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https://doi.org/10.1038/srep08538
Title: | Pulmonary tuberculosis caused by mycobacterium bovis in China | Authors: | Jiang, G Wang, G Chen, S Yu, X Wang, X Zhao, L Ma, Y Dong, L Huang, H |
Keywords: | bacterial protein Cfp32 protein, Mycobacterium tuberculosis RNA 16S transposon bacterium identification China classification clinical trial genetics host pathogen interaction human microbiological examination microbiology multicenter study multiplex polymerase chain reaction Mycobacterium bovis physiology procedures sputum transposon Tuberculosis, Pulmonary Bacterial Proteins Bacterial Typing Techniques Bacteriological Techniques China DNA Transposable Elements Host-Pathogen Interactions Humans Multiplex Polymerase Chain Reaction Mycobacterium bovis RNA, Ribosomal, 16S Sputum Tuberculosis, Pulmonary |
Issue Date: | 2015 | Publisher: | Nature Publishing Group | Citation: | Jiang, G, Wang, G, Chen, S, Yu, X, Wang, X, Zhao, L, Ma, Y, Dong, L, Huang, H (2015). Pulmonary tuberculosis caused by mycobacterium bovis in China. Scientific Reports 5 : 8538. ScholarBank@NUS Repository. https://doi.org/10.1038/srep08538 | Rights: | Attribution 4.0 International | Abstract: | The epidemiology of Mycobacterium bovis infection in humans in China is unknown. In this study, pulmonary tuberculosis caused by M. bovis in China was studied. A total of 4069 clinical strains isolated from sputa during the 2007-2009 nationwide surveillance of drug-resistant tuberculosis in China were analyzed. M. bovis was identified by para-nitrobenzoic acid and thiophen-2-carboxylic acid hydrazide growth tests, spoligotyping and multiplex PCR amplification. In addition, a total of 1828 clinical specimens were recruited from Beijing Chest Hospital (Beijing, China) for Löwenstein-Jensen (LJ) culture, both on standard LJ medium and LJ medium containing 4.5 mg/ml(W/V) sodium pyruvate, the latter being the preferred medium for M. bovis growth. The isolates which demonstrated more vigorous on pyruvate containing medium than on standard LJ medium were then identified by multiplex PCR amplification. Only 1 isolate from the nationwide surveillance was confirmed as M. bovis-BCG. The isolate belonged to a predominant spoligotype SB0120 (ST482). In addition, no M. bovis isolate was acquired by the continuous screening step in Beijing Chest Hospital. M. bovis has a negligible contribution to pulmonary tuberculosis in China, so neither laboratory identification nor clinical treatment of M. bovis infection need be considered in routine work. | Source Title: | Scientific Reports | URI: | https://scholarbank.nus.edu.sg/handle/10635/177762 | ISSN: | 20452322 | DOI: | 10.1038/srep08538 | Rights: | Attribution 4.0 International |
Appears in Collections: | Staff Publications Elements |
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