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GUEST EDITORIAL
Year : 2007  |  Volume : 25  |  Issue : 1  |  Page : 2-3
 

Genetic diversity of pathogenic microorganisms and its medical and public health significance


1 Department of Microbiology, University of Delhi South Campus, Benito Juarez Road, New Delhi - 110 021, India
2 Division of Epidemiology and Biostatistics, McGill University, Montreal, Canada

Date of Submission15-Nov-2006
Date of Acceptance09-Dec-2006

Correspondence Address:
J S Virdi
Department of Microbiology, University of Delhi South Campus, Benito Juarez Road, New Delhi - 110 021
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0255-0857.31052

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How to cite this article:
Virdi J S, Gulati P, Pai M. Genetic diversity of pathogenic microorganisms and its medical and public health significance. Indian J Med Microbiol 2007;25:2-3

How to cite this URL:
Virdi J S, Gulati P, Pai M. Genetic diversity of pathogenic microorganisms and its medical and public health significance. Indian J Med Microbiol [serial online] 2007 [cited 2019 Jun 15];25:2-3. Available from: http://www.ijmm.org/text.asp?2007/25/1/2/31052


In the last decade or so, significant amounts of data have been generated on genetic diversity of a number of pathogens. This has been accomplished largely due to the development of genotyping techniques such as multilocus enzyme electrophoresis, restriction fragment length polymorphism, random amplified polymorphic DNA, pulse field gel electrophoresis, repetitive sequence-based polymerase chain reaction, multilocus sequence typing and DNA sequencing. Why is the study of genetic diversity important and what can it contribute to medicine and public health? Several observations of both fundamental and applied nature have been gleaned from studies on diversity. Thanks to these studies, we now understand that although pathogenic microbes constitute a small proportion of all microbial species, many are characterized by high genetic diversity. For example organisms such as the HIV and influenza virus mutate extensively and pose major challenges to disease control. Further, such studies have dispelled the notion of clonal nature of pathogens. We now realize that population structures of pathogenic microbes range from effectively panmictic to strictly clonal.[1] Therefore, a better understanding of genetic diversity of pathogenic microorganisms may allow us to devise public health interventions that may be more effective.[2]

The field of molecular epidemiology has greatly capitalized on the knowledge gained from genetic diversity of pathogens. The core of molecular epidemiology is genotyping of strains. This has been particularly useful in studying global epidemiology of pathogens and their transmission dynamics. The long-term spread of the pathogens over large geographical areas encompassing continents have been tracked because we have databases of their genetic fingerprints. Genetic diversity studies have been useful in identifying the sources of outbreaks. Such studies have also helped resolve unequivocally whether the recurrence of an infectious disease is due to relapse caused by the same strain or re-infection of the host by a new strain.

In addition to molecular epidemiology, a major application of genetic diversity data has been the development of diagnostics, therapeutics and vaccines. Poorly understood diversity of a pathogen can lead to development of diagnostics that cannot detect the entire set of pathogen genotypes causing a particular disease. For example, the discovery of highly divergent strains of human immunodeficiency virus (HIV) that were not reliably detected by a number of commonly used diagnostic kits emphasized the need for studies to type HIV variants. Another example is the development of new tests for the detection of tuberculosis infection. Comparative genomics has allowed the identification of genomic segments (e.g., region of difference (RD1)) that are present in Mycobacterium tuberculosis but deleted from Mycobacterium bovis BCG sub-strains. Antigens encoded by such regions (e.g., ESAT-6) are currently being used in novel, blood-based interferon-gamma assays and these assays have been shown to be more specific than the tuberculin skin test.[3] Also, to develop more effective therapeutics and vaccines, it is imperative that the candidate drugs/vaccines are evaluated against a set of carefully selected genotypes, which are representative of the pathogen population.[4] Vaccine development for influenza is a classic illustration.

In addition to the medical and public health implications, the long-term benefits which may accrue from the study of pathogen diversity include understanding of the evolution and emergence of new pathogens, pathogenicity per se and phylogenetics.[5] As the oldest inhabitants of the earth, microbes have a highly chequered history of evolution. Comparative genomics of pathogens associated with human, animal and plant hosts may reveal insights into how pathogens evolved. Our recent understanding of the emergence of human pathogens like  Yersinia More Details pestis from Y. pseudotuberculosis has been possible only with the study of large number of genetic variants of these pathogens.[6]

However, genetic diversity studies have been constrained by certain problems. Among these, problems associated with adequate sample selection are paramount. An appropriate sample of the pathogen population is a prerequisite for genetic diversity studies. Presently most studies rely on isolates of a pathogen obtained from culture collection (e.g., referral) centers. Such centers, however, may not represent actual diversity extant in nature, as majority of the strains in such collections are obtained from clinical settings and thus, biased towards the highly pathogenic strains with the exclusion of the opportunistic and accidental pathogenic forms. This problem must be overcome by undertaking structured sampling schemes.[7]

Another concern is the lack of foolproof genotyping methods that are highly accurate in distinguishing between strains. The development of the multilocus sequence typing (MLST) method in recent years has raised hopes in this regard.[8] The sequence data obtained using MLST is reproducible and highly portable among laboratories, allowing development of global databases easily available on the internet so that global comparisons can be made. Lack of a good framework for interpretation of genetic diversity data is another stumbling block in our understanding of pathogen diversity. There is a need for standardized, international guidelines on the interpretation of genetic and molecular diversity data. Lastly, the ability of the host immune system to select certain genotypes also impacts significantly on the genetic diversity of pathogens.

How has India contributed to the study of genetic diversity? In the past decade, genetic diversity studies on selected pathogens have been reported from India. These include Vibrio cholerae , M. tuberculosis, Helicobacter pylori ,  Yersinia enterocolitica More Details , Leptospira and viruses such as rotaviruses, poliovirus and hepatitis. Genetic diversity data pertaining to these pathogens and others isolated from India has been reviewed recently.[9] However, not much data are available on other important pathogens such as HIV,  Neisseria More Details meningitidis , Streptococcus pneumoniae, S. pyogenes and a host of enteropathogenic  Escherichia More Details coli . Similarly, genetic diversity data on parasitic protozoa and fungal pathogens are lacking. Thus, this area needs further impetus, as developing countries including India are a source of rich, hitherto untapped, microbial diversity. Research in this field requires not only adequate funding and training opportunities but also collaborations with international organizations and experts. Overall, in this exciting era of genomics, the study of genetic diversity of pathogens has the potential to contribute greatly in our fight against the disease causing microbes.


 ~ Acknowledgement Top


Supported in part by funding from the Department of Biotechnology (DBT), Department of Science and Technology (DST), Ministry of Environment and Forests (MEF), Defense Research and Development Organisation (DRDO) and the Indian Council of Medical Research (ICMR).

 
 ~ References Top

1.Spratt BG, Maiden MC. Bacterial population genetics, evolution and epidemiology. Phil Trans R Soc London B Biol Sci 1999; 354 :701-10.  Back to cited text no. 1    
2.Read AF, Taylor LH. The ecology of genetically diverse infections. Science 2001; 292 :1099-102.  Back to cited text no. 2  [PUBMED]  [FULLTEXT]
3.Pai M. Alternatives to the tuberculin skin test: Interferon-g assays in the diagnosis of Mycobacterium tuberculosis infection. Indian J Med Microbiol 2005; 23 :151-8.  Back to cited text no. 3  [PUBMED]  [FULLTEXT]
4.Dykhuizen DE, Polin DS, Dunn JJ, Wilske B, Preac-Mursic V, Dattwyler RJ, et al . Borrelia burgdorferi is clonal: Implications for taxonomy and vaccine development. Proc Natl Acad Sci USA 1993; 90 :10163-7.  Back to cited text no. 4  [PUBMED]  [FULLTEXT]
5.Dobrindt U, Hacker J. Whole genome plasticity in pathogenic bacteria. Curr Opin Microbiol 2001; 4 :550-7.  Back to cited text no. 5  [PUBMED]  [FULLTEXT]
6.Achtman M, Zurth K, Morelli G, Torrea G, Guiyoule A, Carniel E. Yersinia pestis , the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis . Proc Natl Acad Sci USA 1999; 96 :14043-8.  Back to cited text no. 6  [PUBMED]  [FULLTEXT]
7.Gupta S, Maiden MC. Exploring the evolution of diversity in pathogen populations. Trends Microbiol 2001; 9 :181-5.  Back to cited text no. 7  [PUBMED]  [FULLTEXT]
8.Maiden MC, Bygraves JA, Feil E, Morelli G, Russell JE, Urwin R, et al . Multilocus sequence typing: A portable approach to the identification of clones within populations of pathogenic microorganisms. Proc Natl Acad Sci USA 1998; 95 :3140-5.  Back to cited text no. 8  [PUBMED]  [FULLTEXT]
9.Virdi JS, Sachdeva P. Genetic diversity of pathogenic microorganisms - Basic insights, public health implications and the Indian initiatives. Curr Sci 2005; 89 :113-23.  Back to cited text no. 9    




 

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