Piscine orthoreovirus

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Piscine orthoreovirus
PRV Virion Feature.png
Analysis of PRV-1 using Transmission Electron Microscopy (Scale bar 100nm).
Virus classification OOjs UI icon edit-ltr.svg
(unranked): Virus
Realm: Riboviria
Kingdom: Orthornavirae
Phylum: Duplornaviricota
Class: Resentoviricetes
Order: Reovirales
Family: Sedoreoviridae
Genus: Orthoreovirus
Species:
Piscine orthoreovirus

Piscine orthoreovirus (PRV) is a species in the genus Orthoreovirus that infects fish exclusively, PRV was first discovered in 2010 in farmed Atlantic salmon exhibiting Heart and Skeletal Muscle Inflammation (HSMI) and has been found present at higher concentration in fish with various diseases. [1] These diseases include HSMI, jaundice syndrome, proliferative darkening syndrome and erythrocytic body inclusion syndrome. [1] [2] [3] [4] PRV is thought to mainly affect aquacultured and maricultured fish stocks, and recent research has been focused around the susceptibility of wild stock. However, whether PRV is virulent with respect to HSMI remains a topic of debate. [5] PRV has been in the public eye mostly due to a potential linkage to farmed Atlantic Salmon exhibiting HSMI. [1] Public concern has been raised regarding the possibility of open ocean-net farms transmitting PRV to wild salmon populations and being a factor in declining populations. [6] PRV has not been confirmed to be pathogenic in wild salmon stocks.

Contents

Classification

Phylogenetic analysis of each segment of the PRV genome initially placed PRV in the Reoviridae family, subfamily Spinareovirinae , based on sequence and structural similarity to known reoviruses. [1] Upon discovery, phylogenetic sequence analysis indicated PRV was equally related to viruses in the genera Orthoreovirus and Aquareovirus . [1] As a result, it was suggested that PRV evolved separately from a common ancestor related to both Orthoreovirus and Aquareovirus in the subfamily Spinareovirinae .

Currently, PRV is officially classified as an Orthoreovirus. [7] Placement into the genus Orthoreovirus has been argued for the following reasons:

Opposing arguments to placement in Orthoreovirus,

Genome and structure

Genome

Piscine orthoreovirus has a segmented dsRNA genome made up of 10 individual linear segments, cumulatively measuring around 23,600bp. [1] [10] It has a GC content of 47%. Each segment has conserved terminal sequences. The 3' end sequence (UCAUC-3') is the same as Orthoreovirus and Aquareovirus. The 5' end sequence (5'-GAUAAA/U) is unique to PRV. [1] [11] These segments are referred to as L1-3 (Long), M1-3(Medium) and S1-4 (Short) based on length and comparison with homologous segments in Orthoreovirus and Aquareovirus. L1 is the longest at 3916bp and S4 the shortest at 1040bp. [1] [10] [8]

Eleven proteins are confirmed to be encoded. [10] S1 exhibits bicistronicity with 2 overlapping open reading frames, while the remaining proteins are either confirmed as monocistronic or have been thought to be bicistronic with no further evidence. [8] [9] [10] The proteins that each segment encodes for are as follows, using a standardized naming system across reovirus genera: [10] [13]

Subdivisions

Dendogram of M2 segment nucleotide sequences for different PRV genotypes and subgenotypes. PRV M2 Sequence compariston.png
Dendogram of M2 segment nucleotide sequences for different PRV genotypes and subgenotypes.

Piscine orthoreovirus has been grouped into multiple different genotypes based on sequence diversity. Although multiple ways of subdividing PRV have been proposed, [3] the system most often used in the literature subdivides PRV into Genotypes I and II, which are further divided into Ia and Ib, and IIa and IIb, respectively. [17] [2] [18] [19] These divisions and subdivisions are based on sequence diversity within segment S1. [18] [8]

Genotype I (PRV-1) [8]

Ia

This sub genotype of PRV is found primarily in farmed Atlantic salmon in Norway, Chile and Canada. It has been associated with populations exhibiting HSMI. It has been found in farmed Chinook salmon in Canada exhibiting Jaundice syndrome, as well as farmed Rainbow trout and Coho showing HSMI like symptoms in Chile and Canada. [20]

Ib

This sub genotype of PRV is found primarily in farmed Atlantic and Coho salmon in Norway and Chile, additionally being found in farmed Rainbow trout in Chile. [4] It has been present in many salmon with HSMI. It has also been found in Coho populations exhibiting Jaundice syndrome.

Genotype II [18]

Genotype II was first discovered when comparing the S1 sequences among farmed Atlantic salmon in Chile, and further reiterated with both M2 and whole genome analysis. [21] [17] Despite being within one genotype, the sub genotypes IIa and IIb exhibit much higher inter-sequence diversity than do Ia and Ib.

IIa (PRV-3)

PRV-3 has been associated with pathological heart lesions in rainbow trout. [22] [17] It has also been found in farmed Coho Salmon, Brown trout, and Rainbow trout exhibiting HSMI across Northern Europe and Chile. [19] It has also been found in wild brown trout with proliferative darkening syndrome in Central Europe. [16] Comparison with PRV-2 shows an 80.1% and 90.5% similarity for nucleotides and amino acids, respectively. [23] Comparison with PRV-1 showed a 72.9% similarity in nucleotide sequence and 80.0% amino acid sequence similarity.

IIb (PRV-2)

PVR-2 has only been found in farmed Coho salmon in Japan exhibiting Erythrocytic Inclusion Body Syndrome (EIBS). [2] Only one genome of PRV-2 has been sequenced thus far, which has reduced confidence in phylogenetic placements. [9] Comparison with PRV-1 showed a 73.4% and 80.3% similarity in nucleotide sequence and amino acid sequence, respectively. [23]

Structure

Electrogram image of PRV with immunogold labelled proteins in black arrows. Left: Viral attachment protein (s1) on outer capsid. Right: Outer clamp protein (s3) on outer capsid. PRV virion proteins.png
Electrogram image of PRV with immunogold labelled proteins in black arrows. Left: Viral attachment protein (σ1) on outer capsid. Right: Outer clamp protein (σ3) on outer capsid.

As a member of genus Orthoreovirus, the virion form of PRV is a non-enveloped icosahedral capsid with two layers, the outer and core. The diameter of the total virion encompassing the outer layer is approximately 70 nm, with the inner core layer measuring around 39 nm in diameter. [24]

The inner layer consists of the shell protein, λ3, as well as the inner clamp protein σ2, which is thought to play a role in the structural stabilization of the icosahedron. [25] The outer layer is thought to play a stabilizing role for the inner capsid and is made up of μ1(Outer Capsid protein) as well as σ3 (Outer Clamp Protein). Additionally, the outer layer has fiber proteins (σ1) that mediate viral attachment and entry into the host.

PRV is a turreted reovirus, exhibiting a turret protein (λ2) on the five-fold axes of its inner capsid icosahedron. [10] [26] The homologous proteins for L2 in MRV and ARV have both guanyltransferase and methyltransferase activity. Although not entirely conserved, the active regions of (λ2) exhibit fidelity to MRV and ARV sequences, suggesting λ2 is the turret protein and that it plays a similar role in the 5' capping of transcribed viral mRNA.

Discovery

PRV was first identified in 2010 via high throughput DNA sequencing and bioinformatics approaches which determined the virus was present in maricultured Atlantic salmon affected by Heart and Skeletal Muscle Inflammation (HSMI), and while control of the spread of PRV was advised, a causal relationship between PRV and HSMI was not demonstrated at that time. [1]

In 2012, several wild fish species off the coast of Norway tested positive for PRV indicating that PRV is present in wild populations, however the majority of sample tests yielded negative results indicating low prevalence of PRV off the Norwegian coast. [27]

There has been speculation that PRV 1a was introduced to the West Coast of North America from a North Atlantic source. PRV 1a was introduced to Chile from North Pacific and North Atlantic sources. [21]

Distribution

Cutthroat trout that tested positive for PRV in Cultus Lake, British Columbia, Canada. Cultus Lake cutthroat trout.jpg
Cutthroat trout that tested positive for PRV in Cultus Lake, British Columbia, Canada.

PRV has been found to have a nearly worldwide distribution with various studies detecting the presence of PRV in fisheries in the Atlantic off the coast of the UK, Ireland, and Norway, as well as in both the Atlantic and Pacific Coasts off of North and South America. PRV has been detected in pacific farmed and wild fish species as far north as Alaska, and as far south as Chile. [8] [21] [28]

PRV-1 is less common in wild salmon than it is in farmed salmon, and while wild Sea Trout tend to exhibit PRV-3 infection, the same can not be said for wild Atlantic Salmon populations. [21]

Interaction with host

Infection dynamics

The kinetics of PRV infection have been identified into three distinct phases:

  1. Early host entry, initial replication without host recognition and systemic dissemination of the virus occurs into the blood cells.
    • This stage determines the general course and overall severity of infection in the early replication phase of MRV. [21] To initiate infection, all three PRV genotypes target the erythrocytes of the host. However, viral inclusions within the erythrocytes and systemic viral recognition by the host cells have not been found to occur during this period, which demonstrates that the virus is being shed into the environment at a low degree and that there is a possible lag in replication or infection of different cell types is initially taking place. [29]
  2. Peak systemic replication, load-dependent host recognition and cytoplasmic viral inclusion formation [30] then occurs.
    • In this phase, the systemic blood loads of PRV RNA occur at its highest. [31] Substantial shedding of the virus also occurs at this phase, as demonstrated by previous cohabitation challenges. [32] The formed cytoplasmic viral inclusions, characteristic to the Orthoreovirus genus, are found to be similar to ones that develop during the mammalian reovirus infection of prevalent cell lines. [29]
  3. Long-term, high-load viral persistence with limited replication occurs, with potential for minor heart inflammation.
    • The duration of this persistence varies depending on the host and/or PRV genotype. Little to no systemic host recognition of PRV occurs and viral inclusions within the erythrocytes disappear. A moderate amount of infectious PRV is still present in the cytoplasm of infected erythrocytes at this late infectious stage, however it is in a reduced or non-replicative state. Shedding of the virus is minimal and may completely stop over time. [29] [21] [32]
    • Heart inflammation can occur early in this phase immediately after the peak viral load or during the infection peak. Depending on many factors, this inflammation can continue on for months, but can disappear even if the PRV infections are still remain. [21]

There are complications in determining the possible outcomes of PRV infection. Each genotype has been shown to lead to circulatory disease; however, high-load PRV infections have also occurred in non-diseased salmon and trout. [21]

Disease

PRV and HSMI

Histopathological assay of PRV (red) in Norwegian farmed Atlantic Salmon heart tissue (blue): a) Salmon exhibiting heart and skeletal muscle inflammation (HSMI) c) Healthy salmon. HSMI2.jpg
Histopathological assay of PRV (red) in Norwegian farmed Atlantic Salmon heart tissue (blue): a) Salmon exhibiting heart and skeletal muscle inflammation (HSMI) c) Healthy salmon.

While Norwegian strains of PRV have led to HSMI outbreaks, it's uncertain if HSMI develops as a result of infection with North American strains of PRV as various salmon and trout have been found to have detectable PRV infections despite an apparent absence of HSMI. [24] [33]

Research in Norway has indicated that injecting tissue from fish exhibiting HSMI into healthy fish leads to HSMI, but this causal relationship seems to be more difficult to demonstrate with PRV variants found off the west coast of Canada. [34] So far, only Atlantic Salmon in Norway have had causation proven, while correlation with disease has been found in other cases, but causation has yet to be proven. [33] Wild salmon from British Columbia, such as Coho, Chinook and Sockeye are susceptible to infection by PRV, and exhibit similar viral loads to farmed Atlantic salmon, but have not been reported to exhibit symptoms of HSMI. [35]

Disease prevention

HSMI is one of the most significant diseases in Atlantic salmon aquaculture in Norway. In efforts to mitigate this disease, attempts have been made to develop vaccines which target PRV-1 using deactivated viral particles, and DNA which codes for proteins with sequences derived from PRV; neither treatment prevented infection with PRV, but the effects of HSMI were lessened with both treatments. Various dietary formulations have been tried in attempts to lower the severity of HSMI, and some efforts have been made to select for fish with genetic variants which confer resistance. [21]

One method of disease prevention may be to disinfect the surface of fish eggs prior to introduction to the farm, as removing PRV from a confined system after the fact requires rigorous disinfection, letting the system rest free of hosts, and thorough regular testing. [21]

Prevalence in aquaculture

PRV has been found to be most prevalent in Europe, and the Americas with relatively few reports in Asia. The prevalence of PRV varies greatly depending on the region and host species. PRV surveillance occurs most significantly in North America and Norway [21]

Europe:

PRV-1 has been present in Norwegian farmed Atlantic Salmon since roughly 1988; within the rest of Europe, PRV is suspected to be common, but reports in some countries remain limited. Iceland has reported finding high PRV-1 prevalence in its Atlantic salmon. In 2018, PRV-3 was reported at Brown Trout and Rainbow trout farms in Denmark and Germany. [21]

North America:

PRV seems to exhibit high infectivity in North America, with a single infected fish often resulting in infection of a farms entire fish stock. PRV-1 tends to be initially detected following the return of farmed salmon from seawater. It’s likely that PRV-1 has been present in North America for decades, or possibly longer. [21]

South America:

In Chile, farmed Atlantic salmon show high rates of PRV-1 infection, while wild fish populations show low rates of infection. Rainbow trout show high rates of infection with PRV-1. [21]

Asia:

Within Asia, PRV-2 has only been found in Japan and it has been linked to Erythrocytic Inclusion Body Syndrome (EIBS) in farmed Coho Salmon. [21]

Host range

PRV has been found in a range of aquacultured/wild host species such as: [33]

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References

  1. 1 2 3 4 5 6 7 8 9 10 11 Palacios G, Lovoll M, Tengs T, Hornig M, Hutchison S, Hui J, et al. (July 2010). "Heart and skeletal muscle inflammation of farmed salmon is associated with infection with a novel reovirus". PLOS ONE. 5 (7): e11487. doi: 10.1371/journal.pone.0011487 . PMC   2901333 . PMID   20634888.
  2. 1 2 3 Takano T, Nawata A, Sakai T, Matsuyama T, Ito T, Kurita J, et al. (2016-10-27). "Full-Genome Sequencing and Confirmation of the Causative Agent of Erythrocytic Inclusion Body Syndrome in Coho Salmon Identifies a New Type of Piscine Orthoreovirus". PLOS ONE. 11 (10): e0165424. doi: 10.1371/journal.pone.0165424 . PMC   5082797 . PMID   27788206.
  3. 1 2 Garseth ÅH, Ekrem T, Biering E (2013-12-11). "Phylogenetic evidence of long distance dispersal and transmission of piscine reovirus (PRV) between farmed and wild Atlantic salmon". PLOS ONE. 8 (12): e82202. doi: 10.1371/journal.pone.0082202 . PMC   3859594 . PMID   24349221.
  4. 1 2 Cartagena J, Jiménez C, Spencer E (November 2020). "Detection of Piscine orthoreoviruses (PRV-1b AND PRV-3a) in farmed Coho salmon with jaundice syndrome from Chile". Aquaculture. 528: 735480. doi:10.1016/j.aquaculture.2020.735480. ISSN   0044-8486. S2CID   219465755.
  5. Zhang Y, Polinski MP, Morrison PR, Brauner CJ, Farrell AP, Garver KA (2019). "High-Load Reovirus Infections Do Not Imply Physiological Impairment in Salmon". Frontiers in Physiology. 10: 114. doi: 10.3389/fphys.2019.00114 . PMC   6425399 . PMID   30930782.
  6. Noakes DJ, Beamish RJ, Kent ML (March 2000). "On the decline of Pacific salmon and speculative links to salmon farming in British Columbia". Aquaculture. 183 (3–4): 363–386. doi:10.1016/s0044-8486(99)00294-x. ISSN   0044-8486.
  7. "ICTV". talk.ictvonline.org. Retrieved 2021-03-16.
  8. 1 2 3 4 5 6 Kibenge MJ, Iwamoto T, Wang Y, Morton A, Godoy MG, Kibenge FS (July 2013). "Whole-genome analysis of piscine reovirus (PRV) shows PRV represents a new genus in family Reoviridae and its genome segment S1 sequences group it into two separate sub-genotypes". Virology Journal. 10 (1): 230. doi: 10.1186/1743-422X-10-230 . PMC   3711887 . PMID   23844948.
  9. 1 2 3 4 Key T, Read J, Nibert ML, Duncan R (May 2013). "Piscine reovirus encodes a cytotoxic, non-fusogenic, integral membrane protein and previously unrecognized virion outer-capsid proteins". The Journal of General Virology. 94 (Pt 5): 1039–1050. doi: 10.1099/vir.0.048637-0 . PMID   23343626.
  10. 1 2 3 4 5 6 7 8 9 10 11 Markussen T, Dahle MK, Tengs T, Løvoll M, Finstad ØW, Wiik-Nielsen CR, et al. (2013-07-29). "Sequence analysis of the genome of piscine orthoreovirus (PRV) associated with heart and skeletal muscle inflammation (HSMI) in Atlantic salmon (Salmo salar)". PLOS ONE. 8 (7): e70075. doi: 10.1371/journal.pone.0070075 . PMC   3726481 . PMID   23922911.
  11. 1 2 Attoui H, Fang Q, Jaafar FM, Cantaloube JF, Biagini P, de Micco P, de Lamballerie X (August 2002). "Common evolutionary origin of aquareoviruses and orthoreoviruses revealed by genome characterization of Golden shiner reovirus, Grass carp reovirus, Striped bass reovirus and golden ide reovirus (genus Aquareovirus, family Reoviridae)". The Journal of General Virology. 83 (Pt 8): 1941–1951. doi: 10.1099/0022-1317-83-8-1941 . PMID   12124458.
  12. Duncan R (August 1999). "Extensive sequence divergence and phylogenetic relationships between the fusogenic and nonfusogenic orthoreoviruses: a species proposal". Virology. 260 (2): 316–28. doi: 10.1006/viro.1999.9832 . PMID   10417266.
  13. 1 2 Yan X, Parent KN, Goodman RP, Tang J, Shou J, Nibert ML, et al. (August 2011). "Virion structure of baboon reovirus, a fusogenic orthoreovirus that lacks an adhesion fiber". Journal of Virology. 85 (15): 7483–95. doi: 10.1128/JVI.00729-11 . PMC   3147939 . PMID   21593159.
  14. Nibert ML, Duncan R (2013-07-04). "Bioinformatics of recent aqua- and orthoreovirus isolates from fish: evolutionary gain or loss of FAST and fiber proteins and taxonomic implications". PLOS ONE. 8 (7): e68607. doi: 10.1371/journal.pone.0068607 . PMC   3701659 . PMID   23861926.
  15. Haatveit HM, Nyman IB, Markussen T, Wessel Ø, Dahle MK, Rimstad E (January 2016). "The non-structural protein μNS of piscine orthoreovirus (PRV) forms viral factory-like structures". Veterinary Research. 47 (1): 5. doi: 10.1186/s13567-015-0302-0 . PMC   4705589 . PMID   26743679.
  16. 1 2 Kuehn R, Stoeckle BC, Young M, Popp L, Taeubert JE, Pfaffl MW, Geist J (2018-10-22). "Identification of a piscine reovirus-related pathogen in proliferative darkening syndrome (PDS) infected brown trout (Salmo trutta fario) using a next-generation technology detection pipeline". PLOS ONE. 13 (10): e0206164. doi: 10.1371/journal.pone.0206164 . PMC   6197672 . PMID   30346982.
  17. 1 2 3 Godoy M, Medina DA, Suarez R, Valenzuela S, Romero J, Kibenge M, et al. (January 2021). "Extensive Phylogenetic Analysis of Piscine Orthoreovirus Genomic Sequences Shows the Robustness of Subgenotype Classification". Pathogens. 10 (1): 41. doi: 10.3390/pathogens10010041 . PMC   7825714 . PMID   33430212.
  18. 1 2 3 Godoy MG, Kibenge MJ, Wang Y, Suarez R, Leiva C, Vallejos F, Kibenge FS (June 2016). "First description of clinical presentation of piscine orthoreovirus (PRV) infections in salmonid aquaculture in Chile and identification of a second genotype (Genotype II) of PRV". Virology Journal. 13 (1): 98. doi: 10.1186/s12985-016-0554-y . PMC   4906990 . PMID   27296722.
  19. 1 2 Kibenge FS (February 2019). "Emerging viruses in aquaculture". Current Opinion in Virology. Emerging viruses: intraspecies transmission • Viral Immunology. 34: 97–103. doi:10.1016/j.coviro.2018.12.008. PMID   30711892. S2CID   73415392.
  20. Di Cicco E, Ferguson HW, Kaukinen KH, Schulze AD, Li S, Tabata A, et al. (2018-10-01). "The same strain of Piscine orthoreovirus (PRV-1) is involved in the development of different, but related, diseases in Atlantic and Pacific Salmon in British Columbia". FACETS. 3 (1): 599–641. doi: 10.1139/facets-2018-0008 . ISSN   2371-1671.
  21. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 Polinski MP, Vendramin N, Cuenca A, Garver KA (November 2020). "Piscine orthoreovirus: Biology and distribution in farmed and wild fish". Journal of Fish Diseases. 43 (11): 1331–1352. doi: 10.1111/jfd.13228 . PMID   32935367.
  22. Vendramin N, Kannimuthu D, Olsen AB, Cuenca A, Teige LH, Wessel Ø, et al. (February 2019). "Piscine orthoreovirus subtype 3 (PRV-3) causes heart inflammation in rainbow trout (Oncorhynchus mykiss)". Veterinary Research. 50 (1): 14. doi: 10.1186/s13567-019-0632-4 . PMC   6380033 . PMID   30777130.
  23. 1 2 Dhamotharan K, Vendramin N, Markussen T, Wessel Ø, Cuenca A, Nyman IB, et al. (April 2018). "Molecular and Antigenic Characterization of Piscine orthoreovirus (PRV) from Rainbow Trout (Oncorhynchus mykiss)". Viruses. 10 (4): 170. doi: 10.3390/v10040170 . PMC   5923464 . PMID   29614838.
  24. 1 2 Wessel Ø, Braaen S, Alarcon M, Haatveit H, Roos N, Markussen T, et al. (2017-08-25). "Infection with purified Piscine orthoreovirus demonstrates a causal relationship with heart and skeletal muscle inflammation in Atlantic salmon". PLOS ONE. 12 (8): e0183781. doi: 10.1371/journal.pone.0183781 . PMC   5571969 . PMID   28841684.
  25. Zhou ZH, Zhang H, Jakana J, Lu XY, Zhang JQ (June 2003). "Cytoplasmic polyhedrosis virus structure at 8 A by electron cryomicroscopy: structural basis of capsid stability and mRNA processing regulation". Structure. 11 (6): 651–63. doi: 10.1016/s0969-2126(03)00091-1 . PMID   12791254.
  26. Miyazaki N, Uehara-Ichiki T, Xing L, Bergman L, Higashiura A, Nakagawa A, et al. (November 2008). "Structural evolution of reoviridae revealed by oryzavirus in acquiring the second capsid shell". Journal of Virology. 82 (22): 11344–53. doi:10.1128/JVI.02375-07. PMC   2573255 . PMID   18787002.
  27. Wiik-Nielsen CR, Løvoll M, Sandlund N, Faller R, Wiik-Nielsen J, Bang Jensen B (January 2012). "First detection of piscine reovirus (PRV) in marine fish species". Diseases of Aquatic Organisms. 97 (3): 255–8. doi: 10.3354/dao02425 . PMID   22422096.
  28. Siah A, Morrison DB, Fringuelli E, Savage P, Richmond Z, Johns R, et al. (2015-11-04). "Piscine Reovirus: Genomic and Molecular Phylogenetic Analysis from Farmed and Wild Salmonids Collected on the Canada/US Pacific Coast". PLOS ONE. 10 (11): e0141475. doi: 10.1371/journal.pone.0141475 . PMC   4633109 . PMID   26536673.
  29. 1 2 3 Polinski MP, Marty GD, Snyman HN, Garver KA (March 2019). "Piscine orthoreovirus demonstrates high infectivity but low virulence in Atlantic salmon of Pacific Canada". Scientific Reports. 9 (1): 3297. doi: 10.1038/s41598-019-40025-7 . PMC   6416343 . PMID   30867461.
  30. Wessel Ø, Olsen CM, Rimstad E, Dahle MK (March 2015). "Piscine orthoreovirus (PRV) replicates in Atlantic salmon (Salmo salar L.) erythrocytes ex vivo". Veterinary Research. 46 (1): 26. doi: 10.1186/s13567-015-0154-7 . PMC   4350956 . PMID   25888832.
  31. Haatveit HM, Wessel Ø, Markussen T, Lund M, Thiede B, Nyman IB, et al. (March 2017). "Viral Protein Kinetics of Piscine Orthoreovirus Infection in Atlantic Salmon Blood Cells". Viruses. 9 (3): 49. doi: 10.3390/v9030049 . PMC   5371804 . PMID   28335455.
  32. 1 2 Garver KA, Johnson SC, Polinski MP, Bradshaw JC, Marty GD, Snyman HN, et al. (January 2016). "Piscine Orthoreovirus from Western North America Is Transmissible to Atlantic Salmon and Sockeye Salmon but Fails to Cause Heart and Skeletal Muscle Inflammation". PLOS ONE. 11 (1): e0146229. doi: 10.1371/journal.pone.0146229 . PMC   4701501 . PMID   26730591.
  33. 1 2 3 Government of Canada, Fisheries and Oceans Canada (2018-04-03). "Piscine Orthoreovirus (PRV) and Heart and Skeletal Muscle Inflammation (HSMI)". www.dfo-mpo.gc.ca. Retrieved 2021-03-13.
  34. Garver, Kyle A.; Johnson, Stewart C.; Polinski, Mark P.; Bradshaw, Julia C.; Marty, Gary D.; Snyman, Heindrich N.; Morrison, Diane B.; Richard, Jon (2016-01-05). "Piscine Orthoreovirus from Western North America Is Transmissible to Atlantic Salmon and Sockeye Salmon but Fails to Cause Heart and Skeletal Muscle Inflammation". PLOS ONE. 11 (1): e0146229. doi: 10.1371/journal.pone.0146229 . ISSN   1932-6203. PMC   4701501 . PMID   26730591.
  35. Purcell, M K; Powers, R L; Evered, J; Kerwin, J; Meyers, T R; Stewart, B; Winton, J R (February 2018). "Molecular testing of adult Pacific salmon and trout ( Oncorhynchus spp.) for several RNA viruses demonstrates widespread distribution of piscine orthoreovirus in Alaska and Washington". Journal of Fish Diseases. 41 (2): 347–355. doi: 10.1111/jfd.12740 .