Genome And Source
Length
993
Type
ssRNA(+)
GC%
40.8%
Completeness
partial_sequence
Country
Brazil
Year
2011
📋 Data Provenance
Genome Browser
No ORF position data available for this genome.
Curation Status
38
Isolates
3
Hosts
1
Proteins
✓
Sequence
Related Viruses
No related viruses found.
Outbreak Events
Brazil
(2004 - 2022)
Infectious myonecrosis virus outbreak in Brazil
Reference
Genetic diversification of penaeid shrimp infectious myonecrosis virus between Indonesia and Brazil.
Naim Sidrotun; Brown Judith K; Nibert Max L
Virus research 2014
PMID: 24874195
DOI: 10.1016/j.virusres.2014.05.013
ICTV Mapping
No ICTV mapping is available or reviewed for this record.
Reviewed Evidence
Only manual-checked evidence records are displayed. Inferred records (without direct isolate linkage) are shown with a yellow badge.
Virulence / pathogenicity
Pathogenicity terms found: lethal
pathogenicity · medium
Pathogenicity terms found: mortality, virulence, symptom
d virus, Decapoda iridovirus 1 (DIV1) can cause a mortality rate of up to 100% in crustaceans, leading to huge economic losses.
pathogenicity · medium
Pathogenicity terms found: lethal
BACKGROUND: Abdominal segment deformity disease (ASDD) of cultivated whiteleg shrimp Penaeus (Litopenaeus) vannamei causes economic loss of approximately 10% in affected specimens because of the unsightliness of distorted abdominal muscles.
pathogenicity · medium
Pathogenicity terms found: experimental infection, tissue tropism
pathogenicity · medium
Preparation of Infectious Study Material To produce materials for disease challenge, moribund larvae were collected from a hatchery that was experiencing mortalities at the time of the study.
pathogenicity · medium
Molluscan cells in culture: Primary cell cultures and cell lines Detection and Description of a Particular Ostreid Herpesvirus 1 Genotype Associated with Massive Mortality Outbreaks of Pacific oysters, Crassostrea gigas, in France in 2008 Identificat
pathogenicity · medium
Genomic selection is particularly promising for selection programs that challenge live animals with infectious agents when survivors cannot later be used as breeders.
pathogenicity · medium
The intramuscular route was selected for infectious challenge using a protocol already described [26, 27].
pathogenicity · medium
Further studies including the determination of infectious virus titer at different time points and in vivo challenge studies will be highly beneficial.
pathogenicity · medium
Development of a reproducible
infectious pancreatic necrosis virus challenge model for Atlantic salmon,
Salmo salar L.
As bioaccumulating organisms, shellfish may also increase disease risk on farms by serving as reservoirs for important finfish pathogens such as infectious pancreatic necrosis virus (IPNV).
pathogenicity · medium
Temperature
Temperature data found: temperature, thermal, °C
d virus, Decapoda iridovirus 1 (DIV1) can cause a mortality rate of up to 100% in crustaceans, leading to huge economic losses.
temperature · medium
Causation and disease: the Henle-Koch postulates revisited Development of a PCR procedure for the detection of a herpes-like virus infecting oysters in France Council Directive 95/70/EC of 22 December 1995 introducing minimum Community measures for t
Since its molecular characterisation, Ostreid herpesvirus 1 (OsHV-1) has been regularly detected in Crassostrea gigas in France.
temperature · medium
Response to selection for survival and its influence on growth and yield Summer mortality of selected juvenile Pacific oyster Crassostrea gigas under laboratory conditions and in comparison with field performance New insight for the genetic evaluatio
temperature · medium
Pertinent examples of pathogens and parasites affecting marine aquaculture and their temperature ranges, optimal conditions, and critical
thresholds affecting their environmental survival
Disease
Pathogen/Parasite
(taxonomy)
Hosts
Temperature
range (
temperature · medium
Fulltext: °C
temperature · medium
Fulltext: heat shock
Protein-protein interaction studies have been widely used in several fields to characterize an unknown protein.
temperature · medium
Fulltext: thermal, °C
temperature · medium
Resistance of hepatitis A virus in mussels subjected to different domestic cookings.
temperature · medium
Temperature data found: temperature, thermal, heat, °C
temperature · high
Temperature data found: temperature, water temperature, degree, °C
temperature · high
Hosts
Diagnostic And Control Records
No curated diagnostic or control records are available for this virus.
Proteins
🧬
No protein annotations available
Loading additional protein data...
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Loading additional literature...
Geographic Distribution
Indonesia
13 isolates
Brazil
11 isolates
India
5 isolates
China
3 isolates
Taxonomy Information
Family
Totiviridae
Host Phylum
Arthropoda
Genome Type
ssRNA(+)
Discovery Method
metagenomic_with_host_evidence
Related Isolates
| Accession | Length | GC | Completeness | Country | Year |
|---|---|---|---|---|---|
| AY570982.3 | 8,226 | 38.6 | complete_genome | Brazil | 2006 |
| EF061744.1 | 7,561 | 37.8 | complete_genome | Indonesia | 2014 |
| HM030799.1 | 685 | 42.3 | partial_sequence | Brazil | 2007 |
| HM357803.1 | 582 | 39.0 | partial_sequence | Brazil | 2007 |
| KC200075.1 | 909 | 40.9 | partial_sequence | Brazil | 2004 |
| KF836757.1 | 8,226 | 38.6 | complete_genome | Indonesia | 2014 |
| KJ556923.1 | 8,226 | 38.6 | complete_genome | Brazil | 2006 |
| KJ636782.2 | 8,230 | 38.6 | complete_genome | Indonesia | 2011 |
| KJ636783.2 | 8,226 | 38.4 | gene_fragment | Indonesia | 2012 |
| KJ636784.1 | 3,000 | 39.9 | partial_sequence | Indonesia | 2012 |
| KJ636785.1 | 3,000 | 40.2 | partial_sequence | Indonesia | 2012 |
| KJ636786.1 | 2,520 | 39.2 | partial_sequence | Indonesia | 2012 |
| KJ636787.1 | 3,000 | 40.0 | partial_sequence | Indonesia | 2012 |
| KJ636788.1 | 3,000 | 40.1 | partial_sequence | Indonesia | 2012 |
| KJ636789.1 | 993 | 40.8 | partial_sequence | Brazil | 2011 |
| KR815474.1 | 8,226 | 38.6 | complete_genome | Brazil | 2009 |
| KT003689.1 | 7,767 | 38.0 | partial_sequence | Brazil | 2015 |
| KY608806.1 | 990 | 41.5 | partial_sequence | India | 2016 |
| KY930468.1 | 327 | 46.2 | partial_sequence | India | 2017 |
| MK308857.1 | 8,226 | 38.6 | complete_genome | India | 2017 |
| MK503766.1 | 2,703 | 39.6 | partial_sequence | Indonesia | 2018 |
| MK503767.2 | 7,037 | 37.6 | complete_genome | Indonesia | 2018 |
| MK503768.1 | 2,703 | 39.6 | partial_sequence | Indonesia | 2018 |
| MK560205.1 | 137 | 41.6 | unverified | N/A | 2019 |
| MK560206.1 | 135 | 43.0 | unverified | N/A | 2019 |
| MN243920.1 | 1,320 | 40.5 | partial_sequence | India | 2017 |
| MN243921.1 | 1,829 | 34.7 | partial_sequence | India | 2017 |
| MZ593846.1 | 8,185 | 38.4 | complete_genome | Brazil | 2018 |
| MZ645876.1 | 8,208 | 38.3 | gene_fragment | Indonesia | 2018 |
| NC_007915.3 | 8,226 | 38.6 | complete_genome | Brazil | 2006 |
| OQ368673.1 | 8,211 | 38.5 | gene_fragment | China | 2020 |
| OQ438431.1 | 288 | 45.5 | partial_sequence | China | 2022 |
| PV054448.1 | 8,206 | 38.4 | complete_genome | Brazil | 2022 |
| PV242991.1 | 8,230 | 38.4 | complete_genome | China | 2022 |
| PZ014968.1 | 2,839 | 49.4 | unknown | N/A | N/A |
| PZ014969.1 | 9,159 | 59.6 | unknown | N/A | N/A |
| PZ014970.1 | 5,377 | 55.9 | unknown | N/A | N/A |
| PZ014971.1 | 7,310 | 56.7 | unknown | N/A | N/A |
Sequence
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