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使用多价凝集试剂对猪链球菌进行血清分型

Use of polyvalent coagglutination reagents for serotyping of Streptococcus suis.

作者信息

Gottschalk M, Higgins R, Boudreau M

机构信息

Groupe de Recherche sur les Maladies Infectieuses du Porc, Faculté de Médecine Vétérinaire, Université de Montréal, St.-Hyacinthe, Québec, Canada.

出版信息

J Clin Microbiol. 1993 Aug;31(8):2192-4. doi: 10.1128/jcm.31.8.2192-2194.1993.

Abstract

Polyvalent coagglutination reagents (PRs) have been evaluated for the serotyping of Streptococcus suis. Monovalent antisera produced against 28 S. suis reference strains have been grouped to obtain five different pools. A total of 249 field isolates previously identified and belonging to different serotypes were tested with PRs prepared by two different procedures: (i) monovalent coagglutination reagents were individually prepared and mixed in equal proportions, and (ii) antisera were mixed in equal proportions before the addition of the Staphylococcus aureus suspension. Only antisera tested by a tube agglutination test with 2-mercaptoethanol and presenting titers of 1:32 or higher were used. Results obtained with PRs prepared by both procedures were similar, and there was a very good correlation between the capsular type of the isolate and the reaction obtained with PRs. Thus, from a practical viewpoint, it is suggested that PRs be prepared by the first procedure. To isolates, were tested in parallel with both the PRs and the monovalent coagglutination reagents over a 1-year period. Ninety-nine percent of the typeable and all of the untypeable isolates were correctly identified. Serotyping with PRs is suggested to be a very useful and reliable screening procedure, particularly when a large number of S. suis isolates have to be serotyped. In addition, the choice of antisera to be included in a given pool is facultative and should be oriented to the needs of a region or a country.

摘要

已对多价凝集试剂(PRs)用于猪链球菌血清分型进行了评估。针对28株猪链球菌参考菌株制备的单价抗血清已分组以获得五个不同的组合。使用通过两种不同程序制备的PRs对总共249株先前鉴定且属于不同血清型的田间分离株进行了检测:(i)分别制备单价凝集试剂并等比例混合,以及(ii)在加入金黄色葡萄球菌悬液之前将抗血清等比例混合。仅使用通过2-巯基乙醇试管凝集试验检测且效价为1:32或更高的抗血清。通过两种程序制备的PRs获得的结果相似,并且分离株的荚膜型与用PRs获得的反应之间存在非常好的相关性。因此,从实际角度来看,建议通过第一种程序制备PRs。在1年的时间内,对分离株同时使用PRs和单价凝集试剂进行检测。99%的可分型分离株和所有不可分型分离株均被正确鉴定。建议使用PRs进行血清分型是一种非常有用且可靠的筛选程序,特别是当必须对大量猪链球菌分离株进行血清分型时。此外,特定组合中包含的抗血清的选择是任意的,应根据一个地区或国家的需求来确定。

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