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首页> 外文期刊>Journal of Clinical Microbiology >Analysis of the role of flagella in the heat-labile Lior serotyping scheme of thermophilic Campylobacters by mutant allele exchange.
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Analysis of the role of flagella in the heat-labile Lior serotyping scheme of thermophilic Campylobacters by mutant allele exchange.

机译:通过突变等位基因交换分析鞭毛在嗜热弯曲杆菌的不耐热Lior血清分型方案中的作用。

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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.
机译:通过基因置换诱变技术(P.Guerry,SM Logan,S.Thornton,and TJ Trust,J.Bacteriol.172:1853-1860,1990)最初在弯曲杆菌VC167(血清型LIO8)中构建的鞭毛蛋白突变从通过自然转化程序将原始宿主分为许多其他Lior血清群的弯曲杆菌菌株。这是使用这种转化方法在弯曲杆菌菌株之间转移突变基因座的首次报道。鞭毛蛋白突变体构建为多种热不稳定的LIO血清型,并进行血清分型并通过免疫电子显微镜与LIO型抗血清进行分析。在六种情况下,同基因的非鞭毛突变体能够在与它们的亲本相同的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结合了亲本和突变体细胞表面的成分。然而,仅在一种情况下,属于血清群LIO4的菌株是无法分型的无鞭毛突变体,免疫金电子显微镜显示抗体与亲本鞭毛细丝结合,而不与细胞表面结合。此外,在该突变体中引入并表达为LIO8鞭毛蛋白基因的鞭毛丝后,不能对该菌株进行血清分型。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簇。

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