Use of Gas Chromatographic Fatty Acid and Mycolic Acid Cleavage Product Determination To Differentiate among Mycobacterium genavense , Mycobacterium fortuitum , Mycobacterium simiae , and Mycobacterium tuberculosis

Author:

Chou S.1,Chedore P.2,Kasatiya S.13

Affiliation:

1. Public Health Laboratory, Ontario Ministry of Health, Ottawa, Ontario, Canada K1G 6C41;

2. Public Health Laboratory, Ontario Ministry of Health, Etobicoke, Ontario, Canada M9P 3T12; and

3. Department of Microbiology and Immunology, University of Ottawa, Ontario, Canada K1N 6N53

Abstract

ABSTRACT Three Mycobacterium genavense strains and three American Type Culture Collection reference strains each of Mycobacterium fortuitum , Mycobacterium simiae , and Mycobacterium tuberculosis were subcultured onto Mycobacteria 7H11 agar (Difco Laboratories, Detroit, Mich.) supplemented with mycobactin J (Allied Laboratories, Fayette, Mo.). After 4 weeks of incubation at 37°C in 10% CO 2 , the cultures were analyzed by gas-liquid chromatography (GLC) for their fatty acids and mycolic acid cleavage products. M. fortuitum was clearly differentiated from M. genavense by the presence of the specific marker 2-methyloctadecenoic acid in M. fortuitum and by the ratio of tetracosanoic acid to hexacosanoic acid. This ratio was <1 for M. genavense and >3 for M. fortuitum. M. fortuitum also contained docosanoic acid, which was not detected in M. genavense. M. genavense , M. simiae , and M. tuberculosis , which have similar GLC profiles, were also differentiated from each other by the presence of either cis -10-hexadecenoic acid or cis -11-hexadecenoic acid and by tetradecanoic acid content.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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