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Cloning and Characterization of Genes Encoding Homologues of the B Subunit of Cholera Toxin and the Escherichia coli Heat-Labile Enterotoxin from Clinical Isolates of Citrobacter freundii and E. coli

机译:弗氏柠檬酸杆菌和大肠杆菌临床分离株霍乱毒素B亚基和大肠杆菌热不稳定肠毒素同源基因的克隆与鉴定

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摘要

We identified and characterized a gene encoding a homologue of the B subunits of cholera toxin (CTB) and heat-labile enterotoxin (LTB) of Escherichia coli from a clinical isolate of Citrobacter freundii that was found to produce a factor in the culture supernatant that cross-reacted with antibodies to CTB and LTB when assayed by enzyme-linked immunosorbent assay (ELISA). The gene encoding the ELISA-positive factor, cfxB, consisted of 375 nucleotides and was located downstream of an 852-nucleotide open reading frame, cfxA, with a 56-nucleotide intergenic space. The cfxB gene was predicted to encode a 125-amino-acid polypeptide, which had 73.8 and 72.8% identities with the amino acid sequences of LTB and CTB, respectively. However, the amino acid sequence of the deduced polypeptide CFXA had no homologies to those of the A subunits of CT or LT. DNA probes developed from the sequences of cfxA and cfxB were used to screen 67 C. freundii isolates and 152 E. coli isolates from diarrheal patients by colony blot hybridization. Two strains, C. freundii 48 and E. coli 176, reacted with both DNA probes under conditions of high stringency. We cloned homologues of the cfxA and cfxB genes from E. coli 176 and designated them ecxA and ecxB, respectively. The ecxA gene and the ecxB gene comprise 855 and 375 nucleotides, respectively, with a 50-nucleotide intergenic space, and encode a 285- and a 125-amino-acid residue polypeptides, respectively. The results of the present study may provide important clues to the origin and evolution of immunologically related factors sharing a common enterotoxin-like A and B subunit structures.
机译:我们从弗氏柠檬酸杆菌的临床分离物中鉴定并鉴定了编码大肠杆菌霍乱毒素(CTB)和热不稳定肠毒素(LTB)B亚基同源物的基因,发现该基因在培养上清中产生交叉通过酶联免疫吸附测定(ELISA)进行测定时,与抗CTB和LTB抗体反应。编码ELISA阳性因子cfxB的基因由375个核苷酸组成,位于852个核苷酸的开放阅读框cfxA的下游,具有56个核苷酸的基因间隔。预计cfxB基因编码125个氨基酸的多肽,与LTB和CTB的氨基酸序列分别具有73.8和72.8%的同一性。但是,推导的多肽CFXA的氨基酸序列与CT或LT的A亚基没有同源性。由cfxA和cfxB序列开发的DNA探针用于通过菌落印迹杂交从腹泻患者中筛选出67种弗氏杆菌和152种大肠杆菌。两种菌株,弗氏梭菌48和大肠杆菌176,在高严格条件下与两种DNA探针反应。我们从大肠杆菌176克隆了cfxA和cfxB基因的同源物,并分别命名为ecxA和ecxB。 ecxA 基因和 ecxB 基因分别包含855和375个核苷酸,具有50个核苷酸的基因间隔,并编码285和125个氨基酸残基多肽。本研究的结果可能为免疫学相关因素的起源和演变提供重要线索,这些因素具有共同的肠毒素样A和B亚基结构。

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