Influenza A viruses initiate infection when the envelope glycoprotein hemagglutinin (HA) binds sialic?acid-containing receptors on host cells and mediates membrane fusion. HA?mediated cross?linking of erythrocytes forms the basis of the hemagglutination (HA) and hemagglutination?inhibition (HI) assays that are widely used to quantify virus and virus?specific antibodies. The choice of erythrocyte species significantly affects these assays, but data for large ratites are limited. This study compared the hemagglutination characteristics of two highly pathogenic avian influenza A (H5N1) isolates, A/H5N1/Bogor 2 and A/H5N1/Lawang, using erythrocytes from ostrich, emu, quail, chicken and horse. Blood was collected from clinically healthy adult animals (n = 5 per species) (wing vein for chickens and quails; jugular vein for ostriches, emus and horses). Washed erythrocytes were examined by bright?field microscopy and used in a microtiter HA assay in which serial two?fold dilutions of erythrocytes were mixed with a constant dose of virus (105 TCID50 per well). Hemagglutination patterns were recorded up to 300 min and expressed as the highest erythrocyte dilution showing complete agglutination. Ostrich and emu erythrocytes were markedly larger than those of chicken and quail, whereas horse erythrocytes were small and anucleate. All five species supported hemagglutination by both A(H5N1) isolates. For A/H5N1/Bogor 2, horse erythrocytes showed delayed agglutination and a subsequent decline in HA titer, whereas avian erythrocytes yielded high, stable titers. For A/H5N1/Lawang, HA titers were more homogeneous and largely time?independent across species. Overall, differences between virus strains were greater than those between erythrocyte species, suggesting that viral HA properties dominate over gross erythrocyte morphology in determining hemagglutination and that the optimal erythrocyte species for HA and HI testing of H5N1 viruses may vary among strains.
References
[1]
Bosch, F.X., Orlich, M., Klenk, H. and Rott, R. (1979) The Structure of the Hemagglutinin, a Determinant for the Pathogenicity of Influenza Viruses. Virology, 95, 197-207. https://doi.org/10.1016/0042-6822(79)90414-8
[2]
Yang, Z., Wei, C., Kong, W., Wu, L., Xu, L., Smith, D.F., et al. (2007) Immunization by Avian H5 Influenza Hemagglutinin Mutants with Altered Receptor Binding Specificity. Science, 317, 825-828. https://doi.org/10.1126/science.1135165
[3]
Suarez, D.L. and Schultz-Cherry, S. (2000) Immunology of Avian Influenza Virus: A Review. Developmental & Comparative Immunology, 24, 269-283. https://doi.org/10.1016/s0145-305x(99)00078-6
[4]
Killian, M.L. (2014) Hemagglutination Assay for Influenza Virus. In: Spackman, E., Ed., Animal Influenza Virus, Springer, 3-9. https://doi.org/10.1007/978-1-4939-0758-8_1
[5]
Pedersen, J.C. (2014) Hemagglutination-inhibition Assay for Influenza Virus Subtype Identification and the Detection and Quantitation of Serum Antibodies to Influenza Virus. In: Spackman, E., Ed., Animal Influenza Virus, Springer, 11-25. https://doi.org/10.1007/978-1-4939-0758-8_2
[6]
Pawar, S.D., Parkhi, S.S., Koratkar, S.S. and Mishra, A.C. (2012) Receptor Specificity and Erythrocyte Binding Preferences of Avian Influenza Viruses Isolated from India. Virology Journal, 9, Article No. 251. https://doi.org/10.1186/1743-422x-9-251
[7]
Trombetta, C.M., Ulivieri, C., Cox, R.J., Remarque, E.J. and Montomoli, E. (2018) Impact of Erythrocyte Species on Assays for Influenza Serology. Journal of Preventive Medicine and Hygiene, 59, E1-E7. https://doi.org/10.15167/2421-4248/jpmh2018.59.1.870
[8]
Wibawa, H., Henning, J., Waluyati, D.E., Usman, T.B., Lowther, S., Bingham, J., et al. (2012) Comparison of Serological Assays for Detecting Antibodies in Ducks Exposed to H5 Subtype Avian Influenza Virus. BMC Veterinary Research, 8, Article No. 117. https://doi.org/10.1186/1746-6148-8-117
[9]
Kayali, G., Setterquist, S.F., Capuano, A.W., Myers, K.P., Gill, J.S. and Gray, G.C. (2008) Testing Human Sera for Antibodies against Avian Influenza Viruses: Horse RBC Hemagglutination Inhibition vs. Microneutralization Assays. Journal of Clinical Virology, 43, 73-78. https://doi.org/10.1016/j.jcv.2008.04.013
[10]
Chatziprodromidou, I.P., Arvanitidou, M., Guitian, J., Apostolou, T., Vantarakis, G. and Vantarakis, A. (2018) Global Avian Influenza Outbreaks 2010-2016: A Systematic Review of Their Distribution, Avian Species and Virus Subtype. Systematic Reviews, 7, Article No. 17. https://doi.org/10.1186/s13643-018-0691-z
[11]
Harfoot, R. and Webby, R.J. (2017) H5 Influenza, a Global Update. Journal of Microbiology, 55, 196-203. https://doi.org/10.1007/s12275-017-7062-7
[12]
WOAH (2021) Manual of Diagnostic Tests and Vaccines for Terrestrial Animals. Chapter 3.3.4: Avian Influenza (Including Infection with High Pathogenicity Avian Influenza Viruses).
[13]
Charostad, J., Rezaei Zadeh Rukerd, M., Mahmoudvand, S., Bashash, D., Hashemi, S.M.A., Nakhaie, M., et al. (2023) A Comprehensive Review of Highly Pathogenic Avian Influenza (HPAI) H5N1: An Imminent Threat at Doorstep. Travel Medicine and Infectious Disease, 55, Article ID: 102638. https://doi.org/10.1016/j.tmaid.2023.102638
[14]
Baz, M., Luke, C.J., Cheng, X., Jin, H. and Subbarao, K. (2013) H5N1 Vaccines in Humans. Virus Research, 178, 78-98. https://doi.org/10.1016/j.virusres.2013.05.006
[15]
Poland, G.A. (2006) Vaccines against Avian Influenza—A Race against Time. New England Journal of Medicine, 354, 1411-1413. https://doi.org/10.1056/nejme068047
[16]
Rimmelzwaan, G.F. and Osterhaus, A.D.M.E. (2001) Influenza Vaccines: New Developments. Current Opinion in Pharmacology, 1, 491-496. https://doi.org/10.1016/s1471-4892(01)00085-6
[17]
McKimm‐Breschkin, J.L. (2012) Influenza Neuraminidase Inhibitors: Antiviral Action and Mechanisms of Resistance. Influenza and Other Respiratory Viruses, 7, 25-36. https://doi.org/10.1111/irv.12047
[18]
Artois, J., Ippoliti, C., Conte, A., Dhingra, M.S., Alfonso, P., Tahawy, A.E., et al. (2018) Avian Influenza a (H5N1) Outbreaks in Different Poultry Farm Types in Egypt: The Effect of Vaccination, Closing Status and Farm Size. BMC Veterinary Research, 14, Article No. 187. https://doi.org/10.1186/s12917-018-1519-8
[19]
McIntosh, E.D.G. (2018) Healthcare-Associated Infections: Potential for Prevention through Vaccination. Therapeutic Advances in Vaccines and Immunotherapy, 6, 19-27. https://doi.org/10.1177/2515135518763183
[20]
Adachi, K., Handharyani, E., Sari, D.K., Takama, K., Fukuda, K., Endo, I., Yamamo-to, R., Sawa, M., Tanaka, M., Konishi, I. and Tsukamoto, Y. (2008) Development of Neutralization Antibodies against Highly Pathogenic H5N1 Avian Influenza Virus Using Ostrich (Struthio camelus) Yolk. Molecular Medicine Reports, 1, 203-209.
[21]
Adachi, K., Takama, K., Tsukamoto, M., Inai, M., Handharyani, E., Hiroi, S., et al. (2010) Ostrich Produce Cross-Reactive Neutralization Antibodies against Pandemic Influenza Virus A/H1N1 Following Immunization with a Seasonal Influenza Vaccine. Experimental and Therapeutic Medicine, 2, 41-45. https://doi.org/10.3892/etm.2010.180
[22]
Tsukamoto, M., et al. (2011) Antibodies against Swine Influenza Virus Neutralize the Pandemic Influenza Virus A/H1N1. Molecular Medicine Reports, 4, 209-214. https://doi.org/10.3892/mmr.2011.410
[23]
Kamiyama, Y., Adachi, K., Handharyani, E., Soejoedono, R.D., Kusano, T., Inai, M., et al. (2011) Protection from Avian Influenza H5N1 Virus Infection with Antibody-Impregnated Filters. Virology Journal, 8, Article No. 54. https://doi.org/10.1186/1743-422x-8-54
[24]
Adachi, K., Suryaman, G.K., Soejoedono, R.D., Handharyani, E. and Tsukamoto, Y. (2018) Prevention of Highly Pathogenic Avian Influenza A/H5N1 Infection by Passive Immunotherapy Using Antiserum. Advances in Microbiology, 8, 874-884. https://doi.org/10.4236/aim.2018.811058
[25]
Adachi, K., Kato, T., Kirimura, N., Kubota, Y., Shiba, H., Soejoedono, R.D., et al. (2014) Double Infections with Avian A/H5N1 and Swine A/H1N1 Influenza Viruses in Chickens. American International Journal of Biology, 2, 58-94. https://doi.org/10.15640/aijb.v2n3-4a6
[26]
Reed, L.J. and Muench, H. (1938) A Simple Method of Estimating Fifty Per Cent Endpoints. American Journal of Epidemiology, 27, 493-497. https://doi.org/10.1093/oxfordjournals.aje.a118408
[27]
Xue, J., Chambers, B.S., Hensley, S.E. and López, C.B. (2016) Propagation and Characterization of Influenza Virus Stocks That Lack High Levels of Defective Viral Genomes and Hemagglutinin Mutations. Frontiers in Microbiology, 7, Article 326. https://doi.org/10.3389/fmicb.2016.00326
[28]
Byrd-Leotis, L. and Cummings, R.D. (2021) Influenza Virus Receptors in the Glycome: Implications for Host Range and Pathogenesis. Current Opinion in Virology, 51, 98-104.
[29]
Long, J.S., Mistry, B., Haslam, S.M. and Barclay, W.S. (2018) Host and Viral Determinants of Influenza a Virus Species Specificity. Nature Reviews Microbiology, 17, 67-81. https://doi.org/10.1038/s41579-018-0115-z