Nesterov Alexander, Mazloum Ali, Byadovskaya Olga, Shumilova Irina, Van Schalkwyk Antoinette, Krotova Alena, Kirpichenko Vladimir, Donnik Irina, Chvala Ilya, Sprygin Alexander
Federal Center for Animal Health, Vladimir, Russia.
Agricultural Research Council-Onderstepoort Veterinary Institute, Pretoria, South Africa.
Front Vet Sci. 2022 Oct 20;9:1001426. doi: 10.3389/fvets.2022.1001426. eCollection 2022.
Lumpy skin disease (LSD) caused by LSD virus (LSDV), is a member of the poxvirus genus . It is classified as a notifiable disease by the World Organization for Animal Health (WOAH) based on its potential for rapid spread and global economic impact. Due to these characteristics, the mode of LSDV transmission has prompted intensive research efforts. Previous experimental studies using the virulent vaccine-derived recombinant LSDV strain Saratov/2017, demonstrated that this strain has the capacity for transmission in a vector-proof environment. This study demonstrated that a second novel recombinant vaccine-derived LSDV strain Udmurtiya/2019, can infect bulls in contact with diseased animals, in the absence of insect vectors. Bulls were housed in an insect proof animal biosafety level 3 facility, where half the animals were inoculated intravenously with the recombinant LSDV (Udmurtiya/2019), whilst the remaining five animals were mock-inoculated but kept in contact with the inoculated group. Both the infected / inoculated group (IN) and uninfected / incontact group (IC), were monitored for 41 days with continuous registration of body temperature, observations for clinical signs and collection of blood samples and nasal swabs for testing of LSDV presence using real-time PCR. Results indicated that cohabitation of animals from both groups was sufficient to transmit the virus from the IN to the IC-group, with the onset of clinical signs including pyrexia (~41°C) and classical LSD nodular skin lesions starting at 10 dpi for the IN group and 16 dpi for the IC-group. Additionally, the presence of LSDV genomes as well as anti-LSDV antibodies were detected in swabs, blood and serum samples from animals belonging to both groups. These results provides additional evidence of LSDV transmission in a controlled environment without direct contact between diseased and healthy animals, yet in the absence of vectors. Based on these observations, the question concerning a hypothetical relation between mutations in the virus genome and its mode of transmission gains more importance and requires additional investigations with direct comparisons between classical and novel recombinant LSDV strains.
由结节性皮肤病病毒(LSDV)引起的结节性皮肤病(LSD)是痘病毒属的成员。基于其快速传播的可能性和全球经济影响,世界动物卫生组织(WOAH)将其列为须申报疾病。由于这些特性,LSDV的传播方式引发了深入的研究。先前使用强毒疫苗衍生的重组LSDV毒株Saratov/2017进行的实验研究表明,该毒株具有在无载体环境中传播的能力。本研究表明,另一种新型疫苗衍生的重组LSDV毒株Udmurtiya/2019,在没有昆虫载体的情况下,能够感染与患病动物接触的公牛。公牛被饲养在一个昆虫防护的动物生物安全3级设施中,其中一半动物静脉注射重组LSDV(Udmurtiya/2019),而其余五只动物接受 mock 接种但与接种组保持接触。对感染/接种组(IN)和未感染/接触组(IC)进行了41天的监测,持续记录体温,观察临床症状,并采集血样和鼻拭子,使用实时PCR检测是否存在LSDV病毒核酸。结果表明,两组动物同居足以将病毒从IN组传播到IC组,临床症状包括发热(约41°C)和典型的LSD结节性皮肤病变,IN组在感染后10天出现,IC组在感染后16天出现。此外,在两组动物的拭子、血液和血清样本中均检测到LSDV病毒核酸以及抗LSDV抗体。这些结果提供了额外的证据,证明LSDV在受控环境中可以传播,患病动物和健康动物没有直接接触,但没有载体。基于这些观察结果,关于病毒基因组突变与其传播方式之间假设关系的问题变得更加重要,需要对经典和新型重组LSDV毒株进行直接比较的进一步研究。