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

Hitoki Yamanaka1, Tai Nakanishi, Toshikazu Takagi

  • 1Division of Comparative Medicine, Center for Frontier Life Sciences, Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan.

Insights

Helicobacter sp. MIT 01-6451 primarily infects newborn mice post-birth, not fetally. This infection can negatively impact birth rates, particularly in immunodeficient mice, suggesting maternal immunity plays a role.

Area of Science:

  • Microbiology
  • Immunology
  • Animal Health

Background:

  • Helicobacter sp. MIT 01-6451 has been identified in specific pathogen-free (SPF) mice in Japan.
  • Understanding the transmission routes and effects of this bacterium is crucial for animal health research.

Purpose of the Study:

  • To characterize Helicobacter sp. MIT 01-6451 infection.
  • To investigate its transmission route during fetal and neonatal stages.
  • To determine its impact on pregnancy and birth rate in different mouse models.

Main Methods:

  • Infection experiments were conducted using immunocompetent (BALB/c, C57BL/6) and immunodeficient (SCID) mouse strains.
  • Maternal and neonatal tissues were analyzed for bacterial presence.
  • Pregnancy outcomes, including fetal infection and birth rates, were assessed.
  • Serum antibody titers (IgA and IgG) were measured.

Main Results:

  • Helicobacter sp. MIT 01-6451 was detected in reproductive tissues of SCID mice but not immunocompetent mice.
  • No evidence of fetal infection was found.
  • Neonatal intestinal infection occurred in C57BL/6 and SCID mice, but not BALB/c mice.
  • Lower antibody titers were observed in C57BL/6 mice compared to BALB/c mice.
  • A reduced birth rate was noted in infected SCID mice.

Conclusions:

  • Helicobacter sp. MIT 01-6451 transmission occurs postnatally, not vertically via the placenta.
  • Infection can negatively affect birth rates, especially in immunodeficient hosts.
  • Maternal immune status and potential transmission through breast milk may influence neonatal infection susceptibility.

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