TY - JOUR
T1 - Genome sequences of Human Adenovirus 14 isolates from mild respiratory cases and a fatal pneumonia, isolated during 2006-2007 epidemics in North America
AU - Houng, Huo Shu H.
AU - Gong, Heping
AU - Kajon, Adriana E.
AU - Jones, Morris S.
AU - Kuschner, Robert A.
AU - Lyons, Arthur
AU - Lott, Lisa
AU - Lin, Kuei Hsiang
AU - Metzgar, David
N1 - Funding Information:
The authors acknowledge the Clinic Commanders and medical staff at Lackland Air Force Base and Wilford Hall Medical Center, San Antonio, TX (US Air Force) and Marine Corps Recruit Depot, San Diego, CA for the permissions, access, and assistance necessary to conduct these studies. The authors also acknowledge the administrative support of the Henry M. Jackson Foundation for Military Medicine and the efforts of the entire WRAIR, NHRC, LRRI, and DGMC teams, especially the technicians and collection personnel whose efforts are represented in this work.
PY - 2010/8/25
Y1 - 2010/8/25
N2 - Background: Human adenovirus 14 (HAdV-14) is a recognized causative agent of epidemic febrile respiratory illness (FRI). Last reported in Eurasia in 1963, this virus has since been conspicuously absent in broad surveys, and was never isolated in North America despite inclusion of specific tests for this serotype in surveillance methods. In 2006 and 2007, this virus suddenly emerged in North America, causing high attack rate epidemics of FRI and, in some cases, severe pneumonias and occasional fatalities. Some outbreaks have been relatively mild, with low rates of progression beyond uncomplicated FRI, while other outbreaks have involved high rates of more serious outcomes.Methodology and Findings: In this paper we present the complete genomic sequence of this emerging pathogen, and compare genomic sequences of isolates from both mild and severe outbreaks. We also compare the genome sequences of the recent isolates with those of the prototype HAdV-14 that circulated in Eurasia 30 years ago and the closely related sequence of HAdV-11a, which has been circulating in southeast Asia.Conclusions: The data suggest that the currently circulating strain of HAdV-14 is closely related to the historically recognized prototype throughout its genome, though it does display a couple of potentially functional mutations in the fiber knob and E1A genes. There are no polymorphisms that suggest an obvious explanation for the divergence in severity between outbreak events, suggesting that differences in outcome are more likely environmental or host determined rather than viral genetics.
AB - Background: Human adenovirus 14 (HAdV-14) is a recognized causative agent of epidemic febrile respiratory illness (FRI). Last reported in Eurasia in 1963, this virus has since been conspicuously absent in broad surveys, and was never isolated in North America despite inclusion of specific tests for this serotype in surveillance methods. In 2006 and 2007, this virus suddenly emerged in North America, causing high attack rate epidemics of FRI and, in some cases, severe pneumonias and occasional fatalities. Some outbreaks have been relatively mild, with low rates of progression beyond uncomplicated FRI, while other outbreaks have involved high rates of more serious outcomes.Methodology and Findings: In this paper we present the complete genomic sequence of this emerging pathogen, and compare genomic sequences of isolates from both mild and severe outbreaks. We also compare the genome sequences of the recent isolates with those of the prototype HAdV-14 that circulated in Eurasia 30 years ago and the closely related sequence of HAdV-11a, which has been circulating in southeast Asia.Conclusions: The data suggest that the currently circulating strain of HAdV-14 is closely related to the historically recognized prototype throughout its genome, though it does display a couple of potentially functional mutations in the fiber knob and E1A genes. There are no polymorphisms that suggest an obvious explanation for the divergence in severity between outbreak events, suggesting that differences in outcome are more likely environmental or host determined rather than viral genetics.
UR - http://www.scopus.com/inward/record.url?scp=79251511635&partnerID=8YFLogxK
U2 - 10.1186/1465-9921-11-116
DO - 10.1186/1465-9921-11-116
M3 - Article
C2 - 20738863
AN - SCOPUS:79251511635
SN - 1465-9921
VL - 11
JO - Respiratory Research
JF - Respiratory Research
M1 - 116
ER -