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Influenza A Virus Isolation, Culture and Identification

Identifieur interne : 000817 ( Pmc/Corpus ); précédent : 000816; suivant : 000818

Influenza A Virus Isolation, Culture and Identification

Auteurs : Amie J. Eisfeld ; Gabriele Neumann ; Yoshihiro Kawaoka

Source :

RBID : PMC:5619698

Abstract

SUMMARY

Influenza A viruses (IAV) cause epidemics and pandemics that result in considerable financial burden and loss of human life. To manage annual IAV epidemics and prepare for future pandemics, improved understanding of how IAVs emerge, transmit, cause disease, and acquire pandemic potential is urgently needed. Fundamental techniques essential for procuring such knowledge are IAV isolation and culture from experimental and surveillance samples. Here, we present a detailed protocol for IAV sample collection and processing, amplification in chicken eggs and mammalian cells, and identification from samples containing unknown pathogens. This protocol is robust, and allows for generation of virus cultures that can be used for downstream analyses. Once experimental or surveillance samples are obtained, virus cultures can be generated and the presence of IAV can be verified in 3–5 days. Increased time-frames may be required for less experienced laboratory personnel, or when large numbers of samples will be processed.


Url:
DOI: 10.1038/nprot.2014.180
PubMed: 25321410
PubMed Central: 5619698

Links to Exploration step

PMC:5619698

Le document en format XML

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<title>SUMMARY</title>
<p id="P1">Influenza A viruses (IAV) cause epidemics and pandemics that result in considerable financial burden and loss of human life. To manage annual IAV epidemics and prepare for future pandemics, improved understanding of how IAVs emerge, transmit, cause disease, and acquire pandemic potential is urgently needed. Fundamental techniques essential for procuring such knowledge are IAV isolation and culture from experimental and surveillance samples. Here, we present a detailed protocol for IAV sample collection and processing, amplification in chicken eggs and mammalian cells, and identification from samples containing unknown pathogens. This protocol is robust, and allows for generation of virus cultures that can be used for downstream analyses. Once experimental or surveillance samples are obtained, virus cultures can be generated and the presence of IAV can be verified in 3–5 days. Increased time-frames may be required for less experienced laboratory personnel, or when large numbers of samples will be processed.</p>
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<article-title>Influenza A Virus Isolation, Culture and Identification</article-title>
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<name>
<surname>Eisfeld</surname>
<given-names>Amie J.</given-names>
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<pmc-comment>aefenney@vetmed.wisc.edu</pmc-comment>
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<name>
<surname>Neumann</surname>
<given-names>Gabriele</given-names>
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<pmc-comment>neumanng@vetmed.wisc.edu</pmc-comment>
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<xref rid="FN1" ref-type="author-notes">*</xref>
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Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, 575 Science Drive, Madison, WI 53711, USA</aff>
<aff id="A2">
<label>2</label>
ERATO Infection-Induced Host Responses Project, Japan Science and Technology Agency, Saitama 332-0012, Japan</aff>
<aff id="A3">
<label>3</label>
Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo 108-8639, Japan</aff>
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Department of Special Pathogens, International Research Center for Infectious Diseases, Institute of Medical Science, University of Tokyo, Minato-ku, Tokyo 108-8639, Japan</aff>
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<bold>Corresponding author’s telephone and fax numbers:</bold>
+1 (608) 265-4925 (office); +1 (608) 262-9641 (fax),
<email>kawaokay@svm.vetmed.wisc.edu</email>
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<fn fn-type="COI-statement" id="FN3">
<p>
<bold>COMPETING FINANCIAL INTERESTS</bold>
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<p>The authors declare that they have no competing financial interests.</p>
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<pub-date pub-type="nihms-submitted">
<day>1</day>
<month>9</month>
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<day>16</day>
<month>10</month>
<year>2014</year>
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<pub-date pub-type="ppub">
<month>11</month>
<year>2014</year>
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<pub-date pub-type="pmc-release">
<day>28</day>
<month>9</month>
<year>2017</year>
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<volume>9</volume>
<issue>11</issue>
<fpage>2663</fpage>
<lpage>2681</lpage>
<pmc-comment>elocation-id from pubmed: 10.1038/nprot.2014.180</pmc-comment>
<abstract>
<title>SUMMARY</title>
<p id="P1">Influenza A viruses (IAV) cause epidemics and pandemics that result in considerable financial burden and loss of human life. To manage annual IAV epidemics and prepare for future pandemics, improved understanding of how IAVs emerge, transmit, cause disease, and acquire pandemic potential is urgently needed. Fundamental techniques essential for procuring such knowledge are IAV isolation and culture from experimental and surveillance samples. Here, we present a detailed protocol for IAV sample collection and processing, amplification in chicken eggs and mammalian cells, and identification from samples containing unknown pathogens. This protocol is robust, and allows for generation of virus cultures that can be used for downstream analyses. Once experimental or surveillance samples are obtained, virus cultures can be generated and the presence of IAV can be verified in 3–5 days. Increased time-frames may be required for less experienced laboratory personnel, or when large numbers of samples will be processed.</p>
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