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迈向致育/损伤性大肠杆菌疫苗:兔肠道致病性大肠杆菌的一种李氏菌属编码调节因子(ler)突变体减毒、具有免疫原性,并能保护兔子免受野生型强毒株的致死性攻击。

Towards a vaccine for attaching/effacing Escherichia coli: a LEE encoded regulator (ler) mutant of rabbit enteropathogenic Escherichia coli is attenuated, immunogenic, and protects rabbits from lethal challenge with the wild-type virulent strain.

作者信息

Zhu Chengru, Feng Shuzhang, Thate Timothy E, Kaper James B, Boedeker Edgar C

机构信息

Center for Vaccine Development, University of Maryland School of Medicine, 685 West Baltimore Street, Baltimore, MD 21201, USA.

出版信息

Vaccine. 2006 May 1;24(18):3845-55. doi: 10.1016/j.vaccine.2005.07.019. Epub 2005 Jul 28.

Abstract

The ler (LEE encoded regulator) gene product is a central regulator for the genes encoded on the locus of enterocyte effacement (LEE) pathogenicity island of attaching/effacing (A/E) pathogens, including human enteropathogenic E. coli (EPEC) and enterohemorrhagic E. coli (EHEC) as well as animal isolates. Although an in vivo role for Ler in bacterial virulence has not been documented, we hypothesized that a Ler deletion mutant should be attenuated for virulence but might retain immunogenicity. The goals of this study were to genetically characterize ler of a rabbit EPEC (rEPEC) strain (O103:H2), to examine the effect of ler on in vivo virulence, and to determine if intragastric inoculation of an attenuated rEPEC ler mutant was immunogenic and could protect rabbits against subsequent challenge with the wild-type virulent parent strain. The predicted ler gene product of rEPEC strain O103:H2 shares high homology (over 95% amino acid identity) with the Lers of another rEPEC strain RDEC-1 (O15:H-) and human EPEC and EHEC. A defined internal ler deletion mutant of rEPEC O103:H2 showed reduced production of secreted proteins. Although orogastric inoculation of rabbits with the virulent parent O103:H2 strain induced severe diarrhea, significant weight loss and early mortality with adherent mucosal bacteria found at sacrifice, the isogeneic ler mutant strain was well tolerated. Animals gained weight and showed no clinical signs of disease. Examination of histological sections of intestinal segments revealed the absence of mucosal bacterial adherence. This result demonstrates an essential role for Ler in in vivo pathogenicity of A/E E. coli. Single dose orogastric immunization with the rEPEC ler mutant induced serum IgG antibody to whole bacteria (but not to intimin). Immunized animals were protected against enteric infection with the WT virulent parent strain exhibiting normal weight gain, absence of diarrhea and absence of mucosally adherent bacteria at sacrifice. Such attenuated ler mutant strains may have potential for use as oral vaccines, or as vaccine vectors for delivery of foreign antigens. It remains to be determined whether such regulatory mutants can protect against infection with A/E bacteria of differing serotypes affecting different hosts.

摘要

Ler(LEE编码调节因子)基因产物是紧密黏附/消除性(A/E)病原菌肠细胞消除位点(LEE)致病岛上所编码基因的核心调节因子,这些病原菌包括人类肠致病性大肠杆菌(EPEC)、肠出血性大肠杆菌(EHEC)以及动物分离株。尽管尚未证实Ler在细菌毒力方面的体内作用,但我们推测Ler缺失突变体的毒力应会减弱,但可能保留免疫原性。本研究的目的是对一株兔EPEC(rEPEC)菌株(O103:H2)的ler进行遗传学特征分析,研究ler对体内毒力的影响,并确定经胃内接种减毒的rEPEC ler突变体是否具有免疫原性,以及能否保护兔子抵御随后野生型强毒株亲本的攻击。rEPEC菌株O103:H2预测的ler基因产物与另一株rEPEC菌株RDEC-1(O15:H-)以及人类EPEC和EHEC的Ler具有高度同源性(氨基酸同一性超过95%)。rEPEC O103:H2的一个明确的内部ler缺失突变体显示分泌蛋白产量降低。尽管用强毒株亲本O103:H2经口接种兔子会引发严重腹泻、显著体重减轻和早期死亡,处死时发现黏膜有黏附细菌,但同基因ler突变体菌株耐受性良好。动物体重增加,未表现出疾病的临床症状。对肠段组织切片的检查显示没有黏膜细菌黏附。这一结果证明Ler在A/E大肠杆菌的体内致病性中起关键作用。用rEPEC ler突变体进行单剂量经口免疫可诱导血清IgG抗体针对全菌(但不针对紧密黏附素)产生反应。免疫的动物受到保护,免受野生型强毒株亲本的肠道感染,表现为体重正常增加、无腹泻且处死时无黏膜黏附细菌。这种减毒的ler突变体菌株可能有潜力用作口服疫苗,或用作递送外源抗原的疫苗载体。此类调节突变体是否能抵御影响不同宿主的不同血清型A/E细菌的感染仍有待确定。

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