Humanized HLA-DR4 mice fed with the protozoan pathogen of oysters Perkinsus marinus (Dermo) do not develop noticeable pathology but elicit systemic immunity.

Perkinsus marinus (Phylum Perkinsozoa) is a marine protozoan parasite responsible for "Dermo" disease in oysters, which has caused extensive damage to the shellfish industry and estuarine environment. The infection prevalence has been estimated in some areas to be as high as 100%, often ca...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Wathsala Wijayalath, Sai Majji, Yuliya Kleschenko, Luis Pow-Sang, Teodor D Brumeanu, Eileen Franke Villasante, Gerardo R Vasta, José-Antonio Fernández-Robledo, Sofia Casares
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2014
Materias:
R
Q
Acceso en línea:https://doaj.org/article/04458b139a4e44bd892b68423ac8193c
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:04458b139a4e44bd892b68423ac8193c
record_format dspace
spelling oai:doaj.org-article:04458b139a4e44bd892b68423ac8193c2021-11-18T08:34:33ZHumanized HLA-DR4 mice fed with the protozoan pathogen of oysters Perkinsus marinus (Dermo) do not develop noticeable pathology but elicit systemic immunity.1932-620310.1371/journal.pone.0087435https://doaj.org/article/04458b139a4e44bd892b68423ac8193c2014-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24498105/?tool=EBIhttps://doaj.org/toc/1932-6203Perkinsus marinus (Phylum Perkinsozoa) is a marine protozoan parasite responsible for "Dermo" disease in oysters, which has caused extensive damage to the shellfish industry and estuarine environment. The infection prevalence has been estimated in some areas to be as high as 100%, often causing death of infected oysters within 1-2 years post-infection. Human consumption of the parasites via infected oysters is thus likely to occur, but to our knowledge the effect of oral consumption of P. marinus has not been investigated in humans or other mammals. To address the question we used humanized mice expressing HLA-DR4 molecules and lacking expression of mouse MHC-class II molecules (DR4.EA(0)) in such a way that CD4 T cell responses are solely restricted by the human HLA-DR4 molecule. The DR4.EA(0) mice did not develop diarrhea or any detectable pathology in the gastrointestinal tract or lungs following single or repeated feedings with live P. marinus parasites. Furthermore, lymphocyte populations in the gut associated lymphoid tissue and spleen were unaltered in the parasite-fed mice ruling out local or systemic inflammation. Notably, naïve DR4.EA(0) mice had antibodies (IgM and IgG) reacting against P. marinus parasites whereas parasite specific T cell responses were undetectable. Feeding with P. marinus boosted the antibody responses and stimulated specific cellular (IFNγ) immunity to the oyster parasite. Our data indicate the ability of P. marinus parasites to induce systemic immunity in DR4.EA(0) mice without causing noticeable pathology, and support rationale grounds for using genetically engineered P. marinus as a new oral vaccine platform to induce systemic immunity against infectious agents.Wathsala WijayalathSai MajjiYuliya KleschenkoLuis Pow-SangTeodor D BrumeanuEileen Franke VillasanteGerardo R VastaJosé-Antonio Fernández-RobledoSofia CasaresPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 1, p e87435 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Wathsala Wijayalath
Sai Majji
Yuliya Kleschenko
Luis Pow-Sang
Teodor D Brumeanu
Eileen Franke Villasante
Gerardo R Vasta
José-Antonio Fernández-Robledo
Sofia Casares
Humanized HLA-DR4 mice fed with the protozoan pathogen of oysters Perkinsus marinus (Dermo) do not develop noticeable pathology but elicit systemic immunity.
description Perkinsus marinus (Phylum Perkinsozoa) is a marine protozoan parasite responsible for "Dermo" disease in oysters, which has caused extensive damage to the shellfish industry and estuarine environment. The infection prevalence has been estimated in some areas to be as high as 100%, often causing death of infected oysters within 1-2 years post-infection. Human consumption of the parasites via infected oysters is thus likely to occur, but to our knowledge the effect of oral consumption of P. marinus has not been investigated in humans or other mammals. To address the question we used humanized mice expressing HLA-DR4 molecules and lacking expression of mouse MHC-class II molecules (DR4.EA(0)) in such a way that CD4 T cell responses are solely restricted by the human HLA-DR4 molecule. The DR4.EA(0) mice did not develop diarrhea or any detectable pathology in the gastrointestinal tract or lungs following single or repeated feedings with live P. marinus parasites. Furthermore, lymphocyte populations in the gut associated lymphoid tissue and spleen were unaltered in the parasite-fed mice ruling out local or systemic inflammation. Notably, naïve DR4.EA(0) mice had antibodies (IgM and IgG) reacting against P. marinus parasites whereas parasite specific T cell responses were undetectable. Feeding with P. marinus boosted the antibody responses and stimulated specific cellular (IFNγ) immunity to the oyster parasite. Our data indicate the ability of P. marinus parasites to induce systemic immunity in DR4.EA(0) mice without causing noticeable pathology, and support rationale grounds for using genetically engineered P. marinus as a new oral vaccine platform to induce systemic immunity against infectious agents.
format article
author Wathsala Wijayalath
Sai Majji
Yuliya Kleschenko
Luis Pow-Sang
Teodor D Brumeanu
Eileen Franke Villasante
Gerardo R Vasta
José-Antonio Fernández-Robledo
Sofia Casares
author_facet Wathsala Wijayalath
Sai Majji
Yuliya Kleschenko
Luis Pow-Sang
Teodor D Brumeanu
Eileen Franke Villasante
Gerardo R Vasta
José-Antonio Fernández-Robledo
Sofia Casares
author_sort Wathsala Wijayalath
title Humanized HLA-DR4 mice fed with the protozoan pathogen of oysters Perkinsus marinus (Dermo) do not develop noticeable pathology but elicit systemic immunity.
title_short Humanized HLA-DR4 mice fed with the protozoan pathogen of oysters Perkinsus marinus (Dermo) do not develop noticeable pathology but elicit systemic immunity.
title_full Humanized HLA-DR4 mice fed with the protozoan pathogen of oysters Perkinsus marinus (Dermo) do not develop noticeable pathology but elicit systemic immunity.
title_fullStr Humanized HLA-DR4 mice fed with the protozoan pathogen of oysters Perkinsus marinus (Dermo) do not develop noticeable pathology but elicit systemic immunity.
title_full_unstemmed Humanized HLA-DR4 mice fed with the protozoan pathogen of oysters Perkinsus marinus (Dermo) do not develop noticeable pathology but elicit systemic immunity.
title_sort humanized hla-dr4 mice fed with the protozoan pathogen of oysters perkinsus marinus (dermo) do not develop noticeable pathology but elicit systemic immunity.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/04458b139a4e44bd892b68423ac8193c
work_keys_str_mv AT wathsalawijayalath humanizedhladr4micefedwiththeprotozoanpathogenofoystersperkinsusmarinusdermodonotdevelopnoticeablepathologybutelicitsystemicimmunity
AT saimajji humanizedhladr4micefedwiththeprotozoanpathogenofoystersperkinsusmarinusdermodonotdevelopnoticeablepathologybutelicitsystemicimmunity
AT yuliyakleschenko humanizedhladr4micefedwiththeprotozoanpathogenofoystersperkinsusmarinusdermodonotdevelopnoticeablepathologybutelicitsystemicimmunity
AT luispowsang humanizedhladr4micefedwiththeprotozoanpathogenofoystersperkinsusmarinusdermodonotdevelopnoticeablepathologybutelicitsystemicimmunity
AT teodordbrumeanu humanizedhladr4micefedwiththeprotozoanpathogenofoystersperkinsusmarinusdermodonotdevelopnoticeablepathologybutelicitsystemicimmunity
AT eileenfrankevillasante humanizedhladr4micefedwiththeprotozoanpathogenofoystersperkinsusmarinusdermodonotdevelopnoticeablepathologybutelicitsystemicimmunity
AT gerardorvasta humanizedhladr4micefedwiththeprotozoanpathogenofoystersperkinsusmarinusdermodonotdevelopnoticeablepathologybutelicitsystemicimmunity
AT joseantoniofernandezrobledo humanizedhladr4micefedwiththeprotozoanpathogenofoystersperkinsusmarinusdermodonotdevelopnoticeablepathologybutelicitsystemicimmunity
AT sofiacasares humanizedhladr4micefedwiththeprotozoanpathogenofoystersperkinsusmarinusdermodonotdevelopnoticeablepathologybutelicitsystemicimmunity
_version_ 1718421602073313280