Perinatal risk factors for fecal antibiotic resistance gene patterns in pregnant women and their infants

被引:19
作者
Sosa-Moreno, Andrea [1 ,6 ]
Comstock, Sarah S. [2 ]
Sugino, Kameron Y. [2 ]
Ma, Teng F. [1 ]
Paneth, Nigel [1 ]
Davis, Yelena [3 ,4 ]
Olivero, Rosemary [4 ,5 ]
Schein, Rebecca [5 ]
Maurer, Joel [3 ]
Zhang, Lixin [1 ]
机构
[1] Michigan State Univ, Dept Epidemiol & Biostat, E Lansing, MI 48824 USA
[2] Michigan State Univ, Dept Food Sci & Human Nutr, E Lansing, MI 48824 USA
[3] Michigan State Univ, Coll Human Med, Dept Obstet Gynecol & Reprod Biol, E Lansing, MI 48824 USA
[4] Helen DeVos Childrens Hosp Spectrum Hlth, Grand Rapids, MI USA
[5] Michigan State Univ, Coll Human Med, Dept Pediat & Human Dev, E Lansing, MI 48824 USA
[6] Univ Michigan, Sch Publ Hlth, Dept Epidemiol, Ann Arbor, MI 48109 USA
来源
PLOS ONE | 2020年 / 15卷 / 06期
基金
美国国家卫生研究院;
关键词
INTESTINAL MICROBIOTA; GUT MICROBIOME; 1ST YEAR; RESISTOME; PREVALENCE; DIVERSITY;
D O I
10.1371/journal.pone.0234751
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Perinatal factors can shape fecal microbiome patterns among pregnant women and their infants. However, there is scarce information about the effect of maternal demographics and perinatal exposures on antibiotic resistance genes (ARG) and mobile genetic element (MGE) patterns in pregnant women and infants. We examined fecal samples from pregnant women during their third trimester of pregnancy (n = 51) and 6-month-old infants (n = 40). Of the 91 participants, 72 represented 36 maternal-infant dyads, 15 were additional pregnant women, and 4 were additional infants. We assessed the effects of demographics, pre-pregnancy BMI, smoking and parity in the pregnancy resistome and the effects of demographics, delivery mode, feeding habits and prenatal antibiotic treatment on the infancy resistome. ARG and MGE richness and abundance were assessed using a SmartChip qPCR-array. Alpha diversity (Shannon and Inverse Simpson index) and beta diversity (Sorensen and Bray-Curtis index) were calculated. The Wilcoxon and the Kruskal non-parametric test were used for comparisons. There is a high variability in shared resistome patterns between pregnant women and their infants. An average of 29% of ARG and 24% of MGE were shared within dyads. Infants had significantly greater abundance and higher diversity of ARG and MGE compared to pregnant women. Pregnancy and infancy samples differed in ARG and MGE gene composition and structure. Composition of the fecal resistome was significantly associated with race in pregnant women, with non-white women having different patterns than white women, and, in infants, with extent of solid food consumption. Our data showed that the pregnancy and infancy resistome had different structure and composition patterns, with maternal race and infant solid food consumption as possible contributors to ARG. By characterizing resistome patterns, our results can inform the mechanism of antibiotic resistome development in pregnant women and their infants.
引用
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页数:21
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