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子宫内及哺乳期暴露于抗逆转录病毒疗法对老年大鼠后代肠道微生物组成及代谢功能的影响。

Effect of in utero and lactational exposure to antiretroviral therapy on the gut microbial composition and metabolic function in aged rat offspring.

作者信息

Muthumula Chandra Mohan Reddy, Yanamadala Yaswanthi, Gokulan Kuppan, Karn Kumari, Cunny Helen, Sutherland Vicki, Santos Janine H, Khare Sangeeta

机构信息

Division of Microbiology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, United States.

Division of Translational Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, NC, United States.

出版信息

Exp Biol Med (Maywood). 2025 May 21;250:10468. doi: 10.3389/ebm.2025.10468. eCollection 2025.

DOI:10.3389/ebm.2025.10468
PMID:40469771
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12135209/
Abstract

Despite the highly effective impact of antiretroviral therapy (ART) in reducing mother-to-child transmission of human immunodeficiency virus (HIV), there are concerns of long-term impacts of ART on the health of the offspring. The implications of perinatal exposure to antiviral drugs on the gut bacterial population and metabolic function in the offspring is unclear but may influence health outcomes given the various reported effects of the microbiome in human health. This study aims to gain insight into the potential effect of and lactational exposure to ART on gut microbiota populations and short-chain fatty acids (SCFAs) production in aged rat offspring. Pregnant rats were administered a combination of antiretroviral drugs (abacavir/dolutegravir/lamivudine) at two different dose levels during gestation and throughout lactation, and the fecal bacterial abundance and SCFA levels of the offspring were analyzed when they reached 12 months of age. Our results showed dose-dependent and sex-based differences in fecal microbial abundance at various taxonomic levels. Specifically, we found a decline in in males, and an increase in among males and females. Furthermore, a sex-specific distribution reorganization of , , and was identified. No significant difference in the concentration of prominent SCFAs and IgA levels were identified. These findings provide preliminary information indicating the need to evaluate perinatal effects of ART more comprehensively on the gut bacterial and metabolic function in future studies, and their potential role in offspring health outcomes.

摘要

尽管抗逆转录病毒疗法(ART)在降低人类免疫缺陷病毒(HIV)母婴传播方面具有高效作用,但人们仍担心ART对后代健康的长期影响。围产期接触抗病毒药物对后代肠道细菌群落和代谢功能的影响尚不清楚,但鉴于微生物群对人类健康的各种报道影响,可能会影响健康结果。本研究旨在深入了解孕期和哺乳期接触ART对老年大鼠后代肠道微生物群数量和短链脂肪酸(SCFAs)产生的潜在影响。在妊娠期间和整个哺乳期,给怀孕大鼠施用两种不同剂量水平的抗逆转录病毒药物组合(阿巴卡韦/多替拉韦/拉米夫定),并在后代达到12个月大时分析其粪便细菌丰度和SCFA水平。我们的结果显示,在不同分类水平上,粪便微生物丰度存在剂量依赖性和基于性别的差异。具体而言,我们发现雄性大鼠中[某种细菌名称]减少,而雄性和雌性大鼠中[另一种细菌名称]增加。此外,还发现了[其他几种细菌名称]的性别特异性分布重组。未发现显著SCFAs浓度和IgA水平存在差异。这些发现提供了初步信息,表明在未来研究中需要更全面地评估ART对肠道细菌和代谢功能的围产期影响,以及它们在后代健康结果中的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/c0124e8f4e5d/ebm-250-10468-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/a30dd61d24d2/ebm-250-10468-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/74faaa9e6dfb/ebm-250-10468-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/9c26697db84e/ebm-250-10468-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/709423eff716/ebm-250-10468-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/1fa4b81e41f8/ebm-250-10468-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/c303dee955d9/ebm-250-10468-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/c5d069d152ec/ebm-250-10468-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/5a9a16634d7a/ebm-250-10468-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/c0124e8f4e5d/ebm-250-10468-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/a30dd61d24d2/ebm-250-10468-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/74faaa9e6dfb/ebm-250-10468-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/9c26697db84e/ebm-250-10468-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/709423eff716/ebm-250-10468-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/1fa4b81e41f8/ebm-250-10468-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/c303dee955d9/ebm-250-10468-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/c5d069d152ec/ebm-250-10468-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/5a9a16634d7a/ebm-250-10468-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/12135209/c0124e8f4e5d/ebm-250-10468-g009.jpg

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