Cargando…

Malnutrition Decreases Antibody Secreting Cell Numbers Induced by an Oral Attenuated Human Rotavirus Vaccine in a Human Infant Fecal Microbiota Transplanted Gnotobiotic Pig Model

Human rotavirus (HRV) is a leading cause of morbidity and mortality in children, especially in developing countries. Malnutrition is prevalent in these countries, which may contribute to the decreased oral vaccine efficacy, posing a concern for global health. Neonatal gnotobiotic (Gn) pigs closely r...

Descripción completa

Detalles Bibliográficos
Autores principales: Michael, Husheem, Langel, Stephanie N., Miyazaki, Ayako, Paim, Francine C., Chepngeno, Juliet, Alhamo, Moyasar A., Fischer, David D., Srivastava, Vishal, Kathayat, Dipak, Deblais, Loic, Rajashekara, Gireesh, Saif, Linda J., Vlasova, Anastasia N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033455/
https://www.ncbi.nlm.nih.gov/pubmed/32117313
http://dx.doi.org/10.3389/fimmu.2020.00196
_version_ 1783499671242539008
author Michael, Husheem
Langel, Stephanie N.
Miyazaki, Ayako
Paim, Francine C.
Chepngeno, Juliet
Alhamo, Moyasar A.
Fischer, David D.
Srivastava, Vishal
Kathayat, Dipak
Deblais, Loic
Rajashekara, Gireesh
Saif, Linda J.
Vlasova, Anastasia N.
author_facet Michael, Husheem
Langel, Stephanie N.
Miyazaki, Ayako
Paim, Francine C.
Chepngeno, Juliet
Alhamo, Moyasar A.
Fischer, David D.
Srivastava, Vishal
Kathayat, Dipak
Deblais, Loic
Rajashekara, Gireesh
Saif, Linda J.
Vlasova, Anastasia N.
author_sort Michael, Husheem
collection PubMed
description Human rotavirus (HRV) is a leading cause of morbidity and mortality in children, especially in developing countries. Malnutrition is prevalent in these countries, which may contribute to the decreased oral vaccine efficacy, posing a concern for global health. Neonatal gnotobiotic (Gn) pigs closely resemble human infants in their anatomy, physiology, and outbred status and are a unique model to investigate malnutrition, oral live attenuated HRV (AttHRV) vaccination, and subsequent virulent HRV (VirHRV) challenge. We evaluated the impact of malnutrition on AttHRV vaccine efficacy and B cell immune responses in neonatal germfree (GF) or Gn pigs transplanted with human infant fecal microbiota (HIFM). Pigs were fed either deficient or sufficient bovine milk diets. Malnutrition did not significantly affect the serum and intestinal contents total or HRV-specific IgG and IgA antibody titers pre VirHRV challenge. However, HRV-specific IgG and IgA antibody secreting cells (ASCs) were reduced in blood or intestinal tissues following AttHRV vaccination and pre VirHRV challenge in deficient HIFM transplanted pigs. Furthermore, post-VirHRV challenge, deficient HIFM pigs had decreased total Ig and HRV-specific IgG and IgA antibody titers in serum or intestinal contents, in addition to decreased HRV-specific IgG and IgA ASCs in blood and ileum, compared with sufficient HIFM pigs. Our results indicate that deficient diet impairs B cell mucosal, and systemic immune responses following HRV vaccination, and challenge. The impaired immune responses contributed to the decreased protective efficacy of the AttHRV vaccine, suggesting that malnutrition may significantly reduce the effectiveness of oral HRV vaccines in children in developing countries.
format Online
Article
Text
id pubmed-7033455
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-70334552020-02-28 Malnutrition Decreases Antibody Secreting Cell Numbers Induced by an Oral Attenuated Human Rotavirus Vaccine in a Human Infant Fecal Microbiota Transplanted Gnotobiotic Pig Model Michael, Husheem Langel, Stephanie N. Miyazaki, Ayako Paim, Francine C. Chepngeno, Juliet Alhamo, Moyasar A. Fischer, David D. Srivastava, Vishal Kathayat, Dipak Deblais, Loic Rajashekara, Gireesh Saif, Linda J. Vlasova, Anastasia N. Front Immunol Immunology Human rotavirus (HRV) is a leading cause of morbidity and mortality in children, especially in developing countries. Malnutrition is prevalent in these countries, which may contribute to the decreased oral vaccine efficacy, posing a concern for global health. Neonatal gnotobiotic (Gn) pigs closely resemble human infants in their anatomy, physiology, and outbred status and are a unique model to investigate malnutrition, oral live attenuated HRV (AttHRV) vaccination, and subsequent virulent HRV (VirHRV) challenge. We evaluated the impact of malnutrition on AttHRV vaccine efficacy and B cell immune responses in neonatal germfree (GF) or Gn pigs transplanted with human infant fecal microbiota (HIFM). Pigs were fed either deficient or sufficient bovine milk diets. Malnutrition did not significantly affect the serum and intestinal contents total or HRV-specific IgG and IgA antibody titers pre VirHRV challenge. However, HRV-specific IgG and IgA antibody secreting cells (ASCs) were reduced in blood or intestinal tissues following AttHRV vaccination and pre VirHRV challenge in deficient HIFM transplanted pigs. Furthermore, post-VirHRV challenge, deficient HIFM pigs had decreased total Ig and HRV-specific IgG and IgA antibody titers in serum or intestinal contents, in addition to decreased HRV-specific IgG and IgA ASCs in blood and ileum, compared with sufficient HIFM pigs. Our results indicate that deficient diet impairs B cell mucosal, and systemic immune responses following HRV vaccination, and challenge. The impaired immune responses contributed to the decreased protective efficacy of the AttHRV vaccine, suggesting that malnutrition may significantly reduce the effectiveness of oral HRV vaccines in children in developing countries. Frontiers Media S.A. 2020-02-14 /pmc/articles/PMC7033455/ /pubmed/32117313 http://dx.doi.org/10.3389/fimmu.2020.00196 Text en Copyright © 2020 Michael, Langel, Miyazaki, Paim, Chepngeno, Alhamo, Fischer, Srivastava, Kathayat, Deblais, Rajashekara, Saif and Vlasova. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Michael, Husheem
Langel, Stephanie N.
Miyazaki, Ayako
Paim, Francine C.
Chepngeno, Juliet
Alhamo, Moyasar A.
Fischer, David D.
Srivastava, Vishal
Kathayat, Dipak
Deblais, Loic
Rajashekara, Gireesh
Saif, Linda J.
Vlasova, Anastasia N.
Malnutrition Decreases Antibody Secreting Cell Numbers Induced by an Oral Attenuated Human Rotavirus Vaccine in a Human Infant Fecal Microbiota Transplanted Gnotobiotic Pig Model
title Malnutrition Decreases Antibody Secreting Cell Numbers Induced by an Oral Attenuated Human Rotavirus Vaccine in a Human Infant Fecal Microbiota Transplanted Gnotobiotic Pig Model
title_full Malnutrition Decreases Antibody Secreting Cell Numbers Induced by an Oral Attenuated Human Rotavirus Vaccine in a Human Infant Fecal Microbiota Transplanted Gnotobiotic Pig Model
title_fullStr Malnutrition Decreases Antibody Secreting Cell Numbers Induced by an Oral Attenuated Human Rotavirus Vaccine in a Human Infant Fecal Microbiota Transplanted Gnotobiotic Pig Model
title_full_unstemmed Malnutrition Decreases Antibody Secreting Cell Numbers Induced by an Oral Attenuated Human Rotavirus Vaccine in a Human Infant Fecal Microbiota Transplanted Gnotobiotic Pig Model
title_short Malnutrition Decreases Antibody Secreting Cell Numbers Induced by an Oral Attenuated Human Rotavirus Vaccine in a Human Infant Fecal Microbiota Transplanted Gnotobiotic Pig Model
title_sort malnutrition decreases antibody secreting cell numbers induced by an oral attenuated human rotavirus vaccine in a human infant fecal microbiota transplanted gnotobiotic pig model
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033455/
https://www.ncbi.nlm.nih.gov/pubmed/32117313
http://dx.doi.org/10.3389/fimmu.2020.00196
work_keys_str_mv AT michaelhusheem malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel
AT langelstephanien malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel
AT miyazakiayako malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel
AT paimfrancinec malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel
AT chepngenojuliet malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel
AT alhamomoyasara malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel
AT fischerdavidd malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel
AT srivastavavishal malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel
AT kathayatdipak malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel
AT deblaisloic malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel
AT rajashekaragireesh malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel
AT saiflindaj malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel
AT vlasovaanastasian malnutritiondecreasesantibodysecretingcellnumbersinducedbyanoralattenuatedhumanrotavirusvaccineinahumaninfantfecalmicrobiotatransplantedgnotobioticpigmodel