Helicobacter sp. MIT 01-6451 infection during fetal and
neonatal life in laboratory mice |
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Authors: | Hitoki Yamanaka Tai Nakanishi Toshikazu Takagi Makiko Ohsawa Noriaki Kubo Naoto Yamamoto Takahira Takemoto Kazutaka Ohsawa |
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Affiliation: | 1)Division of Comparative Medicine, Center for Frontier Life Sciences, Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan;2)Quality Control Department, Bio Technical Center, Japan SLC, Inc., 3-5-1 Aoihigashi, Naka, Hamamatsu, Shizuoka 433-8114, Japan |
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Abstract: | Helicobacter sp. MIT 01-6451 has been detected in SPF mice kept inJapan. To characterize strain MIT 01-6451, its infection route during fetal and neonatallife and effects on pregnancy were investigated using immunocompetent and immunodeficientmouse 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 negativein immunocompetent mice. No fetal infections with MIT 01-6451 were detected at 16–18 daysafter pregnancy in any mouse strain. In newborn mice, MIT 01-6451 was detected inintestinal tissue of C57BL/6 and SCID mice at 9–11 days after birth, but not in BALB/cmice. The IgA and IgG titers to MIT 01-6451 in sera of C57BL/6 female mice weresignificantly lower than those of BALB/c mice. Although no significant differences in thenumber of newborns per litter were observed between MIT 01-6451-infected and MIT01-6451-free dams, the birth rate was lower in infected SCID mice than in control SCIDmice. The present results indicated that MIT 01-6451 infects newborn mice after birthrather than by vertical transmission to the fetus via the placenta and that MIT 01-6451infection shows opportunistically negative effects on the birth rate. In addition, thematernal immune response may affect infection of newborn mice with MIT 01-6451 throughbreast milk. |
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Keywords: | Helicobacter sp. MIT 01-6451 laboratory mice reproductive organ vertical transmission |
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