@article{204446,
  author = {Jurre Siegers and Lucas Ferreri and Dirk Eggink and Edwin Kroeze and Aartjan Velthuis and Marco van de Bildt and Lonneke Leijten and Peter van Run and Dennis de Meulder and Theo Bestebroer and Mathilde Richard and Thijs Kuiken and Anice Lowen and Sander Herfst and Debby van Riel},
  title = {Evolution of highly pathogenic H5N1 influenza A virus in the central nervous system of ferrets.},
  abstract = {<p>Central nervous system (CNS) disease is the most common extra-respiratory tract complication of influenza A virus infections in humans. Remarkably, zoonotic highly pathogenic avian influenza (HPAI) H5N1 virus infections are more often associated with CNS disease than infections with seasonal influenza viruses. Evolution of avian influenza viruses has been extensively studied in the context of respiratory infections, but evolutionary processes in CNS infections remain poorly understood. We have previously observed that the ability of HPAI A/Indonesia/5/2005 (H5N1) virus to replicate in and spread throughout the CNS varies widely between individual ferrets. Based on these observations, we sought to understand the impact of entrance into and replication within the CNS on the evolutionary dynamics of virus populations. First, we identified and characterized three substitutions-PB1 E177G and A652T and NP I119M - detected in the CNS of a ferret infected with influenza A/Indonesia/5/2005 (H5N1) virus that developed a severe meningo-encephalitis. We found that some of these substitutions, individually or collectively, resulted in increased polymerase activity in vitro. Nevertheless, in vivo, the virus bearing the CNS-associated mutations retained its capacity to infect the CNS but showed reduced dispersion to other anatomical sites. Analyses of viral diversity in the nasal turbinate and olfactory bulb revealed the lack of a genetic bottleneck acting on virus populations accessing the CNS via this route. Furthermore, virus populations bearing the CNS-associated mutations showed signs of positive selection in the brainstem. These features of dispersion to the CNS are consistent with the action of selective processes, underlining the potential for H5N1 viruses to adapt to the CNS.</p>},
  year = {2023},
  journal = {PLoS pathogens},
  volume = {19},
  pages = {e1011214},
  month = {03/2023},
  issn = {1553-7374},
  doi = {10.1371/journal.ppat.1011214},
  language = {eng},
}