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首页> 外文期刊>Microbes and Environments >Pathogenic and Saprophytic Leptospira Species in Water and Soils from Selected Urban Sites in Peninsular Malaysia
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Pathogenic and Saprophytic Leptospira Species in Water and Soils from Selected Urban Sites in Peninsular Malaysia

机译:马来西亚半岛某些城市地区水和土壤中的致病和腐生钩端螺旋体物种

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摘要

Leptospira species were studied in water and soils from selected urban sites in Malaysia. A total of 151 water ( n =121) and soil ( n =30) samples were collected from 12 recreational lakes and wet markets. All samples were filtered and inoculated into semi-solid Ellinghausen and McCullough modified by Johnson and Harris (EMJH) media supplemented with additional 5-fluorouracil. The cultures were then incubated at 30°C and observed under a dark field microscope with intervals of 10 days. A PCR assay targeting the rrs gene was used to confirm the genus Leptospira among the isolates. Subsequently, the pathogenic status of the isolates was determined using primer sets G1/G2 and Sapro1/Sapro2, which target the secY and rrs genes, respectively. The isolates were identified at serogroup level using the microscopic agglutination test (MAT) while their genetic diversity was assessed by pulsed field gel electrophoresis (PFGE). Based on dark field microscopy, 23.1% (28/121) water and 23.3% (7/30) soil cultures were positive for Leptospira spp. Of the 35 positive cultures, only 8 were pure and confirmed as Leptospira genus by PCR assay. Two out of 8 isolates were confirmed as pathogenic, 5 were saprophytic and one was intermediate. These 8 isolates were negative for the 25 reference hyperimmune rabbit sera tested in the MAT. PFGE showed that all 8 of these environmental Leptospira spp. were genetically diverse. In conclusion, the presence of pathogenic Leptospira spp. in the urban Malaysian environment may indicate and highlight the importance of water screening, especially in recreational lakes, in order to minimize any chance of Leptospira infection.
机译:在马来西亚选定城市地点的水和土壤中研究了钩端螺旋体物种。从12个休闲湖和湿市场收集了总共151个水(n = 121)和土壤(n = 30)样本。将所有样品过滤并接种到由约翰逊和哈里斯(EMJH)改良的半固体Ellinghausen和McCullough培养基中,并添加了额外的5-氟尿嘧啶。然后将培养物在30℃下孵育,并在暗视野显微镜下以10天的间隔观察。以rrs基因为靶点的PCR测定法被用来确定分离物中的钩端螺旋体属。随后,使用分别针对secY和rrs基因的引物组G1 / G2和Sapro1 / Sapro2确定了分离株的致病状态。使用显微镜凝集试验(MAT)在血清组水平上鉴定出分离株,同时通过脉冲场凝胶电泳(PFGE)评估其遗传多样性。根据暗视野显微镜检查,钩端螺旋体属物种的阳性率为23.1%(28/121)的水和23.3%(7/30)的土壤培养物为阳性。在35种阳性培养物中,只有8种是纯净的,并通过PCR测定确认为钩端螺旋体属。 8株分离株中有2株被确认为致病菌,腐生菌5株,中间菌。这8个分离株对MAT中测试的25个参考超免疫兔血清呈阴性。 PFGE显示所有这些环境钩端螺旋体属中的8种。具有遗传多样性。总之,存在致病性钩端螺旋体。在马来西亚城市环境中,可能表明并强调了水筛查的重要性,尤其是在休闲湖中,以最小化钩端螺旋体感染的机会。

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