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Analysis of the Clinical Course of Experimental Infection with Highly Pathogenic African Swine Fever Strain Isolated from an Outbreak in Poland. Aspects Related to the Disease Suspicion at the Farm Level

机译:从波兰爆发的高致病性非洲猪瘟菌株实验感染的临床过程分析。在农场一级与疾病怀疑有关的方面

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摘要

This paper was aimed to characterize clinical signs and pathomorphological lesions in twenty-two pigs, infected intranasally by different doses of African swine fever virus (Pol18_28298_O111), isolated during the outbreak in a pig farm that occurred in Eastern Poland throughout 2018. This article also attempts to indicate risk, related to virus load and shedding, and present possible difficulties with proper disease recognition at the farm level. The results revealed that even a very low dose (5 HAU) may initiate the infection. Various forms of the disease (acute, subacute, and chronic), mainly with prodromal clinical signs like fever, apathy, and reduced feed intake were observed. The most frequently observed lesions (82%) were: hyperemia and enlargement of lymph nodes and splenomegaly. The minimal incubation period was estimated at five days post-infection (dpi). Mortality ranged from 80–100%. Two pigs survived the infection. Some viremic animals presented delayed fever. In some cases, the fever was not detectable. Shortly after viremia, the virus was secreted ion the urine, feces, and saliva. The highest levels of virus were found in the internal organs and blood; however in the case of one pig (chronic form), viral DNA was not detected in the spleen, liver, bone marrow, and brain. Veterinary diagnosis may be difficult, and the final results should always be based on laboratory investigations.
机译:本文旨在描述在2018年整个波兰东部发生的一次猪场爆发期间分离出的22头猪的临床体征和病理形态学病变,这些猪经鼻内感染了不同剂量的非洲猪瘟病毒(Pol18_28298_O111)。试图指出与病毒载量和脱落有关的风险,并在农场一级正确识别疾病方面存在潜在的困难。结果表明,即使非常低的剂量(5 HAU)也可能引发感染。观察到多种形式的疾病(急性,亚急性和慢性),主要表现为前驱性临床体征,如发烧,冷漠和饲料摄入减少。观察到最多的病变(82%)是:充血,淋巴结肿大和脾肿大。最小潜伏期估计为感染后五天(dpi)。死亡率为80-100%。两只猪在感染后幸存了下来。一些病毒血症动物表现出延迟发烧。在某些情况下,发烧是无法检测到的。病毒血症后不久,病毒便通过尿液,粪便和唾液分泌出来。在内部器官和血液中发现了最高水平的病毒。但是,对于一只猪(慢性),在脾脏,肝脏,骨髓和大脑中均未检测到病毒DNA。兽医诊断可能很困难,最终结果应始终基于实验室调查。

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