Volume 20, Number 2—February 2014
Novel Bunyavirus in Domestic and Captive Farmed Animals, Minnesota, USA
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|EID||Nasci RS, Brault AC, Lambert AJ, Savage HM. Novel Bunyavirus in Domestic and Captive Farmed Animals, Minnesota, USA. Emerg Infect Dis. 2014;20(2):336. https://dx.doi.org/10.3201/eid2002.131360|
|AMA||Nasci RS, Brault AC, Lambert AJ, et al. Novel Bunyavirus in Domestic and Captive Farmed Animals, Minnesota, USA. Emerging Infectious Diseases. 2014;20(2):336. doi:10.3201/eid2002.131360.|
|APA||Nasci, R. S., Brault, A. C., Lambert, A. J., & Savage, H. M. (2014). Novel Bunyavirus in Domestic and Captive Farmed Animals, Minnesota, USA. Emerging Infectious Diseases, 20(2), 336. https://dx.doi.org/10.3201/eid2002.131360.|
To the Editor: Xing et al. (1) conclude that evidence of infection with a severe fever with thrombocytopenia syndrome (SFTS)–like virus or Heartland-like virus (HRTV) was found in many captive large mammals from much of Minnesota, raising the specter of widespread distribution of a novel pathogen. Although it is likely that HRTV can be found beyond the areas in northwestern Missouri, where it was discovered (2), we contend that this conclusion is not substantiated by the data presented by Xing et al., which were generated by an assay that was developed to diagnose SFTS virus infections in China (1,3). The study used an ELISA developed for an SFTS virus recombinant nucleocapsid protein that detects SFTS-reactive antibodies (3). The conclusions reached by Xing et al. are based on the assumption that the SFTS assay developed in China will cross-react with HRTV antibodies (1). This assumption remains unsupported because the SFTS assay has not been evaluated for cross-reaction with antibodies to other non-SFTS members of the genus Phlebovirus (1,3). In addition, it is well recognized that serologic tests, like the ELISA, are often group reactive (4), requiring neutralization tests to confirm antibody presence and provide specificity. Alternative explanations include the possibility that positive results from testing by Xing et al. may have been caused by cross-reaction with antibodies directed against other known tick-associated phleboviruses endemic to North America, such as Lone Star virus (5), which is not known to be pathogenic. In the absence of confirmatory data generated by an independent method, the report by Xing et al. (1) should be considered speculative. Reports suggesting substantial expansion in the geographic range of a pathogenic organism should be based on rigorously validated laboratory methods.
- Xing Z, Schefers J, Schwabenlander M, Jiao Y, Liang M, Qi X, Novel bunyavirus in domestic and captive farmed animals, Minnesota, USA. Emerg Infect Dis. 2013;19:1487–9 .
- McMullan LK, Folk SM, Kelly AJ, MacNeil A, Goldsmith CS, Metcalfe MG, A new phlebovirus associated with severe febrile illness in Missouri. N Engl J Med. 2012;367:834–41 .
- Jiao Y, Zeng X, Guo X, Qi X, Zhang X, Shi Z, Preparation and evaluation of recombinant severe fever with thrombocytopenia syndrome virus nucleocapsid protein for detection of total antibodies in human and animal sera by double-antigen sandwich enzyme-linked immunosorbent assay. J Clin Microbiol. 2012;50:372–7.
- Shope RE. Bunyaviruses. In: Baron S, editor. Medical microbiology. 4th edition. Galveston (TX): University of Texas Medical Branch at Galveston; 1996. Chapter 56 [cited 2013 Dec 10]. http://www.ncbi.nlm.nih.gov/books/NBK8004/
- Swei A, Russell BJ, Naccache SN, Kabre B, Veeraraghavan N, Pilgard MA, The genome sequence of lone star virus, a highly divergent bunyavirus found in the Amblyomma americanum tick. PLoS ONE. 2013;8:e62083 .
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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