Michelle M Cabanatan, Alice Alma C Bungay, Sharon Yvette Angelina M Villanueva, Marohren C Tobias-Altura, Dario D Defensor, Maria Margarita M Lota
{"title":"多重PCR检测菲律宾奎松市耐多药结核病患者中的非结核分枝杆菌","authors":"Michelle M Cabanatan, Alice Alma C Bungay, Sharon Yvette Angelina M Villanueva, Marohren C Tobias-Altura, Dario D Defensor, Maria Margarita M Lota","doi":"10.47895/amp.v59i4.9049","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and objective: </strong>Nontuberculous mycobacteria (NTM) lung disease appears like tuberculosis infection but is resistant to primary anti-tuberculosis drugs. Hence, patients whose sputum sample tests positive for acid-fast bacilli (AFB) and bacterial culture for several times should be assessed for colonization or infection with NTM in a damaged lung secondary to TB. In such cases, though drug-resistant TB may be adequately treated, treatment may need to be directed towards the NTM as well. In NTM therapy, the duration and choice of treatment agent is based upon the specific organism and disease extent. This study used one-step multiplex PCR (mPCR) assay for rapid differentiation of solid cultures in Ogawa medium as <i>Mycobacterium tuberculosis</i> (MTB) and/or NTM.</p><p><strong>Methods: </strong>A total of 80 stocked isolates obtained from the Lung Center of the Philippines from January to December 2018 were screened for NTM in terms of growth in Ogawa medium, acid fastness, and MPT64 TB antigen test result. These were from sputum specimens of multidrug-resistant tuberculosis (MDR-TB) patients. DNA was extracted from cultures (n=55) grown in Ogawa medium and one-step mPCR was performed to identify NTM to the species level.</p><p><strong>Results: </strong>Out of 80 samples screened, a total of 55 isolates were identified as NTM. One-step mPCR identified 12.73% (7/55) as <i>M. abscessus</i>, 34.55% (19/55) as <i>M. massiliense</i>, 1.82% (1/55) as <i>M. kansasii</i>, and 50.91% (28/55) were identified only up to genus <i>Mycobacteria</i> spp. Neither <i>M. avium</i> complex nor <i>M. intracellulare</i> was identified among the samples tested.</p><p><strong>Conclusion: </strong>One-step mPCR was able to identify isolates as MTB or NTM coinciding with the initial screening using MPT64 TB antigen test. Multiplex PCR has given a more specific identification to the species level. The use of mPCR in identifying MTB and clinically significant NTM's is suitable for the adequate treatment of mycobacterial infection.</p>","PeriodicalId":6994,"journal":{"name":"Acta Medica Philippina","volume":"59 4","pages":"103-112"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12037329/pdf/","citationCount":"0","resultStr":"{\"title\":\"Identification of Nontuberculous Mycobacteria in Patients with Multidrug-resistant Tuberculosis in Quezon City, Philippines, Using Multiplex PCR.\",\"authors\":\"Michelle M Cabanatan, Alice Alma C Bungay, Sharon Yvette Angelina M Villanueva, Marohren C Tobias-Altura, Dario D Defensor, Maria Margarita M Lota\",\"doi\":\"10.47895/amp.v59i4.9049\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background and objective: </strong>Nontuberculous mycobacteria (NTM) lung disease appears like tuberculosis infection but is resistant to primary anti-tuberculosis drugs. Hence, patients whose sputum sample tests positive for acid-fast bacilli (AFB) and bacterial culture for several times should be assessed for colonization or infection with NTM in a damaged lung secondary to TB. In such cases, though drug-resistant TB may be adequately treated, treatment may need to be directed towards the NTM as well. In NTM therapy, the duration and choice of treatment agent is based upon the specific organism and disease extent. This study used one-step multiplex PCR (mPCR) assay for rapid differentiation of solid cultures in Ogawa medium as <i>Mycobacterium tuberculosis</i> (MTB) and/or NTM.</p><p><strong>Methods: </strong>A total of 80 stocked isolates obtained from the Lung Center of the Philippines from January to December 2018 were screened for NTM in terms of growth in Ogawa medium, acid fastness, and MPT64 TB antigen test result. These were from sputum specimens of multidrug-resistant tuberculosis (MDR-TB) patients. DNA was extracted from cultures (n=55) grown in Ogawa medium and one-step mPCR was performed to identify NTM to the species level.</p><p><strong>Results: </strong>Out of 80 samples screened, a total of 55 isolates were identified as NTM. One-step mPCR identified 12.73% (7/55) as <i>M. abscessus</i>, 34.55% (19/55) as <i>M. massiliense</i>, 1.82% (1/55) as <i>M. kansasii</i>, and 50.91% (28/55) were identified only up to genus <i>Mycobacteria</i> spp. Neither <i>M. avium</i> complex nor <i>M. intracellulare</i> was identified among the samples tested.</p><p><strong>Conclusion: </strong>One-step mPCR was able to identify isolates as MTB or NTM coinciding with the initial screening using MPT64 TB antigen test. Multiplex PCR has given a more specific identification to the species level. The use of mPCR in identifying MTB and clinically significant NTM's is suitable for the adequate treatment of mycobacterial infection.</p>\",\"PeriodicalId\":6994,\"journal\":{\"name\":\"Acta Medica Philippina\",\"volume\":\"59 4\",\"pages\":\"103-112\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-03-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12037329/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Medica Philippina\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.47895/amp.v59i4.9049\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Medica Philippina","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47895/amp.v59i4.9049","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
Identification of Nontuberculous Mycobacteria in Patients with Multidrug-resistant Tuberculosis in Quezon City, Philippines, Using Multiplex PCR.
Background and objective: Nontuberculous mycobacteria (NTM) lung disease appears like tuberculosis infection but is resistant to primary anti-tuberculosis drugs. Hence, patients whose sputum sample tests positive for acid-fast bacilli (AFB) and bacterial culture for several times should be assessed for colonization or infection with NTM in a damaged lung secondary to TB. In such cases, though drug-resistant TB may be adequately treated, treatment may need to be directed towards the NTM as well. In NTM therapy, the duration and choice of treatment agent is based upon the specific organism and disease extent. This study used one-step multiplex PCR (mPCR) assay for rapid differentiation of solid cultures in Ogawa medium as Mycobacterium tuberculosis (MTB) and/or NTM.
Methods: A total of 80 stocked isolates obtained from the Lung Center of the Philippines from January to December 2018 were screened for NTM in terms of growth in Ogawa medium, acid fastness, and MPT64 TB antigen test result. These were from sputum specimens of multidrug-resistant tuberculosis (MDR-TB) patients. DNA was extracted from cultures (n=55) grown in Ogawa medium and one-step mPCR was performed to identify NTM to the species level.
Results: Out of 80 samples screened, a total of 55 isolates were identified as NTM. One-step mPCR identified 12.73% (7/55) as M. abscessus, 34.55% (19/55) as M. massiliense, 1.82% (1/55) as M. kansasii, and 50.91% (28/55) were identified only up to genus Mycobacteria spp. Neither M. avium complex nor M. intracellulare was identified among the samples tested.
Conclusion: One-step mPCR was able to identify isolates as MTB or NTM coinciding with the initial screening using MPT64 TB antigen test. Multiplex PCR has given a more specific identification to the species level. The use of mPCR in identifying MTB and clinically significant NTM's is suitable for the adequate treatment of mycobacterial infection.
求助内容：
应助结果提醒方式：
京公网安备 11010802042870号
