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山羊羊水中小反刍兽慢病毒的检测与分离

Detection and isolation of small ruminant lentivirus in the amniotic fluid of goats.

作者信息

Furtado Araújo Juscilânia, Andrioli Alice, Pinheiro Raymundo Rizaldo, Peixoto Renato Mesquita, de Sousa Ana Lídia Madeira, de Azevedo Dalva Alana Aragão, Lima Ana Milena Cesar, Nobre Juliana Araújo, Amaral Gabriel Paula, Brandão Iane Sousa, da Silva Teixeira Maria Fátima

机构信息

Doctorate Student in the Northeast Network in Biotechnology, State University of Ceará, Fortaleza, Ceará, Brazil.

Embrapa Goats and Sheep, Sobral, Ceará, Brazil.

出版信息

Comp Immunol Microbiol Infect Dis. 2021 Oct;78:101693. doi: 10.1016/j.cimid.2021.101693. Epub 2021 Jul 29.

Abstract

The objective of this study was to verify the presence of small ruminant lentivirus in the amniotic fluid of goats using molecular tests and viral isolation by cocultivation in the amniotic fluid of naturally infected goats. The study analyzed eight goats: seven were small ruminant lentivirus-positive and one was negative. The amniotic fluid was collected from each of the eight animals during cesarean section at 147 days of pregnancy. Cocultivation was undertaken using secondary goat nictitating membrane cell cultures obtained by explant from a small ruminant lentivirus-negative calf followed by trypsinization and sub-cultivation of the cells for 63 days. During this period, five supernatant collections were performed for DNA extraction and subsequent nested polymerase chain reaction. DNA was extracted from the amniotic fluid after 3 h of cellular sedimentation, from which a sample of 600 μL was taken from the sediment and another 600 μL sample from the supernatant. After DNA extraction, nested polymerase chain reaction was performed. Of the eight goats, 62.5 % (05/08) were small ruminant lentivirus-positive, with 43.75 % (07/16) of the total samples positive when considering the two repetitions (supernatant and cell sediment). Moreover, positivity was confirmed by small ruminant lentivirus pro-viral DNA amplification in the cell supernatant throughout the cocultivation period. Small ruminant lentivirus were present in the amniotic fluid samples from the naturally infected goats indicating an intrauterine transmission route. Moreover, this biological fluid can be adopted for the diagnosis of these lentiviruse because it is an important risk factor related to intrauterine transmission.

摘要

本研究的目的是通过分子检测和在自然感染山羊的羊水中共培养进行病毒分离,来验证山羊羊水中是否存在小反刍兽疫病毒。该研究分析了8只山羊:7只为小反刍兽疫病毒阳性,1只为阴性。在怀孕147天时剖宫产过程中从这8只动物身上采集羊水。使用从小反刍兽疫病毒阴性小牛外植获得的山羊副鼻膜细胞进行二次培养,随后进行胰蛋白酶消化并将细胞传代培养63天。在此期间,进行了5次上清液收集以提取DNA并随后进行巢式聚合酶链反应。细胞沉淀3小时后从羊水中提取DNA,从沉淀中取600μL样品,从上清液中取另一个600μL样品。DNA提取后,进行巢式聚合酶链反应。在这8只山羊中,62.5%(5/8)为小反刍兽疫病毒阳性,考虑两次重复(上清液和细胞沉淀)时,总样本中有43.75%(7/16)为阳性。此外,在整个共培养期间,细胞上清液中的小反刍兽疫病毒前病毒DNA扩增证实了阳性。自然感染山羊的羊水样本中存在小反刍兽疫病毒,表明存在宫内传播途径。此外,这种生物液体可用于这些慢病毒的诊断,因为它是与宫内传播相关的重要风险因素。

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