de Oliveira Bottino Fernanda, Euzebio Pereira Dias de Oliveira Barbara Cristina, Rodrigues Dos Santos João Paulo, Barata Viana Tiradentes Mariana, Rodrigues Maia de Souza Yuli, Silva Galdino de Paula Tainah, da Silva Medeiros Elido Hyago, Barbieri Dos Santos Isabele, Pereira Ribeiro Ieda, Bonaldo Myrna Cristina, Pelajo Machado Marcelo, de Abreu Manso Pedro Paulo
Laboratory of Experimental Medicine and Health (Lames), Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, , Brazil; Laboratory of Professional Education in Laboratory Techniques in Health (Latec), Polytechnic School of Health Joaquim Venancio, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Laboratory of Experimental Medicine and Health (Lames), Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, , Brazil.
Virus Res. 2024 Dec;350:199505. doi: 10.1016/j.virusres.2024.199505. Epub 2024 Dec 7.
The Yellow Fever virus (YFV) wild-type strains studied until now have little or no ability to evade the Syrian hamster interferon antiviral response. Thus, evaluating the susceptibility of this model to new YFV isolates is paramount to aid in the understanding of their viscerotropic phenotype. To this end, Syrian hamsters were inoculated intraperitoneally with two Brazilian wild-type YFV isolates originated from dying or dead howler monkeys obtained during outbreaks in the states of Rio Grande do Sul in 2008 (PR4408) and Rio de Janeiro in 2019 (RJ155). The results were compared with a YFV experimental vaccine strain (17DD). The main findings observed for animals infected with the PR4408 strain were progressive weight loss and persistent viremia (at least up to day seven post-infection), associated with viral RNA detection in the liver, and hepatic, splenic, and pancreatic histological alterations consistent with YF. The infection was eliminated seven days post-infection in animals inoculated with the RJ155 strain. No changes were observed for animals infected with 17DD virus. The findings indicate that both Brazilian isolates are able to infect Syrian hamsters, resulting in histopathological changes compatible with the YF pathology observed in humans. Furthermore, the PR4408 strain exhibited increased virulence in this mammalian model, despite causing a non-fatal infection.
截至目前所研究的黄热病病毒(YFV)野生型毒株几乎没有或完全没有能力逃避叙利亚仓鼠的干扰素抗病毒反应。因此,评估该模型对新的YFV分离株的易感性对于帮助理解它们的嗜内脏表型至关重要。为此,给叙利亚仓鼠腹腔内接种了两种巴西野生型YFV分离株,它们分别源自2008年在南里奥格兰德州疫情期间获得的濒死或死亡的吼猴(PR4408)以及2019年在里约热内卢获得的濒死或死亡的吼猴(RJ155)。将结果与一种YFV实验疫苗株(17DD)进行了比较。对于感染PR4408毒株的动物,观察到的主要结果是体重逐渐减轻和持续性病毒血症(至少持续到感染后第7天),伴有肝脏中病毒RNA的检测,以及与黄热病一致的肝脏、脾脏和胰腺组织学改变。接种RJ155毒株的动物在感染后7天病毒被清除。感染17DD病毒的动物未观察到变化。这些发现表明,两种巴西分离株都能够感染叙利亚仓鼠,导致与人类中观察到的黄热病病理学相符的组织病理学变化。此外,尽管PR4408毒株引起的是非致命性感染,但在这个哺乳动物模型中其毒力有所增强。