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禽致病性大肠杆菌 O78 血清型的减毒突变株:预防禽大肠杆菌病的一种可能的活疫苗株。

An attenuated mutant of avian pathogenic Escherichia coli serovar O78: a possible live vaccine strain for prevention of avian colibacillosis.

机构信息

Nippon Institute for Biological Science, 9-2221-1 Shinmachi, Ome, Tokyo 198-0024, Japan.

出版信息

Microbiol Immunol. 2012 Sep;56(9):605-12. doi: 10.1111/j.1348-0421.2012.00482.x.

DOI:10.1111/j.1348-0421.2012.00482.x
PMID:22708916
Abstract

Here construction of an attenuated mutant of an avian pathogenic Escherichia coli serovar O78 using an allelic exchange procedure is described. The mutant AESN1331, which carries a deletion in the crp gene, lost tryptophan deaminase activity and therefore lacked the ability to produce indole. The mutant strain additionally lacked the ability to adsorb Congo red, no longer fermented sugars other than glucose and L-arabinose, did not harbor four known virulence-associated genes (iss, tsh, cvaA, papC), and was susceptible to many antimicrobials, with the exception of nalidixic acid. The lethal dose (LD(50) value) of the mutant strain on intravenous challenge in chickens was approximately 10-fold higher than that of the parent strain. Additionally, the mutant strain was rapidly eliminated from chickens, being detected in the respiratory tract only on the first day post-inoculation by fine spray. Administration of the mutant strain via various routes such as spray and eye drop for chickens, as well as in ovo inoculation for embryonated egg, evoked an effective immune response that protected against a virulent wild-type E. coli O78 strain. Specifically, after immunization with the mutant strain, chickens challenged intravenously with an E. coli O78 strain exhibited decreases in mortality, clinical scores, organ lesion scores, and recovery of the challenge strain from organs compared to non-immunized chickens. These findings suggest that AESN1331 is a suitable candidate for a live vaccine strain to protect chickens from colibacillosis caused by avian E. coli O78.

摘要

这里描述了使用等位基因交换程序构建禽致病性大肠杆菌 O78 衰减突变株的方法。携带 crp 基因缺失的突变株 AESN1331 失去了色氨酸脱氨酶活性,因此缺乏产生吲哚的能力。该突变株还丧失了刚果红的吸附能力,除葡萄糖和 L-阿拉伯糖外,不再发酵其他糖,不携带四个已知的与毒力相关的基因(iss、tsh、cvaA、papC),并且对许多抗生素敏感,除了萘啶酸。突变株在鸡静脉攻毒的致死剂量(LD 50 值)比亲本株高约 10 倍。此外,突变株在鸡体内迅速被清除,仅在用细喷雾接种后的第一天在呼吸道中检测到。通过喷雾和滴眼等途径将突变株施用于鸡,以及对鸡胚进行卵内接种,均可引发有效的免疫反应,从而预防强毒野生型大肠杆菌 O78 株的感染。具体而言,用突变株免疫后,与未免疫的鸡相比,静脉内攻毒大肠杆菌 O78 株的鸡的死亡率、临床评分、器官损伤评分以及从器官中回收攻毒菌株均降低。这些发现表明 AESN1331 是一种适合的活疫苗株,可以预防禽致病性大肠杆菌 O78 引起的鸡大肠杆菌病。

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