Shiga toxin-producing Escherichia coli (STEC) O22:H8 isolated from cattle reduces E. coli O157:H7 adherence in vitro and in vivo
Problem addressed: Shiga toxin-producing Escherichia coli (STEC) are a group of bacteria responsible for foodassociated diseases. Clinical features include a wide range of symptoms such as diarrhea, hemorrhagic colitis and the hemolytic uremic syndrome (HUS), a life-threatening condition. Objective: Our group has observed that animals naturally colonized with STEC strains of unknown serotype were not efficiently colonized with E. coli O157:H7 after experimental infection. In order to assess the basis of the interference, three STEC strains were isolated from STEC persistently-colonized healthy cattle from a dairy farm in Buenos Aires, Argentina. Methods and results: The three isolated strains are E. coli O22:H8 and carry the stx1 and stx2d genes. The activatable activity of Stx2d was demonstrated in vitro. The three strains carry the adhesins iha, ehaA and lpfO113. E. coli O22:H8 formed stronger biofilms in abiotic surface than E. coli O157:H7 (eae+, stx2+) and displayed a more adherent phenotype in vitro towards HeLa cells. Furthermore, when both serotypes were cultured together O22:H8 could reduce O157:H7 adherence in vitro. When calves were intragastrically pre-challenged with 108 CFU of a mixture of the three STEC strains and two days later challenged with the same dose of the strain E. coli O157:H7 438/99, the shedding of the pathogen was significantly reduced. Conclusions: These results suggest that E. coli O22:H8, a serotype rarely associated with human illness, might compete with O157:H7 at the bovine recto-anal junction, making non-O157 carrying-calves less susceptible to O157:H7 colonization and shedding of the bacteria to the environment.
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Format: | info:eu-repo/semantics/article biblioteca |
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2017-09
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Subjects: | Enfermedades de los Animales, Escherichia Coli, Ganado Bovino, Experimentación In Vitro, Experimentación In Vivo, Animal Disesase, Cattle, In Vitro Experimentation, In Vivo Experimentation, |
Online Access: | http://hdl.handle.net/20.500.12123/1487 http://www.sciencedirect.com/science/article/pii/S0378113517306466 https://doi.org/10.1016/j.vetmic.2017.06.021 |
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Enfermedades de los Animales Escherichia Coli Ganado Bovino Experimentación In Vitro Experimentación In Vivo Animal Disesase Cattle In Vitro Experimentation In Vivo Experimentation Enfermedades de los Animales Escherichia Coli Ganado Bovino Experimentación In Vitro Experimentación In Vivo Animal Disesase Cattle In Vitro Experimentation In Vivo Experimentation |
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Enfermedades de los Animales Escherichia Coli Ganado Bovino Experimentación In Vitro Experimentación In Vivo Animal Disesase Cattle In Vitro Experimentation In Vivo Experimentation Enfermedades de los Animales Escherichia Coli Ganado Bovino Experimentación In Vitro Experimentación In Vivo Animal Disesase Cattle In Vitro Experimentation In Vivo Experimentation Martorelli, Luisina Albanese, Adriana Andrea Vilte, Daniel Alejandro Cantet, Rodolfo Juan Carlos Bentancor, Adriana Beatriz Zolezzi, Gisela Chinen, Isabel Ibarra, Cristina E. Rivas, Marta Mercado, Elsa Cristina Cataldi, Angel Adrian Shiga toxin-producing Escherichia coli (STEC) O22:H8 isolated from cattle reduces E. coli O157:H7 adherence in vitro and in vivo |
description |
Problem addressed: Shiga toxin-producing Escherichia coli (STEC) are a group of bacteria responsible for foodassociated diseases. Clinical features include a wide range of symptoms such as diarrhea, hemorrhagic colitis and the hemolytic uremic syndrome (HUS), a life-threatening condition.
Objective: Our group has observed that animals naturally colonized with STEC strains of unknown serotype were not efficiently colonized with E. coli O157:H7 after experimental infection. In order to assess the basis of the interference, three STEC strains were isolated from STEC persistently-colonized healthy cattle from a dairy farm in Buenos Aires, Argentina.
Methods and results: The three isolated strains are E. coli O22:H8 and carry the stx1 and stx2d genes. The activatable activity of Stx2d was demonstrated in vitro. The three strains carry the adhesins iha, ehaA and lpfO113. E. coli O22:H8 formed stronger biofilms in abiotic surface than E. coli O157:H7 (eae+, stx2+) and displayed a more adherent phenotype in vitro towards HeLa cells. Furthermore, when both serotypes were cultured together O22:H8 could reduce O157:H7 adherence in vitro. When calves were intragastrically pre-challenged with 108
CFU of a mixture of the three STEC strains and two days later challenged with the same dose of the strain E. coli O157:H7 438/99, the shedding of the pathogen was significantly reduced.
Conclusions: These results suggest that E. coli O22:H8, a serotype rarely associated with human illness, might compete with O157:H7 at the bovine recto-anal junction, making non-O157 carrying-calves less susceptible to O157:H7 colonization and shedding of the bacteria to the environment. |
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info:eu-repo/semantics/article |
topic_facet |
Enfermedades de los Animales Escherichia Coli Ganado Bovino Experimentación In Vitro Experimentación In Vivo Animal Disesase Cattle In Vitro Experimentation In Vivo Experimentation |
author |
Martorelli, Luisina Albanese, Adriana Andrea Vilte, Daniel Alejandro Cantet, Rodolfo Juan Carlos Bentancor, Adriana Beatriz Zolezzi, Gisela Chinen, Isabel Ibarra, Cristina E. Rivas, Marta Mercado, Elsa Cristina Cataldi, Angel Adrian |
author_facet |
Martorelli, Luisina Albanese, Adriana Andrea Vilte, Daniel Alejandro Cantet, Rodolfo Juan Carlos Bentancor, Adriana Beatriz Zolezzi, Gisela Chinen, Isabel Ibarra, Cristina E. Rivas, Marta Mercado, Elsa Cristina Cataldi, Angel Adrian |
author_sort |
Martorelli, Luisina |
title |
Shiga toxin-producing Escherichia coli (STEC) O22:H8 isolated from cattle reduces E. coli O157:H7 adherence in vitro and in vivo |
title_short |
Shiga toxin-producing Escherichia coli (STEC) O22:H8 isolated from cattle reduces E. coli O157:H7 adherence in vitro and in vivo |
title_full |
Shiga toxin-producing Escherichia coli (STEC) O22:H8 isolated from cattle reduces E. coli O157:H7 adherence in vitro and in vivo |
title_fullStr |
Shiga toxin-producing Escherichia coli (STEC) O22:H8 isolated from cattle reduces E. coli O157:H7 adherence in vitro and in vivo |
title_full_unstemmed |
Shiga toxin-producing Escherichia coli (STEC) O22:H8 isolated from cattle reduces E. coli O157:H7 adherence in vitro and in vivo |
title_sort |
shiga toxin-producing escherichia coli (stec) o22:h8 isolated from cattle reduces e. coli o157:h7 adherence in vitro and in vivo |
publishDate |
2017-09 |
url |
http://hdl.handle.net/20.500.12123/1487 http://www.sciencedirect.com/science/article/pii/S0378113517306466 https://doi.org/10.1016/j.vetmic.2017.06.021 |
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oai:localhost:20.500.12123-14872019-06-05T18:05:13Z Shiga toxin-producing Escherichia coli (STEC) O22:H8 isolated from cattle reduces E. coli O157:H7 adherence in vitro and in vivo Martorelli, Luisina Albanese, Adriana Andrea Vilte, Daniel Alejandro Cantet, Rodolfo Juan Carlos Bentancor, Adriana Beatriz Zolezzi, Gisela Chinen, Isabel Ibarra, Cristina E. Rivas, Marta Mercado, Elsa Cristina Cataldi, Angel Adrian Enfermedades de los Animales Escherichia Coli Ganado Bovino Experimentación In Vitro Experimentación In Vivo Animal Disesase Cattle In Vitro Experimentation In Vivo Experimentation Problem addressed: Shiga toxin-producing Escherichia coli (STEC) are a group of bacteria responsible for foodassociated diseases. Clinical features include a wide range of symptoms such as diarrhea, hemorrhagic colitis and the hemolytic uremic syndrome (HUS), a life-threatening condition. Objective: Our group has observed that animals naturally colonized with STEC strains of unknown serotype were not efficiently colonized with E. coli O157:H7 after experimental infection. In order to assess the basis of the interference, three STEC strains were isolated from STEC persistently-colonized healthy cattle from a dairy farm in Buenos Aires, Argentina. Methods and results: The three isolated strains are E. coli O22:H8 and carry the stx1 and stx2d genes. The activatable activity of Stx2d was demonstrated in vitro. The three strains carry the adhesins iha, ehaA and lpfO113. E. coli O22:H8 formed stronger biofilms in abiotic surface than E. coli O157:H7 (eae+, stx2+) and displayed a more adherent phenotype in vitro towards HeLa cells. Furthermore, when both serotypes were cultured together O22:H8 could reduce O157:H7 adherence in vitro. When calves were intragastrically pre-challenged with 108 CFU of a mixture of the three STEC strains and two days later challenged with the same dose of the strain E. coli O157:H7 438/99, the shedding of the pathogen was significantly reduced. Conclusions: These results suggest that E. coli O22:H8, a serotype rarely associated with human illness, might compete with O157:H7 at the bovine recto-anal junction, making non-O157 carrying-calves less susceptible to O157:H7 colonization and shedding of the bacteria to the environment. Inst. de Patobiología Fil: Martorelli, Luisina. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Patobiología; Argentina Fil: Albanese, Adriana Andrea. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Fisiología. Laboratorio de Fisiopatogenia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Fisiología y Biofísica Bernardo Houssay; Argentina Fil: Vilte, Daniel Alejandro. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Patobiología; Argentina Fil: Cantet, Rodolfo Juan Carlos. Universidad de Buenos Aires. Facultad de Agronomia. Departamento de Producción Animal; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Bentancor, Adriana B. Universidad de Buenos Aires. Facultad de Ciencias Veterinarias. Cátedra de Microbiología; Argentina Fil: Zolezzi, Gisela. INEI-ANLIS «Dr. Carlos G. Malbrán». Departamento Bacteriología. Servicio Fisiopatogenia; Argentina Fil: Chinen, Isabel. INEI-ANLIS «Dr. Carlos G. Malbrán». Departamento Bacteriología. Servicio Fisiopatogenia; Argentina Fil: Ibarra, Cristina E. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Fisiología. Laboratorio de Fisiopatogenia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Fisiología y Biofísica Bernardo Houssay; Argentina Fil: Rivas, Marta. INEI-ANLIS «Dr. Carlos G. Malbrán». Departamento Bacteriología. Servicio Fisiopatogenia; Argentina Fil: Mercado, Elsa Cristina. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Patobiología; Argentina Fil: Cataldi, Angel Adrian. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Biotecnología; Argentina 2017-10-13T14:09:43Z 2017-10-13T14:09:43Z 2017-09 info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion info:ar-repo/semantics/artículo http://hdl.handle.net/20.500.12123/1487 http://www.sciencedirect.com/science/article/pii/S0378113517306466 0378-1135 (Print) 1873-2542 (Online) https://doi.org/10.1016/j.vetmic.2017.06.021 eng info:eu-repo/semantics/restrictedAccess application/pdf Veterinary microbiology 208 : 8-17. (September 2017) |