School of Animal and Veterinary Sciences, The University of Adelaide, Roseworthy, South Australia, Australia.
School of Veterinary Sciences, The University of Queensland, Gatton, Queensland, Australia.
J Comp Pathol. 2020 Apr;176:50-66. doi: 10.1016/j.jcpa.2020.02.003. Epub 2020 Mar 12.
Koala retrovirus (KoRV) infection shows differences in prevalence and load between northern and southern Australian koala populations; however, the effect of this on diseases such as lymphoma and chlamydial disease is unclear. This study compared clinicopathological findings, haematology and splenic lymphoid area of KoRV-positive koalas from northern (Queensland [Qld], n = 67) and southern (South Australia [SA], n = 92) populations in order to provide further insight into KoRV pathogenesis. Blood was collected for routine haematology and for measurement of KoRV proviral load by quantitative polymerase chain reaction (qPCR). Plasma samples were assessed for KoRV viral load by reverse transcriptase qPCR and conjunctival and cloacal swabs were collected for measurement of the load of Chlamydia pecorum (qPCR). During necropsy examination, spleen was collected for lymphoid area analysis. Lymphoma was morphologically similar between the populations and occurred in koalas with the highest KoRV proviral and viral loads. Severe ocular chlamydial disease was observed in both populations, but urinary tract disease was more severe in Qld, despite similar C. pecorum loads. No associations between KoRV and chlamydial disease severity or load were observed, except in SA where viral load correlated positively with chlamydial disease severity. In both populations, proviral and viral loads correlated positively with lymphocyte and metarubricyte counts and correlated negatively with erythrocyte and neutrophil counts. Splenic lymphoid area was correlated positively with viral load. This study has shown further evidence for KoRV-induced oncogenesis and highlighted that lymphocytes and splenic lymphoid tissue may be key sites for KoRV replication. However, KoRV infection appears to be highly complex and continued investigation is required to fully understand its pathogenesis.
考拉逆转录病毒(KoRV)感染在澳大利亚北部和南部考拉群体中的流行率和负荷存在差异;然而,这对淋巴瘤和衣原体病等疾病的影响尚不清楚。本研究比较了来自北部(昆士兰州[Qld],n=67)和南部(南澳大利亚州[SA],n=92)考拉群体的 KoRV 阳性考拉的临床病理发现、血液学和脾脏淋巴样区,以进一步了解 KoRV 的发病机制。采集血液进行常规血液学检查,并通过定量聚合酶链反应(qPCR)测量 KoRV 前病毒负荷。通过逆转录 qPCR 评估血浆样本中的 KoRV 病毒载量,并采集结膜和泄殖腔拭子测量鹦鹉热衣原体(qPCR)的载量。在尸检检查期间,收集脾脏进行淋巴样区分析。在两个群体中,淋巴瘤的形态相似,并且发生在 KoRV 前病毒和病毒载量最高的考拉中。在两个群体中都观察到严重的眼部衣原体病,但在 Qld 中尿路疾病更为严重,尽管衣原体负荷相似。除了在 SA 中观察到病毒载量与衣原体病严重程度呈正相关外,未观察到 KoRV 与衣原体病严重程度或负荷之间的关联。在两个群体中,前病毒和病毒载量与淋巴细胞和中幼红细胞计数呈正相关,与红细胞和中性粒细胞计数呈负相关。脾脏淋巴样区与病毒载量呈正相关。本研究进一步证明了 KoRV 诱导的致癌作用,并强调了淋巴细胞和脾脏淋巴组织可能是 KoRV 复制的关键部位。然而,KoRV 感染似乎非常复杂,需要进一步研究才能全面了解其发病机制。