4.3 Article

Subunit vaccines based on intimin and Efa-1 polypeptides induce humoral immunity in cattle but do not protect against intestinal colonisation by enterohaemorrhagic Escherichia coli O157:H7 or O26:H-

Journal

VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY
Volume 116, Issue 1-2, Pages 47-58

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.vetimm.2006.12.009

Keywords

enterohaemorrhagic Escherichia coli; O157; O26; cattle; colonisation; subunit vaccines; immune response

Funding

  1. Biotechnology and Biological Sciences Research Council [BBS/E/I/00001013] Funding Source: Medline
  2. Wellcome Trust [076962] Funding Source: Medline
  3. Biotechnology and Biological Sciences Research Council [BBS/E/I/00001013] Funding Source: researchfish

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Enterohaemorrhagic Escherichia coli (EHEC) infections in humans are an important public health concern and are commonly acquired via contact with ruminant faeces. Cattle are a key control point however cross-protective vaccines for the control of EHEC in the bovine reservoir do not yet exist. The EHEC serogroups that are predominantly associated with human infection in Europe and North America are 0 157 and 026. Intimin and EHEC factor for adherence (Efa-1) play important roles in intestinal colonisation of cattle by EHEC and are thus attractive candidates for the development of subunit vaccines. Immunisation of calves with the cell-binding domain of intimin subtypes beta or gamma via the intramuscular route induced anti gen-specific serum lgG1 and, in some cases salivary IgA responses, but did not reduce the magnitude or duration of faecal excretion of EHEC 026:H- (Int(280)-beta) or EHEC O157:1-17 (Int(280)-gamma) upon subsequent experimental challenge. Similarly, immunisation of calves via the intramuscular route with the truncated Efa-1 protein (Eta-1') from EHEC O157:1-17 or a mixture of the amino-terrn inal and central thirds of the full-length protein (Efa-1-N and M) did not protect against intestinal colonisation by EHEC 015TH7 (Eta-1') or EHEC 026:H- (Eta-1-N and M) despite the induction of humoral immunity. A portion of the serum IgG1 elicited by the truncated recombinant antigens in calves was confirmed to recognise native protein exposed on the bacterial surface. Calves immunised with a mixture of Int280-gamma and Efa- Vor an EHEC 015TH7 bacterin via the intramuscular route then boosted via the intranasal route with the same antigens using cholera toxin B subunit as an adjuvant were also not protected against intestinal colonisation by EHEC O157:1-17. These studies highlight the need for further studies to develop and test novel vaccines or treatments for control of this important foodborne pathogen. (c) 2007 Elsevier B.V. All rights reserved.

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