Artificial insemination and laying cycle influence adaptive immune cell numbers and localization in the reproductive tract of turkey breeder hens.

IF 3.8 1区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Yifan Chen, Sunantha Kosonsiriluk, Lillian X Ehresmann, Kent M Reed, Sally L Noll, Ben W Wileman, Marissa M Studniski, Kahina S Boukherroub
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引用次数: 0

Abstract

Weekly artificial insemination (AI) is a common practice on commercial turkey breeder farms. The aim of this study was to determine changes in stress as well as oviduct and systemic immunity in response to weekly artificial inseminations through the laying cycle of turkey hens. Hens were divided into sham (extender only) and semen (extender + sperm) treatments. Blood, uterovaginal junction (UVJ), vagina, and spleen were collected at start of lay, peak lay, and end of lay (n = 8-12 /group for blood and 5 for tissues). The heterophil to lymphocyte ratio (H:L) was significantly higher in the semen-inseminated hens compared with the sham-inseminated hens at peak lay (n = 0.05). Immunohistochemistry revealed a higher number of CD3+ T cells in sperm storage tubules (SSTs) and UVJ submucosa at the end of lay compared with start and peak of lay across insemination treatments (n = 0.07 and 0.01, respectively). Within the end-of-lay group, semen-inseminated hens showed a higher number of CD3+ T cells in SSTs and UVJ submucosa (n = 0.04 and 0.1, respectively). The number of IgM+ B cells was significantly higher at start of lay compared with end of lay in SSTs and spleen (n = 0.01 and 0.0001, respectively) regardless of insemination treatment. In the vaginal submucosa, the number of IgM+ B cells was significantly higher in the semen group compared with the sham group at peak lay (n = 0.04). The number of IgA+ and IgY+ B cells were higher in the UVJ submucosa at the end of lay compared with start of lay, regardless of insemination treatment (n = 0.0001 and 0.03 respectively). In summary, the localization and number of adaptive immune cells change in response to the presence of sperm and laying cycle and depend on factors including immune cell type and tissue compartment. This suggests that the adaptive immune system of the oviduct plays an important role in responding to sperm based on the stage of the laying cycle. Modulating this immune response could improve reproductive performance.

人工授精和产蛋周期对火鸡种母鸡生殖道中适应性免疫细胞数量和定位的影响。
每周人工授精(AI)是商业火鸡饲养场的常见做法。本研究旨在确定火鸡产蛋周期内每周人工授精对应激、输卵管和全身免疫力的影响。母鸡被分为假人工授精(仅人工授精器)和精液人工授精(人工授精器+精子)两种处理。分别在产蛋开始、产蛋高峰和产蛋结束时采集血液、子宫阴道交界处(UVJ)、阴道和脾脏(n = 8-12 只/组,组织 5 只/组)。在产蛋高峰期,输精母鸡的嗜异性细胞与淋巴细胞比率(H:L)明显高于假输精母鸡(n = 0.05)。免疫组化显示,在不同的授精处理中,产蛋末期与产蛋初期和产蛋高峰期相比,精子储存管(SST)和UVJ黏膜下层的CD3+ T细胞数量更高(n = 0.07和0.01)。在产蛋末期组中,精液授精母鸡的SST和UVJ粘膜下层CD3+ T细胞数量较多(n = 0.04和0.1)。无论采用哪种人工授精方法,产蛋初期与产蛋末期相比,SST 和脾脏中的 IgM+ B 细胞数量都明显增加(分别为 n = 0.01 和 0.0001)。在阴道黏膜下层,精液组的 IgM+ B 细胞数量在产卵高峰期明显高于假体组(n = 0.04)。与产卵开始时相比,产卵结束时 UVJ 黏膜下的 IgA+ 和 IgY+ B 细胞数量较高,与人工授精处理无关(n = 0.0001 和 0.03)。总之,适应性免疫细胞的定位和数量随精子的存在和产蛋周期而变化,并取决于免疫细胞类型和组织区系等因素。这表明输卵管的适应性免疫系统在根据产卵周期阶段对精子做出反应方面发挥着重要作用。调节这种免疫反应可以提高繁殖性能。
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来源期刊
Poultry Science
Poultry Science 农林科学-奶制品与动物科学
CiteScore
7.60
自引率
15.90%
发文量
0
审稿时长
94 days
期刊介绍: First self-published in 1921, Poultry Science is an internationally renowned monthly journal, known as the authoritative source for a broad range of poultry information and high-caliber research. The journal plays a pivotal role in the dissemination of preeminent poultry-related knowledge across all disciplines. As of January 2020, Poultry Science will become an Open Access journal with no subscription charges, meaning authors who publish here can make their research immediately, permanently, and freely accessible worldwide while retaining copyright to their work. Papers submitted for publication after October 1, 2019 will be published as Open Access papers. An international journal, Poultry Science publishes original papers, research notes, symposium papers, and reviews of basic science as applied to poultry. This authoritative source of poultry information is consistently ranked by ISI Impact Factor as one of the top 10 agriculture, dairy and animal science journals to deliver high-caliber research. Currently it is the highest-ranked (by Impact Factor and Eigenfactor) journal dedicated to publishing poultry research. Subject areas include breeding, genetics, education, production, management, environment, health, behavior, welfare, immunology, molecular biology, metabolism, nutrition, physiology, reproduction, processing, and products.
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