在 K18-hACE2 转基因小鼠中开发 posadasii 球孢子菌和 SARS-CoV-2 协同感染模型

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Communications medicine Pub Date : 2024-09-30 DOI:10.1038/s43856-024-00610-y
Daniel R. Kollath, Francisca J. Grill, Ashley N. Itogawa, Ana Fabio-Braga, Matthew M. Morales, Kelly M. Shepardson, Mitchell L. Bryant, Jinhee Yi, Marieke L. Ramsey, Emily T. Luberto, Kimberly R. Celona, Paul S. Keim, Erik W. Settles, Douglas Lake, Bridget M. Barker
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引用次数: 0

摘要

背景:早期报告显示,COVID-19患者先前已治愈的球孢子菌病(山谷热,VF)再次复发,有迹象表明合并感染会导致更严重的后果。因此,我们研究了在 K18-hACE2 小鼠模型中连续感染 posadasii 球孢子菌和 SARS-CoV-2 的情况,以评估疾病的后果:方法:在我们的模型中,我们用亚致死剂量的 SARS-CoV-2 连续感染 K18-hACE2 小鼠,24 小时后再用低毒力的 posadasii 球孢子菌株连续感染 K18-hACE2,反之亦然。我们进行了小鼠存活率和致病机理研究,并观察了治疗组之间的全身免疫反应差异:结果:我们在此表明,共同感染组的疾病进展更为严重,存活率也有所下降。重要的是,不同的 SARS-CoV-2 变体(WA-1、Delta 或 Omicron)和感染时间(先感染 SARS-CoV-2,后感染 C. posadasii,反之亦然)会导致不同的结果。我们发现,先感染病毒的群体存活率下降,发病率和体重减轻,真菌和病毒负荷增加,免疫反应以及真菌球的数量和大小存在差异。我们还发现,首先合并感染 C. posadasii 的群体真菌负担和炎症反应均有所减轻:这是首次对 SARS-CoV-2 和球孢子菌的联合感染进行体内模型研究。结论:这是首次对SARS-CoV-2和球孢子菌双重感染进行体内模型研究。由于双重感染可能会增加疾病的严重程度,我们认为生活在球孢子菌病高流行地区的人群可能会经历更高的COVID-19并发症发病率。
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Developing a Coccidioides posadasii and SARS-CoV-2 Co-infection Model in the K18-hACE2 Transgenic Mouse
Early reports showed that patients with COVID-19 had recrudescence of previously resolved coccidioidomycosis (Valley fever, VF), and there were indications that coinfection had more severe outcomes. We therefore investigated serial infection of Coccidioides posadasii and SARS-CoV-2 in a K18-hACE2 mouse model to assess disease outcomes. In our model, we challenged K18-hACE2 mice sequentially with a sub-lethal dose of SARS-CoV-2 and 24 hours later with low virulence strain of Coccidioides posadasii, and vice versa, compared to mice that only received a single infection challenge. We performed survival and pathogenesis mouse studies as well as looked at the systemic immune response differences between treatment groups. Here we show that co-infected groups have a more severe disease progression as well as a decrease in survival. Importantly, results differ depending on the SARS-CoV-2 variant (WA-1, Delta, or Omicron) and infection timing (SARS-CoV-2 first, C. posadasii second or vice versa). We find that groups that are infected with the virus first had a decrease in survival, increased morbidity and weight loss, increased fungal and viral burdens, differences in immune responses, and the amount and size of fungal spherules. We also find that groups coinfected with C. posadasii first have a decrease fungal burden and inflammatory responses. This is the first in vivo model investigation of a coinfection of SARS-CoV-2 and Coccidioides. Because of the potential for increased severity of disease in a coinfection, we suggest populations that live in areas of high coccidioidomycosis endemicity may experience higher incidence of complicated disease progression with COVID-19. The Covid-19 pandemic presented significant challenges to healthcare systems. One of these was the increase in secondary infections, where a patient had both SARS-Cov2 and another infectious disease. Fungal infections co-occurring with or after a Covid-19 infection are of interest due to treatment challenges and more severe illness in patients. Valley fever is a fungal infection prevalent in the southwestern United States and arid regions of Central and South America. Reports from these regions showed an increase in Valley fever cases coinciding with the rise of Covid-19. We therefore investigated how these two pathogens interacted with each other and the host in laboratory-controlled mouse experiments. We observed increased mortality when mice were exposed to the virus first followed by a fungal infection. Although more investigations are needed, our results should be taken into consideration in a clinical setting. Kollath et al. develop a murine model for testing the pathogenesis of a SARS-CoV-2 and Coccidioides posadasii co-infection and find that when mice are infected first with the virus, greater disease severity occurs. This has implications for people living in the endemic area for coccidioidomycosis as well as other emerging viruses.
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