Apakupakul Kathleen, Duncan Mary, Subramaniam Kuttichantran, Brenn-White Maris, Palmer Jamie L, Viadanna Pedro H O, Vann Jordan A, Adamovicz Laura, Waltzek Thomas B, Deem Sharon L
Saint Louis Zoo Institute for Conservation Medicine, 1 Government Dr., St. Louis, Missouri 63110, USA.
Saint Louis Zoo Department of Animal Health, 1 Government Dr., St. Louis, Missouri 63110, USA.
J Wildl Dis. 2024 Jan 1;60(1):151-163. doi: 10.7589/JWD-D-23-00057.
Frog virus 3 (FV3) and related ranaviruses are emerging infectious disease threats to ectothermic vertebrate species globally. Although the impact of these viruses on amphibian health is relatively well studied, less is understood about their effects on reptile health. We report two cases of FV3 infection, 11 mo apart, in three-toed box turtles (Terrapene mexicana triunguis) from a wildlife rehabilitation center. Case 1 had upper respiratory signs upon intake but had no clinical signs at the time of euthanasia 1 mo later. Case 2 presented for vehicular trauma, had ulcerative pharyngitis and glossitis, and died overnight. In case 1, we detected FV3 nucleic acid with qPCR in oral swabs, kidney, liver, spleen, and tongue. In case 2, we detected FV3 in an oral swab, an oral plaque, heart, kidney, lung, liver, spleen, and tongue. We also detected FV3 nucleic acid with in situ hybridization for case 2. For both cases, FV3 was isolated in cell culture and identified with DNA sequencing. Histopathologic examination of postmortem tissue from case 1 was unremarkable, whereas acute hemorrhagic pneumonia and splenic necrosis were noted in case 2. The difference in clinical signs between the two cases may have been due to differences in the temporal course of FV3 disease at the time of necropsy. Failure to detect this infection previously in Missouri reptiles may be due to lack of surveillance, although cases may also represent a novel spillover to box turtles in Missouri. Our findings reiterate previous suggestions that the range of FV3 infection may be greater than previously documented and that infection may occur in host species yet to be tested.
蛙病毒3(FV3)及相关蛙虹彩病毒对全球变温脊椎动物构成了新出现的传染病威胁。尽管这些病毒对两栖动物健康的影响已得到较为充分的研究,但对其对爬行动物健康的影响却知之甚少。我们报告了两例FV3感染病例,相隔11个月,患病动物是来自一家野生动物康复中心的三趾箱龟(Terrapene mexicana triunguis)。病例1在入院时出现上呼吸道症状,但1个月后实施安乐死时未出现临床症状。病例2因车辆撞击受伤前来就诊,患有溃疡性咽炎和舌炎,并在一夜之间死亡。在病例1中,我们通过定量聚合酶链反应(qPCR)在口腔拭子、肾脏、肝脏、脾脏和舌头中检测到FV3核酸。在病例2中,我们在口腔拭子、口腔菌斑、心脏、肾脏、肺、肝脏、脾脏和舌头中检测到FV3。我们还通过原位杂交在病例2中检测到FV3核酸。对于这两个病例,均在细胞培养中分离出FV3,并通过DNA测序进行鉴定。病例1死后组织的组织病理学检查未见明显异常,而病例2则出现急性出血性肺炎和脾脏坏死。两例病例临床症状的差异可能是由于尸检时FV3疾病病程不同所致。此前在密苏里州的爬行动物中未能检测到这种感染,可能是由于缺乏监测,不过这些病例也可能代表了一种新的病毒传播至密苏里州的箱龟。我们的研究结果重申了之前的观点,即FV3感染的范围可能比之前记录的更广,并且感染可能发生在尚未检测的宿主物种中。