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Impact of Infection Dose and Previous Serum Antibodies against the Locus of Enterocyte Effacement Proteins on Escherichia coli O157:H7 Shedding in Calves following Experimental Infection

Escherichia coli O157:H7 is the main causative agent of haemolytic uremic syndrome. Cattle are the main reservoir of these bacteria, and have been shown to develop immune response to colonization. Our aim was to investigate the faecal shedding pattern of E. coli O157:H7 in calves challenged intragas...

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Autores principales: Martorelli, L., Hovde, C. J., Vilte, D. A., Albanese, A., Zotta, E., Ibarra, C., Cantet, R. J. C., Mercado, E. C., Cataldi, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475743/
https://www.ncbi.nlm.nih.gov/pubmed/26167480
http://dx.doi.org/10.1155/2015/290679
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author Martorelli, L.
Hovde, C. J.
Vilte, D. A.
Albanese, A.
Zotta, E.
Ibarra, C.
Cantet, R. J. C.
Mercado, E. C.
Cataldi, A.
author_facet Martorelli, L.
Hovde, C. J.
Vilte, D. A.
Albanese, A.
Zotta, E.
Ibarra, C.
Cantet, R. J. C.
Mercado, E. C.
Cataldi, A.
author_sort Martorelli, L.
collection PubMed
description Escherichia coli O157:H7 is the main causative agent of haemolytic uremic syndrome. Cattle are the main reservoir of these bacteria, and have been shown to develop immune response to colonization. Our aim was to investigate the faecal shedding pattern of E. coli O157:H7 in calves challenged intragastrically with either 10(8) or 10(10) CFU, as well as the ability of specific preexisting antibodies to reduce shedding of the pathogen. Shedding was analysed by direct counting as well as enrichment of rectoanal mucosal swabs. Statistical analysis was performed using a linear model for repeated measures with and without the inclusion of preexisting antibodies against the carboxy-terminal fraction of intimin-γ (γ-intimin C280) as a covariable. Results suggest that there is a statistical difference in the area under the shedding curves between both doses for 14 as well as 28 days after challenge (p = 0.0069 and 0.0209, resp.). This difference is increased when the prechallenge antibodies are taken into account (p = 0.0056 and 0.0185). We concluded that the bacterial dose influences shedding on calves experimentally challenged and that preexisting antibodies against E. coli O157:H7 γ-intimin C280 could partially reduce faecal excretion.
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spelling pubmed-44757432015-07-12 Impact of Infection Dose and Previous Serum Antibodies against the Locus of Enterocyte Effacement Proteins on Escherichia coli O157:H7 Shedding in Calves following Experimental Infection Martorelli, L. Hovde, C. J. Vilte, D. A. Albanese, A. Zotta, E. Ibarra, C. Cantet, R. J. C. Mercado, E. C. Cataldi, A. Biomed Res Int Research Article Escherichia coli O157:H7 is the main causative agent of haemolytic uremic syndrome. Cattle are the main reservoir of these bacteria, and have been shown to develop immune response to colonization. Our aim was to investigate the faecal shedding pattern of E. coli O157:H7 in calves challenged intragastrically with either 10(8) or 10(10) CFU, as well as the ability of specific preexisting antibodies to reduce shedding of the pathogen. Shedding was analysed by direct counting as well as enrichment of rectoanal mucosal swabs. Statistical analysis was performed using a linear model for repeated measures with and without the inclusion of preexisting antibodies against the carboxy-terminal fraction of intimin-γ (γ-intimin C280) as a covariable. Results suggest that there is a statistical difference in the area under the shedding curves between both doses for 14 as well as 28 days after challenge (p = 0.0069 and 0.0209, resp.). This difference is increased when the prechallenge antibodies are taken into account (p = 0.0056 and 0.0185). We concluded that the bacterial dose influences shedding on calves experimentally challenged and that preexisting antibodies against E. coli O157:H7 γ-intimin C280 could partially reduce faecal excretion. Hindawi Publishing Corporation 2015 2015-06-08 /pmc/articles/PMC4475743/ /pubmed/26167480 http://dx.doi.org/10.1155/2015/290679 Text en Copyright © 2015 L. Martorelli et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Martorelli, L.
Hovde, C. J.
Vilte, D. A.
Albanese, A.
Zotta, E.
Ibarra, C.
Cantet, R. J. C.
Mercado, E. C.
Cataldi, A.
Impact of Infection Dose and Previous Serum Antibodies against the Locus of Enterocyte Effacement Proteins on Escherichia coli O157:H7 Shedding in Calves following Experimental Infection
title Impact of Infection Dose and Previous Serum Antibodies against the Locus of Enterocyte Effacement Proteins on Escherichia coli O157:H7 Shedding in Calves following Experimental Infection
title_full Impact of Infection Dose and Previous Serum Antibodies against the Locus of Enterocyte Effacement Proteins on Escherichia coli O157:H7 Shedding in Calves following Experimental Infection
title_fullStr Impact of Infection Dose and Previous Serum Antibodies against the Locus of Enterocyte Effacement Proteins on Escherichia coli O157:H7 Shedding in Calves following Experimental Infection
title_full_unstemmed Impact of Infection Dose and Previous Serum Antibodies against the Locus of Enterocyte Effacement Proteins on Escherichia coli O157:H7 Shedding in Calves following Experimental Infection
title_short Impact of Infection Dose and Previous Serum Antibodies against the Locus of Enterocyte Effacement Proteins on Escherichia coli O157:H7 Shedding in Calves following Experimental Infection
title_sort impact of infection dose and previous serum antibodies against the locus of enterocyte effacement proteins on escherichia coli o157:h7 shedding in calves following experimental infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475743/
https://www.ncbi.nlm.nih.gov/pubmed/26167480
http://dx.doi.org/10.1155/2015/290679
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