Human polyomaviruses and cancer: an overview

The name of the family Polyomaviridae, derives from the early observation that cells infected with murine polyomavirus induced multiple (poly) tumors (omas) in immunocompromised mice. Subsequent studies showed that many members of this family exhibit the capacity of mediating cell transformation and tumorigenesis in different experimental models. The transformation process mediated by these viruses is driven by viral pleiotropic regulatory proteins called T (tumor) antigens. Similar to other viral oncoproteins T antigens target cellular regulatory factors to favor cell proliferation, immune evasion and downregulation of apoptosis. The first two human polyomaviruses were isolated over 45 years ago. However, recent advances in the DNA sequencing technologies led to the rapid identification of additional twelve new polyomaviruses in different human samples. Many of these viruses establish chronic infections and have been associated with conditions in immunosuppressed individuals, particularly in organ transplant recipients. This has been associated to viral reactivation due to the immunosuppressant therapy applied to these patients. Four polyomaviruses namely, Merkel cell polyomavirus (MCPyV), Trichodysplasia spinulosa polyomavirus (TSPyV), John Cunningham Polyomavirus (JCPyV) and BK polyomavirus (BKPyV) have been associated with the development of specific malignant tumors. However, present evidence only supports the role of MCPyV as a carcinogen to humans. In the present review we present a summarized discussion on the current knowledge concerning the role of MCPyV, TSPyV, JCPyV and BKPyV in human cancers

Olhares suíços sobre o Portugal de Salazar. 2 : as guerras (1936-1945)

Entre 1936 e 1945 quase todas as fontes consultadas, quer diplomáticas, quer jornalísticas, dão uma imagem positiva da política de Salazar, a qual defendem sem que praticamente sobre ela exerçam qualquer análise crítica. Durante a guerra civil espanhola, se excluirmos a imprensa comunista, que, no entanto, fala muito pouco de Portugal, os representantes suíços em Lisboa e os editorialistas dos principais quotidianos helvéticos justificam a atitude filofranquista do governo português. No que diz respeito à política externa portuguesa e à neutralidade durante a Segunda Guerra Mundial, as mesmas fontes, obnubiladas, sem dúvida, pelo mito da ditadura «branda e moderada» de Salazar, manifestam uma grande compreensão e simpatia pelas diferentes tomadas de posição do ditador português, por razões ideológicas, pelo facto de Portugal ser um pequeno país como a Suíça e também pelo papel de Portugal no abastecimento da Confederação durante o conflito.ABSTRACT: Between 1936 and 1945, an overwhelming majority of the documents analyzed in this article give a very positive image of Salazar’s regime. During the Spanish civil war, with the exception of a very few left-leaning newspapers, the Swiss journalists and the diplomats in charge at the Swiss Legation in Lisbon defended and justified the support given to the nationalist cause in Spain by the Portuguese government. Concerning the Portuguese neutrality during the Second World War, the same sources adopted the Salazar’s point of view and analyzed his politics with a lot of sympathy and understanding. This was mainly for four reasons: they sympathized partially with the ideology of the Estado Novo; Portugal is a small country, like Switzerland; they were blinded by the myth of the so-called «soft» and «moderate» dictatorship of Salazar; and, finally, because Portugal was an important trade partner for the Confederation during the conflict

dentification of Chelonid alphaherpesvirus 5 (ChHV5) gene sequences in tumor tissues histologically characterized and secretions from green turtles Chelonia mydas captured off the coast of São Paulo State in the period 2001-2012.

A fibropapilomatose é uma neoplasia caracterizada pela formação de múltiplos tumores que acomete, mais frequentemente, a espécie de tartaruga marinha Chelonia mydas. Estudos recentes apontam o Chelonid herpesvirus 5 (ChHV5) como o provável agente etiológico dessa doença, embora a associação com ambientes antropogenicamente alterados parecem contribuir para o desenvolvimento da doença. Nesse estudo, biópsias de tumores e secreções de tartarugas verdes capturadas no litoral do Estado de São Paulo, Brasil, foram submetidas a análises histológicas e moleculares visando detectar e caracterizar ChHV5. Em 45,5 % dos casos, os achados histopatológicos revelaram células epiteliais balonizantes com corpúsculos de inclusão intranucleares. ChHV5 foram detectados nas biópsias de pele e oculares dos animais e em secreções oculares e saliva por PCR. A análise das sequências parciais do gene da polimerase do ChHV5 detectadas revelou duas sequências gênicas distintas entre si. A análise filogenética indicou que as amostras brasileiras são similares às amostras de ChHV5 do grupo filogeográfico do Atlântico, compartilhando o mesmo clado que amostras provenientes do Golfo da Guiné e de Porto Rico, sugerindo um possível fluxo dos vírus entre essas três regiões.Fibropapillomatosis is a neoplastic disease characterized by the formation of multiple tumors affecting different species of sea turtles and, most often, Chelonia mydas. Recent studies indicate that Chelonid herpesvirus 5 (ChHV5) is the etiological agent of this disease, though its association with anthropogenically altered environments also appears to contribute to disease expression and tumor formation. In this study, tumor biopsy and secretions from green turtles captured off the coast of São Paulo State, Brazil, were used in histological and molecular analyses to detect and characterize ChHV5. In 45.5 % of cases, the tumor histopathological findings revealed ballooning degeneration with intranuclear inclusion bodies. ChHV5 was detected using polymerase chain reaction on the animals skin, ocular tumor biopsies, and ocular and oral secretions. The analysis of the detected ChHV5 sequences revealed two distinct genetic sequences together. Phylogenetic analysis indicated that Brazilian samples were similar to ChHV5 samples described for the Atlantic phylogeographic group and are therefore part of the same clade as the Gulf of Guinea and Puerto Rico samples. This similarity suggests a possible flow of the virus between these three regions

Human polyomaviruses and cancer: an overview

The name of the family Polyomaviridae, derives from the early observation that cells infected with murine polyomavirus induced multiple (poly) tumors (omas) in immunocompromised mice. Subsequent studies showed that many members of this family exhibit the capacity of mediating cell transformation and tumorigenesis in different experimental models. The transformation process mediated by these viruses is driven by viral pleiotropic regulatory proteins called T (tumor) antigens. Similar to other viral oncoproteins T antigens target cellular regulatory factors to favor cell proliferation, immune evasion and downregulation of apoptosis. The first two human polyomaviruses were isolated over 45 years ago. However, recent advances in the DNA sequencing technologies led to the rapid identification of additional twelve new polyomaviruses in different human samples. Many of these viruses establish chronic infections and have been associated with conditions in immunosuppressed individuals, particularly in organ transplant recipients. This has been associated to viral reactivation due to the immunosuppressant therapy applied to these patients. Four polyomaviruses namely, Merkel cell polyomavirus (MCPyV), Trichodysplasia spinulosa polyomavirus (TSPyV), John Cunningham Polyomavirus (JCPyV) and BK polyomavirus (BKPyV) have been associated with the development of specific malignant tumors. However, present evidence only supports the role of MCPyV as a carcinogen to humans. In the present review we present a summarized discussion on the current knowledge concerning the role of MCPyV, TSPyV, JCPyV and BKPyV in human cancers

Caracterização antigênica de isolados de parvovirus canino do Brasil utilizando monoclonais específicos

Canine parvovirus (CPV) is an emerged pathogen in dogs, first isolated in 1978 in the USA. The original 1978 strain was designated CPV type 2 (CPV-2). However, analysis of CPV isolates in the USA by restriction enzymes and monoclonal antibodies have shown that around the year 1979 a CPV variant strain, designated CPV type 2a (CPV-2a), became widespread. Subsequently, a new antigenic strain, designated CPV type 2b (CPV-2b), was also observed by analysis of CPV isolates from various parts of the world, although the proportion of each strains was different between countries. In this study, the Haemagglutination Inhibition (HI) test with a panel of monoclonal antibodies was used to type canine parvovirus strains in 29 fecal samples collected from symptomatic dogs from 1980 to 1986 and from 1990 to 1995. The results showed a strong predominance of the antigenic type 2a indicating that the CPV epizooty in Brazil followed the same pattern observed in European and Asian countriesO Parvovírus Canino (CPV) é um patógeno emergente em cães, isolado pela primeira vez em 1978, nos Estados Unidos. A amostra original de 1978 foi designada CPV tipo 2 (CPV-2). Entretanto, análises de isolados de CPV dos Estados Unidos, por enzimas de restrição e anticorpos monoclonais demonstraram que cerca de 1979, uma amostra variante, designada CPV tipo 2a (CPV-2a) tornou-se prevalente. Subseqüentemente, uma nova amostra antigênica, designada CPV tipo 2b (CPV-2b) também foi observada por análises de isolados de CPV de várias partes do mundo, embora a proporção fosse diferente entre os países. Nesse estudo, foi utilizado o teste de Inibição da Hemaglutinação (HI) com um painel de anticorpos monoclonais para a tipagem de 29 amostras fecais de parvovirus canino, coletadas de cães sintomáticos de 1980 a 1986 e de 1990 a 1995. Os resultados indicaram uma forte predominância do tipo antigênico 2a indicando que a epizootia de CPV no Brasil seguiu o mesmo padrão observados na Europa e países Asiático

Identification of circo-like virus-Brazil genomic sequences in raw sewage from the metropolitan area of São Paulo: evidence of circulation two and three years after the first detection

BACKGROUND Two novel viruses named circo-like virus-Brazil (CLV-BR) hs1 and hs2 were previously discovered in a Brazilian human fecal sample through metagenomics. CLV-BR hs1 and hs2 possess a small circular DNA genome encoding a replication initiator protein (Rep), and the two genomes exhibit 92% nucleotide identity with each other. Phylogenetic analysis based on the Rep protein showed that CLV-BRs do not cluster with circoviruses, nanoviruses, geminiviruses or cycloviruses. OBJECTIVE The aim of this study was to search for CLV-BR genomes in sewage and reclaimed water samples from the metropolitan area of São Paulo, Brazil, to verify whether the first detection of these viruses was an isolated finding. METHODS Sewage and reclaimed water samples collected concomitantly during the years 2005-2006 were purified and concentrated using methodologies designed for the study of viruses. A total of 177 treated reclaimed water samples were grouped into five pools, as were 177 treated raw sewage samples. Nucleic acid extraction, polymerase chain reaction (PCR) amplification and Sanger sequencing were then performed.e FINDINGS CLV-BR genomes were detected in two pools of sewage samples, p6 and p9. Approximately 28% and 51% of the CLV-BR genome was amplified from p6 and p9, respectively, including 76% of the Rep gene. The detected genomes are most likely related to CLV-BR hs1. Comparative analysis showed several synonymous substitutions within Rep-encoding sequences, suggesting purifying selection for this gene, as has been observed for other eukaryotic circular Rep-encoding single-stranded DNA (CRESS-DNA) viruses. MAIN CONCLUSION The results therefore indicated that CLV-BR has continued to circulate in Brazil two and three years after first being detected