Amy J. Kinzler , Mary E. Wikswo , G.K. Balasubramani , Helen Eleni Aslanidou D’Agostino , Theresa Sax , Klancie Dauer , Geoffrey A. Weinberg , Peter Szilyagi , Leila C. Sahni , Julie A. Boom , Jennifer E. Schuster , Rangaraj Selvarajan , Christopher J. Harrison , Mary A. Staat , Daniel C. Payne , Natasha B. Halasa , Eileen J. Klein , Janet A. Englund , Judith M. Martin , Robert Hickey , John V. Williams
{"title":"Prevalence of human adenovirus in children with acute gastroenteritis in the New Vaccine Surveillance Network (NVSN) from 2016 to 2019","authors":"Amy J. Kinzler , Mary E. Wikswo , G.K. Balasubramani , Helen Eleni Aslanidou D’Agostino , Theresa Sax , Klancie Dauer , Geoffrey A. Weinberg , Peter Szilyagi , Leila C. Sahni , Julie A. Boom , Jennifer E. Schuster , Rangaraj Selvarajan , Christopher J. Harrison , Mary A. Staat , Daniel C. Payne , Natasha B. Halasa , Eileen J. Klein , Janet A. Englund , Judith M. Martin , Robert Hickey , John V. Williams","doi":"10.1016/j.jcv.2025.105822","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Acute gastroenteritis (AGE) is a leading cause of pediatric morbidity and mortality. However, the AGE burden from human adenoviruses (HAdV) is not fully defined.</div></div><div><h3>Objective</h3><div>To determine the prevalence and characteristics associated with HAdV in U.S. children.</div></div><div><h3>Study design</h3><div>We enrolled AGE case-patients <18 years of age in inpatient and emergency department (ED) settings and healthy controls <11 years of age between December 2016 and November 2019 at seven pediatric medical centers. Demographic and clinical data and stools were prospectively collected. Stools were tested for HAdV F40/41 using multiplex molecular panels. A subset of 120 HAdV-positive samples was genotyped.</div></div><div><h3>Results</h3><div>HAdV was detected in 168 (8 %) of 2229 ED patients, 164 (8 %) of 2151 inpatients, and 23 (1 %) of 2090 healthy controls. AGE case-patients positive for HAdV were more likely to be <3 years of age and more likely to report diarrhea (86 % vs 67 %) and dehydration (43 % vs 31 %) than HAdV-negative case-patients (p < 0.0001, all comparisons). Age did not differ significantly between HAdV-positive and negative controls. HAdV-positive AGE case-patients were less likely to have acute respiratory symptoms than HAdV-negative case-patients (8 % vs 18 %, p < 0.0001). The most frequently detected HAdV genotype was F41 (n = 106, 88 %). Other potential pathogens were detected in 36 % of HAdV-positive AGE case-patients and 43 % of controls; <em>Clostridioides difficile</em> was most common.</div></div><div><h3>Conclusions</h3><div>HAdV accounted for 8 % of medically attended AGE in both inpatient and ED settings in the U.S., primarily in young children. The majority of cases were type F41, which may inform future vaccine development.</div></div>","PeriodicalId":15517,"journal":{"name":"Journal of Clinical Virology","volume":"179 ","pages":"Article 105822"},"PeriodicalIF":4.0000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Virology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1386653225000642","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"VIROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Acute gastroenteritis (AGE) is a leading cause of pediatric morbidity and mortality. However, the AGE burden from human adenoviruses (HAdV) is not fully defined.
Objective
To determine the prevalence and characteristics associated with HAdV in U.S. children.
Study design
We enrolled AGE case-patients <18 years of age in inpatient and emergency department (ED) settings and healthy controls <11 years of age between December 2016 and November 2019 at seven pediatric medical centers. Demographic and clinical data and stools were prospectively collected. Stools were tested for HAdV F40/41 using multiplex molecular panels. A subset of 120 HAdV-positive samples was genotyped.
Results
HAdV was detected in 168 (8 %) of 2229 ED patients, 164 (8 %) of 2151 inpatients, and 23 (1 %) of 2090 healthy controls. AGE case-patients positive for HAdV were more likely to be <3 years of age and more likely to report diarrhea (86 % vs 67 %) and dehydration (43 % vs 31 %) than HAdV-negative case-patients (p < 0.0001, all comparisons). Age did not differ significantly between HAdV-positive and negative controls. HAdV-positive AGE case-patients were less likely to have acute respiratory symptoms than HAdV-negative case-patients (8 % vs 18 %, p < 0.0001). The most frequently detected HAdV genotype was F41 (n = 106, 88 %). Other potential pathogens were detected in 36 % of HAdV-positive AGE case-patients and 43 % of controls; Clostridioides difficile was most common.
Conclusions
HAdV accounted for 8 % of medically attended AGE in both inpatient and ED settings in the U.S., primarily in young children. The majority of cases were type F41, which may inform future vaccine development.
期刊介绍:
The Journal of Clinical Virology, an esteemed international publication, serves as the official journal for both the Pan American Society for Clinical Virology and The European Society for Clinical Virology. Dedicated to advancing the understanding of human virology in clinical settings, the Journal of Clinical Virology focuses on disseminating research papers and reviews pertaining to the clinical aspects of virology. Its scope encompasses articles discussing diagnostic methodologies and virus-induced clinical conditions, with an emphasis on practicality and relevance to clinical practice.
The journal publishes on topics that include:
• new diagnostic technologies
• nucleic acid amplification and serologic testing
• targeted and metagenomic next-generation sequencing
• emerging pandemic viral threats
• respiratory viruses
• transplant viruses
• chronic viral infections
• cancer-associated viruses
• gastrointestinal viruses
• central nervous system viruses
• one health (excludes animal health)