Melatonin alleviates heat stress-induced spermatogenesis dysfunction in male dairy goats by regulating arachidonic acid metabolism mediated by remodeling the gut microbiota.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Xinrui Guo, Jing Xu, Yongkang Zhao, Jie Wang, Tingshu Fu, Mathias L Richard, Harry Sokol, Miao Wang, Yu Li, Yang Liu, Hui Wang, Chenlei Wang, Xueqin Wang, Haiyang He, Yazhou Wang, Baohua Ma, Sha Peng
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Abstract

Background: Heat stress (HS) commonly occurring in summer has gradually become a factor threatening the reproductive performance of male dairy goats by reducing their fecundity. Despite the melatonin is applied to relieve HS, it is still unclear whether melatonin protects against reproductive damage induced by HS in dairy goats and how it works. The purpose of the present study is to evaluate the role of melatonin in alleviating HS-induced spermatogenesis dysfunction in male dairy goats and further explore its mechanism.

Results: HS impaired spermatogenesis, sperm formation in the testes, and sperm maturation in the epididymis of dairy goats, resulting in decreased sperm quality. Melatonin rescued the decrease of sperm quality induced by HS via decreasing inflammatory and oxidative stress levels in testicular tissue and enhancing intercellular barrier function within the testes. Amplicon-based microbiota analysis revealed that despite gut microbiota differences between melatonin-treated dairy goats and NC dairy goats to some extent, melatonin administration tends to return the gut microbiota of male dairy goats under HS to the levels of natural control dairy goats. To explore whether the protective role of melatonin in sperm quality is mediated by regulating gut microbiota, fecal microbiota of HS dairy goats with or without melatonin treatment were transferred to HS mice, respectively. We found HS mice that had received fecal bacteria of HS dairy goats experienced serious testicular injury and dyszoospermia, while this phenomenon was ameliorated in HS mice that had received fecal bacteria of dairy goats treated with melatonin, indicating melatonin alleviates HS-induced spermatogenic damage in a microbiota dependent manner. We further found that the testicular tissue of both HS dairy goats and mice transplanted with HS dairy goat feces produced large amounts of arachidonic acid (AA)-related metabolites, which were closely associated with semen quality. Consistently, supplementation with AA has been shown to elevate the levels of inflammation and oxidative stress in the testicular tissue of mice, disrupting intercellular connections and ultimately leading to spermatogenic disorders.

Conclusion: This study has revealed that melatonin can effectively alleviate spermatogenic disorders in dairy goats caused by HS. This beneficial effect was primarily achieved through the modulation of gut microbiota, which subsequently inhibited the excessive synthesis of AA in testicular tissue. These discoveries are of great significance for preventing or improving the decline in male livestock reproductive performance caused by HS, enhancing the reproductive efficiency of elite male breeds, and ultimately improving the production efficiency of animal husbandry. Video Abstract.

褪黑素通过重塑肠道微生物群来调节花生四烯酸代谢,从而缓解热应激诱发的雄性奶山羊精子发生功能障碍。
背景:夏季常见的热应激(HS)已逐渐成为威胁雄性奶山羊繁殖性能的一个因素,会降低它们的受胎率。尽管褪黑素可用于缓解热应激,但褪黑素是否能保护奶山羊免受热应激引起的生殖损伤以及褪黑素是如何发挥作用的仍不清楚。本研究旨在评估褪黑素在缓解 HS 引起的雄性奶山羊精子发生功能障碍方面的作用,并进一步探讨其作用机制:结果:HS损害了奶山羊的精子发生、睾丸中精子的形成和附睾中精子的成熟,导致精子质量下降。褪黑素通过降低睾丸组织中的炎症和氧化应激水平以及增强睾丸内的细胞间屏障功能,缓解了HS导致的精子质量下降。基于扩增子的微生物群分析表明,尽管褪黑素处理过的奶山羊与NC奶山羊的肠道微生物群存在一定程度的差异,但褪黑素的施用可使HS作用下的雄性奶山羊的肠道微生物群恢复到自然对照奶山羊的水平。为了探索褪黑素对精子质量的保护作用是否是通过调节肠道微生物群介导的,我们将接受或未接受褪黑素治疗的 HS 奶山羊的粪便微生物群分别转移到 HS 小鼠体内。我们发现,接受了 HS 奶山羊粪便细菌的 HS 小鼠出现了严重的睾丸损伤和生精障碍,而接受了经褪黑素处理的 HS 奶山羊粪便细菌的 HS 小鼠的这一现象得到了改善,这表明褪黑素以微生物群依赖的方式减轻了 HS 诱导的生精损伤。我们进一步发现,HS奶山羊和移植了HS奶山羊粪便的小鼠的睾丸组织均产生大量花生四烯酸(AA)相关代谢物,这些代谢物与精液质量密切相关。同样,补充 AA 会提高小鼠睾丸组织的炎症和氧化应激水平,破坏细胞间的联系,最终导致生精障碍:本研究揭示了褪黑素可有效缓解 HS 引起的奶山羊生精障碍,这种有益作用主要是通过调节肠道微生物群来实现的,随后抑制了睾丸组织中 AA 的过度合成。这些发现对于预防或改善HS导致的雄性家畜繁殖性能下降,提高优良雄性品种的繁殖效率,最终提高畜牧业的生产效率具有重要意义。视频摘要
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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