School of Veterinary Science, University of Queensland, Gatton, Qld 4343, Australia.
Centre for Crocodile Research, Noonamah, NT 0837, Australia.
Viruses. 2020 Feb 11;12(2):198. doi: 10.3390/v12020198.
West Nile virus, Kunjin strain (WNV) is endemic in Northern Australia, but rarely causes clinical disease in humans and horses. Recently, WNV genomic material was detected in cutaneous lesions of farmed saltwater crocodiles (), but live virus could not be isolated, begging the question of the pathogenesis of these lesions. Crocodile hatchlings were experimentally infected with either 10 ( = 10) or 10 ( = 11) TCID-doses of WNV and each group co-housed with six uninfected hatchlings in a mosquito-free facility. Seven hatchlings were mock-infected and housed separately. Each crocodile was rotationally examined and blood-sampled every third day over a 3-week period. Eleven animals, including three crocodiles developing typical skin lesions, were culled and sampled 21 days post-infection (dpi). The remaining hatchlings were blood-sampled fortnightly until experimental endpoint 87 dpi. All hatchlings remained free of overt clinical disease, apart from skin lesions, throughout the experiment. Viremia was detected by qRT-PCR in infected animals during 2-17 dpi and in-contact animals 11-21 dpi, indicating horizontal mosquito-independent transmission. Detection of viral genome in tank-water as well as oral and cloacal swabs, collected on multiple days, suggests that shedding into pen-water and subsequent mucosal infection is the most likely route. All inoculated animals and some in-contact animals developed virus-neutralizing antibodies detectable from 17 dpi. Virus-neutralizing antibody titers continued to increase in exposed animals until the experimental endpoint, suggestive of persisting viral antigen. However, no viral antigen was detected by immunohistochemistry in any tissue sample, including from skin and intestine. While this study confirmed that infection of saltwater crocodiles with WNV was associated with the formation of skin lesions, we were unable to elucidate the pathogenesis of these lesions or the nidus of viral persistence. Our results nevertheless suggest that prevention of WNV infection and induction of skin lesions in farmed crocodiles may require management of both mosquito-borne and water-borne viral transmission in addition to vaccination strategies.
西尼罗河病毒,昆金株(WNV)在澳大利亚北部流行,但很少在人类和马中引起临床疾病。最近,在养殖的咸水鳄()的皮肤损伤中检测到 WNV 基因组物质,但无法分离到活病毒,这引发了对这些病变发病机制的疑问。鳄龟孵化后分别用 10(=10)或 10(=11)TCID 剂量的 WNV 进行实验性感染,每组与六只未感染的孵化后鳄龟一起在无蚊设施中共同饲养。七只孵化后鳄龟被模拟感染并单独饲养。在 3 周的时间里,每只鳄龟每隔三天轮换检查和采血。11 只动物,包括 3 只出现典型皮肤病变的鳄龟,在感染后 21 天被扑杀并取样。其余的孵化后鳄龟每两周采血一次,直到实验终点 87 天。除了皮肤病变外,所有孵化后鳄龟在整个实验过程中均未出现明显的临床疾病。感染动物在 2-17 天检测到 qRT-PCR 病毒血症,接触动物在 11-21 天检测到病毒血症,表明存在水平的蚊子非依赖性传播。在水箱水中以及口腔和泄殖腔拭子中多次采集的样本中检测到病毒基因组,提示脱落到围栏水中以及随后的黏膜感染是最可能的途径。所有接种动物和一些接触动物在 17 天可检测到病毒中和抗体。暴露动物的病毒中和抗体滴度持续增加到实验终点,提示持续存在病毒抗原。然而,免疫组织化学检测未在任何组织样本中检测到病毒抗原,包括皮肤和肠道样本。虽然本研究证实 WNV 感染咸水鳄与皮肤病变的形成有关,但我们无法阐明这些病变的发病机制或病毒持续存在的病灶。然而,我们的研究结果表明,除了疫苗接种策略外,预防农场养殖鳄龟感染 WNV 和诱导皮肤病变可能还需要管理蚊子传播和水传播的病毒。