences. 2008; 33(4): 549-555
134 Brucellosis in India - A review
Mantur, B.G., Amarnath, S.K.
Journal of Biosciences. 2008; 33(4): 539-547
135 Neurobrucellosis with thalamic infarction: A case report
Jochum, T., Kliesch, U., Both, R., Leonhardi, J., Bär, K.-J.
Neurological Sciences. 2008; 29(6): 481-483
136 Abnormal liver function in brucellosis | [Alterazioni della funzione epatica in corso di brucellosi]
La Spada, E., Micalizzi, A., La Spada, M., Quartararo, P., Nugara, G., Soresi, M., Affronti, M., Montalto, G.
Infezioni in Medicina. 2008; 16(3): 148-153
137 Case 2: Painful red plagues in a 6-year-old child (Case Presentation)
Tsalkidis, A., Gardikis, S., Cassimos, D., Kambouri, K., Vaos, G., Chatzimichael, A.
Acta Paediatrica, International Journal of Paediatrics. 2008; 97(5): 525-526-685-686
138 Neurobrucellosis with thalamic infarction: a case report
Thomas Jochum,Uta Kliesch,Reinhard Both,Jochen Leonhardi,Karl-Jürgen Bär
Neurological Sciences. 2008; 29(6): 481
[Pubmed] | [DOI]
139 Case 2: Painful red plagues in a 6-year-old child (Discussion and Diagnosis)
A Tsalkidis,S Gardikis,D Cassimos,K Kambouri,G Vaos,A Chatzimichael
Acta Paediatrica. 2008; 97(5): 685
[Pubmed] | [DOI]
140 Brucellosis in India — a review
Basappa G. Mantur,Satish K. Amarnath
Journal of Biosciences. 2008; 33(4): 539
[Pubmed] | [DOI]
141 Brucella sacroiliitis and osteomyelitis of the humeral bone in an adolescent [Sacro-iléite et ostéo-myélite de læhumérus dues à Brucella melitensis chez une adolescente]
Mamalis, I.P. and Panagopoulos, M.I. and Papanastasiou, D.A. and Bricteux, G.
Revue Medicale de Liege. 2008; 63(12): 742-745
142 Abnormal liver function in brucellosis [Alterazioni della funzione epatica in corso di brucellosi]
La Spada, E. and Micalizzi, A. and La Spada, M. and Quartararo, P. and Nugara, G. and Soresi, M. and Affronti, M. and Montalto, G.
Infezioni in Medicina. 2008; 16(3): 148-153


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