Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2011;6(10):e25526.
doi: 10.1371/journal.pone.0025526. Epub 2011 Oct 12.

Deployable laboratory response to influenza pandemic; PCR assay field trials and comparison with reference methods

Affiliations
Comparative Study

Deployable laboratory response to influenza pandemic; PCR assay field trials and comparison with reference methods

Timothy J J Inglis et al. PLoS One. 2011.

Abstract

Background: The influenza A/H1N1/09 pandemic spread quickly during the Southern Hemisphere winter in 2009 and reached epidemic proportions within weeks of the official WHO alert. Vulnerable population groups included indigenous Australians and remote northern population centres visited by international travellers. At the height of the Australian epidemic a large number of troops converged on a training area in northern Australia for an international exercise, raising concerns about their potential exposure to the emerging influenza threat before, during and immediately after their arrival in the area. Influenza A/H1N1/09 became the dominant seasonal variant and returned to Australia during the Southern winter the following year.

Methods: A duplex nucleic acid amplification assay was developed within weeks of the first WHO influenza pandemic alert, demonstrated in northwestern Australia shortly afterwards and deployed as part of the pathology support for a field hospital during a military exercise during the initial epidemic surge in June 2009.

Results: The nucleic acid amplification assay was twice as sensitive as a point of care influenza immunoassay, as specific but a little less sensitive than the reference laboratory nucleic acid amplification assay. Repetition of the field assay with blinded clinical samples obtained during the 2010 winter influenza season demonstrated a 91.7% congruence with the reference laboratory method.

Conclusions: Rapid in-house development of a deployable epidemic influenza assay allowed a flexible laboratory response, effective targeting of limited disease control resources in an austere military environment, and provided the public health laboratory service with a set of verification tools for resource-limited settings. The assay method was suitable for rapid deployment in time for the 2010 Northern winter.

PubMed Disclaimer

Conflict of interest statement

Competing Interests: Applied Biosystems loaned the thermocycler and magnetic bead extraction robot. Field lab equipment for the pandemic response was loaned by PathWest Laboratory Medicine, who also provided reagents gratis. Timothy J. J. Inglis, Adam J. Merritt, Avram Levy, Glenys Chidlow and David W. Smith are employees of PathWest Laboratory Medicine WA. There are no patents, products in development or marketed products to declare. This does not alter the authors' adherence to all the PLoS ONE policies on sharing data and materials, as detailed online in the guide for authors.

Figures

Figure 1
Figure 1. Deployable molecular microbiology laboratory.
Deployable molecular biology equipment used during the exercise. The layout corresponds to the two modules; left table – static field hospital used for real time PCR assays, right table – field portable. Only the hand-held magnetic bead extraction device from the field portable module was used in an attempt to detect influenza A by PCR assay during the military exercise.

Similar articles

Cited by

References

    1. Chidlow G, Harnett G, Williams S, Levy A, Speers D, et al. Duplex real-time RT-PCR assays for the rapid detection and identification of pandemic (H1N1) 2009, seasonal influenza viruses A/H1, A/H3 and B. J Clin Microbiol;48:862-866. Epub 2010 Jan. 2010;13 - PMC - PubMed
    1. Inglis TJJ, Merritt A, Montgomery J, Jayasinghe I, Thevanesam V, et al. Deployable laboratory response to emergence of melioidosis in central Sri Lanka. J Clin Microbiol. 2008;46:3479–3481. - PMC - PubMed
    1. Inglis TJJ, Murray RJ, Watson M. Trouble in paradise: Tropical, Emergency and Disaster Medicine Conference and Tropical Medicine Summit, Broome, WA, 22-25th May, 2009. Conference Report. Med J Aust. 2009;191:597–598. - PubMed
    1. Barry JM, Viboud C, Simonsen L. Cross-protection between successive waves of the 1918-1919 influenza pandemic: epidemiological evidence from US Army camps and from Britain. J Infect Dis. 2008;198:1427–1434. - PMC - PubMed
    1. Lakkstrom GL, Bryce L, Koenig M, Kosha S, Dick W, et al. Development of a department of defense regional viral respiratory surveillance program. Mil Med. 2009;174:35–41. - PubMed

Publication types

MeSH terms