牛胚胎体外生产过程中流产布鲁氏菌的检测

A. Akter, G. Deb, M. Miraz, M. Kabir, Smj Hossain, MR Islam, S. Dey
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摘要

体外胚胎生产(IVP)技术已成为一种潜在的生物技术方法来繁殖遗传高产奶牛。多年来,它在许多发达国家和发展中国家的商业应用正在增加。孟加拉国畜牧研究所(BLRI)采用了屠宰场牛卵巢体外胚胎生产方案。然而,传染性疾病的传播风险,如胚胎流产布鲁氏菌,目前还没有评估。考虑到这些事实,本实验旨在评估屠宰场卵巢体外胚胎生产方案的效率以及生产的胚胎被流产布鲁氏菌污染的风险。为了确定胚胎受流产布鲁氏菌污染的来源(如果有的话),对实验室用水、体外受精过程中使用的不同培养基、精液和卵泡液进行了评估,以确认细菌的存在。此外,对2头因怀疑感染流产布鲁氏菌而流产的水牛采集阴道拭子。采用分子检测方法检测流产布鲁氏菌污染。琼脂糖凝胶电泳未检测到流产布鲁氏菌特异性PCR产物。卵裂率和囊胚发育率分别为75.5±2.7%和16.6±3.9%。本研究推断体外培养的胚胎不存在流产布鲁氏菌感染。j .押尾学。Res. Vol. 27 (1&2), 2020: P. 105-112
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of Brucella abortus during in vitro bovine embryo production
The in vitro embryo production (IVP) technology has emerged as a potential biotechnological approach to multiply genetically high yielding dairy cows. Its commercial application is increasing in many developed and developing countries over the years. Bangladesh livestock Research Institute (BLRI) adopted in vitro embryo production protocol from bovine ovaries of slaughterhouse. However, the risks of transmission of contagious diseases like Brucella abortus with embryos are not evaluated so far. Considering these facts, the present experiments were conducted to evaluate the efficiency of in vitro embryo production protocol with slaughterhouse ovaries as well as risk of contamination of produced embryos with Brucella abortus. To identify sources of contamination of embryos with Brucella abortus (if any), the laboratory water, different media used in the IVP process, semen, and follicular fluids were evaluated for confirmation of the organisms. In addition, vaginal swabs were collected from 2 buffaloes aborted due to suspected Brucella abortus infection. Molecular test were used to detect Brucella abortus contamination. Brucella abortus specific PCR product was not detected on agarose gel electrophoresis. The efficiency of IVP measured by cleavage and blastocyst development rates were 75.5±2.7% and 16.6±3.9%, respectively. The present study inferred that the in vitro produce embryos are free from Brucella abortus infection. Bang. J. Livs. Res. Vol. 27 (1&2), 2020: P. 105-112
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