Skip directly to local search Skip directly to A to Z list Skip directly to navigation Skip directly to site content Skip directly to page options
CDC Home

Volume 16, Number 3—March 2010

Letter

Transmission of West Nile Virus during Horse Autopsy

Suggested citation for this article

To the Editor: West Nile virus (WNV) circulates mainly in birds and ornithophilic mosquitoes. Humans and horses are considered incidental, dead-end hosts (1). Fever, rash, arthralgia, and myalgia develop in ≈20% of cases in humans; severe neurologic disease may develop in <1% (1). In horses, 20% of infections result in clinical disease, of which ≈90% involve neurologic disease with ataxia, weakness, recumbency, muscle fasciculation, and high death rates (30%) (2).

Genetic variants of WNV include lineage 1 found in the Northern Hemisphere and Australia; lineage 2 found mainly in southern Africa and Madagascar (3); lineages 3 and 4 found in central and eastern Europe (4); and lineage 5 found in India (5). Differences in neuroninvasiveness and pathogenic potential are functions of individual genotypes, not lineage (3,68).

We recently reported WNV lineage 2 in several cases of neurologic disease in horses in South Africa (most cases were fatal) (7). We report a case of zoonotic transmission to a veterinary student during the autopsy of a horse. The study was reviewed and approved by the Ethics Committee of the University of Pretoria, and informed consent was provided by the veterinary student.

On April 9, 2008, a 4-month-old Welsh pony from Gauteng in South Africa had fever, Schiff-Sherrington signs, and a leukocyte count of 32 × 109 cells/L. He was treated with dimethyl sulfoxide, dexamethasone, and chloramphenicol and responded well. He was able to stand with help, and did not show neurologic signs at this stage. On May 9, he was sent home and was able to walk with support. On May 12, he had a relapse with neurologic deterioration and rectal prolapse, and was treated with antiinflammatory agents. Symptoms worsened and he was humanely killed on May 15 by using ketamine and MgSO4. The carcass was sent to the Faculty of Veterinary Sciences, University of Pretoria, for autopsy because of unusual neurologic signs in the pony. Autopsy was performed by a veterinary pathologist and 2 students on May 16, 2008.

Macroscopic findings included moderate intermuscular, fascicular, perineural edema, severe diffuse pulmonary edema, mild hydropericardium, and rectal prolapse resulting in marked submucosal edema and mucosal hyperamia, i.e., traumatic proctitis. The spinal cord up to C1 showed marked Wallerian degeneration of the peripheral white matter from the median fissure, which extended along the ventral funiculus up to the most dorsal section of the lateral funiculus. Changes were characterized by white matter spongiosis with numerous digestion chambers containing phagocytosing myelinophages and scattered interstitial gemistocytes. No inflammatory reaction was detected. We also observed septal edema and moderate multifocal perivascular and peribronchiolar lymphocytic infiltration with occasional apoptosis in the lungs.

The brain, which was removed by 1 of the students, was sent to the Department of Medical Virology, University of Pretoria, for WNV reverse transcription–PCR (RT-PCR). The lungs were sent to Onderstepoort Veterinary Institute for African horse sickness RT-PCR. WNV-specific real-time RT-PCR showed positive results. DNA sequencing and phylogenetic analysis identified WNV lineage 2 in several sections of the brain (HS23/2008, GenBank accession no. FJ464376). Results of African horse sickness RT-PCR on lung tissue specimens were inconclusive and could not be confirmed by culture.

On May 22, six days after the autopsy on the horse, fever, malaise, myalgia, stiff neck, and severe headache developed in the veterinary student who had handled the horse brain. A rash appeared 2 days later. Symptoms persisted for ≈10 days. The patient was treated symptomatically by an infectious disease specialist and prescribed bed rest. Because cases of Rift Valley fever were recently reported in veterinarians in South Africa, serum was sent to the National Institute for Communicable Diseases, where a virus isolate was obtained in suckling mice and identified as WNV by RT-PCR.

Figure

Thumbnail of Phylogenetic comparison of West Nile virus (WNV) nonstructural protein 5 partial gene fragment identified in a veterinary student’s serum and in the virus isolate obtained from mouse brain and the horse’s brain after autopsy (triangles) relative to other WNV strains from South Africa and elsewhere. The neighbor-joining tree was compiled by using MEGA version 4 software (www.megasoftware.net/under) and 1,000 bootstrap replicates by using the maximum composite likelihood algorithm. Ge

Figure. Phylogenetic comparison of West Nile virus (WNV) nonstructural protein 5 partial gene fragment identified in a veterinary student’s serum and in the virus isolate obtained from mouse brain and the horse’s...

After diagnosis of WNV infection in the pony, RNA extracted from the original human serum and from the suckling mouse isolate was sent to the Department of Medical Virology, University of Pretoria, for DNA sequencing and phylogenetic analysis of the virus. Comparison of part of the nonstructural protein 5 gene identified identical sequences from the student’s serum, the virus isolate, and the pony’s brain. All sequences clustered with lineage 2 WNV and were closely related to isolates obtained from horses diagnosed with fatal WNV encephalitis in South Africa in 2008 (7) (Figure).

Human infections with WNV have been described after bird autopsies and needle stick injury in laboratory workers (9,10). The case acquired by our patient suggests a zoonotic risk exists for infection with WNV during autopsy of horses that died from neurologic disease. Although humans and horses are considered to have low-grade viremia, virus levels may be higher in nerve tissue.

The patient wore latex gloves, his only protection during the autopsy, and had removed the spinal cord and brain. No protective inhalation or eye equipment was worn. No autopsy assistants or other students who worked with or were near the carcass became sick or seroconverted. The most likely route of infection may have involved exposure of mucous membranes to droplets. After the incident, biosafety measures were improved and included wearing of masks and eye protection gear during autopsies at the facility.

Marietjie VenterComments to Author , Johan Steyl, Stacey Human, Jacqueline Weyer, Dewald Zaayman, Lufcille Blumberg, Patricia A. Leman, Janusz Paweska, and Robert Swanepoel
Author affiliations: University of Pretoria, Pretoria, South Africa (M. Venter, J. Steyl, S. Human, D. Zaayman); National Institute for Communicable Diseases, Sandringham, South Africa (M. Venter, J. Weyer, L. Blumberg, P.A. Lehman, J. Paweska, R. Swanepoel)

Acknowledgments

We thank Janice Croft and Busi Mogodi for technical assistance.

This study was supported by a grant from the National Research Foundation of South Africa.

References

  1. Hayes EB, Sejvar JJ, Zaki SR, Lanciotti RS, Bode AV, Campbell GL. Virology, pathology, and clinical manifestations of West Nile virus disease. Emerg Infect Dis. 2005;11:11749.PubMed
  2. Hayes EB, Gubler DJ. West Nile virus: epidemiology and clinical features of an emerging epidemic in the United States. Annu Rev Med. 2006;57:18194. DOIPubMed
  3. Burt FJ, Grobbelaar AA, Leman PA, Anthony FS, Gibson GV, Swanepoel R. Phylogenetic relationships of southern African West Nile virus isolates. Emerg Infect Dis. 2002;8:8206.PubMed
  4. Lvov DK, Butenko AM, Gromashevsky VL, Kovtunov AI, Prilipov AG, Kinney R, West Nile virus and other zoonotic viruses in Russia: examples of emerging-reemerging situations. Arch Virol Suppl. 2004;18:8596.PubMed
  5. Bondre VP, Jadi RS, Mishra AC, Yergolkar PN, Arankalle VA. West Nile virus isolates from India: evidence for a distinct genetic lineage. J Gen Virol. 2007;88:87584. DOIPubMed
  6. Beasley DW, Li L, Suderman MT, Barrett AD. Mouse neuroinvasive phenotype of West Nile virus strains varies depending upon virus genotype. Virology. 2002;296:1723. DOIPubMed
  7. Venter M, Human S, Zaayman D, Gerdes GH, Williams J, Steyl J, Lineage 2 West Nile virus as cause of fatal neurologic disease in horses, South Africa. Emerg Infect Dis. 2009;15:87784. DOIPubMed
  8. Venter M, Myers TG, Wilson MA, Kindt TJ, Paweska JT, Burt FJ, Gene expression in mice infected with West Nile virus strains of different neurovirulence. Virology. 2005;342:11940. DOIPubMed
  9. Centers for Disease Control and Prevention. Laboratory-acquired West Nile virus infections—United States, 2002. JAMA. 2003;289:4145. DOIPubMed
  10. Venter M, Burt FJ, Blumberg L, Fickl H, Paweska J, Swanepoel R. Cytokine induction after laboratory-acquired West Nile virus infection. N Engl J Med. 2009;360:12602. DOIPubMed

Figure

Suggested citation for this article: Venter M, Steyl J, Human S, Weyer J, Zaayman D, Blumberg L, et al. Transmission of West Nile virus during horse autopsy [letter]. Emerg Infect Dis [serial on the Internet]. 2010 Mar [date cited]. http://wwwnc.cdc.gov/eid/article/16/3/09-1042.htm

DOI: 10.3201/eid1603.091042

Related Links

Top of Page

Table of Contents – Volume 16, Number 3—March 2010

Comments to the Authors

Please use the form below to submit correspondence to the authors or contact them at the following address:

Marietjie Venter, Department of Medical Virology, Faculty of Health Sciences, University of Pretoria, PO Box 2034, Pretoria 0001, South Africa





characters(s) remaining.

Comment submitted successfully, thank you for your feedback.

Comments to the EID Editors

Please contact the EID Editors via our Contact Form.

 

Past Issues

Select a Past Issue:

World Malaria Day - April 25, 2014 - Invest in the future, defeat malaria

20th Anniversary - National Infant Immunization Week - Immunization. Power to Protect.

Art in Science - Selections from Emerging Infectious Diseases
Now available for order



CDC 24/7 – Saving Lives, Protecting People, Saving Money. Learn More About How CDC Works For You…

USA.gov: The U.S. Government's Official Web PortalDepartment of Health and Human Services
Centers for Disease Control and Prevention   1600 Clifton Rd. Atlanta, GA 30333, USA
800-CDC-INFO (800-232-4636) TTY: (888) 232-6348 - Contact CDC–INFO