<i>Porphyromonas gingivalis</i>Infection during Pregnancy Increases Maternal Tumor Necrosis Factor Alpha, Suppresses Maternal Interleukin-10, and Enhances Fetal Growth Restriction and Resorption in Mice
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- Dongming Lin
- Center for Oral and Systemic Diseases
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- Mary Alice Smith
- Center for Oral and Systemic Diseases
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- Catherine Champagne
- Center for Oral and Systemic Diseases
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- John Elter
- Comprehensive Center for Inflammatory Disorders, Department of Dental Ecology, School of Dentistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina
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- James Beck
- Center for Oral and Systemic Diseases
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- Steven Offenbacher
- Center for Oral and Systemic Diseases
書誌事項
- 公開日
- 2003-09
- 権利情報
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- https://journals.asm.org/non-commercial-tdm-license
- DOI
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- 10.1128/iai.71.9.5156-5162.2003
- 公開者
- American Society for Microbiology
この論文をさがす
説明
<jats:title>ABSTRACT</jats:title><jats:p>Epidemiological studies have shown a potential association between maternal periodontitis and pregnancy complications. We used a pregnant murine model to study the effect of infection with the periodontal pathogen<jats:italic>Porphyromonas gingivalis</jats:italic>on pregnancy outcomes. Female BALB/c mice were inoculated with heat-killed<jats:italic>P. gingivalis</jats:italic>(10<jats:sup>9</jats:sup>CFU) in a subcutaneous chamber and mated 2 weeks later. At gestation day (GD) 7.5, mice were challenged with live<jats:italic>P. gingivalis</jats:italic>(10<jats:sup>7</jats:sup>CFU) (<jats:italic>n</jats:italic>= 20) or broth (control;<jats:italic>n</jats:italic>= 8) and sacrificed at GD 16.5. Fetal growth restriction (FGR, <0.46 g) was defined as fetuses with weights 2 standard deviations (SD) smaller than controls (0.56 ± 0.05 g [mean ± SD]). Among the 20 challenged mice, 8 had both normal-weight (0.51 ± 0.11 g) and FGR (0.34 ± 0.1 g) fetuses within the same litter. All other challenged dams had normal-weight fetuses (0.57 ± 0.04 g). Maternal liver, uterus, and spleen samples were examined for<jats:italic>P. gingivalis</jats:italic>DNA using a PCR technique. Of the eight challenged mice with FGR fetuses, three had PCR signals for<jats:italic>P. gingivalis</jats:italic>in liver and uterus, but not in the spleen. Liver, uterus, and spleen were negative for<jats:italic>P. gingivalis</jats:italic>DNA among all other challenged and control mice. In serum of dams with FGR fetuses, tumor necrosis factor alpha levels were elevated significantly, while interluekin-10 levels were significantly reduced compared to levels in dams with normal fetuses.<jats:italic>P. gingivalis</jats:italic>-specific serum immunoglobulin G levels were significantly elevated in dams with FGR fetuses compared to dams without any FGR fetuses. These data demonstrate that<jats:italic>P. gingivalis</jats:italic>-induced murine FGR is associated with systemic dissemination of the organism and activated maternal immune and inflammatory responses.</jats:p>
収録刊行物
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- Infection and Immunity
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Infection and Immunity 71 (9), 5156-5162, 2003-09
American Society for Microbiology
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詳細情報 詳細情報について
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- CRID
- 1361137044877834752
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- NII論文ID
- 30020831404
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- NII書誌ID
- AA00673732
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- ISSN
- 10985522
- 00199567
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- データソース種別
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- Crossref
- CiNii Articles

