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. 2017;5(8):10.18535/jmscr/v5i8.86.
doi: 10.18535/jmscr/v5i8.86.

Comparison of Mycobacterium tuberculosis complex Yield and Contamination Rates using Lowenstein-Jensen with and without Antibiotics in Western Kenya

A Okumu  1 , K McCarthy  2 , J Orwa  1 , J Williamson  3 , S Musau  1 , H Alexander  2 , S Cavanaugh  2 , S Modi  4 , K Cain  1   2
Affiliations

Comparison of Mycobacterium tuberculosis complex Yield and Contamination Rates using Lowenstein-Jensen with and without Antibiotics in Western Kenya

A Okumu et al. J Med Sci Clin Res. 2017.

Abstract

Background: While molecular methods have been recently endorsed for diagnosis of tuberculosis (TB), mycobacterial culture remains the gold standard. Lowenstein-Jensen (LJ) is often used for the cultivation of Mycobacterium tuberculosis complex (MTBC); however contamination often renders a subset of cultures useless. We compared the MTBC yield and contamination rate of processed sputum inoculated on LJ with antibiotics (LJ PACT) to LJ without antibiotics (LJ).

Methodology: Sputum samples were obtained from people living with HIV enrolled in a TB screening study in western Kenya, processed using NALC/NaOH-Na citrate, then inoculated on LJ PACT and LJ media. Cultures were evaluated weekly with growth identified as acid-fast bacilli by Ziehl-Neelsen bright-field microscopy. MTBC and nontuberculous mycobacteria (NTM) were identified by immunochromatographic and line probe assays.

Results: A total of 700 sputum samples were cultured on both LJ PACT and LJ between March and June 2012. Of those cultured on LJ PACT, 29 (4.1%) grew MTBC, 613 (87.6%) were negative, 12 (1.7%) grew NTM, and 46 (6.6%) were contaminated; on LJ, 28 (4%) grew MTBC, 553 (79%) were negative, 9 (1.3%) grew NTM, and 110 (15.7%) were contaminated. The difference in contamination on LJ PACT and LJ was statistically significant (p<0.0001), while the difference in MTBC growth was not (p=0.566).

Keywords: Kenya; Lowenstein-Jensen; Nontuberculous mycobacteria; cross-sectional studies; culture techniques; diagnosis; pulmonary tuberculosis.

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References

    1. Tenover FC, et al. , The resurgence of tuberculosis: is your laboratory ready? J Clin Microbiol, 1993. 31(4): p. 767–70. - PMC - PubMed
    1. World Health Organization Global Tuberculosis Report 2015. http://apps.who.int/iris/bitstream/10665/191102/1/9789241565059_eng.pdf.
    1. Perkins MD, New diagnostic tools for tuberculosis. Int J Tuberc Lung Dis, 2000. 4(12 Suppl 2): p. S182–8. - PubMed
    1. Wilson ML, Recent advances in the laboratory detection of Mycobacterium tuberculosis complex and drug resistance. Clin Infect Dis, 2011. 52(11): p. 1350–5. - PubMed
    1. Parsons LM, et al. , Laboratory diagnosis of tuberculosis in resource-poor countries: challenges and opportunities. Clin Microbiol Rev, 2011. 24(2): p. 314–50. - PMC - PubMed

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