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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Association for Laboratory Animal Science
2015
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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. |
format | Online Article Text |
id | pubmed-4637374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Japanese Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
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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