Abstract

BackgroundGoat milk is very similar to human milk in terms of its abundant nutrients and ease of digestion. To derive greater economic benefit, farmers require more female offspring (does); however, the buck-to-doe offspring sex ratio is approximately 50%. At present, artificial insemination after the separation of X/Y sperm using flow cytometry is the primary means of controlling the sex of livestock offspring. However, flow cytometry has not been successfully utilised for the separation of X/Y sperm aimed at sexing control in dairy goats.ResultsIn this study, a novel, simple goat sperm sexing technology that activates the toll-like receptor 7/8 (TLR7/8), thereby inhibiting X-sperm motility, was investigated. Our results showed that the TLR7/8 coding goat X-chromosome was expressed in approximately 50% of round spermatids in the testis and sperm, as measured from cross-sections of the epididymis and ejaculate, respectively. Importantly, TLR7/8 was located at the tail of the X-sperm. Upon TLR7/8 activation, phosphorylated forms of glycogen synthase kinase α/β (GSK3 α/β) and nuclear factor kappa-B (NF-κB) were detected in the X-sperm, causing reduced mitochondrial activity, ATP levels, and sperm motility. High-motility Y-sperm segregated to the upper layer and the low-motility X-sperm, to the lower layer. Following in vitro fertilisation using the TLR7/8-activated sperm from the lower layer, 80.52 ± 6.75% of the embryos were XX females. The TLR7/8-activated sperm were subsequently used for in vivo embryo production via the superovulatory response; nine embryos were collected from the uterus of two does that conceived. Eight of these were XX embryos, and one was an XY embryo.ConclusionsOur study reveals a novel TLR7/8 signalling mechanism that affects X-sperm motility via the GSK3 α/β-hexokinase pathway; this technique could be used to facilitate the efficient production of sexed dairy goat embryos.

Highlights

  • Goat milk is very similar to human milk in terms of its abundant nutrients and ease of digestion

  • Localisation of TLR7 and TLR8 in dairy goat testes, epididymis, and sperm The percentage and localisation of TLR7 and TLR8 in dairy goat testes, epididymis, and sperm are shown in Figs. 2 and 3

  • TLR7+ cells were observed in approximately half of the round spermatids (47.57 ± 1.79%) and epididymis sperm (43.95 ± 1.02%) stained with PNA, a special dye that binds to the acrosome (Fig. 2a, b, d, and e)

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Summary

Introduction

Goat milk is very similar to human milk in terms of its abundant nutrients and ease of digestion. Artificial insemination after the separation of X/Y sperm using flow cytometry is the primary means of controlling the sex of livestock offspring. Flow cytometry has not been successfully utilised for the separation of X/Y sperm aimed at sexing control in dairy goats. Artificial insemination (AI) after the separation of X and Y chromosome-bearing sperm is one of the primary means of sex control of livestock offspring [3]. The use of flow cytometry to separate X- and Y-sperm in goats has resulted in low sperm motility and poor pregnancy rates [10]. This outcome might be due to species-specific differences in mammalian sperm. We aimed to find a new method to separate dairy goat X- and Y-sperm without flow cytometry

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