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Article: Clinical and molecular epidemiology of human bocavirus in respiratory and fecal samples from children in Hong Kong
Title | Clinical and molecular epidemiology of human bocavirus in respiratory and fecal samples from children in Hong Kong |
---|---|
Authors | |
Issue Date | 2007 |
Publisher | Oxford University Press. The Journal's web site is located at http://jid.oxfordjournals.org |
Citation | Journal Of Infectious Diseases, 2007, v. 196 n. 7, p. 986-993 How to Cite? |
Abstract | Background. Human bocavirus (HBoV) is a recently discovered parvovirus associated with respiratory tract infections in children. We conducted the first systematic prospective clinical and molecular study using nasopharyngeal aspirates (NPAs) and fecal samples. Methods. NPAs negative for influenza virus, parainfluenza virus, respiratory syncytial virus, adenovirus, and coronavirus and fecal samples from patients with acute gastroenteritis were included. On the basis of results from a pilot study using 400 NPAs from all age groups, a prospective 12-month study was conducted to detect HBoV in 1200 NPAs and 1435 fecal samples from patients <18 years old by polymerase chain reaction. The complete genome sequences of HBoVs from 12 NPAs and 12 fecal samples were determined. Results. Of the 400 NPAs collected in the pilot study, 20 (5.0%) were found to contain HBoV, all from children <5 years old. In the subsequent prospective study of pediatric patients, HBoV was detected in 83 (6.9%) of 1200 NPAs. Upper and lower respiratory tract infections were equally common. HBoV was detected in 30 (2.1%) of 1435 fecal samples. Fever and watery diarrhea were the most common symptoms. The seasonality of HBoV in NPAs and fecal samples was similar. Codetection with other pathogens occurred in 33% and 56% of NPAs and fecal samples, respectively, from patients with HBoV infection. Genomes of HBoVs from NPAs and fecal samples displayed minimal sequence variations. Conclusions. HBoV was detected in fecal specimens in children with acute gastroenteritis. A single lineage of HBoV was associated with both respiratory tract and enteric infections. © 2007 by the Infectious Diseases Society of America. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/57297 |
ISSN | 2023 Impact Factor: 5.0 2023 SCImago Journal Rankings: 2.387 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lau, SKP | en_HK |
dc.contributor.author | Yip, CCY | en_HK |
dc.contributor.author | Que, TL | en_HK |
dc.contributor.author | Lee, RA | en_HK |
dc.contributor.author | AuYeung, RKH | en_HK |
dc.contributor.author | Zhou, B | en_HK |
dc.contributor.author | So, LY | en_HK |
dc.contributor.author | Lau, YL | en_HK |
dc.contributor.author | Chan, KH | en_HK |
dc.contributor.author | Woo, PCY | en_HK |
dc.contributor.author | Yuen, KY | en_HK |
dc.date.accessioned | 2010-04-12T01:32:19Z | - |
dc.date.available | 2010-04-12T01:32:19Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | Journal Of Infectious Diseases, 2007, v. 196 n. 7, p. 986-993 | en_HK |
dc.identifier.issn | 0022-1899 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/57297 | - |
dc.description.abstract | Background. Human bocavirus (HBoV) is a recently discovered parvovirus associated with respiratory tract infections in children. We conducted the first systematic prospective clinical and molecular study using nasopharyngeal aspirates (NPAs) and fecal samples. Methods. NPAs negative for influenza virus, parainfluenza virus, respiratory syncytial virus, adenovirus, and coronavirus and fecal samples from patients with acute gastroenteritis were included. On the basis of results from a pilot study using 400 NPAs from all age groups, a prospective 12-month study was conducted to detect HBoV in 1200 NPAs and 1435 fecal samples from patients <18 years old by polymerase chain reaction. The complete genome sequences of HBoVs from 12 NPAs and 12 fecal samples were determined. Results. Of the 400 NPAs collected in the pilot study, 20 (5.0%) were found to contain HBoV, all from children <5 years old. In the subsequent prospective study of pediatric patients, HBoV was detected in 83 (6.9%) of 1200 NPAs. Upper and lower respiratory tract infections were equally common. HBoV was detected in 30 (2.1%) of 1435 fecal samples. Fever and watery diarrhea were the most common symptoms. The seasonality of HBoV in NPAs and fecal samples was similar. Codetection with other pathogens occurred in 33% and 56% of NPAs and fecal samples, respectively, from patients with HBoV infection. Genomes of HBoVs from NPAs and fecal samples displayed minimal sequence variations. Conclusions. HBoV was detected in fecal specimens in children with acute gastroenteritis. A single lineage of HBoV was associated with both respiratory tract and enteric infections. © 2007 by the Infectious Diseases Society of America. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Oxford University Press. The Journal's web site is located at http://jid.oxfordjournals.org | en_HK |
dc.relation.ispartof | Journal of Infectious Diseases | en_HK |
dc.rights | Journal of Infectious Diseases. Copyright © University of Chicago Press. | en_HK |
dc.subject.mesh | Bocavirus - classification - genetics - isolation & purification | en_HK |
dc.subject.mesh | Epidemiology, Molecular | en_HK |
dc.subject.mesh | Gastroenteritis - epidemiology - physiopathology - virology | en_HK |
dc.subject.mesh | Parvoviridae Infections - epidemiology - physiopathology - virology | en_HK |
dc.subject.mesh | Respiratory Tract Infections - epidemiology - virology | en_HK |
dc.title | Clinical and molecular epidemiology of human bocavirus in respiratory and fecal samples from children in Hong Kong | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0022-1899&volume=196&issue=7&spage=986&epage=993&date=2007&atitle=Clinical+and+molecular+epidemiology+of+human+bocavirus+in+respiratory+and+fecal+samples+from+children+in+Hong+Kong | en_HK |
dc.identifier.email | Lau, SKP: skplau@hkucc.hku.hk | en_HK |
dc.identifier.email | Yip, CCY: yipcyril@hku.hk | en_HK |
dc.identifier.email | Lau, YL: lauylung@hku.hk | en_HK |
dc.identifier.email | Woo, PCY: pcywoo@hkucc.hku.hk | en_HK |
dc.identifier.email | Yuen, KY: kyyuen@hkucc.hku.hk | en_HK |
dc.identifier.authority | Lau, SKP=rp00486 | en_HK |
dc.identifier.authority | Yip, CCY=rp01721 | en_HK |
dc.identifier.authority | Lau, YL=rp00361 | en_HK |
dc.identifier.authority | Woo, PCY=rp00430 | en_HK |
dc.identifier.authority | Yuen, KY=rp00366 | en_HK |
dc.description.nature | published_or_final_version | en_HK |
dc.identifier.doi | 10.1086/521310 | en_HK |
dc.identifier.pmid | 17763318 | - |
dc.identifier.scopus | eid_2-s2.0-35348815516 | en_HK |
dc.identifier.hkuros | 136563 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-35348815516&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 196 | en_HK |
dc.identifier.issue | 7 | en_HK |
dc.identifier.spage | 986 | en_HK |
dc.identifier.epage | 993 | en_HK |
dc.identifier.eissn | 1537-6613 | - |
dc.identifier.isi | WOS:000249572500007 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Lau, SKP=7401596211 | en_HK |
dc.identifier.scopusauthorid | Yip, CCY=14016999800 | en_HK |
dc.identifier.scopusauthorid | Que, TL=7003786628 | en_HK |
dc.identifier.scopusauthorid | Lee, RA=7408203830 | en_HK |
dc.identifier.scopusauthorid | AuYeung, RKH=22833521900 | en_HK |
dc.identifier.scopusauthorid | Zhou, B=7401906727 | en_HK |
dc.identifier.scopusauthorid | So, LY=36784797000 | en_HK |
dc.identifier.scopusauthorid | Lau, YL=7201403380 | en_HK |
dc.identifier.scopusauthorid | Chan, KH=7406034307 | en_HK |
dc.identifier.scopusauthorid | Woo, PCY=7201801340 | en_HK |
dc.identifier.scopusauthorid | Yuen, KY=36078079100 | en_HK |
dc.identifier.citeulike | 2878763 | - |
dc.identifier.issnl | 0022-1899 | - |