1887
Surveillance Open Access
Like 0

Abstract

Background

The first autochthonous human West Nile virus (WNV)-positive cases in Germany were confirmed in 2019. Risk minimisation measures (RMM) were introduced in 2020; no WNV transfusion-transmitted infections have been reported to date.

Aim

To analyse German suspected WNV-positive blood donations during annual seasons 2020–23 to review donor testing requirements.

Methods

WNV look-back procedures were initiated as per German regulations and additional donor data were collected. Blood samples were analysed by metagenomic next-generation sequencing (mNGS), individual donor nucleic acid amplification technique (ID-NAT)-based testing and antibody (Ab) testing.

Results

Seventy-four cases were followed up after WNV-positive donor mini-pool screening. Forty-five (83%) of 54 samples tested with the cobas WNV assay and 14 (29%) of 49 samples tested with the RealStar WNV assay showed a reactive ID-NAT-based result; the viral load ranged between 70,251 IU/mL and values below quantification limits. Fifteen (23%) of 64 samples serologically tested were reactive with at least one of the three Ab tests performed; the previous WNV-negative donation was nearly always documented > 28 days before. Of 73 samples sequenced, mNGS detected WNV in 26 (36%) and other flaviviruses in 14 (19%) cases.

Conclusion

In some suspected cases where a WNV infection was not confirmed, mNGS demonstrated a cross-reaction with other flaviviruses. Ab testing could only detect WNV in late stages of infection. A NAT-based WNV donor screening with a detection limit of at least 120 IU/mL seems to be a sufficiently effective RMM at present. However, a continuous re-evaluation of test strategy is always required.

Loading

Article metrics loading...

/content/10.2807/1560-7917.ES.2025.30.8.2400373
2025-02-27
2025-02-27
/content/10.2807/1560-7917.ES.2025.30.8.2400373
Loading
Loading full text...

Full text loading...

/deliver/fulltext/eurosurveillance/30/8/eurosurv-30-8-1.html?itemId=/content/10.2807/1560-7917.ES.2025.30.8.2400373&mimeType=html&fmt=ahah

References

  1. Ebel GD, Kramer LD. West Nile Virus: Molecular Epidemiology and Diversity. In: West Nile Encephalitis Virus Infection. Emerging Infectious Diseases of the 21st Century. New York: Springer; 2009. Available from: https://doi.org/ https://doi.org/10.1007/978-0-387-79840-0_2 
  2. Pesko KN, Ebel GD. West Nile virus population genetics and evolution. Infect Genet Evol. 2012;12(2):181-90. PMID: 22226703 
  3. Koch RT, Erazo D, Folly AJ, Johnson N, Dellicour S, Grubaugh ND, et al. Genomic epidemiology of West Nile virus in Europe. One Health. 2023;18:100664. PMID: 38193029 
  4. Kramer LD, Styer LM, Ebel GD. A global perspective on the epidemiology of West Nile virus. Annu Rev Entomol. 2008;53(1):61-81.  https://doi.org/10.1146/annurev.ento.53.103106.093258  PMID: 17645411 
  5. Seino KK, Long MT, Gibbs EPJ, Bowen RA, Beachboard SE, Humphrey PP, et al. Comparative efficacies of three commercially available vaccines against West Nile Virus (WNV) in a short-duration challenge trial involving an equine WNV encephalitis model. Clin Vaccine Immunol. 2007;14(11):1465-71.  https://doi.org/10.1128/CVI.00249-07  PMID: 17687109 
  6. Ulbert S. West Nile virus vaccines - current situation and future directions. Hum Vaccin Immunother. 2019;15(10):2337-42.  https://doi.org/10.1080/21645515.2019.1621149  PMID: 31116691 
  7. Sambri V, Capobianchi M, Charrel R, Fyodorova M, Gaibani P, Gould E, et al. West Nile virus in Europe: emergence, epidemiology, diagnosis, treatment, and prevention. Clin Microbiol Infect. 2013;19(8):699-704.  https://doi.org/10.1111/1469-0691.12211  PMID: 23594175 
  8. Zou S, Foster GA, Dodd RY, Petersen LR, Stramer SL. West Nile fever characteristics among viremic persons identified through blood donor screening. J Infect Dis. 2010;202(9):1354-61.  https://doi.org/10.1086/656602  PMID: 20874087 
  9. Mostashari F, Bunning ML, Kitsutani PT, Singer DA, Nash D, Cooper MJ, et al. Epidemic West Nile encephalitis, New York, 1999: results of a household-based seroepidemiological survey. Lancet. 2001;358(9278):261-4.  https://doi.org/10.1016/S0140-6736(01)05480-0  PMID: 11498211 
  10. Davis LE, DeBiasi R, Goade DE, Haaland KY, Harrington JA, Harnar JB, et al. West Nile virus neuroinvasive disease. Ann Neurol. 2006;60(3):286-300.  https://doi.org/10.1002/ana.20959  PMID: 16983682 
  11. Debiasi RL. West nile virus neuroinvasive disease. Curr Infect Dis Rep. 2011;13(4):350-9.  https://doi.org/10.1007/s11908-011-0193-9  PMID: 21544522 
  12. McDonald E, Mathis S, Martin SW, Staples JE, Fischer M, Lindsey NP. Surveillance for West Nile virus disease - United States, 2009-2018. MMWR Surveill Summ. 2021;70(1):1-15.  https://doi.org/10.15585/mmwr.ss7001a1  PMID: 33661868 
  13. Centers for Disease Control and Prevention (CDC). Historic Data (1999-2023) | West Nile Virus. Atlanta: CDC. [Accessed: 30 Jan 2025]. Available from: https://www.cdc.gov/west-nile-virus/data-maps/historic-data.html
  14. European Centre for Disease Prevention and Control (ECDC). Historical data by year - West Nile virus seasonal surveillance. Stockholm: ECDC. [Accessed: 30 Jan 2025]. Available from: https://www.ecdc.europa.eu/en/west-nile-fever/surveillance-and-disease-data/historical
  15. Ziegler U, Santos PD, Groschup MH, Hattendorf C, Eiden M, Höper D, et al. West Nile Virus epidemic in Germany triggered by epizootic emergence, 2019. Viruses. 2020;12(4):448.  https://doi.org/10.3390/v12040448  PMID: 32326472 
  16. From the Centers for Disease Control and Prevention. Possible West Nile virus transmission to an infant through breast-feeding--Michigan, 2002. JAMA. 2002;288(16):1976-7. PMID: 12400536 
  17. Cadar D, Maier P, Müller S, Kress J, Chudy M, Bialonski A, et al. Blood donor screening for West Nile virus (WNV) revealed acute Usutu virus (USUV) infection, Germany, September 2016. Euro Surveill. 2017;22(14):30501.  https://doi.org/10.2807/1560-7917.ES.2017.22.14.30501  PMID: 28422005 
  18. Paul-Ehrlich-Institut (PEI) Bundesinstitut für Impfstoffe und biomedizinische Arzneimittel. Bekanntmachung über die Zulassung von Arzneimitteln: Anordnung von Maßnahmen, die das Risiko der Übertragung einer in Deutschland erworbenen West-Nil-Virus (WNV)-Infektion durch Blutkomponenten zur Transfusion (zelluläre Blutzubereitungen und therapeutische Frischplasmen) und durch Stammzellzubereitungen zur hämatopoetischen Rekonstitution minimieren können. Köln: Bundesanzeiger; 04 Jun 2020. German. Available from: https://www.bundesanzeiger.de/pub/publication/C125NFKbnDG9Liyxe7T?0
  19. Paul-Ehrlich-Institut (PEI) Bundesinstitut für Impfstoffe und biomedizinische Arzneimittel. Bekanntmachung über die Zulassung von Arzneimitteln: Abwehr von Arzneimittelrisiken − Anordnung der Nutzung einer Online-Datenbank des Paul-Ehrlich-Instituts zum Ausschluss von Blutspenden für die Herstellung von Blutzubereitungen von Reisenden nach Rückkehr aus Endemiegebieten (Stufenplanverfahren [Bescheid] zu Zika-Virus, West-Nil-Virus, Chikungunya-Virus und Prionen; Plasmodien). Köln: Bundesanzeiger; 8 Nov 2018. German. Available from: https://www.bundesanzeiger.de/pub/publication/JS4MPK1bktM7k9EmjsY?1
  20. Gathof BS, Tauszig ME, Picker SM. Pathogen inactivation/reduction of platelet concentrates: turning theory into practice. ISBT Sci Ser. 2010;5(1):114-9.  https://doi.org/10.1111/j.1751-2824.2010.01417.x  PMID: 32328165 
  21. Domanović D, Gossner CM, Lieshout-Krikke R, Mayr W, Baroti-Toth K, Dobrota AM, et al. West Nile and Usutu virus infections and challenges to blood safety in the European Union. Emerg Infect Dis. 2019;25(6):1050-7.  https://doi.org/10.3201/eid2506.181755  PMID: 31107223 
  22. Dreier J, Vollmer T, Hinse D, Heuser EJ, Pisani G, Knabbe C. Implementation of NAT Screening for West Nile virus and experience with seasonal testing in Germany. Transfus Med Hemother. 2016;43(1):28-36.  https://doi.org/10.1159/000440833  PMID: 27022320 
  23. National Advisory Committee Blood. Verfahren zur Rückverfolgung (Look Back) gemäß § 19 Transfusionsgesetz. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2021;64(1):108-25. German.  https://doi.org/10.1007/s00103-020-03258-w 
  24. Paul-Ehrlich-Institut (PEI) Bundesinstitut für Impfstoffe und biomedizinische Arzneimittel. Hämovigilanzberichte. [Haemovigilance Reports]. Langen: PEI; 27 Nov 2023. German. Available from: https://www.pei.de/EN/newsroom/mandatory-reports/haemovigilance-reports/haemovigilance-reports-node.html
  25. Cameron C, Reeves J, Antonishyn N, Tilley P, Alport T, Eurich B, et al. West Nile virus in Canadian blood donors. Transfusion. 2005;45(4):487-91.  https://doi.org/10.1111/j.0041-1132.2005.04384.x  PMID: 15819667 
  26. Saldanha J, Shead S, Heath A, Drebot M, West Nile Virus Collaborative Study Group. Collaborative study to evaluate a working reagent for West Nile virus RNA detection by nucleic acid testing. Transfusion. 2005;45(1):97-102.  https://doi.org/10.1111/j.1537-2995.2005.04151.x  PMID: 15647024 
  27. Stramer SL, Fang CT, Foster GA, Wagner AG, Brodsky JP, Dodd RY. West Nile virus among blood donors in the United States, 2003 and 2004. N Engl J Med. 2005;353(5):451-9.  https://doi.org/10.1056/NEJMoa044333  PMID: 16079368 
  28. Vamvakas EC, Kleinman S, Hume H, Sher GD. The development of West Nile virus safety policies by Canadian blood services: guiding principles and a comparison between Canada and the United States. Transfus Med Rev. 2006;20(2):97-109.  https://doi.org/10.1016/j.tmrv.2005.11.001  PMID: 16565024 
  29. Pisani G, Cristiano K, Pupella S, Liumbruno GM. West Nile Virus in Europe and Safety of Blood Transfusion. Transfus Med Hemother. 2016;43(3):158-67.  https://doi.org/10.1159/000446219  PMID: 27403087 
  30. Aberle SW, Kolodziejek J, Jungbauer C, Stiasny K, Aberle JH, Zoufaly A, et al. Increase in human West Nile and Usutu virus infections, Austria, 2018. Euro Surveill. 2018;23(43):1800545.  https://doi.org/10.2807/1560-7917.ES.2018.23.43.1800545  PMID: 30376913 
  31. Bakonyi T, Jungbauer C, Aberle SW, Kolodziejek J, Dimmel K, Stiasny K, et al. Usutu virus infections among blood donors, Austria, July and August 2017 - Raising awareness for diagnostic challenges. Euro Surveill. 2017;22(41):17-00644.  https://doi.org/10.2807/1560-7917.ES.2017.22.41.17-00644  PMID: 29043962 
  32. Moureau G, Temmam S, Gonzalez JP, Charrel RN, Grard G, de Lamballerie X. A real-time RT-PCR method for the universal detection and identification of flaviviruses. Vector Borne Zoonotic Dis. 2007;7(4):467-77.  https://doi.org/10.1089/vbz.2007.0206  PMID: 18020965 
  33. Busch MP, Kleinman SH, Tobler LH, Kamel HT, Norris PJ, Walsh I, et al. Virus and antibody dynamics in acute west nile virus infection. J Infect Dis. 2008;198(7):984-93.  https://doi.org/10.1086/591467  PMID: 18729783 
  34. Pezzotti P, Piovesan C, Barzon L, Cusinato R, Cattai M, Pacenti M, et al. Prevalence of IgM and IgG antibodies to West Nile virus among blood donors in an affected area of north-eastern Italy, summer 2009. Euro Surveill. 2011;16(10):19814.  https://doi.org/10.2807/ese.16.10.19814-en  PMID: 21435323 
  35. Girl P, Euringer K, Coroian M, Mihalca AD, Borde JP, Dobler G. Comparison of five serological methods for the detection of West Nile virus antibodies. Viruses. 2024;16(5):788.  https://doi.org/10.3390/v16050788  PMID: 38793670 
  36. Centers for Disease Control and Prevention (CDC). Update: West Nile virus screening of blood donations and transfusion-associated transmission--United States, 2003. MMWR Morb Mortal Wkly Rep. 2004;53(13):281-4. PMID: 15071426 
  37. Lustig Y, Mannasse B, Koren R, Katz-Likvornik S, Hindiyeh M, Mandelboim M, et al. Superiority of West Nile virus RNA detection in whole blood for diagnosis of acute infection. J Clin Microbiol. 2016;54(9):2294-7.  https://doi.org/10.1128/JCM.01283-16  PMID: 27335150 
/content/10.2807/1560-7917.ES.2025.30.8.2400373
Loading

Data & Media loading...

Supplementary data

Submit comment
Close
Comment moderation successfully completed
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error