Shatnawi Shoroq, Gunasekara Sachithra, Bashor Laura, Tamil Selvan Miruthula, Nehring Mary, Cowan Shannon, Ritchey Jerry, VandeWoude Susan, Taylor Brianne, Miller Craig, Rudd Jennifer M
Department of Veterinary Pathobiology, College of Veterinary Medicine, Oklahoma State University, Stillwater, OK 74078, USA.
Department of Microbiology, Immunology, and Pathology, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO 80521, USA.
Microorganisms. 2024 Jun 25;12(7):1289. doi: 10.3390/microorganisms12071289.
People living with human immunodeficiency virus (PLWH) are a significant population globally. Research delineating our understanding of coinfections in PLWH is critical to care for those navigating infection with other pathogens. The recent COVID-19 pandemic underscored the urgent need for studying the effects of SARS-CoV-2 infections in therapy-controlled and uncontrolled immunodeficiency viral infections. This study established the utility of a feline model for the in vivo study of coinfections. Domestic cats are naturally infected with SARS-CoV-2 and Feline Immunodeficiency Virus, a lentivirus molecularly and pathogenically similar to HIV. In this study, comparisons are made between FIV-positive and FIV-negative cats inoculated with SARS-CoV-2 (B.1.617.2.) in an experimental setting. Of the FIV+ cats, three received Zidovudine (AZT) therapy in the weeks leading up to SARS-CoV-2 inoculation, and two did not. SARS-CoV-2 viral RNA was quantified, histopathologic comparisons of respiratory tissues were made, and T-cell populations were analyzed for immune phenotype shifts between groups. CD4+ T lymphocyte responses varied, with FIV+-untreated cats having the poorest CD4+ response to SARS-CoV-2 infection. While all cats had significant pulmonary inflammation, key histopathologic features of the disease differed between groups. Additionally, viral genomic analysis was performed, and results were analyzed for the presence of emerging, absent, amplified, or reduced mutations in SARS-CoV-2 viral RNA after passage through the feline model. Positive selection is noted, especially in FIV+ cats untreated with AZT, and mutations with potential relevance were identified; one FIV+-untreated cat had persistent, increasing SARS-CoV-2 RNA in plasma five days post-infection. These findings and others support the utility of the feline model for studying coinfection in people with HIV and highlight the importance of antiretroviral therapy in clearing SARS-CoV-2 coinfections to minimize transmission and emergence of mutations that may have deleterious effects.
全球范围内,人类免疫缺陷病毒感染者(PLWH)是一个庞大的群体。深入了解PLWH合并感染情况的研究对于护理那些同时感染其他病原体的患者至关重要。近期的新冠疫情凸显了研究严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染在治疗控制和未控制的免疫缺陷病毒感染中的影响的迫切需求。本研究确立了猫科动物模型在体内研究合并感染的实用性。家猫自然感染SARS-CoV-2和猫免疫缺陷病毒(一种在分子和致病机制上与HIV相似的慢病毒)。在本研究中,对在实验环境中接种SARS-CoV-2(B.1.617.2)的FIV阳性和FIV阴性猫进行了比较。在FIV+猫中,三只在接种SARS-CoV-2前几周接受了齐多夫定(AZT)治疗,两只未接受治疗。对SARS-CoV-2病毒RNA进行了定量,对呼吸组织进行了组织病理学比较,并分析了T细胞群体的免疫表型变化。CD4+T淋巴细胞反应各不相同,未接受治疗的FIV+猫对SARS-CoV-2感染的CD4+反应最差。虽然所有猫都有明显的肺部炎症,但各组疾病的关键组织病理学特征有所不同。此外,还进行了病毒基因组分析,并分析了结果,以确定在通过猫科动物模型后SARS-CoV-2病毒RNA中是否存在新出现、缺失、扩增或减少的突变。发现了阳性选择,尤其是在未接受AZT治疗的FIV+猫中,并鉴定出了具有潜在相关性的突变;一只未接受治疗的FIV+猫在感染后五天血浆中SARS-CoV-2 RNA持续增加。这些发现及其他研究结果支持了猫科动物模型在研究HIV感染者合并感染方面的实用性,并强调了抗逆转录病毒疗法在清除SARS-CoV-2合并感染以尽量减少可能产生有害影响的突变的传播和出现方面的重要性。