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Article: Rapid identification of imported influenza viruses at Xiamen International Airport via an active surveillance program

TitleRapid identification of imported influenza viruses at Xiamen International Airport via an active surveillance program
Authors
KeywordsBorder screening
Influenza
Phylogenetic analysis
Rapid test
Vaccine mismatch
Issue Date2018
PublisherElsevier Ltd. The Journal's web site is located at http://www.journals.elsevier.com/clinical-microbiology-and-infection/
Citation
Clinical Microbiology and Infection, 2018, v. 24 n. 3, p. 289-294 How to Cite?
AbstractObjectives: The cross-border transmission of infectious diseases is a worldwide public health issue. Current border screening measures are insufficiently sensitive. The study objectives were to describe the epidemiologic pattern of influenza infection among incoming travellers at Xiamen International Airport during nonpandemic periods and to assess the performance of a rapid influenza diagnostic test in border screening. Methods: Between May 2015 and May 2016, travellers with influenza-like illnesses entering China at Xiamen International Airport were screened with a rapid test, Flu Dot-ELISA, and the collected specimens were further subjected to virus isolation and phylogenetic analysis. Results: Of the 1 540 076 incoming travellers, 1224 cases of influenza-like illness were identified; 261 tested positive in the rapid test, and 176 were confirmed to be influenza through virus culture. The sensitivity and specificity of the rapid test were demonstrated to be 96.6% (170/176) and 91.3% (957/1048), respectively, and the positive predictive and negative predictive values were 65.1% (170/261) and 99.4% (957/963), respectively. The epidemiologic study indicated that H3N2 and (H1N1)pdm09 were dominant in 2015 and 2016, respectively. In 2016, an increased number of influenza B isolates and cocirculation of both Victoria and Yamagata lineage influenza B viruses were observed, and mismatches between circulating influenza A(H1N1)pdm09 and influenza B Victoria lineage strains and vaccine strains also occurred. Conclusions: We demonstrated the suitability and value of a high-sensitivity rapid influenza test in border screening and highlighted the importance of incoming travellers as a source of imported infectious diseases. © 2017 European Society of Clinical Microbiology and Infectious Diseases
Persistent Identifierhttp://hdl.handle.net/10722/248438
ISSN
2021 Impact Factor: 13.310
2020 SCImago Journal Rankings: 2.884
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChen, J-
dc.contributor.authorYang, K-
dc.contributor.authorZhang, M-
dc.contributor.authorShen, C-
dc.contributor.authorChen, J-
dc.contributor.authorWang, G-
dc.contributor.authorHuang, S-
dc.contributor.authorZhang, M-
dc.contributor.authorXiong, H-
dc.contributor.authorChen, H-
dc.contributor.authorChen, Y-
dc.contributor.authorXia, N-
dc.date.accessioned2017-10-18T08:43:11Z-
dc.date.available2017-10-18T08:43:11Z-
dc.date.issued2018-
dc.identifier.citationClinical Microbiology and Infection, 2018, v. 24 n. 3, p. 289-294-
dc.identifier.issn1198-743X-
dc.identifier.urihttp://hdl.handle.net/10722/248438-
dc.description.abstractObjectives: The cross-border transmission of infectious diseases is a worldwide public health issue. Current border screening measures are insufficiently sensitive. The study objectives were to describe the epidemiologic pattern of influenza infection among incoming travellers at Xiamen International Airport during nonpandemic periods and to assess the performance of a rapid influenza diagnostic test in border screening. Methods: Between May 2015 and May 2016, travellers with influenza-like illnesses entering China at Xiamen International Airport were screened with a rapid test, Flu Dot-ELISA, and the collected specimens were further subjected to virus isolation and phylogenetic analysis. Results: Of the 1 540 076 incoming travellers, 1224 cases of influenza-like illness were identified; 261 tested positive in the rapid test, and 176 were confirmed to be influenza through virus culture. The sensitivity and specificity of the rapid test were demonstrated to be 96.6% (170/176) and 91.3% (957/1048), respectively, and the positive predictive and negative predictive values were 65.1% (170/261) and 99.4% (957/963), respectively. The epidemiologic study indicated that H3N2 and (H1N1)pdm09 were dominant in 2015 and 2016, respectively. In 2016, an increased number of influenza B isolates and cocirculation of both Victoria and Yamagata lineage influenza B viruses were observed, and mismatches between circulating influenza A(H1N1)pdm09 and influenza B Victoria lineage strains and vaccine strains also occurred. Conclusions: We demonstrated the suitability and value of a high-sensitivity rapid influenza test in border screening and highlighted the importance of incoming travellers as a source of imported infectious diseases. © 2017 European Society of Clinical Microbiology and Infectious Diseases-
dc.languageeng-
dc.publisherElsevier Ltd. The Journal's web site is located at http://www.journals.elsevier.com/clinical-microbiology-and-infection/-
dc.relation.ispartofClinical Microbiology and Infection-
dc.rightsPosting accepted manuscript (postprint): © <year>. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.subjectBorder screening-
dc.subjectInfluenza-
dc.subjectPhylogenetic analysis-
dc.subjectRapid test-
dc.subjectVaccine mismatch-
dc.titleRapid identification of imported influenza viruses at Xiamen International Airport via an active surveillance program-
dc.typeArticle-
dc.identifier.emailChen, H: hlchen@hku.hk-
dc.identifier.authorityChen, H=rp00383-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.cmi.2017.05.027-
dc.identifier.pmid28587905-
dc.identifier.scopuseid_2-s2.0-85025625747-
dc.identifier.hkuros280835-
dc.identifier.volume24-
dc.identifier.issue3-
dc.identifier.spage289-
dc.identifier.epage294-
dc.identifier.isiWOS:000426417300015-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl1198-743X-

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