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A New Gnotobiotic Pig Model of P[6] Human Rotavirus Infection and Disease for Preclinical Evaluation of Rotavirus Vaccines

Human rotavirus (HRV) is a leading cause of gastroenteritis in children under 5 years of age. Licensed vaccines containing G1P[8] and G1-4P[8] strains are less efficacious against newly emerging P[6] strains, indicating an urgent need for better cross protective vaccines. Here, we report our develop...

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Autores principales: Nyblade, Charlotte, Hensley, Casey, Parreño, Viviana, Zhou, Peng, Frazier, Maggie, Frazier, Annie, Ramesh, Ashwin, Lei, Shaohua, Degiuseppe, Juan Ignacio, Tan, Ming, Yuan, Lijuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9784283/
https://www.ncbi.nlm.nih.gov/pubmed/36560807
http://dx.doi.org/10.3390/v14122803
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author Nyblade, Charlotte
Hensley, Casey
Parreño, Viviana
Zhou, Peng
Frazier, Maggie
Frazier, Annie
Ramesh, Ashwin
Lei, Shaohua
Degiuseppe, Juan Ignacio
Tan, Ming
Yuan, Lijuan
author_facet Nyblade, Charlotte
Hensley, Casey
Parreño, Viviana
Zhou, Peng
Frazier, Maggie
Frazier, Annie
Ramesh, Ashwin
Lei, Shaohua
Degiuseppe, Juan Ignacio
Tan, Ming
Yuan, Lijuan
author_sort Nyblade, Charlotte
collection PubMed
description Human rotavirus (HRV) is a leading cause of gastroenteritis in children under 5 years of age. Licensed vaccines containing G1P[8] and G1-4P[8] strains are less efficacious against newly emerging P[6] strains, indicating an urgent need for better cross protective vaccines. Here, we report our development of a new gnotobiotic (Gn) pig model of P[6] HRV infection and disease as a tool for evaluating potential vaccine candidates. The Arg HRV (G4P[6]) strain was derived from a diarrheic human infant stool sample and determined to be free of other viruses by metagenomic sequencing. Neonatal Gn pigs were orally inoculated with the stool suspension containing 5.6 × 10(5) fluorescent focus units (FFU) of the virus. Small and large intestinal contents were collected at post inoculation day 2 or 3. The virus was passaged 6 times in neonatal Gn pigs to generate a large inoculum pool. Next, 33–34 day old Gn pigs were orally inoculated with 10(−2), 10(3), 10(4), and 10(5) FFU of Arg HRV to determine the optimal challenge dose. All pigs developed clinical signs of infection, regardless of the inoculum dose. The optimal challenge dose was determined to be 10(5) FFU. This new Gn pig model is ready to be used to assess the protective efficacy of candidate monovalent and multivalent vaccines against P[6] HRV.
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spelling pubmed-97842832022-12-24 A New Gnotobiotic Pig Model of P[6] Human Rotavirus Infection and Disease for Preclinical Evaluation of Rotavirus Vaccines Nyblade, Charlotte Hensley, Casey Parreño, Viviana Zhou, Peng Frazier, Maggie Frazier, Annie Ramesh, Ashwin Lei, Shaohua Degiuseppe, Juan Ignacio Tan, Ming Yuan, Lijuan Viruses Brief Report Human rotavirus (HRV) is a leading cause of gastroenteritis in children under 5 years of age. Licensed vaccines containing G1P[8] and G1-4P[8] strains are less efficacious against newly emerging P[6] strains, indicating an urgent need for better cross protective vaccines. Here, we report our development of a new gnotobiotic (Gn) pig model of P[6] HRV infection and disease as a tool for evaluating potential vaccine candidates. The Arg HRV (G4P[6]) strain was derived from a diarrheic human infant stool sample and determined to be free of other viruses by metagenomic sequencing. Neonatal Gn pigs were orally inoculated with the stool suspension containing 5.6 × 10(5) fluorescent focus units (FFU) of the virus. Small and large intestinal contents were collected at post inoculation day 2 or 3. The virus was passaged 6 times in neonatal Gn pigs to generate a large inoculum pool. Next, 33–34 day old Gn pigs were orally inoculated with 10(−2), 10(3), 10(4), and 10(5) FFU of Arg HRV to determine the optimal challenge dose. All pigs developed clinical signs of infection, regardless of the inoculum dose. The optimal challenge dose was determined to be 10(5) FFU. This new Gn pig model is ready to be used to assess the protective efficacy of candidate monovalent and multivalent vaccines against P[6] HRV. MDPI 2022-12-15 /pmc/articles/PMC9784283/ /pubmed/36560807 http://dx.doi.org/10.3390/v14122803 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Nyblade, Charlotte
Hensley, Casey
Parreño, Viviana
Zhou, Peng
Frazier, Maggie
Frazier, Annie
Ramesh, Ashwin
Lei, Shaohua
Degiuseppe, Juan Ignacio
Tan, Ming
Yuan, Lijuan
A New Gnotobiotic Pig Model of P[6] Human Rotavirus Infection and Disease for Preclinical Evaluation of Rotavirus Vaccines
title A New Gnotobiotic Pig Model of P[6] Human Rotavirus Infection and Disease for Preclinical Evaluation of Rotavirus Vaccines
title_full A New Gnotobiotic Pig Model of P[6] Human Rotavirus Infection and Disease for Preclinical Evaluation of Rotavirus Vaccines
title_fullStr A New Gnotobiotic Pig Model of P[6] Human Rotavirus Infection and Disease for Preclinical Evaluation of Rotavirus Vaccines
title_full_unstemmed A New Gnotobiotic Pig Model of P[6] Human Rotavirus Infection and Disease for Preclinical Evaluation of Rotavirus Vaccines
title_short A New Gnotobiotic Pig Model of P[6] Human Rotavirus Infection and Disease for Preclinical Evaluation of Rotavirus Vaccines
title_sort new gnotobiotic pig model of p[6] human rotavirus infection and disease for preclinical evaluation of rotavirus vaccines
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9784283/
https://www.ncbi.nlm.nih.gov/pubmed/36560807
http://dx.doi.org/10.3390/v14122803
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