|Year : 2005 | Volume
| Issue : 2 | Page : 111-113
Evaluation of Biphasic Culture System for Mycobacterial Isolation from the Sputum of Patients with Pulmonary Tuberculosis
M Ghatole, C Sable, P Kamale, S Kandle, V Jahagirdar, V Yemul
Department of Microbiology, Dr. V. M. Medical College, Solapur, India
Department of Microbiology, Dr. V. M. Medical College, Solapur - 413 002, Maharashtra
Source of Support: None, Conflict of Interest: None
Mycobacterial diseases continue to cause high morbidity and mortality. Isolation, identification and sensitivity testing form the backbone of laboratory investigations. M. tuberculosis isolation needs 6-8 weeks on conventional egg containing media. For rapid isolation various methods have been evaluated. We evaluated biphasic system (Middlebrook 7H11 agar slant + Middlebrook 9H broth) in comparison with Lowenstein - Jensen (LJ) medium. In smear positive cases biphasic system showed the recovery rate of 97.05% as against 79.41% on LJ on incubation for 21± 4.44 and 28±3.76 days respectively. In smear negative and culture positive cases biphasic system and LJ showed isolation rates of 91.66% and 66.6% after 36±3.44 and 41± 4.09 days respectively. Biphasic system showed lower contamination rate (1.33%). Biphasic medium is superior to LJ medium in isolation of M. tuberculosis .
Keywords: M. tuberculosis , biphasic system, culture
|How to cite this article:|
Ghatole M, Sable C, Kamale P, Kandle S, Jahagirdar V, Yemul V. Evaluation of Biphasic Culture System for Mycobacterial Isolation from the Sputum of Patients with Pulmonary Tuberculosis. Indian J Med Microbiol 2005;23:111-3
|How to cite this URL:|
Ghatole M, Sable C, Kamale P, Kandle S, Jahagirdar V, Yemul V. Evaluation of Biphasic Culture System for Mycobacterial Isolation from the Sputum of Patients with Pulmonary Tuberculosis. Indian J Med Microbiol [serial online] 2005 [cited 2019 Jun 27];23:111-3. Available from: http://www.ijmm.org/text.asp?2005/23/2/111/16050
Mycobacterial infections continue to cause high mortality. During the year 2000 about 1.66 million people died of tuberculosis and the global burden in terms of DALYs loss was about 35.79 million. India accounts for nearly one third of the global burden i.e., approximately 2.2 million cases. The incidence per lakh population is 184 with 3.4% multidrug resistant cases.,
In all mycobacterial infections, isolation of the aetiological agent forms the definitive investigation. Isolation of mycobacteria is also essential for drug sensitivity testing, epidemiological surveys, case finding and assessment of tuberculosis control programmes. For the isolation of M. tuberculosis conventional egg based media require up to 8-10 weeks of incubation. Thus there is a great need for developing rapid, sensitive, simple and economic culture methods. Introduction of radiometric system with use of selective broth medium in BACTEC 460 has improved the recovery rate and also decreased the incubation period but this system has limitations of being expensive along with disposal of radioactive waste. Similarly, other techniques like fluorescent BACTEC 9000, colorimetric system, MGIT system etc. were introduced.- But in developing country like India, where disease burden is high, these sensitive techniques are not easily available.
The commercial biphasic system (septi chek AFB system or MB chek system) was introduced and evaluated for improving the isolation rate and reducing the recovery time. In the present study we have evaluated the use of biphasic medium in our laboratory using Middlebrook 7H11 agar with OADC supplement (M511 FD018- Hi-Media) slant as solid phase and Middlebrook 9H broth with ADC supplement (M198, FD019-Hi-Media) as liquid phase i.e., MB biphasic system in comparison with conventional Lowenstein - Jensen (LJ) medium.
| ~ Materials and Methods|| |
Between January and December 2002, a total of 151 patients having clinical and radiological evidence of tuberculosis attending the department of tuberculosis and medicine at SCSM hospital, Solapur, who had not taken antitubercular therapy, were selected.
From each patient sputum sample was collected in sterile wide mouthed container for three consecutive mornings and transported to the laboratory. The sputum samples were concentrated and decontaminated by Petroff's method.
LJ medium was prepared by using LJ base obtained from Hi-Media (M162). All ingredients were dissolved by heating and the medium was autoclaved. This medium was mixed with 1000 mL of whole egg emulsion prepared aseptically and 20 mL of 1% malachite green solution. The complete medium was dispensed in McCartney bottles and inspissated at 80oC for one hour.
Middlebrook biphasic medium (MB system) was prepared in two stages. For solid phase, Middlebrook 7H11 agar base obtained from Hi-Media (M511) was used. Slants were prepared as per the manufactured instructions. For liquid phase 2.35 grams of dehydrated Middlebrook 7H9 broth base (Hi-Media, M 198) was dissolved in 450 mL distilled water containing 2mL of glycerol by heating and autoclaved at 121oC for 15 minutes. Medium was cooled to 50oC and one vial of ADC supplement (Hi-Media, FD019) was added. Ten millilitre of this medium was poured over the formed slant.
Before proceeding with the culture of the clinical samples on both the media we did an initial quality control study by inoculating H 37Rv strain of M. tuberculosis , five strains of M. tuberculosis and two strains of M. kansasii isolated and identified in our laboratory.
From each concentrated and decontaminated sample 0.5 mL was inoculated on LJ medium, 0.5 mL on Middlebrook slant and 0.5 mL on Middlebrook broth. Biphasic medium was considered as two systems incorporated into one container so inoculations were done into both. Two smears were prepared on clean grease free slides and stained with Zeihl-Neelsen (ZN) stain and examined. The inoculated media were incubated aerobically at 37oC. All bottles were inspected daily for the detection of growth. The biphasic medium was tilted (for inoculation of slant) on alternate days in the first two weeks, there after once a week.
If a growth was detected, its description along with the duration required was noted. Smears were prepared from the growth, stained with ZN stain and examined. The isolates were identified by conventional biochemical tests. If no growth was detected after eight weeks of incubation then smears were prepared from MB broth, MB slant, LJ slant and examined before reporting as culture negative.
Both the culture methods were compared regarding their recovery rate, duration needed and contamination rate.
| ~ Results|| |
Among the 151 sputum samples 46 (30.46%) detected the organism M. tuberculosis by one or both methods. Thirty four (23.5%) of the samples showed presence of acid fast bacteria in the smear. Thirty four cultures were isolated by both methods. One culture was grown only on LJ and 10 only on biphasic system. Sensitivity and specificity of biphasic system was 97.43% and 93.27% respectively. [Table - 1] summarizes the rate of recovery of M. tuberculosis by each method. MB biphasic system showed recovery rate of 97.05% and LJ 79.41% in smear positive cases. In smear negative cases MB biphasic system yielded 91.66% and LJ 66.66%. According to McNemar's modification of X² test the biphasic medium gave significant (P < 0.05, P <0.001) results in smear positive and negative cases respectively. The over all mean time required for recovery of M. tuberculosis was 21± 4.44 days and 28±3.76 days in smear positive cases, 36±3.44 days and 41±4.09 days in smear negative cases by biphasic system and LJ medium respectively [Table - 1] and [Table - 2].
| ~ Discussion|| |
Resurgence of tuberculosis due to HIV pandemic and multidrug resistant mycobacterial strains has renewed interest in developing more efficient system for isolation, identification and drug susceptibility testing of M. tuberculosis .
In our study of 151 sputum samples the over all detection was 46 (30.46%) by one or more methods. The recovery rate of M. tuberculosis on biphasic medium was 44 (95.65%) and 35 (76.08%) on LJ. Similar observations were made by Luquin et al who has shown recovery rate of 92.5% and 79.6% by MB chek and LJ medium respectively. In their study they have also shown MB chek to be superior to BACTEC. In contrast, Piersimoni et al have shown BACTEC to be superior (91.9%) to MB chek (79.7%). Abe et al have reported same recovery rates of M. tuberculosis by both septi - chek and BACTEC.
We evaluated recovery rates of M. tuberculosis among smear positive and smear negative samples [Table - 2]. Our observations are similar to Sewell et al and Luquin et al. We emphasize the difference in recovery rates of two methods in smear negative cases. Similar observations were also made by Ichiyama et al.
The average number of days required for the recovery of M. Tuberculosis by both culture methods in smear positive and smear negative cases observed by us are similar to those reported by Sewell et al  but Luquin et al  observed shorter incubation period.
Evaluation of any method is incomplete without taking into consideration the contamination rate. We observed 4.63% contamination on LJ medium and only 1.3% on biphasic system, which is consistent with that reported by Luquin et al . However, Isenberg et al have shown higher contamination rate with septi-chek (4.5%) than LJ medium (2%).
Cost of MB biphasic system was calculated to be 1.8 times the cost of LJ medium when prepared indigenously in our laboratory. We did not come across any commercial company in India preparing biphasic system for M. tuberculosis . So we could not compare the cost of commercially available media.
In conclusion, we observed the performance of biphasic system to be superior in recovering M. tuberculosis . Ease of processing the sample and not requiring the special expensive equipment or radioactive media, are its advantages. The biphasic system is feasible and practical method even in medium sized laboratories. It has the advantage of repeated exposure of agar medium to actively proliferating organisms in the liquid broth during subculturing, which is simply by tilting the bottle. In this system different combinations of media can be used for better differentiation of mycobacteria.
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[Table - 1], [Table - 2]
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