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C 型肉毒梭菌禽源菌株的分子特征与比较。

Molecular characterization and comparison of Clostridium botulinum type C avian strains.

机构信息

Department of Bacteriology, National Veterinary Institute, Uppsala, Sweden.

出版信息

Avian Pathol. 2010 Dec;39(6):511-8. doi: 10.1080/03079457.2010.526923.

Abstract

Type C botulinum neurotoxin (BoNT/C)-producing Clostridium botulinum causes animal botulism worldwide and has become a serious problem in poultry flocks and waterfowl in Sweden. The objectives of the present study were to isolate, characterize and subtype C. botulinum type C avian isolates in order to increase the knowledge of the genetic diversity. Isolates from 13 birds were identified by 16S rRNA sequencing and BoNT/C gene detection by real-time polymerase chain reaction (PCR). Conventional PCR was used to distinguish a chimeric BoNTC/D gene, often associated with avian botulism, from the BoNT/C gene. The isolates analysed all contained the gene coding for a chimeric toxin type C/D. Two fingerprinting techniques, pulsed-field gel electrophoresis (PFGE) and randomly amplified polymorphic DNA analysis (RAPD), were optimized and used to investigate the epidemiological relatedness among the strains. The isolates were divided into three different pulsotypes based upon their restriction profiles for SmaI and SalI. The RAPD system proved to be as discriminative as PFGE. This study reveals a small genetic diversity among Swedish type C strains, with a high similarity between strains from broilers and herring gulls.

摘要

C 型肉毒梭菌(BoNT/C)产生的肉毒梭菌在世界范围内引起动物肉毒中毒,在瑞典已成为家禽和水禽的严重问题。本研究的目的是分离、鉴定和亚型 C. botulinum 禽源分离株,以增加对遗传多样性的了解。通过 16S rRNA 测序和实时聚合酶链反应(PCR)检测 BoNT/C 基因,从 13 只鸟类中鉴定出分离株。常规 PCR 用于区分与禽肉中毒相关的嵌合 BoNTC/D 基因与 BoNT/C 基因。分析的分离株均含有编码嵌合毒素 C/D 的基因。优化了两种指纹技术,即脉冲场凝胶电泳(PFGE)和随机扩增多态性 DNA 分析(RAPD),用于研究菌株之间的流行病学相关性。根据 SmaI 和 SalI 的限制图谱,将分离株分为三种不同的脉冲类型。RAPD 系统与 PFGE 一样具有区分能力。本研究揭示了瑞典 C 型菌株之间遗传多样性较小,肉鸡和海鸥来源的菌株之间高度相似。

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