RESUMEN
The aim of this study was to compare the accuracy of breeding values (EBVs) predicted using the traditional pedigree based Best Linear Unbiased Prediction (PBLUP) and the single-step genomic Best Linear Unbiased Prediction (ssGBLUP) for resistance against infectious pancreatic necrosis virus (IPNV) in rainbow trout. A total of 2278 animals were challenged against IPNV and 768 individuals were genotyped using a 57â¯K single nucleotide polymorphism array for rainbow trout. Accuracies for both methods were assessed using five-fold cross-validation. The heritabilities were higher for PBLUP compared to ssGBLUP. The ssGBLUP accuracies outperformed PBLUP in 7 and 11% for days to death and binary survival, respectively. The ssGBLUP could be an alternative approach to improve the accuracy of breeding values for resistance against infectious pancreatic necrosis virus in rainbow trout, using information from genotyped and non-genotyped animals.
Asunto(s)
Infecciones por Birnaviridae/genética , Resistencia a la Enfermedad , Enfermedades de los Peces/genética , Estudio de Asociación del Genoma Completo/métodos , Selección Artificial , Trucha/genética , Animales , Infecciones por Birnaviridae/inmunología , Enfermedades de los Peces/inmunología , Estudio de Asociación del Genoma Completo/normas , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Trucha/virologíaRESUMEN
In order to obtain an insight into genomic changes and associated evolution and adaptation of Infectious Pancreatic Necrosis Virus (IPNV), the complete coding genomes of 57 IPNV isolates collected from Scottish aquafarms from 1982 to 2014 were sequenced and analysed. Phylogenetic analysis of the sequenced IPNV strains showed separate clustering of genogroups I, II, III and V. IPNV isolates with genetic reassortment of segment A/B of genogroup III/II were determined. About 59â% of the IPNV isolates belonged to the persistent type and 32â% to the low-virulent type, and only one highly pathogenic strain (1.79â%) was identified. Codon adaptation index calculations indicated that the IPNV major capsid protein VP2 has adapted to its salmonid host. Under-representation of CpG dinucleotides in the IPNV genome to minimize detection by the innate immunity receptors, and observed positive selection in the virulence determination sites of VP2 embedded in the variable region of the main antigenic region, suggest an immune escape mechanism driving virulence evolution. The prevalence of mostly persistent genotypes, together with the assumption of adaptation and immune escape, indicates that IPNV is evolving with the host.
Asunto(s)
Infecciones por Birnaviridae/veterinaria , Enfermedades de los Peces/epidemiología , Enfermedades de los Peces/virología , Variación Genética , Virus de la Necrosis Pancreática Infecciosa/clasificación , Virus de la Necrosis Pancreática Infecciosa/genética , Adaptación Biológica , Animales , Acuicultura , Infecciones por Birnaviridae/epidemiología , Infecciones por Birnaviridae/virología , Proteínas de la Cápside/genética , Codón , Genotipo , Evasión Inmune , Virus de la Necrosis Pancreática Infecciosa/aislamiento & purificación , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Epidemiología Molecular , Prevalencia , Escocia/epidemiología , Selección Genética , Análisis de Secuencia de ADN , Virulencia , Secuenciación Completa del GenomaRESUMEN
Infectious pancreatic necrosis (IPN) is a significant disease of farmed salmonids resulting in direct economic losses due to high mortality in China. However, no gene sequence of any Chinese infectious pancreatic necrosis virus (IPNV) isolates was available. In the study, moribund rainbow trout fry samples were collected during an outbreak of IPN in Yunnan province of southwest China in 2013. An IPNV was isolated and tentatively named ChRtm213. We determined the full genome sequence of the IPNV ChRtm213 and compared it with previously identified IPNV sequences worldwide. The sequences of different structural and non-structural protein genes were compared to those of other aquatic birnaviruses sequenced to date. The results indicated that the complete genome sequence of ChRtm213 strain contains a segment A (3099 nucleotides) coding a polyprotein VP2-VP4-VP3, and a segment B (2789 nucleotides) coding a RNA-dependent RNA polymerase VP1. The phylogenetic analyses showed that ChRtm213 strain fell within genogroup 1, serotype A9 (Jasper), having similarities of 96.3% (segment A) and 97.3% (segment B) with the IPNV strain AM98 from Japan. The results suggest that the Chinese IPNV isolate has relative closer relationship with Japanese IPNV strains. The sequence of ChRtm213 was the first gene sequence of IPNV isolates in China. This study provided a robust reference for diagnosis and/or control of IPNV prevalent in China.
Asunto(s)
Enfermedades de los Peces/genética , Virus de la Necrosis Pancreática Infecciosa/genética , Oncorhynchus mykiss/virología , Secuencia de Aminoácidos/genética , Animales , Secuencia de Bases , China , Enfermedades de los Peces/virología , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Anotación de Secuencia Molecular , Oncorhynchus mykiss/genética , FilogeniaRESUMEN
Infectious pancreatic necrosis (IPN) is a contagious viral disease of fish that causes economic losses in aquaculture worldwide. In Finland, IPN virus (IPNV) has been isolated since 1987 from adult fish showing no signs of clinical disease at fish farms located in the coastal areas of the Baltic Sea. The inland area of Finland, however, remained free of IPN until 2012, when fish on several rainbow trout farms were diagnosed IPNV-positive. The fish mortalities detected at the farms were low, but clinical signs and histopathological changes typical for IPNV infection were seen in juvenile salmonids. IPNV was isolated at high water temperatures up to 22°C. In 2013 and 2014, IPNV detections continued at inland farms, indicating that infections have spread. The aim of this study was to describe the epidemiology of the outbreak and to characterise the Finnish inland IPNV isolates using histopathological, immunohistochemical and genetic approaches. In order to determine the epidemiological origin of the inland IPNV infections, the partial viral capsid protein (VP2) gene sequences of the inland IPNV isolates were compared with the sequences of the isolates from the coastal farms. Based on the genetic analysis, the inland isolates belong to IPNV Genogroup 2 (Serotype A3/Ab), and the origin of the isolates appears to be one or several coastal fish farms.
Asunto(s)
Acuicultura , Infecciones por Birnaviridae/veterinaria , Enfermedades de los Peces/virología , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Oncorhynchus mykiss , Animales , Infecciones por Birnaviridae/epidemiología , Infecciones por Birnaviridae/virología , Finlandia/epidemiología , Enfermedades de los Peces/epidemiología , Virus de la Necrosis Pancreática Infecciosa/genética , FilogeniaRESUMEN
Goldfish Carassius auratus are commonly used in scientific research and have a significant economic value in the pet trade. In this study, two cell lines were established from the snout and kidney tissue of goldfish, in order to create a biological monitoring tool for viral diseases. Cell lines were optimally maintained at 25 °C in M199 medium supplemented with 15-20 % fetal bovine serum. Chromosomal analysis indicated that both cell lines remained diploid, with a mean chromosomal count of 100. Results of viral inoculation assays revealed that both cell lines shared similar patterns of viral susceptibility and production to infectious pancreatic necrosis virus (IPNV). The viral titers of IPNV in goldfish snout cell line (GFSe) and goldfish kidney cell line (GFKf) reached 10(6.8) and 10(5.9) TCID50/0.1 mL, respectively, within 7 days. The cytopathic effect could be observed when Cyprinid herpesvirus 2 was inoculated into these cells; however, the CPE disappeared after four passages. No CPE was observed in the cells infected by spring viremia carp virus or grass carp reovirus. These newly established cell lines will be a useful diagnostic tool for viral diseases in this fish species and also for the isolation and study of goldfish viruses in future.
Asunto(s)
Línea Celular/virología , Carpa Dorada , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Riñón/citología , Nariz/citología , Animales , Infecciones por Birnaviridae/veterinaria , Proliferación Celular , Células Cultivadas , Cromosomas , Enfermedades de los PecesRESUMEN
Infectious pancreatic necrosis virus (IPNV) is a prevalent pathogen in fish worldwide. The virus causes substantial mortality in Atlantic salmon juveniles and smolts when transferred to sea water and persistent infection in surviving fish after disease outbreaks. Here, we have investigated the occurrence of the virus as well as the innate immune marker Mx in the head kidney (HK) of Atlantic salmon throughout an experimental challenge covering both a fresh and a seawater phase. The fish were challenged with a high (HV) and low virulence (LV) IPNV. Both isolates caused mortality due to reactivation of the virus after transfer to sea water. In the freshwater phase, higher levels of virus transcripts were detected in the HK of fish infected with LV IPNV compared to HV, suggesting that the HV isolate is able to limit its own replication to a level where the innate immune system is not alerted. Further, ex vivoHK leucocytes derived from fish infected with the two isolates were stimulated with CpG DNA. Significantly, higher IFN levels were found in the LV compared to the HV group in the freshwater phase. This suggests that the viruses attenuate the antiviral host immune response at different levels which may contribute to the observed differences in disease outcome.
Asunto(s)
Infecciones por Birnaviridae/veterinaria , Enfermedades de los Peces/microbiología , Interacciones Huésped-Patógeno/inmunología , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Salmo salar/microbiología , Animales , Infecciones por Birnaviridae/microbiología , Infecciones por Birnaviridae/mortalidad , Enfermedades de los Peces/mortalidad , Datos de Secuencia Molecular , Proteínas de Resistencia a Mixovirus/metabolismoRESUMEN
Infectious pancreatic necrosis virus (IPNV) causes economic losses with a highly variable mortality rate worldwide, especially in rainbow trout. The virus has a double-stranded bi-partite RNA genome designated segment A and B. New complete genome sequences of nine rainbow trout isolates from Turkey were determined and subjected to phylogenetic analysis, identifying all as genotype 5 (serotype Sp). A time-dependent change in the extended pathogenicity motif of VP2 from P217T221A247 (PTA) to PTE P217T221E247 over a period of 10 years was identified. A wider analysis of 99 IPNV sequences from Turkey and Iran revealed the emergence of the motif PTE from 2007 to 2017, inducing significant morbidity in fry by 2013. In fact, displacement of the PTA motif, by the PTE motif in IPNV isolates appeared to be connected to a production peak of rainbow trout in 2013. An additional CAI analysis provided more evidence, indicating that rainbow trout culture in Turkey has an influence on the evolution of IPNV.
Asunto(s)
Infecciones por Birnaviridae , Enfermedades de los Peces , Virus de la Necrosis Pancreática Infecciosa , Oncorhynchus mykiss , Animales , Secuencias de Aminoácidos , Acuicultura , Infecciones por Birnaviridae/veterinaria , Infecciones por Birnaviridae/virología , Evolución Molecular , Enfermedades de los Peces/virología , Genoma Viral , Genotipo , Virus de la Necrosis Pancreática Infecciosa/genética , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Virus de la Necrosis Pancreática Infecciosa/aislamiento & purificación , Virus de la Necrosis Pancreática Infecciosa/clasificación , Oncorhynchus mykiss/virología , Filogenia , Turquía , Proteínas Estructurales Virales/genética , VirulenciaRESUMEN
In order to study the variety of infectious pancreatic necrosis virus (IPNV) strains involved in outbreaks of infectious pancreatic necrosis (IPN) in Atlantic salmon fish farms, samples were collected from 19 different outbreaks of IPN in the northern part of Norway. The main objective of this study was to examine whether IPNV isolates of different virulence were involved in the outbreaks and could explain the variable IPN protection observed in vaccinated post-smolts in the field. Both the molecular basis of virulence of all field isolates and virulence expressed by mortality after bath challenge of unvaccinated post-smolts with eight of the isolates were studied. Very little variation among the field isolates was detected when the 578-bp variable region encoding the VP2 protein known to be involved in virulence was sequenced. The cumulative mortality after experimental challenge with field isolates genetically characterized as highly virulent was always high (40-56%), while the cumulative mortality of the same strains in vaccinated post-smolts during the field outbreaks varied from 1 to 50%. Although the tested samples came from fish vaccinated with the same vaccine product, the protection against IPN varied. These results demonstrate that differences in virulence of the isolates were not the main reason for the variation in mortality in the field outbreaks. Most of the field isolates were of high virulence, which is shown in experimental challenges to be important for mortality, but clearly other factors that might affect the susceptibility of IPN also play an important role in the outcome of an IPNV infection.
Asunto(s)
Infecciones por Birnaviridae/veterinaria , Enfermedades de los Peces/virología , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Secuencia de Aminoácidos , Animales , Infecciones por Birnaviridae/mortalidad , Infecciones por Birnaviridae/virología , Enfermedades de los Peces/mortalidad , Peces , Virus de la Necrosis Pancreática Infecciosa/genética , Virus de la Necrosis Pancreática Infecciosa/aislamiento & purificación , Datos de Secuencia Molecular , Noruega , Alineación de Secuencia , Proteínas Estructurales Virales/genética , Virulencia/genéticaRESUMEN
Infectious pancreatic necrosis virus (IPNV), a pathogen of salmon and trout, imposes a severe toll on the aquaculture and sea farming industries. IPNV belongs to the Aquabirnavirus genus in the Birnaviridae family of bisegmented double-stranded RNA viruses. The virions are nonenveloped with a T=13l icosahedral capsid made by the coat protein VP2, the three-dimensional (3D) organization of which is known in detail for the family prototype, the infectious bursal disease virus (IBDV) of poultry. A salient feature of the birnavirus architecture is the presence of 260 trimeric spikes formed by VP2, projecting radially from the capsid. The spikes carry the principal antigenic sites as well as virulence and cell adaptation determinants. We report here the 3.4-A resolution crystal structure of a subviral particle (SVP) of IPNV, containing 20 VP2 trimers organized with icosahedral symmetry. We show that, as expected, the SVPs have a very similar organization to the IBDV counterparts, with VP2 exhibiting the same overall 3D fold. However, the spikes are significantly different, displaying a more compact organization with tighter packing about the molecular 3-fold axis. Amino acids controlling virulence and cell culture adaptation cluster differently at the top of the spike, i.e., in a central bowl in IBDV and at the periphery in IPNV. In contrast, the spike base features an exposed groove, conserved across birnavirus genera, which contains an integrin-binding motif. Thus, in addition to revealing the viral antigenic determinants, the structure suggests that birnaviruses interact with different receptors for attachment and for cell internalization during entry.
Asunto(s)
Antígenos Virales/química , Virus de la Necrosis Pancreática Infecciosa/química , Virus de la Necrosis Pancreática Infecciosa/inmunología , Secuencia de Aminoácidos , Animales , Variación Antigénica , Antígenos Virales/genética , Cápside/química , Cápside/inmunología , Cristalografía por Rayos X , Virus de la Necrosis Pancreática Infecciosa/genética , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Modelos Moleculares , Datos de Secuencia Molecular , Estructura Cuaternaria de Proteína , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/inmunología , Homología de Secuencia de Aminoácido , Serotipificación , Proteínas Estructurales Virales/química , Proteínas Estructurales Virales/genética , Proteínas Estructurales Virales/inmunología , Virulencia/genética , Virulencia/inmunologíaRESUMEN
BACKGROUND: Infectious pancreatic necrosis virus (IPNV) is an aquatic member of the Birnaviridae family that causes widespread disease in salmonids. IPNV is represented by multiple strains with markedly different virulence. Comparison of isolates reveals hyper variable regions (HVR), which are presumably associated with pathogenicity. However little is known about the rates and modes of sequence divergence and molecular mechanisms that determine virulence. Also how the host response may influence IPNV virulence is poorly described. METHODS: In this study we compared two field isolates of IPNV (NFH-Ar and NFH-El). The sequence changes, replication and mortality were assessed following experimental challenge of Atlantic salmon. Gene expression analyses with qPCR and microarray were applied to examine the immune responses in head kidney. RESULTS: Significant differences in mortality were observed between the two isolates, and viral load in the pancreas at 13 days post infection (d p.i.) was more than 4 orders of magnitude greater for NFH-Ar in comparison with NFH-El. Sequence comparison of five viral genes from the IPNV isolates revealed different mutation rates and Ka/Ks ratios. A strong tendency towards non-synonymous mutations was found in the HRV of VP2 and in VP3. All mutations in VP5 produced precocious stop codons. Prior to the challenge, NFH-Ar and NFH-El possessed high and low virulence motifs in VP2, respectively. Nucleotide substitutions were noticed already during passage of viruses in CHSE-214 cells and their accumulation continued in the challenged fish. The sequence changes were notably directed towards low virulence. Co-ordinated activation of anti-viral genes with diverse functions (IFN-a1 and c, sensors - Rig-I, MDA-5, TLR8 and 9, signal transducers - Srk2, MyD88, effectors - Mx, galectin 9, galectin binding protein, antigen presentation - b2-microglobulin) was observed at 13 d p.i. (NFH-Ar) and 29 d p.i. (both isolates). CONCLUSIONS: Mortality and expression levels of the immune genes were directly related to the rate of viral replication, which was in turn associated with sequences of viral genes. Rapid changes in the viral genome that dramatically reduced virus proliferation might indicate a higher susceptibility to protective mechanism employed by the host. Disease outbreak and mortality depend on a delicate balance between host defence, regulation of signalling cascades and virus genomic properties.
Asunto(s)
Infecciones por Birnaviridae/inmunología , Enfermedades de los Peces/inmunología , Virus de la Necrosis Pancreática Infecciosa/inmunología , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Mutación , Salmo salar/virología , Animales , Infecciones por Birnaviridae/mortalidad , Infecciones por Birnaviridae/patología , Infecciones por Birnaviridae/virología , Enfermedades de los Peces/mortalidad , Enfermedades de los Peces/patología , Enfermedades de los Peces/virología , Perfilación de la Expresión Génica , Virus de la Necrosis Pancreática Infecciosa/genética , Virus de la Necrosis Pancreática Infecciosa/aislamiento & purificación , Riñón/virología , Análisis por Micromatrices , ARN Viral/genética , Reacción en Cadena en Tiempo Real de la Polimerasa , Análisis de Supervivencia , Virulencia , Replicación ViralRESUMEN
The possible importance of the O-linked glycosylation in virion stability and infectivity of infectious pancreatic necrosis virus (IPNV) was analysed. Enzymatic treatment with O-glycosidase of radiolabelled virions under different ionic conditions, to allow for possible alternative exposure of glycosidic enzyme cleavage sites, did not alter the specific infectivity of virions re-isolated after rate-zonal centrifugation in glycerol gradients. As an alternative method to assess the significance of carbohydrates in IPNV integrity, periodate oxidation in the presence of an aldehyde quencher was chosen. Following re-isolation of viruses, a 3-5 (10)log-unit reduction in specific infectivity was revealed and, at higher concentrations, a total disruption or virion aggregation was observed. The loss of infectivity of intact virions was not because of a lack of attachment to cells. Additionally, re-evaluation of reading values from UV-spectra of purified IPNV yielded a specific infectivity of 3 × 10(11) TCID(50)-units mg(-1) of protein and a ratio of 40 virions per TCID(50)-unit in the CHSE-214 cell system.
Asunto(s)
Inestabilidad Genómica/efectos de los fármacos , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Virión/metabolismo , Animales , Células Cultivadas , Colorimetría , Embrión no Mamífero/citología , Glicósido Hidrolasas/farmacología , Glicosilación , Lectinas/metabolismo , Salmón , Espectrofotometría Ultravioleta , Virión/genéticaRESUMEN
In salmon farming, viruses are responsible for outbreaks that produce significant economic losses for which there is a lack of control tools other than vaccines. Type I interferon has been successfully used for treating some chronic viral infections in humans. However, its application in salmonids depends on the proper design of a vehicle that allows its massive administration, ideally orally. In mammals, administration of recombinant probiotics capable of expressing cytokines has shown local and systemic therapeutic effects. In this work, we evaluate the use of Lactococcus lactis as a type I Interferon expression system in Atlantic salmon, and we analyze its ability to stimulate the antiviral immune response against IPNV, in vivo and in vitro. The interferon expressed in L. lactis, even though it was located mainly in the bacterial cytoplasm, was functional, stimulating Mx and PKR expression in CHSE-214 cells, and reducing the IPNV viral load in SHK-1 cells. In vivo, the oral administration of this L. lactis producer of Interferon I increases Mx and PKR expression, mainly in the spleen, and to a lesser extent, in the head kidney. The oral administration of this strain also reduces the IPNV viral load in Atlantic salmon specimens challenged with this pathogen. Our results show that oral administration of L. lactis producing Interferon I induces systemic effects in Atlantic salmon, allowing to stimulate the antiviral immune response. This probiotic could have effects against a wide variety of viruses that infect Atlantic salmon and also be effective in other salmonids due to the high identity among their type I interferons.
Asunto(s)
Infecciones por Birnaviridae/prevención & control , Proteínas de Peces/metabolismo , Inmunidad Innata , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Interferón Tipo I/metabolismo , Lactococcus lactis/metabolismo , Probióticos , Salmo salar/microbiología , Animales , Infecciones por Birnaviridae/inmunología , Infecciones por Birnaviridae/microbiología , Infecciones por Birnaviridae/virología , Línea Celular , Proteínas de Peces/genética , Explotaciones Pesqueras , Interacciones Huésped-Patógeno , Virus de la Necrosis Pancreática Infecciosa/crecimiento & desarrollo , Virus de la Necrosis Pancreática Infecciosa/inmunología , Interferón Tipo I/genética , Lactococcus lactis/genética , Lactococcus lactis/inmunología , Proteínas de Resistencia a Mixovirus/metabolismo , Salmo salar/genética , Salmo salar/inmunología , Salmo salar/virología , Carga Viral , eIF-2 Quinasa/metabolismoRESUMEN
Infectious pancreatic necrosis virus (IPNV) causes economic losses in Mexican rainbow trout industry. In this study, virulence and genetic fingerprints of Mexican IPNV isolates was investigated for the first time. Two Mexican IPNV isolates were analyzed in rainbow trout fry and the Sp strain was included as high virulence. One of the Mexican IPNV isolate was obtained from diseased fish and the other from fish without clinical signs. The infection was performed using a standardized immersion. Clinical signs were observed at 4 days post infection in fry group infected with strain Sp, two days earlier than in trout infected with IPNV isolates Mexican. Severe lesions were found in 100% of the individuals of Sp group, but only in 25% of each isolated Mexican group. Results suggest that Mexican IPNV isolates are pathogenic, but less virulent than strain Sp. The amino acid motif residues of both Mexican isolates, corresponded to a subclinical disease. Nevertheless, the accumulated motility observed in the field, suggest that other factors play a role in the virulence of the disease.
Asunto(s)
Infecciones por Birnaviridae/veterinaria , Enfermedades de los Peces/virología , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Secuencias de Aminoácidos , Animales , Infecciones por Birnaviridae/virología , Virus de la Necrosis Pancreática Infecciosa/genética , Virus de la Necrosis Pancreática Infecciosa/aislamiento & purificación , México , Oncorhynchus mykiss , VirulenciaRESUMEN
Acute pancreatitis is an inflammatory disease of the pancreas. Acute abdominal pain is the most common symptom, and increased concentrations of serum amylase and lipase confirm the diagnosis. Pancreatic injury is mild in 80% of patients, who recover without complications. The remaining patients have a severe disease with local and systemic complications. Gallstone migration into the common bile duct and alcohol abuse are the most frequent causes of pancreatitis in adults. About 15-25% of pancreatitis episodes are of unknown origin. Treatment of mild disease is supportive, but severe episodes need management by a multidisciplinary team including gastroenterologists, interventional radiologists, intensivists, and surgeons. Improved understanding of pathophysiology and better assessments of disease severity should ameliorate the management and outcome of this complex disease.
Asunto(s)
Amilasas/sangre , Infecciones por Birnaviridae/fisiopatología , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Lipasa/sangre , Pancreatitis , Enfermedad Aguda , Antibacterianos/uso terapéutico , Infecciones por Birnaviridae/clasificación , Infecciones por Birnaviridae/metabolismo , Colecistectomía , Cálculos Biliares/complicaciones , Cálculos Biliares/tratamiento farmacológico , Humanos , Incidencia , Pancreatitis/diagnóstico , Pancreatitis/fisiopatología , Pancreatitis/terapia , Índice de Severidad de la EnfermedadRESUMEN
Infectious pancreatic necrosis virus (IPNV) is a major pathogen in the aquaculture industry worldwide. Factors contributing to IPNV pathogenicity are yet poorly understood. Indications of IPNV being able to evade or counteract innate host defense come from its lack of ability to induce strong type I interferon (IFN) responses in cell culture. We show here that addition of salmon rIFN-alpha1 to cells prior to IPNV infection halts the viral protein synthesis and prevents processing of pVP2 into mature VP2. Furthermore, compared to pre-treatment with IFN-alpha1 the antiviral state in cells infected with IPNV prior to IFN-treatment, was antagonized by IPNV, as detected by higher viral titers, faster viral protein synthesis and also by reduced Mx expression. The longer headstart the virus gets, the more prominent is the weakening of IFN signaling. IPNV VP4 and VP5 inhibit IFN-induced expression from the Mx promoter, indicating that these proteins contribute to the antagonistic effect.
Asunto(s)
Infecciones por Birnaviridae/veterinaria , Enfermedades de los Peces/tratamiento farmacológico , Enfermedades de los Peces/virología , Virus de la Necrosis Pancreática Infecciosa/efectos de los fármacos , Interferón-alfa/farmacología , Transducción de Señal , Animales , Antivirales/farmacología , Infecciones por Birnaviridae/tratamiento farmacológico , Infecciones por Birnaviridae/metabolismo , Infecciones por Birnaviridae/virología , Línea Celular , Enfermedades de los Peces/metabolismo , Proteínas de Unión al GTP/biosíntesis , Proteínas de Unión al GTP/genética , Regulación de la Expresión Génica , Interacciones Huésped-Patógeno , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Virus de la Necrosis Pancreática Infecciosa/fisiología , Proteínas de Resistencia a Mixovirus , Salmón , Serina Endopeptidasas/metabolismo , Proteínas no Estructurales Virales/metabolismo , Proteínas Estructurales Virales/metabolismo , Virulencia , Replicación Viral/efectos de los fármacosRESUMEN
Intraperitoneal (IP) injection, cohabitation and immersion routes of infection were used to determine if Atlantic cod, Gadus morhua (L.), of 1 and 3 g are susceptible to infectious pancreatic necrosis (IPN). Mortalities of cod injected IP were significantly higher when challenged with infectious pancreatic necrosis virus (IPNV) than with phosphate buffered saline. This is the first report of Atlantic cod mortalities caused by IPNV. Fish challenged by cohabitation had significantly higher mortalities than the controls, but mortalities of Atlantic cod challenged with IPNV by immersion were not significantly different from controls. Titres of IPNV in the tissues of infected fish were sometimes very high (range 10(2)-10(10) infectious units per gram of tissue) suggesting virus replication and titres of fish that died were generally higher than those of fish which survived. However, the relatively low mortality rates when challenged by cohabitation and immersion (20% and 17%, respectively), compared to the IP injection challenge (100%) suggest that 1 and 3 g cod have low susceptibility to IPN when challenged by more natural routes. These data strongly suggest that the cause of death of experimentally challenged cod was IPNV and further histological evidence for this came from 1 g cod challenged IP with IPNV in which the pancreas showed severe necrosis and heavy immunostaining for IPNV coincidentally with the peak of mortalities.
Asunto(s)
Infecciones por Birnaviridae/veterinaria , Susceptibilidad a Enfermedades/veterinaria , Enfermedades de los Peces/virología , Gadus morhua/virología , Virus de la Necrosis Pancreática Infecciosa/fisiología , Salmo salar/virología , Animales , Infecciones por Birnaviridae/mortalidad , Infecciones por Birnaviridae/patología , Infecciones por Birnaviridae/transmisión , Infecciones por Birnaviridae/virología , Enfermedades de los Peces/mortalidad , Enfermedades de los Peces/patología , Enfermedades de los Peces/transmisión , Inmersión , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Inyecciones IntraperitonealesRESUMEN
This study investigated the genotypes and sub-groups of infectious pancreatic necrosis virus (IPNV) present in farmed and wild salmonid fish in Ireland. An 1100-bp portion of the VP2 region of segment A from each of 55 IPNV isolates collected over 2003-2007 was amplified by reverse-transcription-polymerase chain reaction and the product directly sequenced. The nucleotide sequences of each isolate were aligned and compared with each other and with the corresponding sequences of a number of reference isolates. All the 55 sequenced isolates belonged to genogroup 5 (Sp serotype) and could be divided into two subgroups. Irish subgroup 1 consisted of isolates from farmed salmon originating from an Irish salmon broodstock. Irish subgroup 2 consisted of isolates from imported farmed stock and all reported clinical outbreaks of IPN were associated with isolates from subgroup 2. Isolates from wild fish were identical to some isolates from subgroup 2, and therefore are believed to have originated from infected farms. These results highlight the importance of import risk analysis for diseases not listed under current legislation.
Asunto(s)
Animales Salvajes/virología , Infecciones por Birnaviridae/veterinaria , Enfermedades de los Peces/virología , Explotaciones Pesqueras , Virus de la Necrosis Pancreática Infecciosa/genética , Sustitución de Aminoácidos , Animales , Infecciones por Birnaviridae/epidemiología , Enfermedades de los Peces/epidemiología , Variación Genética , Virus de la Necrosis Pancreática Infecciosa/clasificación , Virus de la Necrosis Pancreática Infecciosa/aislamiento & purificación , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Irlanda/epidemiología , Filogenia , Salmonidae/virología , Proteínas Virales/genéticaRESUMEN
Infectious pancreatic necrosis (IPN) is a viral disease with considerable negative impact on the rainbow trout (Oncorhynchus mykiss) aquaculture industry. The aim of the present work was to detect genomic regions that explain resistance to infectious pancreatic necrosis virus (IPNV) in rainbow trout. A total of 2,278 fish from 58 full-sib families were challenged with IPNV and 768 individuals were genotyped (488 resistant and 280 susceptible), using a 57K SNP panel Axiom, Affymetrix. A genome-wide association study (GWAS) was performed using the phenotypes time to death (TD) and binary survival (BS), along with the genotypes of the challenged fish using a Bayesian model (Bayes C). Heritabilities for resistance to IPNV estimated using genomic information, were 0.53 and 0.82 for TD and BS, respectively. The Bayesian GWAS detected a SNP located on chromosome 5 explaining 19% of the genetic variance for TD. The proximity of Sentrin-specific protease 5 (SENP5) to this SNP makes it a candidate gene for resistance against IPNV. In case of BS, a SNP located on chromosome 23 was detected explaining 9% of the genetic variance. However, the moderate-low proportion of variance explained by the detected marker leads to the conclusion that the incorporation of all genomic information, through genomic selection, would be the most appropriate approach to accelerate genetic progress for the improvement of resistance against IPNV in rainbow trout.
Asunto(s)
Resistencia a la Enfermedad/genética , Enfermedades de los Peces/virología , Proteínas de Peces/genética , Virus de la Necrosis Pancreática Infecciosa/fisiología , Oncorhynchus mykiss/genética , Animales , Teorema de Bayes , Infecciones por Birnaviridae/genética , Infecciones por Birnaviridae/inmunología , Infecciones por Birnaviridae/mortalidad , Infecciones por Birnaviridae/veterinaria , Enfermedades de los Peces/inmunología , Enfermedades de los Peces/mortalidad , Proteínas de Peces/inmunología , Estudio de Asociación del Genoma Completo , Interacciones Huésped-Patógeno/genética , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Oncorhynchus mykiss/inmunología , Oncorhynchus mykiss/virología , Polimorfismo de Nucleótido Simple , Replicación Viral/fisiologíaRESUMEN
In this study, we investigated changes in protein expression of fish cells induced by infection of infectious pancreatic necrosis virus (IPNV) using two-dimensional electrophoresis and matrix-assisted laser desorption-time of flight proton motive force analysis and identified a novel type of salmon annexin 1 that is induced in fish cells by infection with IPNV. Northern blotting showed that this annexin is overexpressed in IPNV-infected cells compared to control cells, and further analysis revealed that it has a 1,509-bp full-length cDNA sequence with an open reading frame encoding 339 amino acids (GenBank accession no. AY944135). Amino acid sequence analysis revealed that this protein belongs to the annexin 1 subfamily. By applying RNA interference, the mRNA levels of salmon annexin 1 were suppressed and, under these conditions, apoptosis of IPNV-infected cells was significantly increased. While small interfering RNA (siRNA) treatment did not affect the levels of the viral proteins significantly until 10 h postinfection, it reduced the titer of extracellular virus to 25% of that of a scrambled siRNA-treated control. These data provide evidence of an antiapoptotic function for salmon annexin 1 that is important for IPNV growth in cultured cells.
Asunto(s)
Anexinas , Regulación de la Expresión Génica , Virus de la Necrosis Pancreática Infecciosa/patogenicidad , Salmón/virología , Secuencia de Aminoácidos , Animales , Anexinas/química , Anexinas/genética , Anexinas/metabolismo , Anexinas/farmacología , Apoptosis/efectos de los fármacos , Células Cultivadas , Electroforesis en Gel Bidimensional , Datos de Secuencia Molecular , Filogenia , ARN Mensajero/genética , ARN Mensajero/metabolismo , ARN Interferente Pequeño/genética , ARN Interferente Pequeño/metabolismo , Análisis de Secuencia de ADN , Espectrometría de Masa por Láser de Matriz Asistida de Ionización DesorciónRESUMEN
Reassortment is one of the main mechanisms of evolution in dsRNA viruses with segmented genomes. It contributes to generate genetic diversity and plays an important role in the emergence and spread of new strains with altered virulence. Natural reassorment has been demonstrated among infectious pancreatic necrosis-like viruses (genus Aquabirnavirus, Birnaviridae). In the present study, coinfections between different viral strains, and genome sequencing by the Sanger and Illumina methods were applied to analyze the frequency of reassortment of this virus in vitro, the possible mechanisms involved, and its effect on virulence. Results have demonstrated that reassortment is a cell-dependent and non-random process, probably through differential expression of the different mRNA classes in the ribosomes of a specific cell, and by specific associations between the components to construct the ribonucleoprotein (RNP) complexes and/or RNP cross-inhibition. However, the precise mechanisms involved, known in other viruses, still remain to be demonstrated in birnaviruses.