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首页> 外文期刊>Transactions of the Royal Society of Tropical Medicine and Hygiene >Rapid molecular typing of Burkholderia pseudomallei, isolated in an outbreak of melioidosis in Singapore in 2004, based on variable-number tandem repeats.
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Rapid molecular typing of Burkholderia pseudomallei, isolated in an outbreak of melioidosis in Singapore in 2004, based on variable-number tandem repeats.

机译:根据可变数目的串联重复序列,在2004年新加坡发生的类鼻虫病暴发中分离出的伯克霍尔德菌假苹果花的快速分子分型。

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摘要

An increase in the number of reported melioidosis cases was observed in the first 4 months of 2004. These cases were associated with a significant increase in case-fatality rate compared with the past 5 years. In order to exclude the possibility of a single source, including the possibility of intentional release of Burkholderia pseudomallei, we applied a multiplex PCR-based multilocus variable-number tandem repeat (VNTR) assay to determine the clonality of the clinical isolates. Our investigation indicated that a total of 30 different VNTR types could be distinguished in the 32 clinical isolates of B. pseudomallei obtained during this period, thus indicating that infection was unlikely to have occurred from a single source. Our experience underscores the usefulness of a rapid strain typing method in augmenting an epidemiological investigation into an infectious disease outbreak, particularly at a time where the intentional use of biological agents is a potential threat to public health.
机译:在2004年的前4个月,报告的类me虫病病例有所增加。与过去5年相比,这些病例的病死率显着增加。为了排除单一来源的可能性,包括有意释放假单胞伯克氏菌的可能性,我们应用了基于多重PCR的多基因座可变数目串联重复序列(VNTR)分析法来确定临床分离株的克隆性。我们的研究表明,在此期间获得的32株假芽孢杆菌临床分离株中,总共可以区分出30种不同的VNTR类型,因此表明感染不可能是单一来源发生的。我们的经验强调了快速菌株分型方法在加强对传染病暴发的流行病学调查方面的有用性,特别是在故意使用生物制剂对公共卫生构成潜在威胁的时候。

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