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Volume 14, Number 8—August 2008
Letter

Rarity of Influenza A Virus in Spring Shorebirds, Southern Alaska

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To the Editor: Knowledge of avian influenza (AI) virus and its host epidemiology and ecology is essential for effective monitoring and mitigation (1). Applicability of global and continental-scale models will be key for expanding this knowledge base. Research in the Delaware Bay area, eastern United States, suggests an ecologic and epidemiologic viewpoint of AI virus in wild birds in which shorebirds (family Scolopacidae) are predominant hosts in spring; however, research in Alberta, Canada, suggests that waterfowl are such in autumn (2,3). AI virus surveillance in Europe (4) suggests that the spring aspect of this scenario does not apply there. To increase knowledge of AI transport among shorebirds in spring in the North Pacific, we conducted AI virus surveillance during the springs of 2006 and 2007 at the Copper River Delta area of Alaska. Millions of birds congregate at this location in the spring, resulting in the highest spring shorebird concentrations in the New World (5). We also sampled gulls (Laridae), which are common and heretofore unsurveyed for AI in this ecosystem.

In 2006 and 2007, 1,050 shorebirds (Western Sandpiper, Calidris mauri, and Least Sandpiper, C. minutilla) and 770 Glaucous-winged Gulls (Larus glaucescens) were sampled during peak spring migration at Hartney Bay, Cordova, Alaska (60°28′N 146°8′W; Table). Fresh fecal samples were obtained from tidal flats within <1 to 90 min after identified flocks were dispersed, and samples were placed in sterile medium (brain heart infusion buffer with 10,000 U/mL penicillin G, 1 mg/mL gentamicin, and 20 μg/mL amphotericin B) and either kept cool (<1 week) before transport to Fairbanks (2006) or placed into liquid nitrogen within 2 h of collection (2007). Samples were stored at –70° C; shipped frozen overnight to Athens, Georgia; and maintained frozen until analyzed.

Samples were screened by real-time reverse transcriptase–PCR (RT-PCR) for influenza A virus, and virus isolation was performed on samples that were positive. RNA was extracted by adding 250 μL of sample to 750 μL Trizol LS reagent (Invitrogen, Inc., Carlsbad, CA, USA). Samples were mixed and incubated at room temperature for 10 min. A total of 200 μL of chloroform was then added, incubation was continued for 5 min, and samples were centrifuged for 15 min at 12,000 × g at 4° C. Supernatant was removed, and 50 μL was extracted with the MagMax AI/ND viral RNA extraction kit (Ambion, Inc. Austin, TX, USA). RNA was tested for AI virus matrix (M) gene. A positive test result for this gene indicates the presence of any influenza viruses (6) when an internal positive control is used (7). Positive samples were processed for virus isolation in embryonated chicken eggs by standard methods (8). Real-time RT-PCR results were corroborated by processing 50 randomly selected negative samples for virus isolation with 3 egg passages.

Screening for AI virus was conducted on 1,820 samples (Table). Among these, 1 AI virus was identified (A/Glaucous-wingedGull/AK/4906A/2006; H16N?), reflecting an overall prevalence of 0.055% (0% in shorebirds and 0.13% in gulls).

Results of power analysis (9) suggested that our shorebird samples would detect infection rates >0.9% with 99% probability (95% probability of detecting rates 1%–2% or higher in each year). In gulls, probability of detecting infection rates >1% across both years of the study (>6% in 2006 and >1%–2% in 2007) was 95%.

Virus prevalence in spring shorebirds in Alaska was substantially lower than prevalence in spring shorebirds in the Delaware Bay area (3) and more similar to prevalence in spring shorebirds in Europe (4). Our shorebird samples (1,050) were fewer than those in other studies (3; 4,266 samples from 4 species over 16 years, and 4; 3,159 samples from 47 species over 8 years, with 35% from spring), representing 25% and 33% of those studies, respectively. Our study covered only 2 years, but it would detect AI virus infections in shorebirds at rates >1%–2% within each year with 95% probability and at rates >0.9% across years with 99% probability. Thus, the prevalence rate among Copper River Delta shorebirds in our study is lower than that found in the 16-year Delaware Bay study (3). In the Delaware Bay area, 4 shorebird species were sampled: 3 Calidris and 1 Arenaria (3). Precise statistics are unavailable, but the average 16-year prevalence rate was 14.2%, fluctuating annually from ≈2% to ≈38% (3).

In Europe AI viruses were absent among spring shorebirds (4). Differences in prevalence rates found among studies may be influenced by species sampled, sampling procedures, and seasonal timing (4). However, with >1,000 spring shorebirds sampled, results suggest that differences might exist between the world’s major migration systems (3,4).

Our results corroborate other recent results (10) suggesting that AI prevalence rates among shorebirds at Delaware Bay are not typical within North America. Present evidence indicates (this study; 3,10) that the role of shorebirds in AI virus ecology and epidemiology is heterogeneous within North America and within a genus (Calidris). These findings confirm that knowledge of how AI viruses cycle in wild bird hosts remains incomplete at continental and family-level taxonomic scales. Only further surveillance can fill these knowledge gaps.

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Acknowledgments

We thank C. Pruett and J. Maley for assisting with field work and D.E. Stallknecht and an anonymous reviewer for providing helpful comments.

This research was supported by US Department of Agriculture Service Center Agencies 58-6612-2-217 and 58-6612-6-244, and AI supplemental Current Research Information System 6612-32000-051-00D.

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Kevin Winker*Comments to Author , Erica Spackman†, and David E. Swayne†
Author affiliations: *University of Alaska Museum, Fairbanks, Alaska, USA; †US Department of Agriculture, Athens, Georgia, USA;

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References

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DOI: 10.3201/eid1408.080083

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Kevin Winker, University of Alaska Museum, 907 Yukon Dr, Fairbanks, AK 99775, USA;

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Page created: July 12, 2010
Page updated: July 12, 2010
Page reviewed: July 12, 2010
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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