Genetic diversity of Mycobacterium tuberculosis, drug resistance and atypical mycobacteria in Rwanda
Abstract
348 words
The genus Mycobacterium has two main groups, Mycobacterium tuberculosis
complex (MTBC) and atypical mycobacteria. The MTBC species, the causative agents of
tuberculosis (TB), has been further typed into different genotypes. Genotyping
methods of M. tuberculosis help in identifying the most predominant circulating
genotypes and their transmission dynamics and this helps in planning for a better
tuberculosis drug resistance surveillance system. In Rwanda, little is known about the
most predominant M. tuberculosis genotypes and there is limited data on drug resistance
especially pyrazinamide drug resistance profile. Moreover, the distribution of atypical
mycobacteria and their underlying epidemiological factors are also unknown. Our main
goal is to characterize epidemiologically and genotypically M. tuberculosis, establish drug
resistance and determine the distribution of atypical mycobacteria countrywide. Smear
positives collected from suspected TB patients from Januray to July 2015
were submitted for primary culture on both solid and liquid culture media. All
positive cultures on Lowenstein Jensen and BACTEC MGIT 960 liquid culture system
were followed by phenotypic drug susceptibility testing (DST) to characterize resistance
for first line anti-tuberculosis drugs. Isolates were tested for susceptibility to first line
anti-TB drugs using Isoniazid, Rifampin, Streptomycin, and Ethambutol. Speciation of
atypical mycobacteria was done using GenoType MTB DRplus Assay CM and AS. The
present review presents preliminary results from primary culture, drug resistance and
atypical mycobacteria. Out of 994 positive culture, MTBC accounted for 99.6% while
atypical mycobacteria represented 0.4%. Of the 990 samples, 932 (94.1%) were new
patients and 58 (5.9%) were patients with previous history of treatment for tuberculosis.
MDR-TB was detected in 1.4% cases among new patients and 8.6% in previous treated
patients. Among the mono-resistance pattern, Ethambutol represented the majority of
all mono-resistance, averaging 17.4%. Non- Tuberclosis Mycobacteria (NTM) included
M. celatum (0.1%), M. lentiflavum (0.1%), M. peregrinum (0.1%) and M. intracellulare
(0.1%). In light of the present preliminary results, further investigations are needed to
confirm the pan-resistance of Ethambutol. Molecular characterization is needed to decipher
the most predominant M. tuberculosis genotypes, drug resistance and understand the
extent of atypical mycobacteria in Rwanda. This would aid in strengthening TB treatment
and control.
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