Regional immune response to immunization with Escherichia coli O157:H7-derived intimin in cattle - PubMed
Regional immune response to immunization with Escherichia coli O157:H7-derived intimin in cattle
Kathryn G Boland et al. Clin Vaccine Immunol. 2013 Apr.
Abstract
Escherichia coli O157:H7 is an enteric pathogen of animals and humans that can result in deadly sequelae. Cattle are asymptomatic carriers and shedders of the bacteria and serve as an important reservoir of human infection. E. coli O157:H7 colonizes the gastrointestinal tract, most frequently at the rectoanal junction mucosa in cattle. Vaccination is a potentially highly effective means of decreasing cattle colonization and shedding and thereby decreasing human infections. Currently available vaccines are administered subcutaneously or intramuscularly, and immune responses have been evaluated solely by systemic immunoglobulin responses. This study evaluated local and systemic lymphoproliferative responses in addition to immunoglobulin responses following subcutaneous or mucosal (rectal) immunization with E. coli O157:H7 outer membrane protein intimin over three trials. In all three trials, significant local and systemic lymphoproliferative responses (P < 0.05) occurred following immunization in the majority of animals, as well as significant immunoglobulin responses (P < 0.001) in all animals. Surprisingly, local responses in the mesorectal lymph nodes were very similar between the subcutaneous and mucosal immunization groups. Moreover, the responses in mesorectal lymph nodes appeared targeted rather than generalized, as minimal or no significant responses were observed in the associated prescapular lymph nodes of subcutaneously immunized animals. The results indicate that both subcutaneous and mucosal immunizations are effective methods of inducing immune responses against E. coli O157:H7 in cattle.
Figures

Trial 1 local and systemic lymphoproliferative responses: PBMC or cells from the MRLN were incubated with intimin (medium-gray bars), ovalbumin (dark-gray bars), concanavalin A (white bars), and TCGF (light-gray bars) as positive controls to determine lymphoproliferative responses to proteins. (A) PBMC from week 0, prior to immunization; (B) cells from MRLN at week 9; (C) PBMC from week 9. Asterisks indicate significant responses of cells incubated with antigen compared to cells incubated with medium by a one-tailed Student t test at P values of <0.05 and SI greater than 2.0.

Trial 2 local and systemic lymphoproliferative responses: PBMC or cells from the MRLN were incubated with intimin (medium-gray bars), ovalbumin (dark-gray bars), concanavalin A (white bars), or TCGF (light-gray bars) as positive controls to assess lymphoproliferative responses to proteins. (A) PBMC from week 0, prior to immunization; (B) cells from MRLN at week 9; C) PBMC from week 9. Asterisks indicate significant responses of cells incubated with antigen compared to cells incubated with medium by a one-tailed Student t test at P values of <0.05 and SI greater than 2.0.

Trial 3 local and systemic lymphoproliferative responses: PBMC or cells from the MRLN were incubated with intimin (medium-gray bars), ovalbumin (dark-gray bars), or concanavalin A (white bars) as a positive control. Lymphoproliferative responses were then measured. (A) PBMC from week 0, prior to immunization; (B) cells from MRLN at week 11; (C) PBMC from week 11. Asterisks indicate significant responses of cells incubated with antigen compared to cells incubated with medium by a one-tailed Student t test at P values of <0.05 and SI greater than 2.0.

Trial 3 lymphoproliferative responses in draining and contralateral PLN: cells from the lymph node draining the subcutaneous immunization site (left PLN) and contralateral lymph node (right PLN) were harvested 3 days after final immunization at week 11, incubated with intimin (medium-gray bars), ovalbumin (dark-gray bars), or concanavalin A (white bars) as a positive control to determine lymphoproliferative responses to proteins. (A) Cells from draining PLN; (B) cells from contralateral PLN. Asterisks indicate significant responses of cells incubated with antigen compared to cells incubated with medium by a one-tailed Student t test at P values of <0.05 and SI greater than 2.0.
Similar articles
-
Vilte DA, Larzábal M, Garbaccio S, Gammella M, Rabinovitz BC, Elizondo AM, Cantet RJ, Delgado F, Meikle V, Cataldi A, Mercado EC. Vilte DA, et al. Vaccine. 2011 May 23;29(23):3962-8. doi: 10.1016/j.vaccine.2011.03.079. Epub 2011 Apr 6. Vaccine. 2011. PMID: 21477674
-
Khare S, Alali W, Zhang S, Hunter D, Pugh R, Fang FC, Libby SJ, Adams LG. Khare S, et al. BMC Vet Res. 2010 Jul 7;6:35. doi: 10.1186/1746-6148-6-35. BMC Vet Res. 2010. PMID: 20609252 Free PMC article.
-
Martorelli L, Garimano N, Fiorentino GA, Vilte DA, Garbaccio SG, Barth SA, Menge C, Ibarra C, Palermo MS, Cataldi A. Martorelli L, et al. Vaccine. 2018 Jun 22;36(27):3949-3959. doi: 10.1016/j.vaccine.2018.05.059. Epub 2018 May 26. Vaccine. 2018. PMID: 29807709
-
Vaccination of Cattle against Escherichia coli O157:H7.
Smith DR. Smith DR. Microbiol Spectr. 2014 Dec;2(6). doi: 10.1128/microbiolspec.EHEC-0006-2013. Microbiol Spectr. 2014. PMID: 26104456 Review.
-
Vande Walle K, Vanrompay D, Cox E. Vande Walle K, et al. Vet Immunol Immunopathol. 2013 Mar 15;152(1-2):109-20. doi: 10.1016/j.vetimm.2012.09.028. Epub 2012 Sep 26. Vet Immunol Immunopathol. 2013. PMID: 23084625 Review.
Cited by
-
Buskirk AD, Ndungo E, Shimanovich AA, Lam D, Blackwelder WC, Ikumapayi UN, Ma B, Powell H, Antonio M, Nataro JP, Kaper JB, Pasetti MF. Buskirk AD, et al. mBio. 2022 Aug 30;13(4):e0053822. doi: 10.1128/mbio.00538-22. Epub 2022 Aug 4. mBio. 2022. PMID: 35924851 Free PMC article.
-
Chitosan-Based Nanomaterial as Immune Adjuvant and Delivery Carrier for Vaccines.
Gong X, Gao Y, Shu J, Zhang C, Zhao K. Gong X, et al. Vaccines (Basel). 2022 Nov 11;10(11):1906. doi: 10.3390/vaccines10111906. Vaccines (Basel). 2022. PMID: 36423002 Free PMC article. Review.
-
Desin TS, Townsend HG, Potter AA. Desin TS, et al. PLoS One. 2015 Oct 9;10(10):e0139803. doi: 10.1371/journal.pone.0139803. eCollection 2015. PLoS One. 2015. PMID: 26451946 Free PMC article.
References
-
- Boyce TG, Swerdlow DL, Griffin PM. 1995. Escherichia coli O157:H7 and the hemolytic-uremic syndrome. N. Engl. J. Med. 333:364–368 - PubMed
-
- Cohen MB. 1996. Escherichia coli O157:H7 infections: a frequent cause of bloody diarrhea and the hemolytic-uremic syndrome. Adv. Pediatr. 43:171–207 - PubMed
-
- CDC 1985. Hemolytic-uremic syndrome associated with Escherichia coli O157:H7 enteric infections—United States, 1984. MMWR Morb. Mortal. Wkly. Rep. 34:20–21 - PubMed
-
- Noel JM, Boedeker EC. 1997. Enterohemorrhagic Escherichia coli: a family of emerging pathogens. Dig. Dis. 15:67–91 - PubMed
-
- Dundas S, Todd WT, Stewart AI, Murdoch PS, Chaudhuri AK, Hutchinson SJ. 2001. The central Scotland Escherichia coli O157:H7 outbreak: risk factors for the hemolytic uremic syndrome and death among hospitalized patients. Clin. Infect. Dis. 33:923–931 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical