Rapid Diagnosis of Extensively Drug-Resistant Tuberculosis by Use of a Reverse Line Blot Hybridization Assay

被引:29
作者
Ajbani, Kanchan [2 ]
Shetty, Anjali
Mehta, Ajita
Rodrigues, Camilla [1 ]
机构
[1] PD Hinduja Natl Hosp & Med Res Ctr, Dept Microbiol, Res Labs, Bombay 400016, Maharashtra, India
[2] PD Hinduja Natl Hosp & Med Res Ctr, Dept Res, Bombay 400016, Maharashtra, India
关键词
MYCOBACTERIUM-TUBERCULOSIS; ISONIAZID RESISTANCE; RIFAMPIN RESISTANCE; MUTATIONS; DNA; SUSCEPTIBILITY; COMPLEX; PCR; TB;
D O I
10.1128/JCM.02511-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Drug resistance in tuberculosis (TB) is a matter of grave concern for TB control programs, as there is currently no cure for some extensively drug-resistant (XDR) strains. There is concern that this resistance could transmit, stressing the need for additional control measures, rapid diagnostic methods, and newer drugs for treatment. We developed an in-house assay that can rapidly detect resistance to drugs involved in the definition of XDR-TB directly from smear-positive specimens. Two hundred fifteen phenotypically XDR-TB isolates and 50 pansusceptible isolates were analyzed using a reverse line blot hybridization (RLBH) assay. The assay was also successfully applied to 73 smear-positive clinical specimens. The RLBH assay exhibited good sensitivity for the detection of resistance to isoniazid (99%), rifampin (99%), fluoroquinolones (95.3%), and second-line aminoglycosides (94.8%). The results from application of this assay on direct smear-positive clinical specimens revealed 93% concordance with the phenotypic drug susceptibility test (DST) results for the above-mentioned drugs. The time to accurate DST results was significantly reduced from weeks to 3 days. This molecular assay is a highly accurate tool for screening for XDR-TB, which achieves a substantial reduction in diagnostic delays.
引用
收藏
页码:2546 / 2551
页数:6
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