Cargando…

Voluntary Wheel Running Does Not Alter Mortality to or Immunogenicity of Vaccinia Virus in Mice: A Pilot Study

Exercise has been shown to improve immune responses to viral infections and vaccines in several mouse models. However, previous pathogen studies have primarily used infections limited to the respiratory tract. Additionally, previous studies have utilized forced treadmill exercise paradigms, and volu...

Descripción completa

Detalles Bibliográficos
Autores principales: Pence, Brandt D., Ryerson, Melissa R., Bravo Cruz, Ariana G., Woods, Jeffrey A., Shisler, Joanna L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760534/
https://www.ncbi.nlm.nih.gov/pubmed/29354074
http://dx.doi.org/10.3389/fphys.2017.01123
_version_ 1783291375352020992
author Pence, Brandt D.
Ryerson, Melissa R.
Bravo Cruz, Ariana G.
Woods, Jeffrey A.
Shisler, Joanna L.
author_facet Pence, Brandt D.
Ryerson, Melissa R.
Bravo Cruz, Ariana G.
Woods, Jeffrey A.
Shisler, Joanna L.
author_sort Pence, Brandt D.
collection PubMed
description Exercise has been shown to improve immune responses to viral infections and vaccines in several mouse models. However, previous pathogen studies have primarily used infections limited to the respiratory tract. Additionally, previous studies have utilized forced treadmill exercise paradigms, and voluntary wheel running (VWR) has been shown to have differential effects on the immune system in non-infection models. We examined whether VWR could improve morbidity and mortality to a 50% lethal dose of vaccinia virus (VACV), a systemic pathogen commonly used to examine immune responses. Additionally, we examined whether VWR could improve antibody response to a replication-deficient strain of VACV, mimicking a vaccination. Male C57Bl/6J mice underwent 8 weeks of VWR or remained sedentary, then were infected intranasally with 10(5) PFU VACV strain WR and followed 14 days for weight loss. Mice in the vaccination study ran or were sedentary for 8 weeks, then were given 10(6) PFU of replication-deficient VACV strain MVA intraperitoneally. Blood was collected at 1, 2, and 4 weeks post-inoculation, and anti-VACV IgG titer was determined by ELISA. VWR did not improve mortality due to VACV infection (p = 0.26), although fewer VWR mice (4/10) died compared to sedentary (SED, 6/10). VWR did not prevent body weight loss due to infection compared to SED (p = 0.20), although VWR mice loss slightly less weight compared to SED through the first 6 days post-infection. Food intake was significantly reduced in SED post-infection compared to VWR (p = 0.05). VWR mice developed a greater IgG antibody response, although this was not significant (p = 0.22). In summary, VWR did not protect against mortality to VACV or prevent infection-induced weight loss, and VWR did not enhance antibody responses. However, there were non-significant trends toward VWR-related improvements in these outcomes, and post-infection food intake was improved by VWR.
format Online
Article
Text
id pubmed-5760534
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-57605342018-01-19 Voluntary Wheel Running Does Not Alter Mortality to or Immunogenicity of Vaccinia Virus in Mice: A Pilot Study Pence, Brandt D. Ryerson, Melissa R. Bravo Cruz, Ariana G. Woods, Jeffrey A. Shisler, Joanna L. Front Physiol Physiology Exercise has been shown to improve immune responses to viral infections and vaccines in several mouse models. However, previous pathogen studies have primarily used infections limited to the respiratory tract. Additionally, previous studies have utilized forced treadmill exercise paradigms, and voluntary wheel running (VWR) has been shown to have differential effects on the immune system in non-infection models. We examined whether VWR could improve morbidity and mortality to a 50% lethal dose of vaccinia virus (VACV), a systemic pathogen commonly used to examine immune responses. Additionally, we examined whether VWR could improve antibody response to a replication-deficient strain of VACV, mimicking a vaccination. Male C57Bl/6J mice underwent 8 weeks of VWR or remained sedentary, then were infected intranasally with 10(5) PFU VACV strain WR and followed 14 days for weight loss. Mice in the vaccination study ran or were sedentary for 8 weeks, then were given 10(6) PFU of replication-deficient VACV strain MVA intraperitoneally. Blood was collected at 1, 2, and 4 weeks post-inoculation, and anti-VACV IgG titer was determined by ELISA. VWR did not improve mortality due to VACV infection (p = 0.26), although fewer VWR mice (4/10) died compared to sedentary (SED, 6/10). VWR did not prevent body weight loss due to infection compared to SED (p = 0.20), although VWR mice loss slightly less weight compared to SED through the first 6 days post-infection. Food intake was significantly reduced in SED post-infection compared to VWR (p = 0.05). VWR mice developed a greater IgG antibody response, although this was not significant (p = 0.22). In summary, VWR did not protect against mortality to VACV or prevent infection-induced weight loss, and VWR did not enhance antibody responses. However, there were non-significant trends toward VWR-related improvements in these outcomes, and post-infection food intake was improved by VWR. Frontiers Media S.A. 2018-01-05 /pmc/articles/PMC5760534/ /pubmed/29354074 http://dx.doi.org/10.3389/fphys.2017.01123 Text en Copyright © 2018 Pence, Ryerson, Bravo Cruz, Woods and Shisler. 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) or licensor 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 Physiology
Pence, Brandt D.
Ryerson, Melissa R.
Bravo Cruz, Ariana G.
Woods, Jeffrey A.
Shisler, Joanna L.
Voluntary Wheel Running Does Not Alter Mortality to or Immunogenicity of Vaccinia Virus in Mice: A Pilot Study
title Voluntary Wheel Running Does Not Alter Mortality to or Immunogenicity of Vaccinia Virus in Mice: A Pilot Study
title_full Voluntary Wheel Running Does Not Alter Mortality to or Immunogenicity of Vaccinia Virus in Mice: A Pilot Study
title_fullStr Voluntary Wheel Running Does Not Alter Mortality to or Immunogenicity of Vaccinia Virus in Mice: A Pilot Study
title_full_unstemmed Voluntary Wheel Running Does Not Alter Mortality to or Immunogenicity of Vaccinia Virus in Mice: A Pilot Study
title_short Voluntary Wheel Running Does Not Alter Mortality to or Immunogenicity of Vaccinia Virus in Mice: A Pilot Study
title_sort voluntary wheel running does not alter mortality to or immunogenicity of vaccinia virus in mice: a pilot study
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760534/
https://www.ncbi.nlm.nih.gov/pubmed/29354074
http://dx.doi.org/10.3389/fphys.2017.01123
work_keys_str_mv AT pencebrandtd voluntarywheelrunningdoesnotaltermortalitytoorimmunogenicityofvacciniavirusinmiceapilotstudy
AT ryersonmelissar voluntarywheelrunningdoesnotaltermortalitytoorimmunogenicityofvacciniavirusinmiceapilotstudy
AT bravocruzarianag voluntarywheelrunningdoesnotaltermortalitytoorimmunogenicityofvacciniavirusinmiceapilotstudy
AT woodsjeffreya voluntarywheelrunningdoesnotaltermortalitytoorimmunogenicityofvacciniavirusinmiceapilotstudy
AT shislerjoannal voluntarywheelrunningdoesnotaltermortalitytoorimmunogenicityofvacciniavirusinmiceapilotstudy