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Frontiers in veterinary science2023; 10; 1126199; doi: 10.3389/fvets.2023.1126199

Serological and molecular surveillance of West Nile virus in domesticated mammals of peninsular Malaysia.

Abstract: West Nile virus is a mosquito-borne neurotropic pathogen with a wide host range that constitutes a significant risk to public and animal health. There is limited information on WNV infection in domesticated mammals in Malaysia; however, current reports indicate infections in birds, macaques, bats and pigs from Malaysia. In this study, 203 serum samples from cattle, goats, and horses were tested for the presence of anti-WNV IgG using a competitive enzyme-linked immunosorbent assay (c-ELISA). Additionally, using one-step RT-PCR, nasopharyngeal swabs were analyzed for WNV RNA from all 203 animals in this study. The WNV seroprevalence was 32.53% (27/83) at 95% CI (0.2342-0.4319) in cattle, 48.27% (14/29) at 95% CI (0.3139-0.6557) in goats and 53.84% (49/91) at 95% CI (0.4366-0.6373) in horses. Cross-reactive JEV antibodies were detected in two cattle and 34 horses. None of the cattle or goats tested positive for WNV RT-PCR. Seven horses were positive for WNV RT-PCR, a molecular prevalence of 7.69% (7/91) at 95% CI (0.0353-0.1528). This is the first reported detection of WNV in domesticated mammals of Malaysia, a significant addition to the growing evidence that WNV is being transmitted from vectors to susceptible hosts in Malaysia.
Publication Date: 2023-06-29 PubMed ID: 37456951PubMed Central: PMC10343450DOI: 10.3389/fvets.2023.1126199Google Scholar: Lookup
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  • Journal Article

Summary

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This research article investigates the prevalence of the West Nile virus in domesticated animals – specifically cattle, goats, and horses – in Malaysia, providing the first notable evidence of the virus in this context.

Introduction

  • The West Nile virus (WNV) is a mosquito-borne virus that affects a wide range of hosts, posing a substantial threat to both public and animal health.
  • Currently, there is limited information on WNV infections in domesticated animals in Malaysia, with existing studies primarily documenting infections in birds, macaques, bats, and pigs within the country.

Methodology

  • The researchers collected serum samples from 203 animals, which included cattle, goats, and horses.
  • These samples were then tested for the presence of antibodies against the WNV (anti-WNV IgG) using a competitive enzyme-linked immunosorbent assay (c-ELISA).
  • Furthermore, nasopharyngeal swabs were analyzed for WNV RNA from all 203 animals involved in the study using a one-step RT-PCR process.

Results

  • The results showed a seroprevalence of WNV of 32.53% in cattle, 48.27% in goats, and 53.84% in horses.
  • Also, evidence of cross-reactivity with Japanese Encephalitis virus (JEV) was found in two cattle and 34 horses.
  • While none of the cattle or goats tested positive for WNV using the RT-PCR test, seven horses did, showing a molecular prevalence of 7.69%.

Conclusion

  • The study provides the first reported evidence of WNV in domesticated mammals in Malaysia.
  • This discovery significantly contributes to the growing body of evidence that indicates WNV being transmitted from vectors (such as mosquitoes) to susceptible hosts within Malaysia.

Cite This Article

APA
Mohammed MN, Yasmin AR, Ramanoon SZ, Noraniza MA, Ooi PT, Ain-Najwa MY, Natasha JA, Nur-Fazila SH, Arshad SS, Mohammed HO. (2023). Serological and molecular surveillance of West Nile virus in domesticated mammals of peninsular Malaysia. Front Vet Sci, 10, 1126199. https://doi.org/10.3389/fvets.2023.1126199

Publication

ISSN: 2297-1769
NlmUniqueID: 101666658
Country: Switzerland
Language: English
Volume: 10
Pages: 1126199

Researcher Affiliations

Mohammed, Mohammed Nma
  • Department of Veterinary Laboratory Diagnosis, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang, Malaysia.
  • Department of Animal Production, School of Agriculture and Agricultural Technology, Federal University of Technology, Minna, Nigeria.
Yasmin, Abd Rahaman
  • Department of Veterinary Laboratory Diagnosis, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang, Malaysia.
  • Laboratory of Vaccines and Biomolecules, Institute of Bioscience, Universiti Putra Malaysia, Serdang, Malaysia.
Ramanoon, Siti Zubaidah
  • Department of Farm and Exotic Animal Medicine and Surgery, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang, Malaysia.
Noraniza, Mohd Adzahan
  • Department of Farm and Exotic Animal Medicine and Surgery, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang, Malaysia.
Ooi, Peck Toung
  • Department of Veterinary Clinical Studies, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang, Malaysia.
Ain-Najwa, Mohd Yuseri
  • Department of Veterinary Laboratory Diagnosis, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang, Malaysia.
Natasha, Jafar Ali
  • Department of Veterinary Laboratory Diagnosis, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang, Malaysia.
Nur-Fazila, Saulol Hamid
  • Department of Veterinary Pathology and Microbiology, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang, Malaysia.
Arshad, Siti Suri
  • Department of Veterinary Pathology and Microbiology, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang, Malaysia.
Mohammed, Hussni Omar
  • Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, United States.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

This article includes 44 references
  1. Girard M, Nelson CB, Picot V, Gubler DJ. Arboviruses: A global public health threat.. Vaccine 2020 May 19;38(24):3989-3994.
  2. Smithburn KC, Hughes TP, Burke AW, Paul JH. A neurotropic virus isolated from the blood of a native of Uganda1. Am J Trop Med Hyg (1940) 20:471–92.
  3. Chancey C, Grinev A, Volkova E, Rios M. The global ecology and epidemiology of West Nile virus.. Biomed Res Int 2015;2015:376230.
    doi: 10.1155/2015/376230pmc: PMC4383390pubmed: 25866777google scholar: lookup
  4. Chowers MY, Lang R, Nassar F, Ben-David D, Giladi M, Rubinshtein E, Itzhaki A, Mishal J, Siegman-Igra Y, Kitzes R, Pick N, Landau Z, Wolf D, Bin H, Mendelson E, Pitlik SD, Weinberger M. Clinical characteristics of the West Nile fever outbreak, Israel, 2000.. Emerg Infect Dis 2001 Jul-Aug;7(4):675-8.
    doi: 10.3201/eid0704.017414pmc: PMC2631759pubmed: 11585531google scholar: lookup
  5. Ronca SE, Ruff JC, Murray KO. A 20-year historical review of West Nile virus since its initial emergence in North America: Has West Nile virus become a neglected tropical disease?. PLoS Negl Trop Dis 2021 May;15(5):e0009190.
  6. Young JJ, Haussig JM, Aberle SW, Pervanidou D, Riccardo F, Sekulić N, Bakonyi T, Gossner CM. Epidemiology of human West Nile virus infections in the European Union and European Union enlargement countries, 2010 to 2018.. Euro Surveill 2021 May;26(19).
  7. Trock SC, Meade BJ, Glaser AL, Ostlund EN, Lanciotti RS, Cropp BC, Kulasekera V, Kramer LD, Komar N. West Nile virus outbreak among horses in New York State, 1999 and 2000.. Emerg Infect Dis 2001 Jul-Aug;7(4):745-7.
    doi: 10.3201/eid0704.017427pmc: PMC2631776pubmed: 11585543google scholar: lookup
  8. Nash D, Mostashari F, Fine A, Miller J, O'Leary D, Murray K, Huang A, Rosenberg A, Greenberg A, Sherman M, Wong S, Layton M. The outbreak of West Nile virus infection in the New York City area in 1999.. N Engl J Med 2001 Jun 14;344(24):1807-14.
    doi: 10.1056/NEJM200106143442401pubmed: 11407341google scholar: lookup
  9. Steele KE, Linn MJ, Schoepp RJ, Komar N, Geisbert TW, Manduca RM, Calle PP, Raphael BL, Clippinger TL, Larsen T, Smith J, Lanciotti RS, Panella NA, McNamara TS. Pathology of fatal West Nile virus infections in native and exotic birds during the 1999 outbreak in New York City, New York.. Vet Pathol 2000 May;37(3):208-24.
    doi: 10.1354/vp.37-3-208pubmed: 10810985google scholar: lookup
  10. Ahlers LRH, Goodman AG. The Immune Responses of the Animal Hosts of West Nile Virus: A Comparison of Insects, Birds, and Mammals.. Front Cell Infect Microbiol 2018;8:96.
    doi: 10.3389/fcimb.2018.00096pmc: PMC5891621pubmed: 29666784google scholar: lookup
  11. Assaid N, Mousson L, Moutailler S, Arich S, Akarid K, Monier M, Beck C, Lecollinet S, Failloux AB, Sarih M. Evidence of circulation of West Nile virus in Culex pipiens mosquitoes and horses in Morocco.. Acta Trop 2020 May;205:105414.
  12. Autorino GL, Battisti A, Deubel V, Ferrari G, Forletta R, Giovannini A, Lelli R, Murri S, Scicluna MT. West Nile virus epidemic in horses, Tuscany region, Italy.. Emerg Infect Dis 2002 Dec;8(12):1372-8.
    doi: 10.3201/eid0812.020234pmc: PMC2738505pubmed: 12498650google scholar: lookup
  13. Castillo-Olivares J, Wood J. West Nile virus infection of horses.. Vet Res 2004 Jul-Aug;35(4):467-83.
    doi: 10.1051/vetres:2004022pubmed: 15236677google scholar: lookup
  14. Hemida MG, Perera RAPM, Chu DKW, Ko RLW, Alnaeem AA, Peiris M. West Nile virus infection in horses in Saudi Arabia (in 2013-2015).. Zoonoses Public Health 2019 Mar;66(2):248-253.
    doi: 10.1111/zph.12532pubmed: 30402969google scholar: lookup
  15. Sule WF, Oluwayelu DO, Adedokun RA, Rufai N, McCracken F, Mansfield KL, Johnson N. High seroprevelance of West Nile virus antibodies observed in horses from southwestern Nigeria.. Vector Borne Zoonotic Dis 2015 Mar;15(3):218-20.
    doi: 10.1089/vbz.2014.1706pmc: PMC4369928pubmed: 25793479google scholar: lookup
  16. Selim A, Abdelhady A. The first detection of anti-West Nile virus antibody in domestic ruminants in Egypt.. Trop Anim Health Prod 2020 Nov;52(6):3147-3151.
    doi: 10.1007/s11250-020-02339-xpubmed: 32588359google scholar: lookup
  17. Rimoldi G, Mete A, Adaska JM, Anderson ML, Symmes KP, Diab S. West Nile Virus Infection in Sheep.. Vet Pathol 2017 Jan;54(1):155-158.
    doi: 10.1177/0300985816653796pubmed: 27312367google scholar: lookup
  18. Asebe G, Mamo G, Michlmayr D, Abegaz WE, Endale A, Medhin G, Larrick JW, Legesse M. Seroprevalence of Rift Valley Fever and West Nile Fever in Cattle in Gambella Region, South West Ethiopia.. Vet Med (Auckl) 2020;11:119-130.
    doi: 10.2147/VMRR.S278867pmc: PMC7683499pubmed: 33244452google scholar: lookup
  19. Ain-Najwa MY, Yasmin AR, Omar AR, Arshad SS, Abu J, Mohammed HO, Kumar K, Loong SK, Rovie-Ryan JJ, Mohd-Kharip-Shah AK. Evidence of West Nile virus infection in migratory and resident wild birds in west coast of peninsular Malaysia.. One Health 2020 Dec;10:100134.
  20. Ain-Najwa MY, Yasmin AR, Arshad SS, Omar AR, Abu J, Kumar K, Mohammed HO, Natasha JA, Mohammed MN, Bande F, Abdullah ML, J Rovie-Ryan J. Exposure to Zoonotic West Nile Virus in Long-Tailed Macaques and Bats in Peninsular Malaysia.. Animals (Basel) 2020 Dec 10;10(12).
    doi: 10.3390/ani10122367pmc: PMC7764493pubmed: 33321964google scholar: lookup
  21. Mohammed MN, Yasmin AR, Noraniza MA, Ramanoon SZ, Arshad SS, Bande F, Mohammed HO. Serological evidence of West Nile viral infection in archived swine serum samples from Peninsular Malaysia.. J Vet Sci 2021 May;22(3):e29.
    doi: 10.4142/jvs.2021.22.e29pmc: PMC8170214pubmed: 33908203google scholar: lookup
  22. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool.. J Mol Biol 1990 Oct 5;215(3):403-10.
    doi: 10.1016/S0022-2836(05)80360-2pubmed: 2231712google scholar: lookup
  23. Katoh K, Standley DM. MAFFT multiple sequence alignment software version 7: improvements in performance and usability.. Mol Biol Evol 2013 Apr;30(4):772-80.
    doi: 10.1093/molbev/mst010pmc: PMC3603318pubmed: 23329690google scholar: lookup
  24. Criscuolo A, Gribaldo S. BMGE (Block Mapping and Gathering with Entropy): a new software for selection of phylogenetic informative regions from multiple sequence alignments.. BMC Evol Biol 2010 Jul 13;10:210.
    doi: 10.1186/1471-2148-10-210pmc: PMC3017758pubmed: 20626897google scholar: lookup
  25. Guindon S, Dufayard JF, Lefort V, Anisimova M, Hordijk W, Gascuel O. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0.. Syst Biol 2010 May;59(3):307-21.
    doi: 10.1093/sysbio/syq010pubmed: 20525638google scholar: lookup
  26. Letunic I, Bork P. Interactive Tree Of Life (iTOL) v5: an online tool for phylogenetic tree display and annotation.. Nucleic Acids Res 2021 Jul 2;49(W1):W293-W296.
    doi: 10.1093/nar/gkab301pmc: PMC8265157pubmed: 33885785google scholar: lookup
  27. Ciota AT. West Nile virus and its vectors.. Curr Opin Insect Sci 2017 Aug;22:28-36.
    doi: 10.1016/j.cois.2017.05.002pubmed: 28805636google scholar: lookup
  28. LaPointe DA. Culex Quinquefasciatus (Southern House Mosquito) CABI Compendium. (2022) 86848. doi: 10.1079/cabicompendium.86848
  29. Chen C. D., Lee H. L., Stella-Wong S. P., Lau K. W., Sofian-Azirun M. Container survey of mosquito breeding sites in a university campus in Kuala Lumpur, Malaysia. Dengue Bulletin. WHO Regional Office for South-East Asia (2009), 33, 187–193.
  30. Nazni WA, Lee HL, Azahari AH. Adult and larval insecticide susceptibility status of Culex quinquefasciatus (Say) mosquitoes in Kuala Lumpur Malaysia.. Trop Biomed 2005 Jun;22(1):63-8.
    pubmed: 16880755
  31. Ching CY, Casals J, Bowen ET, Simpson DI, Platt GS, Way HJ, Smith CE. Arbovirus infections in Sarawak: the isolation of Kunjin virus from mosquitoes of the Culex pseudovishnui group.. Ann Trop Med Parasitol 1970 Sep;64(3):263-8.
    doi: 10.1080/00034983.1970.11686690pubmed: 5500097google scholar: lookup
  32. Rais MN, Omar AR, Abu J, Omar MH. Prevalence of West Nile virus antibody in captive bird populations in selected areas in Selangor, Malaysia. In: 6th Seminar on Veterinary Sciences, 11-14 Jan. 2011. Malaysia: Faculty of Veterinary Medicine, Universiti Putra Malaysia; (2011) p. 127.
  33. Marlina S, Radzi SF, Lani R, Sieng KC, Rahim NF, Hassan H, Li-Yen C, AbuBakar S, Zandi K. Seroprevalence screening for the West Nile virus in Malaysia's Orang Asli population.. Parasit Vectors 2014 Dec 17;7:597.
    doi: 10.1186/s13071-014-0597-0pmc: PMC4311511pubmed: 25515627google scholar: lookup
  34. Murin CD, Wilson IA, Ward AB. Antibody responses to viral infections: a structural perspective across three different enveloped viruses.. Nat Microbiol 2019 May;4(5):734-747.
    doi: 10.1038/s41564-019-0392-ypmc: PMC6818971pubmed: 30886356google scholar: lookup
  35. Steyn J, Botha E, Stivaktas VI, Buss P, Beechler BR, Myburgh JG, Steyl J, Williams J, Venter M. West Nile Virus in Wildlife and Nonequine Domestic Animals, South Africa, 2010-2018.. Emerg Infect Dis 2019 Dec;25(12):2290-2294.
    doi: 10.3201/eid2512.190572pmc: PMC6874268pubmed: 31742510google scholar: lookup
  36. Olaleye OD, Omilabu SA, Ilomechina EN, Fagbami AH. A survey for haemagglutination-inhibiting antibody to West Nile virus in human and animal sera in Nigeria.. Comp Immunol Microbiol Infect Dis 1990;13(1):35-9.
    doi: 10.1016/0147-9571(90)90006-Fpubmed: 2323182google scholar: lookup
  37. Atadiose EO, Kabir J, Adamu SG, Umoh JU. Serosurvey of West Nile virus in horses and detection of West Nile virus antigen in mosquitoes in Kaduna State, Nigeria.. J Equine Sci 2020 Oct;31(3):61-66.
    doi: 10.1294/jes.31.61pmc: PMC7538258pubmed: 33061786google scholar: lookup
  38. Schvartz G, Tirosh-Levy S, Erester O, Shenhar R, Levy H, Bazanow B, Gelman B, Steinman A. Exposure of Horses in Israel to West Nile Virus and Usutu Virus.. Viruses 2020 Sep 28;12(10).
    doi: 10.3390/v12101099pmc: PMC7650752pubmed: 32998459google scholar: lookup
  39. Levett PN, Sonnenberg K, Sidaway F, Shead S, Niedrig M, Steinhagen K, Horsman GB, Drebot MA. Use of immunoglobulin G avidity assays for differentiation of primary from previous infections with West Nile virus.. J Clin Microbiol 2005 Dec;43(12):5873-5.
  40. Vilibic-Cavlek T, Kristofic B, Savic V, Kolaric B, Barbic L, Tabain I, Peric L, Sabadi D, Miklausic B, Potocnik-Hunjadi T, Zember S, Stevanovic V, Listes E, Savini G. Diagnostic significance of immunoglobulin G avidity in symptomatic and asymptomatic West Nile virus infection.. Rev Soc Bras Med Trop 2018 Sep-Oct;51(5):591-595.
    doi: 10.1590/0037-8682-0482-2017pubmed: 30304263google scholar: lookup
  41. Kumar K, Arshad SS, Selvarajah GT, Abu J, Toung OP, Abba Y, Bande F, Yasmin AR, Sharma R, Ong BL, Rasid AA, Hashim N, Peli A, Heshini EP, Shah AKMK. Prevalence and risk factors of Japanese encephalitis virus (JEV) in livestock and companion animal in high-risk areas in Malaysia.. Trop Anim Health Prod 2018 Apr;50(4):741-752.
    doi: 10.1007/s11250-017-1490-6pmc: PMC5866273pubmed: 29243139google scholar: lookup
  42. Venter M, Pretorius M, Fuller JA, Botha E, Rakgotho M, Stivaktas V, Weyer C, Romito M, Williams J. West Nile Virus Lineage 2 in Horses and Other Animals with Neurologic Disease, South Africa, 2008-2015.. Emerg Infect Dis 2017 Dec;23(12):2060-2064.
    doi: 10.3201/eid2312.162078pmc: PMC5708237pubmed: 29148375google scholar: lookup
  43. Kleiboeker SB, Loiacono CM, Rottinghaus A, Pue HL, Johnson GC. Diagnosis of West Nile virus infection in horses.. J Vet Diagn Invest 2004 Jan;16(1):2-10.
    doi: 10.1177/104063870401600102pubmed: 14974840google scholar: lookup
  44. Botha EM, Markotter W, Wolfaardt M, Paweska JT, Swanepoel R, Palacios G, Nel LH, Venter M. Genetic determinants of virulence in pathogenic lineage 2 West Nile virus strains.. Emerg Infect Dis 2008 Feb;14(2):222-30.
    doi: 10.3201/eid1402.070457pmc: PMC2600181pubmed: 18258114google scholar: lookup

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