MPT 64 Antigen detection for Rapid confirmation of M.tuberculosis isolates
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,...
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| Published in: | BMC research notes Vol. 4; no. 1; p. 79 |
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| Abstract | 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. |
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| AbstractList | Abstract Background: 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. Material/methods: 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. Findings: 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%. Conclusion: 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. 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. 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 and 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. Material/methods: 54 culture isolates of M. tuberculosis in broth and on LJ medium, 12 Non mycobacterial isolates, 10 Non tubercular (NTM) rapidly growing Mycobacteria isolated from pus and 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 and 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. BACKGROUNDA 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. MATERIAL/METHODS54 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. FINDINGSH37 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%. CONCLUSIONTuberculosis 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. BACKGROUND: 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. Material/methods: 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. FINDINGS: 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%. CONCLUSION: 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. Background 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 and 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. Material/methods: 54 culture isolates of M. tuberculosis in broth and on LJ medium, 12 Non mycobacterial isolates, 10 Non tubercular (NTM) rapidly growing Mycobacteria isolated from pus and 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. Findings 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 and NPV were 100%. Conclusion 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. |
| ArticleNumber | 79 |
| Audience | Academic |
| Author | Ranganath, Rajani R Kumar, Vijay Gs Urs, Tejashree A |
| AuthorAffiliation | 2 Professor of Microbiology, JSS Medical College, Mysore, 570 015, India 3 Post graduate student, Department of Microbiology, JSS Medical College, Mysore, 570 015, India 1 Professor & Head of Clinical Microbiology, JSS Medical College, Mysore, 570 015, India |
| AuthorAffiliation_xml | – name: 3 Post graduate student, Department of Microbiology, JSS Medical College, Mysore, 570 015, India – name: 2 Professor of Microbiology, JSS Medical College, Mysore, 570 015, India – name: 1 Professor & Head of Clinical Microbiology, JSS Medical College, Mysore, 570 015, India |
| Author_xml | – sequence: 1 givenname: Vijay Gs surname: Kumar fullname: Kumar, Vijay Gs email: gsvijaykumar@yahoo.com organization: Professor & Head of Clinical Microbiology, JSS Medical College, Mysore, 570 015, India. gsvijaykumar@yahoo.com – sequence: 2 givenname: Tejashree A surname: Urs fullname: Urs, Tejashree A – sequence: 3 givenname: Rajani R surname: Ranganath fullname: Ranganath, Rajani R |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/21429231$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1046/j.1365-3083.1997.d01-429.x 10.1128/IAI.57.1.283-288.1989 10.1016/j.jmb.2006.11.039 10.1128/CVI.00486-08 10.1128/IAI.52.1.293-302.1986 10.1111/j.1365-3156.2009.02284.x 10.1128/JCM.40.3.908-912.2002 10.1038/gt.2008.13 10.1128/IAI.62.5.2058-2064.1994 10.1128/JCM.42.1.390-392.2004 |
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| References_xml | – volume: 13 start-page: 1045 issue: 8 year: 2009 ident: 833_CR13 publication-title: Int J Tuberc Lung Dis contributor: fullname: NA Ismail – volume: 45 start-page: 499 issue: 5 year: 1997 ident: 833_CR2 publication-title: Scand J immunol doi: 10.1046/j.1365-3083.1997.d01-429.x contributor: fullname: T Oettinger – volume: 57 start-page: 283 issue: 1 year: 1989 ident: 833_CR6 publication-title: Infect Immun doi: 10.1128/IAI.57.1.283-288.1989 contributor: fullname: R Yamaguchi – volume: 9 start-page: 1409 issue: 12 year: 2005 ident: 833_CR15 publication-title: Int J Tuberc Lung Dis contributor: fullname: D Hillemann – volume: 366 start-page: 375 issue: 2 year: 2007 ident: 833_CR5 publication-title: J Mol Biol doi: 10.1016/j.jmb.2006.11.039 contributor: fullname: Z Wang – volume: 16 start-page: 686 year: 2009 ident: 833_CR11 publication-title: Clin Vaccine Immunol doi: 10.1128/CVI.00486-08 contributor: fullname: Wang Ruiling Fu Chun – volume: 52 start-page: 293 issue: 1 year: 1986 ident: 833_CR10 publication-title: Infect Immun doi: 10.1128/IAI.52.1.293-302.1986 contributor: fullname: M Harboe – ident: 833_CR14 – volume: 14 start-page: 748 issue: 7 year: 2009 ident: 833_CR4 publication-title: Trop Med Int Health doi: 10.1111/j.1365-3156.2009.02284.x contributor: fullname: K Ngamlert – volume: 14 start-page: 748 issue: 7 year: 2009 ident: 833_CR16 publication-title: Trop Med Int Health doi: 10.1111/j.1365-3156.2009.02284.x contributor: fullname: Ngamlert Keerataya – volume: 40 start-page: 908 issue: 3 year: 2002 ident: 833_CR1 publication-title: J Clin Microbiol doi: 10.1128/JCM.40.3.908-912.2002 contributor: fullname: N Hasegawa – volume: 15 start-page: 652 year: 2008 ident: 833_CR9 publication-title: Gene Therapy doi: 10.1038/gt.2008.13 contributor: fullname: Yu D-H – volume: 13 start-page: 371 issue: 3 year: 2009 ident: 833_CR12 publication-title: Int J Tuberc Lung Dis contributor: fullname: GH Shen – volume: 30 start-page: 243 issue: 3 year: 2000 ident: 833_CR8 publication-title: J Infect Dis. Proceedings of International Symposium on Tuberculosis Vaccine Development and Evaluation contributor: fullname: ML Gennaro – volume: 62 start-page: 2058 year: 1994 ident: 833_CR7 publication-title: Infect Immun doi: 10.1128/IAI.62.5.2058-2064.1994 contributor: fullname: T Oettinger – volume: 42 start-page: 390 issue: 1 year: 2004 ident: 833_CR3 publication-title: J Clin Microbiol doi: 10.1128/JCM.42.1.390-392.2004 contributor: fullname: K Hirano |
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| Snippet | 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... Background A new rapid Immunochromatographic test kit(SD MPT64TB Ag Kit) for detection of MPT 64 Antigen in M. tuberculosis isolates using mouse monoclonal MPT... Abstract Background: A new rapid Immunochromatographic test kit(SD MPT64TB Ag Kit) for detection of MPT 64 Antigen in M. tuberculosis isolates using mouse... BACKGROUNDA new rapid Immunochromatographic test kit(SD MPT64TB Ag Kit) for detection of MPT 64 Antigen in M. tuberculosis isolates using mouse monoclonal MPT... BACKGROUND: A new rapid Immunochromatographic test kit(SD MPT64TB Ag Kit) for detection of MPT 64 Antigen in M. tuberculosis isolates using mouse monoclonal... Abstract Background A new rapid Immunochromatographic test kit(SD MPT64TB Ag Kit) for detection of MPT 64 Antigen in M. tuberculosis isolates using mouse... |
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| StartPage | 79 |
| SubjectTerms | Antigens Bacteria Drug resistance Immune system Medical research Methods Mutation Mycobacteria Mycobacterium Physiological aspects Technical Note Testing Tuberculosis |
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| Title | MPT 64 Antigen detection for Rapid confirmation of M.tuberculosis isolates |
| URI | https://www.ncbi.nlm.nih.gov/pubmed/21429231 https://www.proquest.com/docview/902411225 https://search.proquest.com/docview/862005093 http://dx.doi.org/10.1186/1756-0500-4-79 https://pubmed.ncbi.nlm.nih.gov/PMC3074510 https://doaj.org/article/244cf389890f4ab08809df55bd8c8096 |
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