Effect of Simulated Cosmic Radiation on Cytomegalovirus Reactivation and Lytic Replication

Human exploration of the solar system will expose crew members to galactic cosmic radiation (GCR), with a potential for adverse health effects. GCR particles (protons and ions) move at nearly the speed of light and easily penetrate space station walls, as well as the human body. Previously, we have shown reactivation of latent herpesviruses, including herpes simplex virus, Varicella zoster virus, Epstein-Barr virus, and cytomegalovirus (CMV), during stays at the International Space Station. Given the prevalence of latent CMV and the known propensity of space radiation to cause alterations in many cellular processes, we undertook this study to understand the role of GCR in reactivating latent CMV. Latently infected Kasumi cells with CMV were irradiated with <sup>137</sup>Cs gamma rays, 150 MeV protons, 600 MeV/n carbon ions, 600 MeV/n iron ions, proton ions, and simulated GCR. The CMV copy number increased significantly in the cells exposed to radiation as compared with the non-irradiated controls. Viral genome sequencing did not reveal significant nucleotide differences among the compared groups. However, transcriptome analysis showed the upregulation of transcription of the UL49 ORF, implicating it in the switch from latent to lytic replication. These findings support our hypothesis that GCR may be a strong contributor to the reactivation of CMV infection seen in ISS crew members.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2024-09-26
DOI
https://doi.org/10.3390/ijms251910337
Citations
3
Primary Topic
Cytomegalovirus and herpesvirus research
Type
article
Field-Weighted Citation Impact
1.16

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article

Effect of Simulated Cosmic Radiation on Cytomegalovirus Reactivation and Lytic Replication

Ianik Plante, Satish Mehta, Brian E. Crucian, Ritesh Tandon et al.
3 citations
International Journal of Molecular Sciences
Cytomegalovirus and herpesvirus research
1.16
article

Effect of Simulated Cosmic Radiation on Cytomegalovirus Reactivation and Lytic Replication

Ianik Plante, Satish Mehta, Brian E. Crucian, Ritesh Tandon, Douglass M. Diak, Mayra Nelman‐Gonzalez, Sara Bustos-Lopez, Xi Chen, Stephen J. Stray
article en
3 citations

Abstract

Human exploration of the solar system will expose crew members to galactic cosmic radiation (GCR), with a potential for adverse health effects. GCR particles (protons and ions) move at nearly the speed of light and easily penetrate space station walls, as well as the human body. Previously, we have shown reactivation of latent herpesviruses, including herpes simplex virus, Varicella zoster virus, Epstein-Barr virus, and cytomegalovirus (CMV), during stays at the International Space Station. Given the prevalence of latent CMV and the known propensity of space radiation to cause alterations in many cellular processes, we undertook this study to understand the role of GCR in reactivating latent CMV. Latently infected Kasumi cells with CMV were irradiated with <sup>137</sup>Cs gamma rays, 150 MeV protons, 600 MeV/n carbon ions, 600 MeV/n iron ions, proton ions, and simulated GCR. The CMV copy number increased significantly in the cells exposed to radiation as compared with the non-irradiated controls. Viral genome sequencing did not reveal significant nucleotide differences among the compared groups. However, transcriptome analysis showed the upregulation of transcription of the UL49 ORF, implicating it in the switch from latent to lytic replication. These findings support our hypothesis that GCR may be a strong contributor to the reactivation of CMV infection seen in ISS crew members.

International Journal of Molecular SciencesVol. 25(19)
KBR (United States) (US), AEgis Technologies (United States) (US), University of Mississippi Medical Center (US), Johnson Space Center (US), JES Tech (United States) (US), University of Houston (US)
National Aeronautics and Space Administration, Nuclear Safety and Security Commission, Brookhaven National Laboratory
Openalex Percentile: Top 20%
Cytomegalovirus and herpesvirus research
1.16
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