RESUMO
Piscine orthoreovirus (PRV) mediated diseases have emerged throughout salmonid aquaculture. Three PRV subtypes are currently reported as causative agents of or in association with diseases in different salmonid species. PRV-1 causes heart and skeletal muscle inflammation (HSMI) in Atlantic salmon (Salmo salar) and is associated with jaundice syndrome in farmed chinook salmon (Oncorhynchus tshawytscha). PRV-2 causes erythrocytic inclusion body syndrome (EIBS) in coho salmon in Japan. PRV-3 has recently been associated with a disease in rainbow trout (Oncorhynchus mykiss) characterized by anaemia, heart and red muscle pathology; to jaundice syndrome in coho salmon (Oncorhynchus kisutch). In this study, we conducted a 10-week long experimental infection trial in rainbow trout with purified PRV-3 particles to assess the causal relationship between the virus and development of heart inflammation. The monitoring the PRV-3 load in heart and spleen by RT-qPCR shows a progressive increase of viral RNA to a peak, followed by clearance without a measurable change in haematocrit. The development of characteristic cardiac histopathological findings occurred in the late phase of the trial and was associated with increased expression of CD8+, indicating cytotoxic T cell proliferation. The findings indicate that, under these experimental conditions, PRV-3 infection in rainbow trout act similarly to PRV-1 infection in Atlantic salmon with regards to immunological responses and development of heart pathology, but not in the ability to establish a persistent infection.
Assuntos
Doenças dos Peixes/imunologia , Cardiopatias/veterinária , Inflamação/veterinária , Oncorhynchus mykiss , Orthoreovirus/fisiologia , Infecções por Reoviridae/veterinária , Animais , Doenças dos Peixes/virologia , Cardiopatias/imunologia , Cardiopatias/virologia , Imunidade Inata , Inflamação/imunologia , Inflamação/virologia , Infecções por Reoviridae/imunologia , Infecções por Reoviridae/virologiaRESUMO
Infectious hematopoietic necrosis virus (IHNV) is endemic in farmed rainbow trout in continental Europe and in various salmonid fish species at the Pacific coast of North America. IHN has never occurred in European Atlantic salmon (Salmo salar) farms, but is considered as a major threat for the European salmon industry. Another virus, Piscine orthoreovirus (PRV), is widespread in the sea phase of Atlantic salmon, and is identified as the causative agent of heart and skeletal muscle inflammation. The aim of this study was to investigate the interactions between a primary PRV infection and a secondary IHNV infection under experimental conditions. A PRV cohabitation challenge was performed with Atlantic salmon. At peak of PRV viremia the fish were challenged by immersion with an IHNV genogroup E isolate. Clinical signs and morbidity were monitored. Target organs were sampled at selected time points to assess viral loads of both pathogens. Antiviral immune response and presence of histopathological findings were also investigated. Whereas the PRV-negative/IHNV positive group suffered significant decrease in survival caused by IHNV, the PRV infected groups did not suffer any morbidity and showed negligible levels of IHNV infection. Antiviral response genes were induced, as measured in spleen samples, from PRV infected fish prior to IHNV challenge. In conclusion, PRV-infection protects Atlantic salmon against IHNV infection and morbidity, most likely by inducing a protective innate antiviral response.
Assuntos
Doenças dos Peixes/imunologia , Vírus da Necrose Hematopoética Infecciosa/fisiologia , Infecções por Reoviridae/veterinária , Infecções por Rhabdoviridae/veterinária , Salmo salar , Animais , Doenças dos Peixes/virologia , Genótipo , Vírus da Necrose Hematopoética Infecciosa/genética , Orthoreovirus/fisiologia , Infecções por Reoviridae/imunologia , Infecções por Reoviridae/virologia , Infecções por Rhabdoviridae/imunologia , Infecções por Rhabdoviridae/virologiaRESUMO
Heart and skeletal muscle inflammation (HSMI) and pancreas disease (PD) cause substantial losses in Atlantic salmon (Salmo salar) aquaculture. The respective causative agents, Piscine orthoreovirus (PRV) and Salmonid alphavirus (SAV), are widespread and often concurrently present in farmed salmon. An experimental infection in Atlantic salmon was conducted to study the interaction between the two viruses, including the immunological mechanisms involved. The co-infected fish were infected with PRV four or ten weeks before they were infected with SAV. The SAV RNA level and the PD specific lesions were significantly lower in co-infected groups compared to the group infected by only SAV. The expression profiles of a panel of innate antiviral response genes and the plasma SAV neutralization titers were examined. The innate antiviral response genes were in general upregulated for at least ten weeks after the primary PRV infection. Plasma from co-infected fish had lower SAV neutralizing titers compared to the controls infected with only SAV. Plasma from some individuals infected with only PRV neutralized SAV, but heat treatment removed this effect. Field studies of co-infected fish populations indicated a negative correlation between the two viruses in randomly sampled apparently healthy fish, in line with the experimental findings, but a positive correlation in moribund or dead fish. The results indicate that the innate antiviral response induced by PRV may temporary protect against a secondary SAV infection.
Assuntos
Infecções por Alphavirus/veterinária , Proteção Cruzada , Doenças dos Peixes/imunologia , Imunidade Inata , Infecções por Reoviridae/veterinária , Salmo salar , Alphavirus/fisiologia , Infecções por Alphavirus/imunologia , Infecções por Alphavirus/virologia , Animais , Doenças dos Peixes/virologia , Proteínas de Peixes/genética , Proteínas de Peixes/metabolismo , Orthoreovirus/fisiologia , Infecções por Reoviridae/imunologia , Infecções por Reoviridae/virologiaRESUMO
Piscine orthoreovirus (PRV) is associated with heart- and skeletal muscle inflammation in farmed Atlantic salmon. The virus is ubiquitous and found in both farmed and wild salmonid fish. It belongs to the family Reoviridae, closely related to the genus Orthoreovirus. The PRV genome comprises ten double-stranded RNA segments encoding at least eight structural and two non-structural proteins. Erythrocytes are the major target cells for PRV. Infected erythrocytes contain globular inclusions resembling viral factories; the putative site of viral replication. For the mammalian reovirus (MRV), the non-structural protein µNS is the primary organizer in factory formation. The analogous PRV protein was the focus of the present study. The subcellular location of PRV µNS and its co-localization with the PRV σNS, µ2 and λ1 proteins was investigated. We demonstrated that PRV µNS forms dense globular cytoplasmic inclusions in transfected fish cells, resembling the viral factories of MRV. In co-transfection experiments with µNS, the σNS, µ2 and λ1 proteins were recruited to the globular structures. The ability of µNS to recruit other PRV proteins into globular inclusions indicates that it is the main viral protein involved in viral factory formation and pivotal in early steps of viral assembly.
Assuntos
Regulação Viral da Expressão Gênica/fisiologia , Orthoreovirus/metabolismo , Proteínas não Estruturais Virais/metabolismo , Replicação Viral/fisiologia , Sequência de Aminoácidos , Animais , Linhagem Celular , Peixes , Dados de Sequência Molecular , Orthoreovirus/genética , Proteínas não Estruturais Virais/genéticaRESUMO
Viral diseases are among the main challenges in farming of Atlantic salmon (Salmo salar). The most prevalent viral diseases in Norwegian salmon aquaculture are heart and skeletal muscle inflammation (HSMI) caused by Piscine orthoreovirus (PRV), and pancreas disease (PD) caused by Salmonid alphavirus (SAV). Both PRV and SAV target heart and skeletal muscles, but SAV additionally targets exocrine pancreas. PRV and SAV are often present in the same locations and co-infections occur, but the effect of this crosstalk on disease development has not been investigated. In the present experiment, the effect of a primary PRV infection on subsequent SAV infection was studied. Atlantic salmon were infected with PRV by cohabitation, followed by addition of SAV shedder fish 4 or 10 weeks after the initial PRV infection. Histopathological evaluation, monitoring of viral RNA levels and host gene expression analysis were used to assess disease development. Significant reduction of SAV RNA levels and of PD specific histopathological changes were observed in the co-infected groups compared to fish infected by SAV only. A strong correlation was found between histopathological development and expression of disease related genes in heart. In conclusion, experimentally PRV infected salmon are less susceptible to secondary SAV infection and development of PD.
Assuntos
Doenças dos Peixes/virologia , Orthoreovirus , Pancreatopatias/veterinária , Infecções por Reoviridae/veterinária , Salmo salar/virologia , Alphavirus , Infecções por Alphavirus/complicações , Infecções por Alphavirus/patologia , Infecções por Alphavirus/veterinária , Infecções por Alphavirus/virologia , Animais , Doenças dos Peixes/patologia , Pancreatopatias/etiologia , Pancreatopatias/patologia , Pancreatopatias/virologia , Infecções por Reoviridae/patologia , Reação em Cadeia da Polimerase Via Transcriptase Reversa/veterináriaRESUMO
Piscine orthoreovirus (PRV) is a reovirus that has predominantly been detected in Atlantic salmon (Salmo salar L.). PRV is associated with heart and skeletal muscle inflammation (HSMI) in farmed Atlantic salmon, and recently erythrocytes were identified as major target cells. The study of PRV replication and pathogenesis of the infection has been impeded by the inability to propagate PRV in vitro. In this study we developed an ex vivo cultivation system for PRV in Atlantic salmon erythrocytes. PRV was successfully passaged to naïve erythrocytes using lysates of blood cells from infected salmon. During cultivation a significant increase in viral load was observed by RT-qPCR and flow cytometry, which coincided with the formation of cytoplasmic inclusions. The inclusions resembled viral factories and contained both PRV protein and dsRNA. In addition, the erythrocytes generated an antiviral immune gene activation after PRV infection, with significant up-regulation of IFN-α, RIG-I, Mx and PKR transcripts. Supernatants from the first passage successfully transmitted virus to naïve erythrocytes. This study demonstrates that PRV replicates in Atlantic salmon erythrocytes ex vivo. The ex vivo infection model closely reflects the situation in vivo and can be used to study the infection and replication mechanisms of PRV, as well as the antiviral immune responses of salmonid erythrocytes.
Assuntos
Doenças dos Peixes/virologia , Proteínas de Peixes/genética , Orthoreovirus/fisiologia , Infecções por Reoviridae/veterinária , Salmo salar , Regulação para Cima , Animais , Eritrócitos/virologia , Doenças dos Peixes/genética , Proteínas de Peixes/metabolismo , Infecções por Reoviridae/genética , Infecções por Reoviridae/virologia , Carga Viral/veterináriaRESUMO
Heart and skeletal muscle inflammation (HSMI) is a widespread disease of farmed Atlantic salmon (Salmo salar L.) and is associated with piscine orthoreovirus (PRV) infection. PRV is detectable in blood long before development of pathology in cardiac- and skeletal muscle appear, and erythrocytes have been identified as important target cells for the virus. The effects of PRV infection on cellular processes of erythrocytes are not known, but haemolytic anemia or systemic lysis of erythrocytes does not seem to occur, even with high virus loads in erythrocytes. In this study, gene expression profiling performed with high-density oligonucleotide microarray showed that PRV infection of erythrocytes induced a large panel of virus responsive genes. These involved interferon-regulated antiviral genes, as well as genes involved in antigen presentation via MHC class I. PRV infection also stimulated negative immune regulators. In contrast, a large number of immune genes expressed prior to infection were down-regulated. Moderate reduction of expression was also found for many genes encoding components of cytoskeleton and myofiber, proteins involved in metabolism, ion exchange, cell-cell interactions as well as growth factors and regulators of differentiation. PRV did not affect expression of genes involved in heme biosynthesis, gas exchange or erythrocyte-specific markers, but some regulators of erythropoiesis showed decreased transcription levels. These results indicate that PRV infection activates innate antiviral immunity in salmon erythrocytes, but suppresses other gene expression programs. Gene expression profiles suggest major phenotypic changes in PRV infected erythrocytes, but the functional consequences remain to be explored.
Assuntos
Eritrócitos/metabolismo , Doenças dos Peixes/imunologia , Regulação da Expressão Gênica , Orthoreovirus/fisiologia , Infecções por Reoviridae/veterinária , Salmo salar , Transcriptoma , Animais , Eritrócitos/virologia , Doenças dos Peixes/genética , Doenças dos Peixes/virologia , Perfilação da Expressão Gênica/veterinária , Análise de Sequência com Séries de Oligonucleotídeos/veterinária , Fenótipo , Reação em Cadeia da Polimerase/veterinária , Infecções por Reoviridae/genética , Infecções por Reoviridae/imunologia , Infecções por Reoviridae/virologiaRESUMO
Piscine orthoreovirus (PRV) belongs to the Reoviridae family and is the only known fish virus related to the Orthoreovirus genus. The virus is the causative agent of heart and skeletal muscle inflammation (HSMI), an emerging disease in farmed Atlantic salmon (Salmo salar L.). PRV is ubiquitous in farmed Atlantic salmon and high loads of PRV in the heart are consistent findings in HSMI. The mechanism by which PRV infection causes disease remains largely unknown. In this study we investigated the presence of PRV in blood and erythrocytes using an experimental cohabitation challenge model. We found that in the early phases of infection, the PRV loads in blood were significantly higher than in any other organ. Most virus was found in the erythrocyte fraction, and in individual fish more than 50% of erythrocytes were PRV-positive, as determined by flow cytometry. PRV was condensed into large cytoplasmic inclusions resembling viral factories, as demonstrated by immunofluorescence and confocal microscopy. By electron microscopy we showed that these inclusions contained reovirus-like particles. The PRV particles and inclusions also had a striking resemblance to previously reported viral inclusions described as Erythrocytic inclusion body syndrome (EIBS). We conclude that the erythrocyte is a major target cell for PRV infection. These findings provide new information about HSMI pathogenesis, and show that PRV is an important factor of viral erythrocytic inclusions.
Assuntos
Eritrócitos/virologia , Doenças dos Peixes/virologia , Orthoreovirus/fisiologia , Infecções por Reoviridae/veterinária , Salmo salar , Animais , Antígenos Virais/análise , Proteínas do Capsídeo/genética , Proteínas do Capsídeo/metabolismo , Microscopia Confocal/veterinária , Microscopia Eletrônica de Transmissão/veterinária , Microscopia de Fluorescência/veterinária , Noruega , RNA Viral/genética , RNA Viral/metabolismo , Infecções por Reoviridae/virologia , Carga Viral/veterinária , Viremia/veterinária , Viremia/virologiaRESUMO
Cyclic AMP (cAMP) is an important physiological growth inhibitor of lymphoid cells, and the cAMP/protein kinase A (PKA) pathway is disrupted in several immunological disorders and cancers. Epstein Barr virus (EBV) infection of B lymphocytes is responsible for the development of lymphoproliferative disease as well as certain B-lymphoid malignancies. Here we hypothesized that EBV infection might render B lymphocytes resistant to cAMP/PKA-mediated growth inhibition. To test this, we assessed the growth-inhibitory response of cAMP-elevating compounds such as forskolin and isoproterenol, as well as the PKA activator 8-CPT-cAMP in normal B lymphocytes, EBV-infected B cells and in the EBV-negative B lymphoid cell line Reh. We could demonstrate that EBV infection indeed abolished cAMP-mediated growth inhibition of B cells. The defect was pinpointed to defective adenylyl cyclase (AC) activation by forskolin and isoproterenol, resulting in reduced formation of cAMP and lack of PKA activation and CREB phosphorylation. In contrast, 8-CPT-cAMP which directly activates PKA was able to inhibit EBV-infected B cell growth. The physiological implications of these results were underlined by the observation that the ability of forskolin to inhibit camptothecin-induced apoptosis was abolished in EBV-infected B cells. We conclude that EBV infection of B cells abrogates the activation of AC and thereby cAMP formation, and that this dysfunction renders the cells resistant to growth inhibition via the cAMP/PKA pathway.
Assuntos
Adenilil Ciclases/metabolismo , Linfócitos B/virologia , Herpesvirus Humano 4/fisiologia , Apoptose/efeitos dos fármacos , Linfócitos B/efeitos dos fármacos , Linfócitos B/enzimologia , Camptotecina/toxicidade , Linhagem Celular , Proliferação de Células/efeitos dos fármacos , Células Cultivadas , Colforsina/antagonistas & inibidores , AMP Cíclico/antagonistas & inibidores , Proteínas Quinases Dependentes de AMP Cíclico/antagonistas & inibidores , Proteínas Quinases Dependentes de AMP Cíclico/metabolismo , Humanos , Isoproterenol/farmacologia , Transdução de SinaisRESUMO
A new disease in farmed rainbow trout (Onchorhyncus mykiss) was described in Norway in 2013. The disease mainly affected the heart and resembled heart and skeletal muscle inflammation (HSMI) in Atlantic salmon (Salmo salar L.). HSMI is associated with Piscine orthoreovirus (PRV), and a search for a similar virus in the diseased rainbow trout led to detection of a sequence with 85% similarity to PRV. This finding called for a targeted effort to assess the risk the new PRV-variant pose on farmed rainbow trout and Atlantic salmon by studying infection and disease pathogenesis, aiming to provide more diagnostic knowledge. Based on the genetic relationship to PRV, the novel virus is referred to as PRV-Oncorhynchus mykiss (PRV-Om) in contrast to PRV-Salmo salar (PRV-Ss). In experimental trials, intraperitoneally injected PRV-Om was shown to replicate in blood in both salmonid species, but more effectively in rainbow trout. In rainbow trout, the virus levels peaked in blood and heart of cohabitants 6 weeks post challenge, along with increased expression of antiviral genes (Mx and viperin) in the spleen, with 80-100% of the cohabitants infected. Heart inflammation was diagnosed in all cohabitants examined 8 weeks post challenge. In contrast, less than 50% of the Atlantic salmon cohabitants were infected between 8 and 16 weeks post challenge and the antiviral response in these fish was very low. From 12 weeks post challenge and onwards, mild focal myocarditis was demonstrated in a few virus-positive salmon. In conclusion, PRV-Om infects both salmonid species, but faster transmission, more notable antiviral response and more prominent heart pathology were observed in rainbow trout.
Assuntos
Doenças dos Peixes/virologia , Oncorhynchus mykiss/virologia , Orthoreovirus/fisiologia , Infecções por Reoviridae/virologia , Salmo salar/virologia , Animais , Dinamarca , Doenças dos Peixes/diagnóstico , Doenças dos Peixes/transmissão , Proteínas de Peixes/sangue , Proteínas de Peixes/genética , Expressão Gênica , Coração/virologia , Hemoglobinas/análise , Interações Hospedeiro-Patógeno , Músculo Esquelético/virologia , Noruega , Oncorhynchus mykiss/sangue , Oncorhynchus mykiss/genética , Orthoreovirus/genética , Orthoreovirus/patogenicidade , RNA Viral/genética , Infecções por Reoviridae/diagnóstico , Infecções por Reoviridae/transmissão , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Salmo salar/sangue , Salmo salar/genética , VirulênciaRESUMO
Piscine orthoreovirus (PRV) is ubiquitous in farmed Atlantic salmon (Salmo salar) and the cause of heart and skeletal muscle inflammation. Erythrocytes are important target cells for PRV. We have investigated the kinetics of PRV infection in salmon blood cells. The findings indicate that PRV causes an acute infection of blood cells lasting 1-2 weeks, before it subsides into persistence. A high production of viral proteins occurred initially in the acute phase which significantly correlated with antiviral gene transcription. Globular viral factories organized by the non-structural protein µNS were also observed initially, but were not evident at later stages. Interactions between µNS and the PRV structural proteins λ1, µ1, σ1 and σ3 were demonstrated. Different size variants of µNS and the outer capsid protein µ1 appeared at specific time points during infection. Maximal viral protein load was observed five weeks post cohabitant challenge and was undetectable from seven weeks post challenge. In contrast, viral RNA at a high level could be detected throughout the eight-week trial. A proteolytic cleavage fragment of the µ1 protein was the only viral protein detectable after seven weeks post challenge, indicating that this µ1 fragment may be involved in the mechanisms of persistent infection.
Assuntos
Eritrócitos/virologia , Doenças dos Peixes/virologia , Orthoreovirus , Infecções por Reoviridae/veterinária , Salmo salar/virologia , Proteínas Virais/metabolismo , Animais , Eritrócitos/ultraestrutura , Doenças dos Peixes/sangue , Expressão Gênica , Genes Virais , Doenças Musculares/sangue , Doenças Musculares/veterinária , Doenças Musculares/virologia , Orthoreovirus/genética , Orthoreovirus/ultraestrutura , Proteólise , RNA Viral/metabolismo , Infecções por Reoviridae/sangue , Infecções por Reoviridae/virologia , Salmo salar/sangue , Carga Viral/veterináriaRESUMO
Heart and skeletal muscle inflammation (HSMI) are a disease of farmed Atlantic salmon (Salmo salar) associated with Piscine orthoreovirus (PRV). The disease appears mainly during the marine production phase. This study examined if smoltification and transfer to seawater could compromise immune responses to PRV. Parr and smolts of the same origin were challenged by cohabitation with intraperitoneally injected salmon. Peak levels of PRV in spleen of cohabitants were reached after 8 weeks, but at a lower level in parr compared to smolts. Thereafter the virus levels declined, but remained significantly lower in parr than in smolts. Both groups developed typical HSMI histopathological heart lesions, which were most prominent after 10 weeks. Microarray and qPCR analyses revealed slightly lower expression of immune genes in spleen and head kidney of smolts before challenge. Infected parr showed earlier induction of genes involved in innate antiviral immunity, as well as for genes related to B and T cell responses. Gene expression profiles also indicated stimulation of heme and iron metabolism and erythropoiesis in smolts, which may indicate replacement of PRV-infected erythrocytes.
Assuntos
Doenças dos Peixes/imunologia , Expressão Gênica/imunologia , Infecções por Reoviridae/veterinária , Salmo salar/imunologia , Salmo salar/virologia , Animais , Aquicultura/métodos , Doenças dos Peixes/virologia , Análise de Sequência com Séries de Oligonucleotídeos , Orthoreovirus , Reação em Cadeia da PolimeraseRESUMO
Piscine orthoreovirus (PRV) has a double-stranded, segmented RNA genome and belongs to the family Reoviridae. PRV is associated with heart and skeletal muscle inflammation (HSMI) in farmed Atlantic salmon (Salmo salar L.) and cause intraerythrocytic inclusions. The virus is widespread in both wild and farmed salmonid fish in Europe, North- and South America. In mammalian orthoreovirus (MRV), the outer capsid protein Æ¡3 has dsRNA binding properties, which serve to inhibit the early innate immune response of the host. Important structural motifs and key amino acid residues are conserved between MRV Æ¡3 and the homologous PRV protein, and we hypothesized that PRV Æ¡3 binds dsRNA. Gene regions and amino acid residues predicted to be important for dsRNA binding were determined through bioinformatic analysis and investigated functionally following site-directed mutagenesis and the generation of truncated Æ¡3 variants. Our results provide evidence that the PRV protein Æ¡3 binds dsRNA in a sequence independent manner, thus sharing this function with MRV Æ¡3. Although no specific domain solely responsible for dsRNA binding was determined, the results point to residues within a predominantly basic region to be important for this functional property. We conclude that multiple sites are involved in the dsRNA binding activity of PRV Æ¡3.
Assuntos
Proteínas do Capsídeo/metabolismo , Orthoreovirus/fisiologia , RNA de Cadeia Dupla/metabolismo , Proteínas de Ligação a RNA/metabolismo , Animais , Proteínas do Capsídeo/genética , Linhagem Celular , Biologia Computacional , Análise Mutacional de DNA , Peixes , Mutagênese Sítio-Dirigida , Orthoreovirus/genética , Ligação Proteica , Proteínas de Ligação a RNA/genéticaRESUMO
BACKGROUND: Cyclic AMP-dependent protein kinase (PKA) plays a central role in regulation of energy metabolism. Upon stimulation of testicular Sertoli cells by follicle stimulating hormone (FSH), glycolysis is activated to increase the production of nutrients for the germ cells, and a new regulatory subunit of cAMP-dependent protein kinase, RIIbeta, is induced. We have previously shown that production of the transcription factor C/EBPbeta is rapidly increased by FSH and cAMP in primary Sertoli cell cultures, and that C/EBPbeta induces the RIIbeta promoter. RESULTS: In this work we show that USF1, USF2 and truncated USF isoforms bind to a conserved E-box in the RIIbeta gene. Interestingly, overexpression of USF2, but not USF1, led to inhibition of both cAMP- and C/EBPbeta-mediated induction of RIIbeta. Furthermore, Western blots show that a novel USF1 isoform is induced by cAMP in Sertoli cells. CONCLUSIONS: These results indicate that the expression of various USF isoforms may be regulated by cAMP, and that the interplay between USF and C/EBPbeta is important for cAMP-mediated regulation of RIIbeta expression. The counteracting effects of USF2 and C/EBPbeta observed on the RIIbeta promoter is in accordance with the hypothesis that C/EBP and USF play opposite roles in regulation of glucose metabolism.
RESUMO
We have examined protein kinase A (PKA) subunit expression in adult rat skeletal muscles. Northern blots identified PKA catalytic alpha and regulatory (R) I alpha and RII alpha subunits as the major subunits expressed in slowly contracting soleus (SOL) and rapidly contracting extensor digitorum longus (EDL) muscles. In addition, the steady-state RNA levels of PKA subunit mRNAs and activities of RI alpha and RII alpha promoters are similar in SOL and EDL. These data indicate that posttranscriptional mechanisms account for the twofold differences in PKA subunit protein levels reported earlier. Electrical stimulation of denervated SOL with an EDL-like activity pattern (fast pattern) transformed SOL into an EDL-like muscle with regard to PKA protein levels. These experiments suggest that the posttranscriptional regulation is activity pattern-dependent. Denervation specifically increased RI alpha promoter activity and RI alpha mRNA levels in SOL and EDL. Further experiments indicated that the RI alpha 1a upstream sequences were activated following denervation. Direct electrical stimulation prevented the rise in RI alpha mRNA levels following denervation, demonstrating that electrical muscle activity regulates transcription.