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  • Natural Sciences  (2)
  • TD 7650  (2)
  • 1
    In: Annals of the New York Academy of Sciences, Wiley, Vol. 1465, No. 1 ( 2020-04), p. 89-98
    Abstract: The prevalence of maternal and child overweight/obesity and gestational hyperglycemia has increased greatly in China in recent years. However, studies examining the relationship between maternal hyperglycemia, maternal prepregnancy body mass index (ppBMI), and offspring obesity in China are limited. Here, we conducted a prospective study of 6684 mother−child pairs in Wuhan, China in 2012–2015. Maternal glucose concentrations were measured at approximately 24–28 weeks of gestation; children's weight and length were measured at birth and at 6, 12, and 24 months of age; and BMI‐for‐age Z‐scores (BMIZ) were calculated for different time points. We found that maternal fasting plasma glucose (FPG) concentrations were positively associated with offspring ponderal index and the risk of macrosomia at birth, but not with BMIZ or the risk of overweight/obesity at 6, 12, and 24 months of age. By contrast, maternal ppBMI was positively associated with both an increased risk of macrosomia at birth and overweight/obesity at 6, 12, and 24 months of age. Here, we observed an interaction effect of the association of FPG and ppBMI on offspring macrosomia and a mediating effect of gestational diabetes mellitus on the pathway between ppBMI and macrosomia. Our findings suggest that maternal ppBMI is a more pronounced predictor than gestational FPG concentrations in both the relation to BMIZ and the risk of overweight/obesity in early childhood.
    Type of Medium: Online Resource
    ISSN: 0077-8923 , 1749-6632
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2834079-6
    detail.hit.zdb_id: 211003-9
    detail.hit.zdb_id: 2071584-5
    SSG: 11
    Location Call Number Limitation Availability
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  • 2
    In: Annals of the New York Academy of Sciences, Wiley, Vol. 1465, No. 1 ( 2020-04), p. 146-160
    Abstract: Aeromonas veronii is an important aquatic zoonotic pathogen in humans and animals. In recent years, extracellular proteins from bacteria have been found to be the major pathogenic factors for aquatic animals. The aim of this study was to systematically analyze the extracellular proteins of nine sources of A. veronii and the effects of hisJ on virulence. We screened only the common proteins from nine different sources of A. veronii by liquid chromatography−tandem mass spectrometry and identified the gene hisJ . We then constructed Δ hisJ (deleted) and C‐ hisJ (complemented) variants of A. veronii TH0426 to assess the biological function of hisJ . While the Δ hisJ strain did not show altered growth ( P 〉 0.05), we observed that it had reduced colony formation and biofilm formation and reduced adhesion to and invasion of epithelioma papulosum cyprini cells by 2.0‐, 1.9‐, and 10.8‐fold, respectively. Additionally, infection experiments on zebrafish and mouse infection experiments showed that the virulence of the Δ hisJ strain was decreased by 865‐fold ( P 〈 0.001) compared with the wild‐type strain; virulence of the complemented C‐ hisJ strain was reduced only 2.8‐fold. Furthermore, in the context of hisJ deletion, flagella of A. veronii TH0426 were easily detached and the expression of virulence genes was downregulated. A persistence test (of bacterial colonies in crucian carp) showed that the number of bacteria in the immune organs of the Δ hisJ ‐infected group was lower than that in the wild‐type–infected group. Overall, these results show that hisJ affects flagellar shedding, virulence, biofilm formation, adhesion, and invasion of A. veronii TH0426, and that hisJ is closely associated with virulence and plays a crucial role in its pathogenicity of A. veronii TH0426.
    Type of Medium: Online Resource
    ISSN: 0077-8923 , 1749-6632
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2834079-6
    detail.hit.zdb_id: 211003-9
    detail.hit.zdb_id: 2071584-5
    SSG: 11
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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