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Helicobacter sp. MIT 01-6451 infection during fetal and neonatal life in laboratory mice

Helicobacter sp. MIT 01-6451 has been detected in SPF mice kept in Japan. To characterize strain MIT 01-6451, its infection route during fetal and neonatal life and effects on pregnancy were investigated using immunocompetent and immunodeficient mouse strains (BALB/c, C57BL/6, and SCID). MIT 01-6451...

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Autores principales: Yamanaka, Hitoki, Nakanishi, Tai, Takagi, Toshikazu, Ohsawa, Makiko, Kubo, Noriaki, Yamamoto, Naoto, Takemoto, Takahira, Ohsawa, Kazutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Association for Laboratory Animal Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637374/
https://www.ncbi.nlm.nih.gov/pubmed/26134357
http://dx.doi.org/10.1538/expanim.15-0034
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author Yamanaka, Hitoki
Nakanishi, Tai
Takagi, Toshikazu
Ohsawa, Makiko
Kubo, Noriaki
Yamamoto, Naoto
Takemoto, Takahira
Ohsawa, Kazutaka
author_facet Yamanaka, Hitoki
Nakanishi, Tai
Takagi, Toshikazu
Ohsawa, Makiko
Kubo, Noriaki
Yamamoto, Naoto
Takemoto, Takahira
Ohsawa, Kazutaka
author_sort Yamanaka, Hitoki
collection PubMed
description Helicobacter sp. MIT 01-6451 has been detected in SPF mice kept in Japan. To characterize strain MIT 01-6451, its infection route during fetal and neonatal life and effects on pregnancy were investigated using immunocompetent and immunodeficient mouse strains (BALB/c, C57BL/6, and SCID). MIT 01-6451 was detected in the uterus, vagina, and mammary glands of 50% of infected SCID mice, whereas these tissues were all negative in immunocompetent mice. No fetal infections with MIT 01-6451 were detected at 16–18 days after pregnancy in any mouse strain. In newborn mice, MIT 01-6451 was detected in intestinal tissue of C57BL/6 and SCID mice at 9–11 days after birth, but not in BALB/c mice. The IgA and IgG titers to MIT 01-6451 in sera of C57BL/6 female mice were significantly lower than those of BALB/c mice. Although no significant differences in the number of newborns per litter were observed between MIT 01-6451-infected and MIT 01-6451-free dams, the birth rate was lower in infected SCID mice than in control SCID mice. The present results indicated that MIT 01-6451 infects newborn mice after birth rather than by vertical transmission to the fetus via the placenta and that MIT 01-6451 infection shows opportunistically negative effects on the birth rate. In addition, the maternal immune response may affect infection of newborn mice with MIT 01-6451 through breast milk.
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spelling pubmed-46373742015-11-09 Helicobacter sp. MIT 01-6451 infection during fetal and neonatal life in laboratory mice Yamanaka, Hitoki Nakanishi, Tai Takagi, Toshikazu Ohsawa, Makiko Kubo, Noriaki Yamamoto, Naoto Takemoto, Takahira Ohsawa, Kazutaka Exp Anim Original Helicobacter sp. MIT 01-6451 has been detected in SPF mice kept in Japan. To characterize strain MIT 01-6451, its infection route during fetal and neonatal life and effects on pregnancy were investigated using immunocompetent and immunodeficient mouse strains (BALB/c, C57BL/6, and SCID). MIT 01-6451 was detected in the uterus, vagina, and mammary glands of 50% of infected SCID mice, whereas these tissues were all negative in immunocompetent mice. No fetal infections with MIT 01-6451 were detected at 16–18 days after pregnancy in any mouse strain. In newborn mice, MIT 01-6451 was detected in intestinal tissue of C57BL/6 and SCID mice at 9–11 days after birth, but not in BALB/c mice. The IgA and IgG titers to MIT 01-6451 in sera of C57BL/6 female mice were significantly lower than those of BALB/c mice. Although no significant differences in the number of newborns per litter were observed between MIT 01-6451-infected and MIT 01-6451-free dams, the birth rate was lower in infected SCID mice than in control SCID mice. The present results indicated that MIT 01-6451 infects newborn mice after birth rather than by vertical transmission to the fetus via the placenta and that MIT 01-6451 infection shows opportunistically negative effects on the birth rate. In addition, the maternal immune response may affect infection of newborn mice with MIT 01-6451 through breast milk. Japanese Association for Laboratory Animal Science 2015-07-02 2015 /pmc/articles/PMC4637374/ /pubmed/26134357 http://dx.doi.org/10.1538/expanim.15-0034 Text en ©2015 Japanese Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Original
Yamanaka, Hitoki
Nakanishi, Tai
Takagi, Toshikazu
Ohsawa, Makiko
Kubo, Noriaki
Yamamoto, Naoto
Takemoto, Takahira
Ohsawa, Kazutaka
Helicobacter sp. MIT 01-6451 infection during fetal and neonatal life in laboratory mice
title Helicobacter sp. MIT 01-6451 infection during fetal and neonatal life in laboratory mice
title_full Helicobacter sp. MIT 01-6451 infection during fetal and neonatal life in laboratory mice
title_fullStr Helicobacter sp. MIT 01-6451 infection during fetal and neonatal life in laboratory mice
title_full_unstemmed Helicobacter sp. MIT 01-6451 infection during fetal and neonatal life in laboratory mice
title_short Helicobacter sp. MIT 01-6451 infection during fetal and neonatal life in laboratory mice
title_sort helicobacter sp. mit 01-6451 infection during fetal and neonatal life in laboratory mice
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637374/
https://www.ncbi.nlm.nih.gov/pubmed/26134357
http://dx.doi.org/10.1538/expanim.15-0034
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