Viral and host factors associated with SARS-CoV-2 disease severity in Georgia, USA
While SARS-CoV-2 vaccines have shown strong efficacy, the continued emergence of new viral variants raises concerns about the ongoing and future public health impact of COVID-19, especially in locations with suboptimal vaccination uptake. We investigated viral and host factors, including vaccination...
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Published in | PloS one Vol. 20; no. 4; p. e0317972 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Public Library of Science
01.04.2025
Public Library of Science (PLoS) |
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Abstract | While SARS-CoV-2 vaccines have shown strong efficacy, the continued emergence of new viral variants raises concerns about the ongoing and future public health impact of COVID-19, especially in locations with suboptimal vaccination uptake. We investigated viral and host factors, including vaccination status, that were associated with SARS-CoV-2 disease severity in a setting with low vaccination rates. We analyzed clinical and demographic data from 1,957 individuals in the state of Georgia, USA, coupled with viral genome sequencing from 1,185 samples. We found no specific mutations associated with disease severity. Compared to those who were unvaccinated, vaccinated individuals experienced less severe SARS-CoV-2 disease, and the effect was similar for both variants. Vaccination within the prior 3-9 months was associated with decreased odds of moderate disease, severe disease, and death. Older age and underlying health conditions, especially immunosuppression and renal disease, were associated with increased disease severity. Overall, this study provides insights into the impact of vaccination status, variants/mutations, and clinical factors on disease severity in SARS-CoV-2 infection when vaccination rates are low. Understanding these associations will help refine and reinforce messaging around the crucial importance of vaccination in mitigating the severity of SARS-CoV-2 disease. |
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AbstractList | While SARS-CoV-2 vaccines have shown strong efficacy, the continued emergence of new viral variants raises concerns about the ongoing and future public health impact of COVID-19, especially in locations with suboptimal vaccination uptake. We investigated viral and host factors, including vaccination status, that were associated with SARS-CoV-2 disease severity in a setting with low vaccination rates. We analyzed clinical and demographic data from 1,957 individuals in the state of Georgia, USA, coupled with viral genome sequencing from 1,185 samples. We found no specific mutations associated with disease severity. Compared to those who were unvaccinated, vaccinated individuals experienced less severe SARS-CoV-2 disease, and the effect was similar for both variants. Vaccination within the prior 3-9 months was associated with decreased odds of moderate disease, severe disease, and death. Older age and underlying health conditions, especially immunosuppression and renal disease, were associated with increased disease severity. Overall, this study provides insights into the impact of vaccination status, variants/mutations, and clinical factors on disease severity in SARS-CoV-2 infection when vaccination rates are low. Understanding these associations will help refine and reinforce messaging around the crucial importance of vaccination in mitigating the severity of SARS-CoV-2 disease.While SARS-CoV-2 vaccines have shown strong efficacy, the continued emergence of new viral variants raises concerns about the ongoing and future public health impact of COVID-19, especially in locations with suboptimal vaccination uptake. We investigated viral and host factors, including vaccination status, that were associated with SARS-CoV-2 disease severity in a setting with low vaccination rates. We analyzed clinical and demographic data from 1,957 individuals in the state of Georgia, USA, coupled with viral genome sequencing from 1,185 samples. We found no specific mutations associated with disease severity. Compared to those who were unvaccinated, vaccinated individuals experienced less severe SARS-CoV-2 disease, and the effect was similar for both variants. Vaccination within the prior 3-9 months was associated with decreased odds of moderate disease, severe disease, and death. Older age and underlying health conditions, especially immunosuppression and renal disease, were associated with increased disease severity. Overall, this study provides insights into the impact of vaccination status, variants/mutations, and clinical factors on disease severity in SARS-CoV-2 infection when vaccination rates are low. Understanding these associations will help refine and reinforce messaging around the crucial importance of vaccination in mitigating the severity of SARS-CoV-2 disease. While SARS-CoV-2 vaccines have shown strong efficacy, the continued emergence of new viral variants raises concerns about the ongoing and future public health impact of COVID-19, especially in locations with suboptimal vaccination uptake. We investigated viral and host factors, including vaccination status, that were associated with SARS-CoV-2 disease severity in a setting with low vaccination rates. We analyzed clinical and demographic data from 1,957 individuals in the state of Georgia, USA, coupled with viral genome sequencing from 1,185 samples. We found no specific mutations associated with disease severity. Compared to those who were unvaccinated, vaccinated individuals experienced less severe SARS-CoV-2 disease, and the effect was similar for both variants. Vaccination within the prior 3-9 months was associated with decreased odds of moderate disease, severe disease, and death. Older age and underlying health conditions, especially immunosuppression and renal disease, were associated with increased disease severity. Overall, this study provides insights into the impact of vaccination status, variants/mutations, and clinical factors on disease severity in SARS-CoV-2 infection when vaccination rates are low. Understanding these associations will help refine and reinforce messaging around the crucial importance of vaccination in mitigating the severity of SARS-CoV-2 disease. |
Audience | Academic |
Author | Johnson, Laura M. Zhang, Rebecca Bombin, Andrei Langsjoen, Rose M. Ahmed, Alaa Kraft, Colleen Khosravi, Dara Westbrook, Adrianna Carmola, Ludy R. Chen, Cara Wang, Ethan Fitts, Eric Openo, Kyle P. Nguyen, Phuong-Vi Taz, Azmain Roebling, Allison Dorothy Zheng, Ziduo Waggoner, Jesse J. Reid, Alex Lam, Wilbur A. Arthur, Robert A. Lu, Yang Higginbotham, Dustin Babiker, Ahmed Piantadosi, Anne Crumpler, John Hunter Gulick, Dalia Arafat Bixler, Bri |
AuthorAffiliation | 9 Emory Integrated Genomics Core, Emory University School of Medicine, Atlanta, Georgia, United States of America Yale University School of Medicine, UNITED STATES OF AMERICA 8 Georgia Clinical & Translational Science Alliance, Emory University School of Medicine, Atlanta, Georgia, United States of America 2 Georgia Department of Health, Georgia Emerging Infections Program, Atlanta, Georgia, United States of America 11 Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia, United States of America 4 Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, United States of America 10 The Atlanta Center for Microsystems-Engineered Point-of-Care Technologies, Atlanta, Georgia, United States of America 14 Department of Pediatrics, Pediatric Biostatistics Core, School of Medicine, Emory University, Atlanta, Georgia, United States of America 3 Atlanta Veterans Affairs Medical Center, Decatur, Georgia, United States of A |
AuthorAffiliation_xml | – name: 3 Atlanta Veterans Affairs Medical Center, Decatur, Georgia, United States of America – name: 6 Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, Georgia, United States of America – name: 9 Emory Integrated Genomics Core, Emory University School of Medicine, Atlanta, Georgia, United States of America – name: 13 Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, Georgia, United States of America – name: 2 Georgia Department of Health, Georgia Emerging Infections Program, Atlanta, Georgia, United States of America – name: 4 Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, United States of America – name: Yale University School of Medicine, UNITED STATES OF AMERICA – name: 7 Emory Integrated Computational Core, Emory University School of Medicine, Atlanta, Georgia, United States of America – name: 12 Aflac Cancer and Blood Disorders Center at Children’s Healthcare of Atlanta, Atlanta, Georgia, United States of America – name: 1 Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, United States of America – name: 10 The Atlanta Center for Microsystems-Engineered Point-of-Care Technologies, Atlanta, Georgia, United States of America – name: 5 Graduate Program in Genetics and Molecular Biology, Emory University, Atlanta, Georgia, United States of America – name: 8 Georgia Clinical & Translational Science Alliance, Emory University School of Medicine, Atlanta, Georgia, United States of America – name: 14 Department of Pediatrics, Pediatric Biostatistics Core, School of Medicine, Emory University, Atlanta, Georgia, United States of America – name: 11 Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia, United States of America |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40168303$$D View this record in MEDLINE/PubMed |
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Copyright | Copyright: © 2025 Carmola et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. COPYRIGHT 2025 Public Library of Science 2025 Carmola et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2025 Carmola et al 2025 Carmola et al 2025 Carmola et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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