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Volume 20, Number 9—September 2014
Letter

Porcine Coronavirus HKU15 Detected in 9 US States, 2014

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To the Editor: Porcine coronavirus (PorCoV) HKU15 is a single-stranded, positive-sense, enveloped RNA virus belonging to the genus Deltacoronavirus (family Coronaviridae). PorCoV HKU15 was first identified in 2012 in a surveillance study from China (1). Until February 2014, however, the role of this virus strain in clinical diseases of pigs had not been reported.

We recently reported the detection of PorCoV strain HKU15-OH1987 in feces samples from sows and intestine samples from piglets in Ohio, United States; the infected animals were from swine farms where outbreaks of diarrheal disease had occurred in late January and early February 2014 (2). Genetic analysis showed that HKU15-OH1987 is closely related to 2 deltacoronavirus strains that were detected in Hong Kong, China, in 2012: HKU15-155 and HKU15-44 (2). We also demonstrated the presence of histopathologic lesions in the small intestines of PorCoV HKU15–infected piglets with diarrhea (L. Wang, unpub. data). In April 2014, a novel swine enteric coronavirus disease caused by PorCoV HKU15 or porcine epidemic diarrhea virus was reported to the World Animal Health Organization by the US Department of Agriculture (http://www.oie.int/wahis_2/public/wahid.php/Reviewreport/Review?page_refer=MapFullEventReport&reportid=15133).

PorCoV HKU15 is now recognized as a key pathogenic cause of diarrheal diseases in pigs in the United States. However, the geographic distribution and genotype diversity of PorCoV HKU15 in this country are still not clear. To further our knowledge of the virus, we analyzed swine samples that had been submitted for diagnosis of diarrheal disease from farms in 10 US states. We report the detection and phylogenetic analyses of PorCoV HKU15 strains from these samples.

Figure

Thumbnail of US states with swine samples positive for porcine coronavirus (PorCoV) HKU15, between February and April 2014. A total of 435 samples from 10 states were selected to be tested for the presence of PorCoV. Of those samples, 109 (25%) from 9 states (dark gray) were positive for PorCoV HKU15. Another recent article reported the presence of PorCoV HKU15 in Iowa (white) (3). Strain names are indicated below state abbreviations.

Figure. US states with swine samples positive for porcine coronavirus (PorCoV) HKU15, between February and April 2014. A total of 435 samples from 10 states were selected to be tested for the...

Between February 7, 2014, when PorCoV HKU15-OH1987 was first identified in Ohio (2), and April 9, 2014, the Animal Disease Diagnostic Laboratory of the Ohio Department of Agriculture received >2,000 swine samples from farms in 10 US states for diagnosis of diarrheal disease. The states from which samples had been submitted were Minnesota, South Dakota, Nebraska, Illinois, Indiana, Michigan, Kentucky, Pennsylvania, Maryland, and Ohio. Among those samples, 435 were selected to be tested for the presence of PorCoV HKU15. A real-time reverse transcription PCR assay targeting the membrane protein gene was used to identify PorCoV HKU15. Samples with a cycle threshold value of <35 were considered positive on the basis of validation data using the cloned membrane protein gene (data not shown). Of the 435 samples, 109 (25%) from 9 states (all states mentioned above, excluding Maryland) were positive for PorCoV HKU15 by real-time reverse transcription PCR (Figure). Of those 109 samples, 19 (17%) were also positive for porcine epidemic diarrhea virus. This result suggests that PorCoV HKU15 is prevalent among pig populations in the major pig-producing US states.

To determine the genetic diversity of PorCoV HKU15 strains from the 9 states, we conducted whole-genome sequencing for 1 strain from each state by using 16 pairs of previously described, overlapping primers (2). Strain names were designated by the state abbreviation and case number. The complete sequence for HKU15-OH1987 was reported previously (2). Sequence analysis showed that strains from South Dakota (SD3424), Nebraska (NE3579), Illinois (IL2768), Indiana (IN2847), Kentucky (KY4813), Michigan (MI6148), and Pennsylvania (PA3148) have the same genome size (25,422 nt) as OH1987, and whole-genome pairwise comparison showed that they share a high nucleotide similarity (>99.8%). Furthermore, all of the isolates share high nucleotide similarity (98.9%–99.2%) with the 2 PorCoV HKU15 strains in GenBank, HKU15-155 and HKU15-44.

A phylogenetic tree constructed by using the entire sequence showed that all PorCoV HKU15 strains from the United States clustered together in 1 clade of the genus Deltacoronavirus with HKU15-155 and HKU15-44 (Technical Appendix Figure, panel A). This finding indicates that 1 genotype of PorCoV HKU15 is currently circulating in multiple US states. This result was further supported by phylogenetic trees constructed by using the full-length amino acids of spike and nucleocapsid proteins (Technical Appendix Figure, panels B, C). Because of limitation of the samples received, only a partial genome sequence was determined for strain MN3092 from Minnesota. However, on the basis of the spike and nucleocapsid protein sequence analyses, it is highly likely that the entire genome of the Minnesota strain is genetically identical to that of the other 8 strains (Technical Appendix Figure, panels B, C).

In addition to the 9 states reported in this study, Iowa has also had a recent detection of PorCoV HKU15 (3). Thus, PorCoV HKU15 has been detected in 10 of the 50 US states, and those 10 states mainly cluster in the midwestern United States (Figure). As with data collected for porcine epidemic diarrhea outbreaks by the US National Animal Health Laboratory Network (http://www.nahln.org/default/), data collected on the geographic location and numbers of PorCoV HKU15 cases is also required to be reported weekly.

Earlier reports support avian coronaviruses as the gene source for Deltacoronavirus spp. (1,4). To confirm this, surveillance for PorCoV should be carried out among birds. Moreover, effective control strategies, including vaccine development, should be in place for prevention and control of infections caused by PorCoV HKU15.

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Acknowledgment

We acknowledge and appreciate the excellent technical help provided by Jason Herr and Kerri Lawrence.

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Leyi Wang1, Beverly Byrum, and Yan Zhang1Comments to Author 
Author affiliations: Ohio Department of Agriculture, Reynoldsburg, Ohio, USA

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References

  1. Woo  PC, Lau  SK, Lam  CS, Lau  CC, Tsang  AK, Lau  JH, Discovery of seven novel mammalian and avian coronaviruses in the genus Deltacoronavirus supports bat coronaviruses as the gene source of Alphacoronavirus and Betacoronavirus and avian coronaviruses as the gene source of Gammacoronavirus and Deltacoronavirus. J Virol. 2012;86:39954008 . DOIPubMedGoogle Scholar
  2. Wang  L, Byrum  B, Zhang  Y. Detection and genetic characterization of a deltacoronavirus in pigs in the United States. Emerg Infect Dis. 2014;20:12271230. DOIPubMedGoogle Scholar
  3. Li  G, Chen  Q, Harmon  KM, Yoon  KJ, Schwartz  KJ, Hoogland  MJ, Full-length genome sequence of porcine deltacoronavirus strain USA/IA/2014/8734. Genome Announc. 2014;2:e00278-14.
  4. Chu  DK, Leung  CY, Gilbert  M, Joyner  PH, Ng  EM, Tse  TM, Avian coronavirus in wild aquatic birds. J Virol. 2011;85:1281520 . DOIPubMedGoogle Scholar

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Cite This Article

DOI: 10.3201/eid2009.140756

1These authors were co–principal investigators.

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Table of Contents – Volume 20, Number 9—September 2014

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

Yan Zhang, Animal Disease Diagnostic Laboratory, Ohio Department of Agriculture, 8995 East Main St, Bldg. 6, Reynoldsburg, OH 43068, USA

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Page created: April 23, 2015
Page updated: April 23, 2015
Page reviewed: April 23, 2015
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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