| Literature DB >> 25349393 |
Robert H Yolken1, Lorraine Jones-Brando2, David D Dunigan3, Geetha Kannan4, Faith Dickerson5, Emily Severance2, Sarven Sabunciyan2, C Conover Talbot6, Emese Prandovszky2, James R Gurnon3, Irina V Agarkova3, Flora Leister2, Kristin L Gressitt2, Ou Chen2, Bryan Deuber2, Fangrui Ma3, Mikhail V Pletnikov4, James L Van Etten7.
Abstract
Chloroviruses (family Phycodnaviridae) are large DNA viruses known to infect certain eukaryotic green algae and have not been previously shown to infect humans or to be part of the human virome. We unexpectedly found sequences homologous to the chlorovirus Acanthocystis turfacea chlorella virus 1 (ATCV-1) in a metagenomic analysis of DNA extracted from human oropharyngeal samples. These samples were obtained by throat swabs of adults without a psychiatric disorder or serious physical illness who were participating in a study that included measures of cognitive functioning. The presence of ATCV-1 DNA was confirmed by quantitative PCR with ATCV-1 DNA being documented in oropharyngeal samples obtained from 40 (43.5%) of 92 individuals. The presence of ATCV-1 DNA was not associated with demographic variables but was associated with a modest but statistically significant decrease in the performance on cognitive assessments of visual processing and visual motor speed. We further explored the effects of ATCV-1 in a mouse model. The inoculation of ATCV-1 into the intestinal tract of 9-11-wk-old mice resulted in a subsequent decrease in performance in several cognitive domains, including ones involving recognition memory and sensory-motor gating. ATCV-1 exposure in mice also resulted in the altered expression of genes within the hippocampus. These genes comprised pathways related to synaptic plasticity, learning, memory formation, and the immune response to viral exposure.Entities:
Keywords: chlorovirus ATCV-1; cognitive functioning; infection; metagenomic sequencing; oropharyngeal virome
Mesh:
Year: 2014 PMID: 25349393 PMCID: PMC4234575 DOI: 10.1073/pnas.1418895111
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205