Bárria Cátia, Mil-Homens Dalila, Pinto Sandra N, Fialho Arsénio M, Arraiano Cecília M, Domingues Susana
Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, 2780-157 Oeiras, Portugal.
iBB-Institute for Bioengineering and Biosciences and i4HB-Institute for Health and Bioeconomy, Instituto Superior Técnico, Universidade de Lisboa, 1049-001 Lisboa, Portugal.
Microorganisms. 2022 Jan 29;10(2):317. doi: 10.3390/microorganisms10020317.
Pneumococcal infections have increasingly high mortality rates despite the availability of vaccines and antibiotics. Therefore, the identification of new virulence determinants and the understanding of the molecular mechanisms behind pathogenesis have become of paramount importance in the search of new targets for drug development. The exoribonuclease RNase R has been involved in virulence in a growing number of pathogens. In this work, we used as an infection model to demonstrate that the presence of RNase R increases the pneumococcus virulence. Larvae infected with the RNase R mutant show an increased expression level of antimicrobial peptides. Furthermore, they have a lower bacterial load in the hemolymph in the later stages of infection, leading to a higher survival rate of the larvae. Interestingly, pneumococci expressing RNase R show a sudden drop in bacterial numbers immediately after infection, resembling the eclipse phase observed after intravenous inoculation in mice. Concomitantly, we observed a lower number of mutant bacteria inside larval hemocytes and a higher susceptibility to oxidative stress when compared to the wild type. Together, our results indicate that RNase R is involved in the ability of pneumococci to evade the host immune response, probably by interfering with internalization and/or replication inside the larval hemocytes.
尽管有疫苗和抗生素,肺炎球菌感染的死亡率仍日益升高。因此,鉴定新的毒力决定因素并理解发病机制背后的分子机制,在寻找新的药物开发靶点方面已变得至关重要。外切核糖核酸酶RNase R已在越来越多的病原体的毒力中发挥作用。在这项研究中,我们以[此处原文缺失具体感染模型信息]作为感染模型,来证明RNase R的存在会增加肺炎球菌的毒力。感染RNase R突变体的幼虫显示抗菌肽表达水平增加。此外,在感染后期它们血淋巴中的细菌载量较低,从而导致幼虫的存活率更高。有趣的是,表达RNase R的肺炎球菌在感染后细菌数量会立即突然下降,类似于在小鼠静脉接种后观察到的隐蔽期。同时,与野生型相比,我们观察到幼虫血细胞内的突变细菌数量较少,且对氧化应激更敏感。总之,我们的结果表明RNase R可能通过干扰幼虫血细胞内的内化和/或复制,参与了肺炎球菌逃避宿主免疫反应的能力。