Please use this identifier to cite or link to this item: 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
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