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High prevalence of pathogenicLeptospira in wild and domesticated animals in an endemic area of China

机译:中国流行区野生和家养动物中致病性钩端螺旋体的高流行

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Objective:To assess the prevalence ofLeptospira detected in wildlife and domesticated animals in Jiangxi Province, China, in2009.Methods:Urine samples from 28 buffaloes and kidney samples from50 pigs,50 dogs and38 rats were collected from Fuliang and Shangrao County, Jiangxi Province, China, in October2009. Polymerase chain reaction(PCR) and culture analyses were used to detectLeptospira. The cultured isolates were typed using the microscopic agglutination test (MAT).Results:The results showed that rats potentially serve as the main reservoir of leptospiral infection, followed by dogs. Although16% of rats (6/38) were positive using culture analysis, PCR analysis using the diagnostic primersG1/G2 and B64I/B64II or lipL32 showed identification as50% and24%, respectively, of the rat samples as positive for the presence of leptospiralDNA.Conclusions:PCR-based detection of leptospiralDNA in infected kidney tissues of reservoirs is more efficient when usingG1/G2 primers thanlipL32 primers. However, the latter primers have a potential application for detection in urine samples. The alarmingly high prevalence of leptospiralDNAin the wild rat population near human habitation underscores the utility of routineLeptospira surveillance, preferably usingPCR methods, which are more sensitive than traditional culture-based methods.
机译:目的:评估2009年江西省野生动物和家畜中检出的Leptospira患病率。方法:从江西省富良县和上饶县采集28只水牛的尿液样本和50头猪,50只狗和38只大鼠的肾脏样本。 ,于2009年10月发布。聚合酶链反应(PCR)和培养分析被用来检测细螺旋体。结果:结果表明,大鼠可能是钩端螺旋体感染的主要宿主,其次是狗。尽管使用培养分析显示有16%的大鼠(6/38)为阳性,但使用诊断引物G1 / G2和B64I / B64II或lipL32进行的PCR分析显示,分别鉴定出50%和24%的大鼠样本为钩端螺旋体DNA阳性。结论:使用G1 / G2引物比lipL32引物更有效地检测受感染肾脏组织中钩端螺旋体DNA。但是,后一种引物在尿液样品检测中具有潜在的应用。钩端螺旋体DNA在人类居住区附近的野生大鼠种群中的惊人流行率突出了常规钩端螺旋体监测的实用性,最好使用PCR方法,这种方法比传统的基于培养的方法更为敏感。

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    《亚太热带医药杂志(英文版)》 |2011年第011期|841-845|共5页
  • 作者单位

    Department of Medical Microbiology and Parasitology, Institutes of Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China;

    Department of Medical Microbiology and Parasitology, Institutes of Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China;

    Department of Medical Microbiology and Parasitology, Institutes of Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China;

    Jiangxi Provincial Center for Disease Control and Prevention, Nanchang 330029, China;

    Department of Medical Microbiology and Parasitology, Institutes of Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China;

    Department of Medical Microbiology and Parasitology, Institutes of Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China;

    Department of Veterinary Medicine, University of Maryland, College Park, Maryland, 20742, USA;

    Department of Medical Microbiology and Parasitology, Institutes of Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China;

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