Marcílio Jorge Fumagalli
University of São Paulo
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Featured researches published by Marcílio Jorge Fumagalli.
Virology | 2018
William Marciel de Souza; Marcílio Jorge Fumagalli; Jansen de Araujo; Gilberto Sabino-Santos; Felipe Gonçalves Motta Maia; Marilia Farignoli Romeiro; Sejal Modha; Marcello Schiavo Nardi; Luzia Helena Queiroz; Edison Luiz Durigon; Márcio Roberto Teixeira Nunes; Pablo R. Murcia; Luiz Tadeu Moraes Figueiredo
The Anelloviridae comprises single-stranded DNA viruses currently grouped in sixty-eight species classified in twelve genera. They have been found in many vertebrate hosts including primates. In this study, we describe the application of the high-throughput sequencing to examine the frequency and diversity of anelloviruses in rodents, bats and opossums captured in São Paulo State, Brazil. We report a total of twenty-six anelloviruses with sixteen nearly complete genomes and ten partial genomes, which include eleven potential novel species identified in rodents (Cricetidae), bats (Molossidae and Phyllostomidae), and opossums (Didelphidae). We also propose the inclusion of two potential new genera within the Anelloviridae family, provisionally named Omegatorquevirus and Sigmatorquevirus, including six and three novel species of anelloviruses, respectively. In summary, this study expands the diversity and the host range of the known anelloviruses.
Journal of General Virology | 2017
William Marciel de Souza; Marilia Farignoli Romeiro; Marcílio Jorge Fumagalli; Sejal Modha; Jansen de Araujo; Luzia Helena Queiroz; Edison Luiz Durigon; Luiz Tadeu Moraes Figueiredo; Pablo R. Murcia; Robert J. Gifford
Chapparvoviruses are a highly divergent group of parvoviruses (family Parvoviridae) that have recently been identified via metagenomic sampling of animal faeces. Here, we report the sequences of six novel chapparvoviruses identified through both metagenomic sampling of bat tissues and in silico screening of published vertebrate genome assemblies. The novel chapparvoviruses share several distinctive genomic features and group together as a robustly supported monophyletic clade in phylogenetic trees. Our data indicate that chapparvoviruses have a broad host range in vertebrates and a global distribution.Chapparvoviruses are a highly divergent group of parvoviruses (family Parvoviridae) that have recently been identified via metagenomic sampling of animal faeces. Here we report the sequences of six novel chapparvoviruses identified through both metagenomic sampling of bat tissues and in silico screening of published vertebrate genome assemblies. The novel chapparvoviruses share several distinctive genomic features, and group together as a robustly supported monophyletic clade in phylogenetic trees. Our data indicate that chapparvoviruses have a broad host range in vertebrates, and a global distribution.
Viruses | 2018
William Marciel de Souza; Tristan P.W. Dennis; Marcílio Jorge Fumagalli; Jansen de Araujo; Gilberto Sabino-Santos; Felipe Gonçalves Motta Maia; Gustavo Olszanski Acrani; Adriano de Oliveira Torres Carrasco; Marilia Farignoli Romeiro; Sejal Modha; Luiz Carlos Vieira; Tatiana Ometto; Luzia Helena Queiroz; Edison Luiz Durigon; Márcio Roberto Teixeira Nunes; Luiz Tadeu Moraes Figueiredo; Robert J. Gifford
Parvoviruses (family Parvoviridae) are small, single-stranded DNA viruses. Many parvoviral pathogens of medical, veterinary and ecological importance have been identified. In this study, we used high-throughput sequencing (HTS) to investigate the diversity of parvoviruses infecting wild and domestic animals in Brazil. We identified 21 parvovirus sequences (including twelve nearly complete genomes and nine partial genomes) in samples derived from rodents, bats, opossums, birds and cattle in Pernambuco, São Paulo, Paraná and Rio Grande do Sul states. These sequences were investigated using phylogenetic and distance-based approaches and were thereby classified into eight parvovirus species (six of which have not been described previously), representing six distinct genera in the subfamily Parvovirinae. Our findings extend the known biogeographic range of previously characterized parvovirus species and the known host range of three parvovirus genera (Dependovirus, Aveparvovirus and Tetraparvovirus). Moreover, our investigation provides a window into the ecological dynamics of parvovirus infections in vertebrates, revealing that many parvovirus genera contain well-defined sub-lineages that circulate widely throughout the world within particular taxonomic groups of hosts.
Virology | 2018
William Marciel de Souza; Marilia Farignoli Romeiro; Gilberto Sabino-Santos; Felipe Gonçalves Motta Maia; Marcílio Jorge Fumagalli; Sejal Modha; Márcio R. T. Nunes; Pablo R. Murcia; Luiz Tadeu Moraes Figueiredo
The Hepeviridae comprise single-stranded positive-sense RNA viruses classified into two genera, Orthohepevirus and Piscihepevirus. Orthohepeviruses have a wide host range that includes rodents, but previous studies had been restricted to rodents of the Muridae family. In this study, we applied a high-throughput sequencing approach to examine the presence of orthohepeviruses in rodents from São Paulo State, Brazil. We also used RT-PCR to determine the frequency of orthohepeviruses in our sampled population. We identified novel orthohepeviruses in blood samples derived from Necromys lasiurus (1.19%) and Calomys tener (3.66%). Therefore, our results expand the host range and viral diversity of the Hepeviridae family.
Archives of Virology | 2017
Glauciane Garcia de Figueiredo; Alberto Anastacio Amarilla; William Marciel de Souza; Marcílio Jorge Fumagalli; Mario Luis Garcia de Figueiredo; Matias Pablo Juan Szabó; Soraya Jabur Badra; Yin Xiang Setoh; Alexander A. Khromykh; Victor Hugo Aquino; Luiz Tadeu Moraes Figueiredo
Cacipacoré virus (CPCV) is a potential emerging virus classified in the genus Flavivirus, family Flaviviridae. In the present study, we present the genetic characterization of a CPCV isolated from ticks (Amblyomma cajennense) collected from a sick capybara (Hydrochoerus hydrochaeris) in São Paulo State, Brazil. The CPCV isolate shares the typical genomic organization of flaviviruses with 10,857 nucleotides in length and a single open reading frame of 10,284 nucleotides encoding a polyprotein of 3,427 amino acids. Phylogenetic analysis revealed that CPCV is unique, as a potentially tick-borne virus, in the Japanese encephalitis virus serogroup.
bioRxiv | 2018
William Marciel de Souza; Tristan P.W. Dennis; Marcílio Jorge Fumagalli; Jansen de Araujo; Gilberto Sabino-Santos; Felipe Gonçalves Motta Maia; Gustavo Olszanski Acrani; Adriano de Oliveira Torres Carrasco; Marilia Farignoli Romeiro; Sejal Modha; Luiz Carlos Vieira; Tatiana Ometto; Luzia Helena Queiroz; Edison Luiz Durigon; Márcio R. T. Nunes; Luiz Tadeu Moraes Figueiredo; Robert J. Gifford
Parvoviruses (family Parvoviridae) are small, single-stranded DNA viruses. Many parvoviral pathogens of medical, veterinary and ecological importance have been identified. In this study, we used high-throughput sequencing (HTS) to investigate the diversity of parvoviruses infecting wild and domestic animals in Brazil. We identified 21 parvovirus sequences (including twelve nearly complete genomes and nine partial genomes) in samples derived from rodents, bats, opossums, birds and cattle in Pernambuco, São Paulo, Paraná and Rio Grande do Sul states. These sequences were investigated using phylogenetic and distance-based approaches, and were thereby classified into eight parvovirus species (six of which have not been described previously), representing six distinct genera in the subfamily Parvovirinae. Our findings extend the known biogeographic range of previously characterized parvovirus species, and the known host range of three parvovirus genera (Dependovirus, Aveparvovirus, and Tetraparvovirus). Moreover, our investigation provides a window into the ecological dynamics of parvovirus infections in vertebrates, revealing that many parvovirus genera contain well-defined sub-lineages that circulate widely throughout the world within particular taxonomic groups of hosts.
Virus Evolution | 2018
William Marciel de Souza; G O Acrani; A Carrasco; Marcílio Jorge Fumagalli; Marilia Farignoli Romeiro; Sejal Modha; J Hughes; Márcio Roberto Teixeira Nunes; Pablo R. Murcia; Luiz Tadeu Moraes Figueiredo
Trabalho apresentado no 22nd International BioInformatics Workshop on Virus Evolution and Molecular Epidemiology, 2017. Lisboa, Portugal.
Virology Journal | 2018
Marcílio Jorge Fumagalli; William Marciel de Souza; Danillo Lucas Alves Espósito; Angélica Silva; Marilia Farignoli Romeiro; Edson Zangiacomi Martinez; Benedito Antônio Lopes da Fonseca; Luiz Tadeu Moraes Figueiredo
BackgroundChikungunya (CHIKV) virus is an important mosquito-borne virus causing outbreaks of acute febrile illness with arthropathy. The detection of specific antibodies against CHIKV is used for diagnosis after the acute viremic phase of the disease. However, a major challenge for serologic diagnosis of CHIKV and other alphaviruses is the cross-reactivity of antibodies to common antigens among these viruses. In the present study, we have developed an enzyme-linked immunosorbend assay using a recombinant envelope protein 2 of CHIKV produced in Escherichia coli system, as a capture antigen.ResultsHigh titers (1600 to 12,800) of anti-CHIKV antibodies were detected in human sera analyzed by the CHIKV assay, suggesting it may detect low levels of the antibodies presence. On the other side, cross-reactivity was not observed in mouse hyperimmune sera to Mayaro virus and other alphaviruses analyzed by the CHIKV immunosorbend assay, suggesting it is a CHIKV-specific test. Fifty-nine human serum samples of CHIKV infection suspected cases were tested for immunoglobulin G (IgG) and M (IgM) antibodies detection using the CHIKV immunosorbend assay. A total of 44% (26/59) of samples were positive for IgG to CHIKV, determining 89.66% sensitivity and 100% specificity when the assay is compared to a CHIKV-specific neutralization assay. In addition, 40.6% (24/59) of samples were positive for IgM, determining 92.48% sensitivity and 79.04% specificity by a Bayesian method in the absence of a gold standard. Moreover, CHIKV immunosorbend assay showed similar sensibilities to a commercial immunochromatography assay (Lumiquick, USA) for CHIKV IgG and IgM detection.ConclusionIn short, we have developed a rapid, simple, specific and sensitive CHIKV immunosorbend assay for IgG and IgM detection and our results showed potential applicability on the diagnosis of infections by this virus.
PLOS ONE | 2018
Alberto Anastacio Amarilla; Marcílio Jorge Fumagalli; Mario Luis Garcia de Figueiredo; Djalma S. Lima-Junior; Nilton Nascimento dos Santos-Junior; Helda Liz Alfonso; Veronica Lippi; Amanda Cristina Trabuco; Flávio Lauretti; Vanessa Danielle Menjon Muller; David F. Colón; João P. M. Luiz; Andreas Suhrbier; Yin Xiang Setoh; Alexander A. Khromykh; Luiz Tadeu Moraes Figueiredo; Victor Hugo Aquino
Rocio virus (ROCV) was the causative agent of an unprecedented outbreak of encephalitis during the 1970s in the Vale do Ribeira, Sao Paulo State, in the Southeast region of Brazil. Surprisingly, no further cases of ROCV infection were identified after this outbreak; however, serological surveys have suggested the circulation of ROCV among humans and animals in different regions of Brazil. Cross-protective immunity among flaviviruses is well documented; consequently, immunity induced by infections with other flaviviruses endemic to Brazil could potentially be responsible for the lack of ROCV infections. Herein, we evaluated the cross-protection mediated by other flaviviruses against ROCV infection using an experimental C57BL/6 mouse model. Cross-protection against ROCV infection was observed when animals had prior exposure to Ilheus virus or Saint Louis encephalitis virus, suggesting that cross-reactive anti-flavivirus antibodies may limit ROCV disease outbreaks.
Archives of Virology | 2018
Felipe Gonçalves Motta Maia; William Marciel de Souza; Gilberto Sabino-Santos; Marcílio Jorge Fumagalli; Sejal Modha; Pablo R. Murcia; Luiz Tadeu Moraes Figueiredo
The nearly complete genome sequence of a novel polyomavirus from blood samples of Akodon montensis and Calomys tener collected in Brazil was determined by high-throughput sequencing. This virus showed a typical polyomaviruses genome organization, and it was classified as a member of the genus Betapolyomavirus. Our results expand the host range and viral diversity of the family Polyomaviridae.