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Distribution gene sequence and expression in vivo of the plasmid encoded fimbrial antigen of Salmonella serotype Enteritidis.

机译:沙门氏菌血清型肠炎沙门氏菌纤维状抗原编码质粒的体内分布基因序列和表达。

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摘要

The pefA gene which encoded the serotype associated plasmid (SAP) mediated fimbrial major subunit antigen of Salmonella enterica serotype Typhimurium shared genetic identity with 128 of 706 salmonella isolates as demonstrated by dot (colony) hybridization. Seventy-seven of 113 isolates of Typhimurium and individual isolates of serotypes Bovis-morbificans, Cholerae-suis and Enteritidis phage type 9b hybridized pefA strongly, whereas 48 isolates of Enteritidis hybridized pefA weakly and one Enteritidis isolate of phage type 14b failed to hybridize. Individual isolates of 294 serotypes and 247 individual isolates of serotype Dublin did not hybridize pefA. Southern hybridization of plasmids extracted from Enteritidis demonstrated that the pefA gene probe hybridized strongly an atypical SAP of 80 kb in size harboured by one Enteritidis isolate of phage-type 9b, whereas the typical SAP of 58 kb in size harboured by 48 Enteritidis isolates hybridized weakly. One Enteritidis isolate of phage type 14b which failed to hybridize pefA in dot (colony) hybridization experiments was demonstrated to be plasmid free. A cosmid library of Enteritidis phage type 4 expressed in Escherichia coli K12 was screened by hybridization for the presence of pef sequences. Recombinant clones which were deduced to harbour the entire pef operon elaborated a PEF-like fimbrial structure at the cell surface. The PEF-like fimbrial antigen was purified from one cosmid clone and used in western blot experiments with sera from chickens infected with Enteritidis phage-type 4. Seroconversion to the fimbrial antigen was observed which indicated that the Enteritidis PEF-like fimbrial structure was expressed at some stage during infection. Nucleotide sequence analysis demonstrated that the pefA alleles of Typhimurium and Enteritidis phage-type 4 shared 76% DNA nucleotide and 82% deduced amino acid sequence identity.
机译:通过点(菌落)杂交证明,编码血清型相关质粒(SAP)介导的鼠伤寒沙门氏菌血清型鼠伤寒沙门氏菌的纤维主要亚基抗原的pefA基因与706个沙门氏菌分离物中的128个具有遗传同一性。 113鼠伤寒分离株中有77个与血清型Bovis-morbificans,霍乱弧菌和肠炎肠炎噬菌体9b型噬菌体分别强力杂交,而p肠炎弱毒株中48株与pefA弱杂交,而1噬菌体14b型肠炎病菌则没有杂交。 294种血清型的个体分离株和247种都柏林的血清型分离株没有与pefA杂交。从肠炎沙门氏菌提取的质粒的Southern杂交表明,pefA基因探针与一个噬菌体9b型肠炎沙门氏菌分离株所藏的大小为80 kb的非典型SAP强烈杂交,而由48个肠炎沙门氏菌分离株所藏的58kb的典型SAP杂交很弱。在点(菌落)杂交实验中未能与pefA杂交的一种噬菌体14b肠炎分离株被证明不含质粒。通过杂交筛选pef序列的存在,筛选在大肠杆菌K12中表达的肠炎噬菌体4型粘粒文库。推测含有整个pef操纵子的重组克隆在细胞表面形成了PEF样纤维结构。从一个粘粒克隆中纯化出PEF样纤维抗原,并将其用于感染4型肠炎沙门氏菌噬菌体鸡的血清进行Western blot实验,观察到血清纤维转化为纤维抗原,这表明肠炎PEF样纤维结构在感染期间的某个阶段。核苷酸序列分析表明,鼠伤寒和肠炎4型噬菌体的pefA等位基因共享76%的DNA核苷酸和82%的推导氨基酸序列同一性。

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