Comparative cell free salivary miRNA profile in Bubalus bubalis between diestrus and estrus stages

RAJEEV CHANDEL, Dheer Singh, Suneel Kumar Onteru
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Abstract

Despite buffaloes being primary farm animals, their reproductive performance remains poor mainly due to inaccurate estrus detection methods that ultimately has an economic impact on dairy industry as well as farmers. Recently, numerous studies showed potential of miRNAs as estrus biomarker. However, a miRNA profile of buffalo cell free saliva, a non-invasive fluid, at estrus and diestrus stages is missing. Hence, the present study was planned to identify differential levels of salivary cell free miRNAs in estrus as compared to the diestrus phase of buffalo oestrous cycle (n=3) in order to discover a possible estrus specific miRNAs as biomarkers. miRNA-Seq data analysis showed that in total 10 miRNAs i.e bta-miR-375, bta-miR-200c, bta-miR-30d, bta-let-7f, bta-miR-200a, bta-miR-12034, bta-let-7b, bta-miR-142-5p, bta-miR-2467-3p, bta-miR-30a-5p are significantly altered (log2foldchange >3 and p<0.05) during estrus in comparison to the diestrus phase in buffaloes, suggesting their estrus biomarker potential. Overall, 8 miRNAs i.e bta-miR-375 (6.87 Fold; p-value 0.003), bta-miR-200c (5.98 Fold; p-value 0.003), bta-miR-30d (4.17 Fold; p-value 0.015), bta-let-7f (3.34 Fold; p-value 0.022), bta-miR-200a (4.92 Fold; p-value 0.024), bta-miR-12034 (3.58 Fold; p-value 0.0025), bta-let-7b (3.06 Fold; p-value 0.031), bta-miR-30a-5p (4.7 Fold; p-value 0.036) were upregulated, whereas bta-miR-142-5p (-3.4 Fold; p-value 0.032) and bta-miR-2467-3p (-5.24 Fold; p-value 0.035) were downregulated during estrus. However, further validation study using qPCR is required in a large sample size in order to determine their estrus biomarker potential. In summary, our results revealed differential salivary cell free miRNAs profile during the oestrous cycle that may lead to the development of estrus specific miRNAs based point-of-care test applicable for the reproductive management of buffaloes in the field condition in the near future.
发情期和发情期小黄牛游离细胞唾液 miRNA 图谱的比较
尽管水牛是主要的农场动物,但它们的繁殖性能仍然很差,这主要是由于发情检测方法不准确,最终对乳品业和农民造成了经济影响。最近,许多研究表明 miRNAs 具有作为发情生物标志物的潜力。然而,水牛无细胞唾液(一种非侵入性液体)在发情和发情期的 miRNA 图谱尚属空白。因此,本研究计划鉴定水牛发情周期(n=3)中发情期与发情后期的唾液细胞游离 miRNAs 水平差异,以发现可能的发情特异性 miRNAs 作为生物标志物。e bta-miR-375、bta-miR-200c、bta-miR-30d、bta-let-7f、bta-miR-200a、bta-miR-12034、bta-let-7b、bta-miR-142-5p、bta-miR-2467-3p、bta-miR-30a-5p 在发情期与发情期相比有显著变化(log2foldchange >3和p<0.05),这表明它们具有发情生物标志物的潜力。总体而言,8 个 miRNA,即 bta-miR-375 (6.87 Fold; p-value 0.003)、bta-miR-200c (5.98 Fold; p-value 0.003)、bta-miR-30d (4.17 Fold; p-value 0.015)、bta-let-7f(3.34 Fold; p-value 0.022)、bta-miR-200a(4.92 Fold; p-value 0.024)、bta-miR-12034(3.58 Fold; p-value 0.0025)、bta-let-7b (3.06 Fold; p-value 0.031)、bta-miR-30a-5p (4.7 Fold; p-value 0.036)在发情期上调,而 bta-miR-142-5p (-3.4 Fold; p-value 0.032)和 bta-miR-2467-3p (-5.24 Fold; p-value 0.035)在发情期下调。然而,为了确定其发情生物标志物的潜力,还需要使用大样本量的 qPCR 进行进一步的验证研究。总之,我们的研究结果揭示了发情周期中唾液细胞游离 miRNAs 的差异,这可能有助于开发基于发情特异性 miRNAs 的护理点测试,在不久的将来用于野外水牛的繁殖管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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