Limited Interference at the Early Stage of Infection between Two Recombinant Novirhabdoviruses: Viral Hemorrhagic Septicemia Virus and Infectious Hematopoietic Necrosis Virus

The genome sequence of a hypervirulent novirhabdovirus, viral hemorrhagic septicemia virus (VHSV) French strain 23-75, was determined. Compared to the genome of the prototype Fil3 strain, a number of substitutions, deletions, and insertions were observed. Following the establishment of a plasmid-based minigenome replication assay, recombinant VHSV (rVHSV) was successfully recovered. rVHSV exhibits wild-type-like growth properties in vitro as well as in vivo in rainbow trout. The dispensable role of NV for the novirhabdovirus replication was confirmed by generating rVHSV-ΔNV, in which the NV gene was deleted. This deletion mutant was shown to be as debilitated as that previously described for infectious hematopoietic necrosis virus (IHNV), a distantly related novirhabdovirus (S. Biacchesi, M. I. Thoulouze, M. Bearzotti, Y. X. Yu, and M. Bremont, J. Virol. 74:11247-11253, 2000). Recombinant VHSV and IHNV expressing tdTomato and GFP_max reporter genes, respectively, were generated, demonstrating the potential of these rhabdoviruses to serve as viral vectors. Interestingly, rIHNV-GFP_max could be recovered using the replicative complex proteins of either virus, whereas rVHSV-Tomato could be recovered only by using its own replicative complex, reflecting that the genome signal sequences of VHSV are relatively distant from those of IHNV and do not allow their cross-recognition. Moreover, the use of heterologous protein combinations underlined the importance of strong protein-protein interactions for the formation of a functional ribonucleoprotein complex. The rIHNV-GFP_max and rVHSV-Tomato viruses were used to simultaneously coinfect cell monolayers. It was observed that up to 74% of the cell monolayer was coinfected by both viruses, demonstrating that a limited interference phenomenon exists during the early stage of primary infection, and it was not mediated by a cellular antiviral protein or by some of the viral proteins.Viral hemorrhagic septicemia virus (VHSV) is a member of the Novirhabdovirus genus in the Rhabdoviridae family. VHSV is considered by many countries and international organizations to be one of the most important viral pathogens of finfish (38). During recent years, VHSV has been isolated from at least 50 different species from marine and freshwater fish and is present throughout the northern hemisphere (45). The transmission of the virus from fish to fish occurs directly through the water or by contact between infected and healthy individuals. VHSV is thought to enter the body through the gills or possibly through wounds on the skin. However, we recently showed that fins may represent the main portal of entry for the novirhabdoviruses (25). The virus usually causes severe hemorrhages in the skin, muscles, eyes, kidney, and liver, with mortality rates as high as 90%. As for all members of the Rhabdoviridae family, the VHSV genome consists of a negative-sense single-stranded RNA molecule of about 11 kb encoding five structural proteins: N, the nucleoprotein; P, a polymerase-associated protein; M, the matrix protein; G, the unique viral surface glycoprotein; and L, the large RNA-dependent RNA polymerase. In addition, like the other members of the Novirhabdovirus genus, such as infectious hematopoietic necrosis virus (IHNV), the VHSV genome encodes a small nonstructural NV protein, which has been shown to be dispensable for IHNV replication in cell culture and is involved in virus-induced pathogenicity in rainbow trout (8, 50).The sequence analysis of the glycoprotein (G) and nucleoprotein (N) genes of VHSV has shown that VHSV isolates can be divided into four genotypes that generally correlate with geographic location rather than the host species (4, 19, 47, 49). Isolates belonging to VHSV genotypes I, II, and III are present in continental Europe, the north Atlantic Ocean, the Baltic Sea, the North Sea, and waters around Scotland. Genotype IV consists of isolates from the marine environment in North America. Recently, viral hemorrhagic septicemia has become an emerging disease of freshwater fish in the Great Lakes region of North America (2, 54). Thus, it is quite obvious that VHSV is becoming a worldwide and very-broad-host-range fish virus and that the development of efficient vaccines is needed. Reverse genetics, allowing the introduction of targeted modifications into the viral genome and the production of attenuated live vaccine, may help to fight this rapidly spreading and emerging virus. It is routinely observed in farm trouts exposed to viral diseases that VHSV and IHNV coexist (26). By developing experimental coinfections by VHSV and IHNV in rainbow trout, Brudeseth et al. studied the pathogenesis and virus distribution (10). They found that both viruses established an infection and raised similar virus titers in kidneys, but the distribution of IHNV was more restricted in internal organs during the acute stage of the infection and was not detected in the brain. However, it generally is admitted that infection by one virus renders host cells resistant to a superinfecting virus.Superinfection exclusion, also known as homologous interference, is the phenomenon in which a cell infected with one type of virus or transfected with a viral replicon becomes resistant to a secondary infection with the same virus, whereas infection with unrelated viruses normally is unaffected (40, 51). Superinfection exclusion has been observed in a broad range of viruses, including vaccinia virus (14, 18), human immunodeficiency virus (HIV) (36, 37), vesicular stomatitis virus (VSV) (32, 43, 53), Borna disease virus (BDV) (24), measles virus (34), Sindbis virus (28), Semliki Forest virus (44), rubella virus (15), hepatitis C virus (HCV) (40, 51), and bovine viral diarrhea virus (BVDV) (31). Mechanisms of exclusion are diverse and have not been determined in all cases, but mechanisms described so far are caused by competition among different viruses for critical replicative pathways (for example, the use of the same receptors for the entry) or depend on the direct interaction of products of the primary infection with the secondary infecting virus. For example, the superinfection exclusion of VSV was found to be caused by a combination of three distinct effects on endocytosis by VSV-infected cells: (i) a decreased rate of the formation of endocytic vesicles, (ii) a decreased rate of the internalization of receptor-bound ligands, and (iii) a competition with newly synthesized virus for the occupancy of coated pits (43). In contrast, the cytoplasmic accumulation of BDV nucleocapsid components appeared to prevent subsequent infection through a blockage of the polymerase activity of incoming viruses (24). Superinfection exclusion by BVDV was the result of dual mechanisms that were mediated by the structural protein E2, which blocks the entry of a homologous second virus, and by a blockage at the level of replication dependent on the level of primary viral RNA replication but not influenced by the expression of viral structural proteins, as observed for BDV (31). HIV employs its early gene product Nef to efficiently interfere with superinfection at the virus entry step by downregulating cell surface receptors (36). Finally, vaccinia virus expresses in newly infected cells two surface proteins that mark cells as infected and induce the repulsion of superinfecting viruses (18).In the present study, we described a reverse-genetics system for VHSV allowing the generation of a wild-type-like recombinant VHSV and a recombinant virus expressing a red fluorescent protein (Tomato). The system is based on the French strain 23/75 of VHSV, which is a hypervirulent and devastating strain for farmed rainbow trout belonging to genotype I (serotype III) and was isolated in France in 1975 from a brown trout (16, 23). Thus, this system provides a suitable starting point for identifying potential virulence determinants, as demonstrated by the deletion of the NV gene, and for developing attenuated derivatives as candidate vaccines. Using the available reverse-genetics system elaborated with IHNV, a recombinant IHNV expressing a green fluorescent protein (GFP) also was produced (8), and it was of interest to study whether a superinfection exclusion phenomenon could be observed between both VHSV and IHNV, whose cohabitation has been recorded often. We showed that up to 74% of a cell monolayer could be simultaneously infected by the viruses, demonstrating a limited viral interference between salmonid novirhabdoviruses and that, based on previous data, chimeric or pseudotyped viruses could be generated (6).     

Mice expressing HLA-DQ6alpha8beta transgenes develop polychondritis spontaneously

Relapsing polychondritis (RP) is a human autoimmune disease of unknown etiology in which cartilaginous sites are destroyed by cyclic inflammatory episodes beginning, most commonly, during the fourth or fifth decade of life. We have previously described collagen-induced polychondritis that closely mirrors RP occurring in young (6-8 weeks old) HLA-DQ6alphabeta 8alphabeta transgenic Abeta0 mice, following immunization with heterologous type II collagen (CII). We present evidence here that transgenic strains expressing the DQ6alpha8beta transgene develop spontaneous polychondritis (SP) at the mouse equivalent of human middle age (4.5-6 months and 40-50 years old, respectively) and display polyarthritis, auricular chondritis and nasal chondritis--three of the most common sites affected in RP. Auricular chondritis in SP, like RP but unlike CII-induced polychondritis, exhibited a relapsing/remitting phenotype, requiring several inflammatory cycles before the cartilage is destroyed. Elevated serum levels of total IgG corresponded with the onset of disease in SP, as in RP and CII-induced polychondritis. No CII-specific immune response was detected in SP, however--more closely mirroring RP, in which as few as 30% of RP patients have been reported to have CII-specific IgG. CII-induced polychondritis displays a strong CII-specific immune response. SP also demonstrated a strong female preponderance, as some workers have reported in RP but has not observed in CII-induced polychondritis. These characteristics of SP allow for the examination of the immunopathogenesis of polychondritis in the absence of an overwhelming CII-specific immune response and the strong adjuvant-induced immunostimulatory influence in CII-induced polychondritis. This spontaneous model of polychondritis provides a new and unique tool to investigate both the initiatory events as well as the immunopathogenic mechanisms occurring at cartilaginous sites during the cyclic inflammatory assaults of polychondritis.     

AIDS in Haitian immigrants and in a Caucasian woman closely associated with Haitians.

In Montreal the acquired immune deficiency syndrome (AIDS) was seen in eight Haitian immigrants and one Caucasian woman who had lived with Haitian immigrants for 3 years before the onset of her illness. AIDS was characterized by opportunistic infections alone in seven patients, by opportunistic infection and Kaposi''s sarcoma in one patient and by chronic generalized lymphadenopathy in one patient. Five of the patients had presented with Mycobacterium tuberculosis infections 1 to 12 months before the onset of opportunistic infections. All nine patients were found to have recall anergy by skin testing for delayed hypersensitivity. Enumeration of the lymphocyte subpopulations in three patients showed a marked inversion of the ratio of helper to suppressor T lymphocytes. Six of the patients died as a result of the opportunistic infections; autopsies showed no recognizable causes of immunodeficiency. Thus, there is in Montreal a third clustering of AIDS cases in North America related to Haitian immigrants.     

Arcellacea (Testate Lobose Amoebae) as pH Indicators in a Pyrite Mine-Acidified Lake, Northeastern Ontario, Canada

Arcellacea (testate lobose amoebae) were examined in 24 sediment–water interface samples collected over two late August field seasons in 2010 and 2011, from James and Granite lakes, Temagami Region, Northeastern Ontario. The work was carried out to quantitatively test species–environment relationships in a lake system known to be characterized by a significant pH gradient, partially the result of contamination from the early twentieth century Northland Pyrite Mine Co., located on the shoreline in the southern basin of James Lake. Redundancy analysis confirmed that arcellacean assemblage structure was most strongly controlled by pH, explaining 14.06 % (p?<?0.002) of the total variance. Q- and R-mode cluster analysis supported by detrended correspondence analysis yielded two major faunal assemblages. The Oligotrophic Assemblage (1) had a Shannon Diversity Index (SDI) ranging up to 2.45, typical of healthy boreal lakes. This assemblage characterized samples collected from higher pH stations within James and Granite lakes away from the immediate area of the mine site, while the Low pH Assemblage 2010 (2a) and Low pH Assemblage 2011 (2b) groupings were from the very low pH environments of James Lake adjacent to the former mine site. Both low diversity assemblages (SDI ranging from 0.62 to 1.22) were characterized by Arcella vulgaris, a species known to thrive in hostile lacustrine environments. Differing depositional conditions during August 2010, a probable result of different prevailing wind patterns that summer, led to allochthonous specimens of the seasonally planktic Cucurbitella tricuspis dominating the Low pH Assemblage 2010 (2a) fauna.     

Synapse Formation Activates a Transcriptional Program for Persistent Enhancement in the Bi-directional Transport of Mitochondria

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Factors affecting the accuracy of urine-based biomarkers of BSE

Background  

Transmissible spongiform encephalopathy diseases are untreatable, uniformly fatal degenerative syndromes of the central nervous system that can be transmitted both within as well as between species. The bovine spongiform encephalopathy (BSE) epidemic and the emergence of a new human variant of Creutzfeldt-Jakob disease (vCJD), have profoundly influenced beef production processes as well as blood donation and surgical procedures. Simple, robust and cost effective diagnostic screening and surveillance tools are needed for both the preclinical and clinical stages of TSE disease in order to minimize both the economic costs and zoonotic risk of BSE and to further reduce the risk of secondary vCJD.     

Quantitative proteomic analysis of cyclosporine-induced toxicity in a human kidney cell line and comparison with tacrolimus

The calcineurin-inhibitors (CNIs) cyclosporine (CsA) and tacrolimus (TAC) remain the pillars of modern immunosuppression regimens used in solid organ transplantation. Nephrotoxicity is an adverse effect that limits their successful use. The precise molecular mechanisms underlying this nephrotoxicity remain unclear. Using SILAC together with LC-MALDI-TOF/TOF, we investigated the CNIs-induced proteomic perturbations in renal cells. Among the 495 proteins quantifiable in both forward and reverse SILAC, 69 displayed CsA-induced perturbations: proteins involved in ER-stress/protein folding, apoptosis, metabolism/transport or cytoskeleton pathways were up-regulated, while cyclophilin B as well as nuclear and RNA-processing proteins were down-regulated. Co-administration of CsA with the antioxidant N-acetylcysteine significantly decreased lipid peroxidation and also partially corrected the CsA-induced unfolded protein response. TAC toxicity profile was apparently different from that of CsA, especially without perturbation of cyclophilins A and B, up-regulation of ER-chaperones nor down-regulation of a number of nuclear proteins. These results provide a new insight and are consistent with recent data regarding the molecular mechanisms of CNIs-induced nephrotoxicity. Our findings offer new directions for future research aiming to identify specific biomarkers of CsA nephrotoxicity.