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基于多重聚合酶链反应的最常见沙门氏菌第二阶段鞭毛抗原的检测与鉴定。

Multiplex PCR-based detection and identification of the most common Salmonella second-phase flagellar antigens.

作者信息

Echeita M Aurora, Herrera Silvia, Garaizar Javier, Usera Miguel A

机构信息

Servicio de Bacteriología, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Madrid, Spain.

出版信息

Res Microbiol. 2002 Mar;153(2):107-13. doi: 10.1016/s0923-2508(01)01295-5.

Abstract

Most Salmonella serotypes alternatively express phase 1 or phase 2 flagellar antigens encoded by fliC and fljB genes respectively. Flagellar phase reversal to identify both flagellar antigens is not necessary at the genetic level. Variable internal regions of the fljB genes encoding H:1,w, H:e,n,x and H:e,n,z15 antigens have been sequenced and the specific sites for each antigen determined in selected Salmonella serotypes. These results, together with flagellar H1 complex variable internal sequences previously published, have been used to design a multiplex-PCR to identify H:1,2, H:1,5, H:1,6, H:1,7, H:1,w, H:e,n,x and H:e,n,z15 second-phase antigens. These antigens are part of the most common Salmonella serotypes possessing second-phase flagellar antigens. This multiplex-PCR includes 10 primers. A total of 140 Salmonella strains associated with 49 different serotypes were tested. Each strain generated one second-phase-specific antigen fragment, ranging between 50 and 400 bps. Twenty-five strains associated with 17 serotypes, with no second-phase antigen or with an antigen different from those tested in this work, did not generate any fragments. The method is quick, specific and reproducible and is independent of the phase expressed by the bacteria when tested.

摘要

大多数沙门氏菌血清型交替表达分别由fliC和fljB基因编码的1相或2相鞭毛抗原。在基因水平上,无需进行鞭毛相逆转来鉴定两种鞭毛抗原。已对编码H:1,w、H:e,n,x和H:e,n,z15抗原的fljB基因的可变内部区域进行了测序,并在选定的沙门氏菌血清型中确定了每种抗原的特定位点。这些结果与先前发表的鞭毛H1复合体可变内部序列一起,已被用于设计一种多重PCR,以鉴定H:1,2、H:1,5、H:1,6、H:1,7、H:1,w、H:e,n,x和H:e,n,z15第二相抗原。这些抗原是具有第二相鞭毛抗原的最常见沙门氏菌血清型的一部分。这种多重PCR包括10种引物。共测试了与49种不同血清型相关的140株沙门氏菌菌株。每个菌株产生一个50至400个碱基对的第二相特异性抗原片段。与17种血清型相关的25株菌株,没有第二相抗原或具有与本研究中测试的抗原不同的抗原,未产生任何片段。该方法快速、特异且可重复,并且在测试时与细菌表达的相无关。

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