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通过突变等位基因交换分析鞭毛在嗜热弯曲杆菌热不稳定Lior血清分型方案中的作用。

Analysis of the role of flagella in the heat-labile Lior serotyping scheme of thermophilic Campylobacters by mutant allele exchange.

作者信息

Alm R A, Guerry P, Power M E, Lior H, Trust T J

机构信息

Department of Biochemistry and Microbiology, University of Victoria, British Columbia.

出版信息

J Clin Microbiol. 1991 Nov;29(11):2438-45. doi: 10.1128/jcm.29.11.2438-2445.1991.

Abstract

Flagellin mutations originally constructed in Campylobacter coli VC167 (serotype LIO8) by a gene replacement mutagenesis technique (P. Guerry, S. M. Logan, S. Thornton, and T. J. Trust, J. Bacteriol. 172:1853-1860, 1990) were moved from the original host into Campylobacter strains of a number of other Lior serogroups by a natural transformation procedure. This is the first report of the use of this transformation method to transfer a mutated locus among Campylobacter strains. Flagellin mutants were constructed in a number of heat-labile LIO serotypes and were serotyped and analyzed by immunoelectron microscopy with LIO typing antisera. In six cases, isogenic nonflagellated mutants were able to be serotyped in the same serogroup as their parent, and immunogold electron microscopy confirmed that antibodies in the typing antisera bound to components on the surface of both parent and mutant cells. However, in only one case, a strain belonging to serogroup LIO4, was a nonflagellated mutant untypeable, and immunogold electron microscopy showed that antibodies bound to the flagella filament of the parent but not to the cell surface. Furthermore, after introduction and expression as a flagellar filament of a LIO8 flagellin gene in this mutant, the strain could not be serotyped. These results indicate that a nonflagellar antigen is often the serodeterminant in the heat-labile Lior serotyping scheme.

摘要

最初通过基因置换诱变技术(P. Guerry、S. M. Logan、S. Thornton和T. J. Trust,《细菌学杂志》172:1853 - 1860,1990年)在空肠弯曲菌VC167(血清型LIO8)中构建的鞭毛蛋白突变体,通过自然转化程序从原始宿主转移到许多其他Lior血清群的弯曲杆菌菌株中。这是关于使用这种转化方法在弯曲杆菌菌株间转移突变位点的首次报道。在多种热不稳定的LIO血清型中构建了鞭毛蛋白突变体,并使用LIO分型抗血清通过免疫电子显微镜进行血清分型和分析。在六个案例中,同基因的无鞭毛突变体能够与其亲本在同一血清群中进行血清分型,免疫金电子显微镜证实分型抗血清中的抗体与亲本和突变体细胞表面的成分结合。然而,仅在一个案例中,属于血清群LIO4的一个菌株,其无鞭毛突变体无法进行血清分型,免疫金电子显微镜显示抗体与亲本的鞭毛丝结合,但不与细胞表面结合。此外,在该突变体中引入并表达LIO8鞭毛蛋白基因作为鞭毛丝后,该菌株无法进行血清分型。这些结果表明,在热不稳定的Lior血清分型方案中,非鞭毛抗原通常是血清决定因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afc9/270352/a28329ca813f/jcm00047-0095-a.jpg

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