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Evidence of reduced viremia, pathogenicity and vector competence in a re-emerging European strain of bluetongue virus serotype 8 in sheep

机译:在羊的重新出现欧洲菌株8中减少病毒血症,致病性和载体能力的证据

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The outbreak of bluetongue virus (BTV) serotype 8 (BTV-8) during 2006-2009 in Europe was the most costly epidemic of the virus in recorded history. In 2015, a BTV-8 strain re-emerged in France which has continued to circulate since then. To examine anecdotal reports of reduced pathogenicity and transmission efficiency, we investigated the infection kinetics of a 2007 UK BTV-8 strain alongside the re-emerging BTV-8 strain isolated from France in 2017. Two groups of eight BTV-naive British mule sheep were inoculated with 5.75 log(10)TCID(50)/ml of either BTV-8 strain. BTV RNA was detected by 2 dpi in both groups with peak viraemia occurring between 5-9 dpi. A significantly greater amount of BTV RNA was detected in sheep infected with the 2007 strain (6.0-8.8 log(10) genome copies/ml) than the re-emerging BTV-8 strain (2.9-7.9 log(10) genome copies/ml). All infected sheep developed BTV-specific antibodies by 9 dpi. BTV was isolated from 2 dpi to 12 dpi for 2007 BTV-8-inoculated sheep and from 5 to 10 dpi for sheep inoculated with the remerging BTV-8. In Culicoides sonorensis feeding on the sheep over the period 7-12 dpi, vector competence was significantly higher for the 2007 strain than the re-emerging strain. Both the proportion of animals showing moderate (as opposed to mild or no) clinical disease (6/8 vs. 1/8) and the overall clinical scores (median 5.25 vs. 3) were significantly higher in sheep infected with the 2007 strain, compared to those infected with the re-emerging strain. However, one sheep infected with the re-emerging strain was euthanized at 16 dpi having developed severe lameness. This highlights the potential of the re-emerging BTV-8 to still cause illness in naive ruminants with concurrent costs to the livestock industry.
机译:BlueTongue病毒(BTV)血清型8(BTV-8)在欧洲2006 - 2009年的爆发是记录历史中最昂贵的病毒疫情。 2015年,在法国重新出现的BTV-8菌株继续自那时继续流通。为了检查降低致病性和传输效率的轶事报告,我们研究了2007年英国BTV-8应变的感染动力学以及2017年重新出现的BTV-8菌株。两组八组八个BTV-naive英国骡子绵羊接种5.75个log(10)BTV-8菌株的TCID(50)/ mL。 BTV RNA在两组中检测到2个DPI,其峰值病毒症发生在5-9 dpi之间。在用2007株(6.0-8.8对数(10)基因组拷贝/ mL)中检测到比重新出现的BTV-8菌株(2.9-7.9 log(10)基因组拷贝/ ml在绵羊中检测到显着更大的BTV RNA )。所有受感染的绵羊通过9 dpi开发了BTV特异性抗体。将BTV从2007年BTV-8接种的绵羊中分离为2dPI至12 dpi,以及用搅拌BTV-8接种的绵羊5至10dpi。在7-12 DPI期间,在7-12 dPI上喂养绵羊的辛雌醇,对于2007年应变的菌株比重新出现的应变显着更高。显示中等(与温和或不)临床疾病(6/8与1/8)和整体临床评分(中位数5.25 vs.3)的动物的比例均在感染2007年菌株的绵羊显着高,与感染重新出现的菌株的菌株相比。然而,在16DPI产生严重跛行的16dPI下对感染重新出现菌株感染的一只绵羊。这突出了重新出现BTV-8的潜力,仍然在幼稚反刍动物中造成疾病,并经常成本对畜牧业。

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