tuberculosis in the presence of the respective antibiotics. Depending on the method, this process requires at least 10 days to 8 weeks before JPH203 in vitro drug sensitivity results are available. During this time the infected patient may be treated incorrectly which may have serious health implications in particular in patients with HIV-TB coinfection. The disclosure of the genetic basis of resistance to anti-tuberculous agents has enabled development of new molecular tests to detect mutations associated with reduced susceptibility to antituberculous drugs [9, 10]. In order to detect and validate the drug resistance associated mutations, DNA

sequencing is the most accurate among the molecular techniques. We used PCR fragment sequencing since molecular mechanisms explaining resistance to anti-tuberculous agents are not fully understood [24]. It presents the advantage, over methods that use DNA probes, to detect unknown mutations. Recently the GeneXpert has been endorsed by the WHO for point of care testing [25]. Drug sensitivity testing with this method is based on the detection of mutations in the core selleck chemicals llc region of the rpoB gene, thus only RIF-resistance or MDR

would be detected. In this study, we set out to investigate the association of phenotypic resistance with genetic mutations in drug resistance TB isolates in Cameroon. Salubrinal concentration The majority of the isolates in this study were from the Jamot Hospital (Central Region of Cameroon), the reference hospital for diagnostic and treatment of pulmonary diseases throughout the country. Therefore, C-X-C chemokine receptor type 7 (CXCR-7) the data obtained in this study can be considered to be representative of the make-up of resistance conferring mutations present in M. tuberculosis strains in this region. A 158-bp fragment of the rpoB gene from codon 507 to 533 was amplified and sequenced to detect mutations in RIFR

strains. Of the 7 phentotypically RIFR strains, mutations were found in the rifampicin resistant determining region (RRDR) for all the 7 isolates. These alterations affected the codons Ser531Thr (71.4%), His526Asp (14.3%) and Asp516Val (14.3%). The rpoB codons 531, 526, and 516 are the most frequently mutated codons worldwide, although variations in the relative frequencies of mutations in these codons have been described for M. tuberculosis isolates from different geographic locations. The most common site of nucleotide substitutions in RIFR isolates was codon 531. This finding was similar to those reported in Russia [26], the US [27], Tunisia [28] Ghana [21] and Germany [29]. The codon 531 mutation was also reported as the most frequent (68%) in M. tuberculosis isolates of the LAM family in Cameroon [30]. For codons 526 and 516 involved in RIFR, mutations in our strains occurred at equal frequencies than in strains from other geographical regions [31–33].