Serologic survey for hantavirus infection in domestic animals and coyotes from New Mexico and northeastern Arizona

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Abstract

Objective - To determine whether animals had serologic evidence of infection with Sin Nombre virus (SNV). Design - Prospective serosurvey. Sample Population - Serum samples were obtained from 145 cats, 85 dogs, 120 horses, and 24 cattle between April 1993 and August 1994 and 54 coyotes between December 1994 and February 1995. Procedure - Serum samples were analyzed by western immunoblot assays for reaction with SNV nucleocapsid antigen. Samples with reactivity to SNV nucleocapsid proteins were used to probe multiple-antigen blots containing recombinant fusion proteins derived from prototypic hantaviruses. Lung tissue or blood clots were used in nested reverse-transcriptase polymerase chain reaction assays for a 320-nucleotide portion of the SNV G1 gene. Results - Sera from 4 of 145 (2.8%) cats and 4 of 85 (3.5%) dogs had trace reactivity to full-length SNV-encoded nucleocapsid proteins. All samples from horses, cattle, and coyotes were nonreactive. Sera from cats and dogs that had trace IgG-antibody reactivity to nucleocapsid proteins were then tested for IgG-antibody reactivity to nucleocapsid proteins of prototypic hantaviruses. One cat had multiple cross-reactivities with these hantaviruses, consistent with exposure to a hantavirus; however, epitope mapping studies did not support this conclusion. Reverse-transcriptase polymerase chain reaction studies of blood clots or lung tissue from 2 animals that had weak reactivity to SNV failed to amplify any hantavirus sequence. Clinical Implications - Domestic animals, particularly dogs and cats, as well as coyotes do not appear to have a major role in the maintenance and transmission of SNV.

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APA

Malecki, T. M., Jillson, G. P., Thilsted, J. P., Elrod, J., Torrez-Martinez, N., & Hjelle, B. (1998). Serologic survey for hantavirus infection in domestic animals and coyotes from New Mexico and northeastern Arizona. Journal of the American Veterinary Medical Association, 212(7), 970–973. https://doi.org/10.2460/javma.1998.212.07.970

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