MPT 64 Antigen detection for Rapid confirmation of M.tuberculosis isolates

• Published in: BMC research notes Vol. 4; no. 1; p. 79
• Main Authors: Kumar, Vijay Gs, Urs, Tejashree A, Ranganath, Rajani R
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 24-03-2011; BioMed Central; BMC
• Subjects: Antigens; Bacteria; Drug resistance; Immune system; Medical research; Methods; Mutation; Mycobacteria; Mycobacterium; Physiological aspects; Technical Note; Testing; Tuberculosis; India
• ISSN: 1756-0500; 1756-0500
• DOI: 10.1186/1756-0500-4-79

A new rapid Immunochromatographic test kit(SD MPT64TB Ag Kit) for detection of MPT 64 Antigen in M. tuberculosis isolates using mouse monoclonal MPT 64 Antibody developed by SD Bioline, South Korea was evaluated for rapid identification of M. tuberculosis isolates. We also assessed the sensitivity, specificity and predictive values of this kit. The test kit has an excellent sensitivity, specificity, negative predictive value & positive predictive value. This rapid method is found to be a reliable, rapid and cheaper method for confirming MTB culture isolates in resource poor laboratories.
54 culture isolates of M. tuberculosis in broth & on LJ medium, 12 Non mycobacterial isolates, 10 Non tubercular (NTM) rapidly growing Mycobacteria isolated from pus & 5 smear positive sputum samples were tested for detection of MPT64 antigen using the SD Bioline immunochromatography (ICT)test kit. H37 RV strain was employed as the positive reference control.
H37 RV strain showed the presence of MPT64 antigen band. Similar band was formed in all the 54 MTB isolates tested proving 100% sensitivity. MPT64 band formation was not detected in any of the other test isolates which proved the 100% specificity of the test kit. Both PPV & NPV were 100%.
Tuberculosis is a global pandemic. Rapid identification of MTB culture isolate is very important for drug susceptibility testing. MPT 64 TB Ag detection ICT kit is a rapid, reliable method; it can be a substitute for the molecular identification methods.