Pietschmann Jana, Guinat Claire, Beer Martin, Pronin Valery, Tauscher Kerstin, Petrov Anja, Keil Günther, Blome Sandra
Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Suedufer 10, 17493, Greifswald-Insel Riems, Germany.
Arch Virol. 2015 Jul;160(7):1657-67. doi: 10.1007/s00705-015-2430-2. Epub 2015 Apr 29.
In 2007, African swine fever virus (ASFV) was introduced into the Transcaucasian countries and Russia. Since then, it has spread alarmingly and reached the European Union. ASFV strains are highly virulent and lead to almost 100% mortality under experimental conditions. However, the possibility of dose-dependent disease courses has been discussed. For this reason, a study was undertaken to assess the risk of chronic disease and the establishment of carriers upon low-dose oronasal infection of domestic pigs and European wild boar. It was demonstrated that very low doses of ASFV are sufficient to infect especially weak or runted animals by the oronasal route. Some of these animals did not show clinical signs indicative of ASF, and they developed almost no fever. However, no changes were observed in individual animal regarding the onset, course and outcome of infection as assessed by diagnostic tests. After amplification of ASFV by these animals, pen- and stablemates became infected and developed acute lethal disease with similar characteristics in all animals. Thus, we found no indication of prolonged or chronic individual courses upon low-dose infection in either species. The scattered onset of clinical signs and pathogen detection within and among groups confirms moderate contagiosity that is strongly linked with blood contact. In conclusion, the prolonged course at the "herd level" together with the exceptionally low dose that proved to be sufficient to infect a runted wild boar could be important for disease dynamics in wild-boar populations and in backyard settings.
2007年,非洲猪瘟病毒(ASFV)传入外高加索国家和俄罗斯。自那时起,它惊人地传播开来并蔓延至欧盟。ASFV毒株具有高度毒性,在实验条件下可导致近100%的死亡率。然而,已经有人讨论了剂量依赖性病程的可能性。因此,开展了一项研究,以评估家猪和欧洲野猪经低剂量口鼻感染后出现慢性病和形成带毒动物的风险。结果表明,极低剂量的ASFV就足以经口鼻途径感染特别虚弱或发育不良的动物。其中一些动物没有表现出非洲猪瘟的临床症状,几乎也没有发烧。然而,通过诊断测试评估,在个体动物的感染起始、病程和结局方面未观察到变化。这些动物使ASFV增殖后,同栏和同圈的猪被感染,并在所有动物中都发展出具有相似特征的急性致死性疾病。因此,我们没有发现任何迹象表明这两个物种经低剂量感染后会出现病程延长或慢性病程。临床症状和病原体检测在组内和组间的分散出现证实了与血液接触密切相关的中等传染性。总之,“群体水平”上的病程延长以及被证明足以感染一头发育不良野猪的极低剂量,可能对野猪种群和后院环境中的疾病动态具有重要意义。