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  1. Article ; Online: Recombination between poliovirus and coxsackie A viruses of species C: a model of viral genetic plasticity and emergence.

    Combelas, Nicolas / Holmblat, Barbara / Joffret, Marie-Line / Colbère-Garapin, Florence / Delpeyroux, Francis

    Viruses

    2011  Volume 3, Issue 8, Page(s) 1460–1484

    Abstract: Genetic recombination in RNA viruses was discovered many years ago for poliovirus (PV), an enterovirus of the Picornaviridae family, and studied using PV or other picornaviruses as models. Recently, recombination was shown to be a general phenomenon ... ...

    Abstract Genetic recombination in RNA viruses was discovered many years ago for poliovirus (PV), an enterovirus of the Picornaviridae family, and studied using PV or other picornaviruses as models. Recently, recombination was shown to be a general phenomenon between different types of enteroviruses of the same species. In particular, the interest for this mechanism of genetic plasticity was renewed with the emergence of pathogenic recombinant circulating vaccine-derived polioviruses (cVDPVs), which were implicated in poliomyelitis outbreaks in several regions of the world with insufficient vaccination coverage. Most of these cVDPVs had mosaic genomes constituted of mutated poliovaccine capsid sequences and part or all of the non-structural sequences from other human enteroviruses of species C (HEV-C), in particular coxsackie A viruses. A study in Madagascar showed that recombinant cVDPVs had been co-circulating in a small population of children with many different HEV-C types. This viral ecosystem showed a surprising and extensive biodiversity associated to several types and recombinant genotypes, indicating that intertypic genetic recombination was not only a mechanism of evolution for HEV-C, but an usual mode of genetic plasticity shaping viral diversity. Results suggested that recombination may be, in conjunction with mutations, implicated in the phenotypic diversity of enterovirus strains and in the emergence of new pathogenic strains. Nevertheless, little is known about the rules and mechanisms which govern genetic exchanges between HEV-C types, as well as about the importance of intertypic recombination in generating phenotypic variation. This review summarizes our current knowledge of the mechanisms of evolution of PV, in particular recombination events leading to the emergence of recombinant cVDPVs.
    MeSH term(s) Coxsackievirus Infections/transmission ; Coxsackievirus Infections/virology ; Disease Eradication ; Enterovirus C, Human/genetics ; Enterovirus C, Human/pathogenicity ; Evolution, Molecular ; Genome, Viral ; Genomic Instability ; Humans ; Models, Genetic ; Mutation ; Poliomyelitis/immunology ; Poliomyelitis/transmission ; Poliomyelitis/virology ; Poliovirus/genetics ; Poliovirus/immunology ; Poliovirus/pathogenicity ; Poliovirus Vaccines/adverse effects ; Poliovirus Vaccines/economics ; RNA, Viral/genetics ; Recombination, Genetic ; Species Specificity
    Chemical Substances Poliovirus Vaccines ; RNA, Viral
    Language English
    Publishing date 2011-08-17
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2516098-9
    ISSN 1999-4915 ; 1999-4915
    ISSN (online) 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v3081460
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Identification of the neutralizing epitopes of Merkel cell polyomavirus major capsid protein within the BC and EF surface loops.

    Fleury, Maxime J J / Nicol, Jérôme T J / Samimi, Mahtab / Arnold, Françoise / Cazal, Raphael / Ballaire, Raphaelle / Mercey, Olivier / Gonneville, Hélène / Combelas, Nicolas / Vautherot, Jean-Francois / Moreau, Thierry / Lorette, Gérard / Coursaget, Pierre / Touzé, Antoine

    PloS one

    2015  Volume 10, Issue 3, Page(s) e0121751

    Abstract: Merkel cell polyomavirus (MCPyV) is the first polyomavirus clearly associated with a human cancer, i.e. the Merkel cell carcinoma (MCC). Polyomaviruses are small naked DNA viruses that induce a robust polyclonal antibody response against the major capsid ...

    Abstract Merkel cell polyomavirus (MCPyV) is the first polyomavirus clearly associated with a human cancer, i.e. the Merkel cell carcinoma (MCC). Polyomaviruses are small naked DNA viruses that induce a robust polyclonal antibody response against the major capsid protein (VP1). However, the polyomavirus VP1 capsid protein epitopes have not been identified to date. The aim of this study was to identify the neutralizing epitopes of the MCPyV capsid. For this goal, four VP1 mutants were generated by insertional mutagenesis in the BC, DE, EF and HI loops between amino acids 88-89, 150-151, 189-190, and 296-297, respectively. The reactivity of these mutants and wild-type VLPs was then investigated with anti-VP1 monoclonal antibodies and anti-MCPyV positive human sera. The findings together suggest that immunodominant conformational neutralizing epitopes are present at the surface of the MCPyV VLPs and are clustered within BC and EF loops.
    MeSH term(s) Animals ; Antibodies, Monoclonal/immunology ; Antibodies, Neutralizing/immunology ; Antibodies, Viral/immunology ; Capsid Proteins/chemistry ; Capsid Proteins/genetics ; Capsid Proteins/immunology ; Cell Line ; Cross Reactions/immunology ; Epitope Mapping ; Epitopes/immunology ; Female ; Humans ; Immunodominant Epitopes/immunology ; Merkel cell polyomavirus/genetics ; Merkel cell polyomavirus/immunology ; Mice ; Models, Molecular ; Mutation ; Protein Conformation ; Protein Interaction Domains and Motifs/immunology
    Chemical Substances Antibodies, Monoclonal ; Antibodies, Neutralizing ; Antibodies, Viral ; Capsid Proteins ; Epitopes ; Immunodominant Epitopes
    Language English
    Publishing date 2015
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0121751
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Recombination between Poliovirus and Coxsackie A Viruses of Species C

    Francis Delpeyroux / Nicolas Combelas / Marie-Line Joffret / Barbara Holmblat / Florence Colbère-Garapin

    Viruses, Vol 3, Iss 8, Pp 1460-

    A Model of Viral Genetic Plasticity and Emergence

    2011  Volume 1484

    Abstract: Genetic recombination in RNA viruses was discovered many years ago for poliovirus (PV), an enterovirus of the Picornaviridae family, and studied using PV or other picornaviruses as models. Recently, recombination was shown to be a general phenomenon ... ...

    Abstract Genetic recombination in RNA viruses was discovered many years ago for poliovirus (PV), an enterovirus of the Picornaviridae family, and studied using PV or other picornaviruses as models. Recently, recombination was shown to be a general phenomenon between different types of enteroviruses of the same species. In particular, the interest for this mechanism of genetic plasticity was renewed with the emergence of pathogenic recombinant circulating vaccine-derived polioviruses (cVDPVs), which were implicated in poliomyelitis outbreaks in several regions of the world with insufficient vaccination coverage. Most of these cVDPVs had mosaic genomes constituted of mutated poliovaccine capsid sequences and part or all of the non-structural sequences from other human enteroviruses of species C (HEV-C), in particular coxsackie A viruses. A study in Madagascar showed that recombinant cVDPVs had been co-circulating in a small population of children with many different HEV-C types. This viral ecosystem showed a surprising and extensive biodiversity associated to several types and recombinant genotypes, indicating that intertypic genetic recombination was not only a mechanism of evolution for HEV-C, but an usual mode of genetic plasticity shaping viral diversity. Results suggested that recombination may be, in conjunction with mutations, implicated in the phenotypic diversity of enterovirus strains and in the emergence of new pathogenic strains. Nevertheless, little is known about the rules and mechanisms which govern genetic exchanges between HEV-C types, as well as about the importance of intertypic recombination in generating phenotypic variation. This review summarizes our current knowledge of the mechanisms of evolution of PV, in particular recombination events leading to the emergence of recombinant cVDPVs.
    Keywords enterovirus ; poliovirus ; poliomyelitis ; live vaccine ; vaccine-derived poliovirus ; VDPV ; genetic plasticity ; recombination ; emergence ; Microbiology ; QR1-502 ; Science ; Q ; DOAJ:Microbiology ; DOAJ:Biology ; DOAJ:Biology and Life Sciences
    Subject code 580
    Language English
    Publishing date 2011-08-01T00:00:00Z
    Publisher Molecular Diversity Preservation International
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: Papillomavirus pseudovirions packaged with the L2 gene induce cross-neutralizing antibodies.

    Combelas, Nicolas / Saussereau, Emilie / Fleury, Maxime J J / Ribeiro, Tatiana / Gaitan, Julien / Duarte-Forero, Diego F / Coursaget, Pierre / Touzé, Antoine

    Journal of translational medicine

    2010  Volume 8, Page(s) 28

    Abstract: Background: Current vaccines against HPVs are constituted of L1 protein self-assembled into virus-like particles (VLPs) and they have been shown to protect against natural HPV16 and HPV18 infections and associated lesions. In addition, limited cross- ... ...

    Abstract Background: Current vaccines against HPVs are constituted of L1 protein self-assembled into virus-like particles (VLPs) and they have been shown to protect against natural HPV16 and HPV18 infections and associated lesions. In addition, limited cross-protection has been observed against closely related types. Immunization with L2 protein in animal models has been shown to provide cross-protection against distant papillomavirus types, suggesting that the L2 protein contains cross-neutralizing epitopes. However, vaccination with L2 protein or L2 peptides does not induce high titers of anti-L2 antibodies. In order to develop a vaccine with the potential to protect against other high-risk HPV types, we have produced HPV58 pseudovirions encoding the HPV31 L2 protein and compared their capacity to induce cross-neutralizing antibodies with that of HPV L1 and HPV L1/L2 VLPs.
    Methods: The titers of neutralizing antibodies against HPV16, HPV18, HPV31 and HPV58 induced in Balb/c mice were compared after immunization with L2-containing vaccines.
    Results: Low titers of cross-neutralizing antibodies were detected in mice when immunized with L1/L2 VLPs, and the highest levels of cross-neutralizing antibodies were observed in mice immunized with HPV 58 L1/L2 pseudovirions encoding the HPV 31 L2 protein.
    Conclusions: The results obtained indicate that high levels of cross-neutralizing antibodies are only observed after immunization with pseudovirions encoding the L2 protein. HPV pseudovirions thus represent a possible new strategy for the generation of a broad-spectrum vaccine to protect against high-risk HPVs and associated neoplasia.
    MeSH term(s) Animals ; Antibodies, Neutralizing/immunology ; Antigens, Viral/immunology ; Capsid Proteins/immunology ; Female ; Humans ; Mice ; Mice, Inbred BALB C ; Oncogene Proteins, Viral/immunology ; Papillomaviridae/immunology ; Papillomaviridae/ultrastructure ; Papillomavirus Infections/immunology ; Papillomavirus Infections/virology ; Viral Vaccines/immunology ; Virion/immunology ; Virion/ultrastructure
    Chemical Substances Antibodies, Neutralizing ; Antigens, Viral ; Capsid Proteins ; Oncogene Proteins, Viral ; Viral Vaccines
    Language English
    Publishing date 2010-03-24
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1479-5876
    ISSN (online) 1479-5876
    DOI 10.1186/1479-5876-8-28
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: The Golgi protein ACBD3, an interactor for poliovirus protein 3A, modulates poliovirus replication.

    Téoulé, François / Brisac, Cynthia / Pelletier, Isabelle / Vidalain, Pierre-Olivier / Jégouic, Sophie / Mirabelli, Carmen / Bessaud, Maël / Combelas, Nicolas / Autret, Arnaud / Tangy, Frédéric / Delpeyroux, Francis / Blondel, Bruno

    Journal of virology

    2013  Volume 87, Issue 20, Page(s) 11031–11046

    Abstract: We have shown that the circulating vaccine-derived polioviruses responsible for poliomyelitis outbreaks in Madagascar have recombinant genomes composed of sequences encoding capsid proteins derived from poliovaccine Sabin, mostly type 2 (PVS2), and ... ...

    Abstract We have shown that the circulating vaccine-derived polioviruses responsible for poliomyelitis outbreaks in Madagascar have recombinant genomes composed of sequences encoding capsid proteins derived from poliovaccine Sabin, mostly type 2 (PVS2), and sequences encoding nonstructural proteins derived from other human enteroviruses. Interestingly, almost all of these recombinant genomes encode a nonstructural 3A protein related to that of field coxsackievirus A17 (CV-A17) strains. Here, we investigated the repercussions of this exchange, by assessing the role of the 3A proteins of PVS2 and CV-A17 and their putative cellular partners in viral replication. We found that the Golgi protein acyl-coenzyme A binding domain-containing 3 (ACBD3), recently identified as an interactor for the 3A proteins of several picornaviruses, interacts with the 3A proteins of PVS2 and CV-A17 at viral RNA replication sites, in human neuroblastoma cells infected with either PVS2 or a PVS2 recombinant encoding a 3A protein from CV-A17 [PVS2-3A(CV-A17)]. The small interfering RNA-mediated downregulation of ACBD3 significantly increased the growth of both viruses, suggesting that ACBD3 slowed viral replication. This was confirmed with replicons. Furthermore, PVS2-3A(CV-A17) was more resistant to the replication-inhibiting effect of ACBD3 than the PVS2 strain, and the amino acid in position 12 of 3A was involved in modulating the sensitivity of viral replication to ACBD3. Overall, our results indicate that exchanges of nonstructural proteins can modify the relationships between enterovirus recombinants and cellular interactors and may thus be one of the factors favoring their emergence.
    MeSH term(s) Adaptor Proteins, Signal Transducing/metabolism ; Cell Line ; Host-Pathogen Interactions ; Humans ; Membrane Proteins/metabolism ; Neurons/virology ; Poliovirus/physiology ; Viral Core Proteins/metabolism ; Virus Replication
    Chemical Substances 3A protein, Poliovirus ; ACBD3 protein, human ; Adaptor Proteins, Signal Transducing ; Membrane Proteins ; Viral Core Proteins
    Language English
    Publishing date 2013-08-07
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80174-4
    ISSN 1098-5514 ; 0022-538X
    ISSN (online) 1098-5514
    ISSN 0022-538X
    DOI 10.1128/JVI.00304-13
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Papillomavirus pseudovirions packaged with the L2 gene induce cross-neutralizing antibodies

    Duarte-Forero Diego F / Gaitan Julien / Ribeiro Tatiana / Fleury Maxime JJ / Saussereau Emilie / Combelas Nicolas / Coursaget Pierre / Touzé Antoine

    Journal of Translational Medicine, Vol 8, Iss 1, p

    2010  Volume 28

    Abstract: Abstract Background Current vaccines against HPVs are constituted of L1 protein self-assembled into virus-like particles (VLPs) and they have been shown to protect against natural HPV16 and HPV18 infections and associated lesions. In addition, limited ... ...

    Abstract Abstract Background Current vaccines against HPVs are constituted of L1 protein self-assembled into virus-like particles (VLPs) and they have been shown to protect against natural HPV16 and HPV18 infections and associated lesions. In addition, limited cross-protection has been observed against closely related types. Immunization with L2 protein in animal models has been shown to provide cross-protection against distant papillomavirus types, suggesting that the L2 protein contains cross-neutralizing epitopes. However, vaccination with L2 protein or L2 peptides does not induce high titers of anti-L2 antibodies. In order to develop a vaccine with the potential to protect against other high-risk HPV types, we have produced HPV58 pseudovirions encoding the HPV31 L2 protein and compared their capacity to induce cross-neutralizing antibodies with that of HPV L1 and HPV L1/L2 VLPs. Methods The titers of neutralizing antibodies against HPV16, HPV18, HPV31 and HPV58 induced in Balb/c mice were compared after immunization with L2-containing vaccines. Results Low titers of cross-neutralizing antibodies were detected in mice when immunized with L1/L2 VLPs, and the highest levels of cross-neutralizing antibodies were observed in mice immunized with HPV 58 L1/L2 pseudovirions encoding the HPV 31 L2 protein. Conclusions The results obtained indicate that high levels of cross-neutralizing antibodies are only observed after immunization with pseudovirions encoding the L2 protein. HPV pseudovirions thus represent a possible new strategy for the generation of a broad-spectrum vaccine to protect against high-risk HPVs and associated neoplasia.
    Keywords Medicine ; R
    Subject code 616
    Language English
    Publishing date 2010-03-01T00:00:00Z
    Publisher BMC
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Identification of the neutralizing epitopes of Merkel cell polyomavirus major capsid protein within the BC and EF surface loops.

    Maxime J J Fleury / Jérôme T J Nicol / Mahtab Samimi / Françoise Arnold / Raphael Cazal / Raphaelle Ballaire / Olivier Mercey / Hélène Gonneville / Nicolas Combelas / Jean-Francois Vautherot / Thierry Moreau / Gérard Lorette / Pierre Coursaget / Antoine Touzé

    PLoS ONE, Vol 10, Iss 3, p e

    2015  Volume 0121751

    Abstract: Merkel cell polyomavirus (MCPyV) is the first polyomavirus clearly associated with a human cancer, i.e. the Merkel cell carcinoma (MCC). Polyomaviruses are small naked DNA viruses that induce a robust polyclonal antibody response against the major capsid ...

    Abstract Merkel cell polyomavirus (MCPyV) is the first polyomavirus clearly associated with a human cancer, i.e. the Merkel cell carcinoma (MCC). Polyomaviruses are small naked DNA viruses that induce a robust polyclonal antibody response against the major capsid protein (VP1). However, the polyomavirus VP1 capsid protein epitopes have not been identified to date. The aim of this study was to identify the neutralizing epitopes of the MCPyV capsid. For this goal, four VP1 mutants were generated by insertional mutagenesis in the BC, DE, EF and HI loops between amino acids 88-89, 150-151, 189-190, and 296-297, respectively. The reactivity of these mutants and wild-type VLPs was then investigated with anti-VP1 monoclonal antibodies and anti-MCPyV positive human sera. The findings together suggest that immunodominant conformational neutralizing epitopes are present at the surface of the MCPyV VLPs and are clustered within BC and EF loops.
    Keywords Medicine ; R ; Science ; Q
    Language English
    Publishing date 2015-01-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Generation of Merkel cell polyomavirus (MCV)-like particles and their application to detection of MCV antibodies.

    Touzé, Antoine / Gaitan, Julien / Arnold, Françoise / Cazal, Raphaël / Fleury, Maxime J / Combelas, Nicolas / Sizaret, Pierre-Yves / Guyetant, Serge / Maruani, Annabel / Baay, Marc / Tognon, Mauro / Coursaget, Pierre

    Journal of clinical microbiology

    2010  Volume 48, Issue 5, Page(s) 1767–1770

    Abstract: The genome of a new human polyomavirus, known as Merkel cell polyomavirus (MCV), has recently been reported to be integrated within the cellular DNA of Merkel cell carcinoma (MCC), a rare human skin cancer. To investigate MCV seroprevalence in the ... ...

    Abstract The genome of a new human polyomavirus, known as Merkel cell polyomavirus (MCV), has recently been reported to be integrated within the cellular DNA of Merkel cell carcinoma (MCC), a rare human skin cancer. To investigate MCV seroprevalence in the general population, we expressed three different MCV VP1 in insect cells using recombinant baculoviruses. Viruslike particles (VLPs) were obtained with only one of the three VP1 genes. High-titer antibodies against VP1 VLPs were detected in mice immunized with MCV VLPs, and limited cross-reactivity was observed with BK polyomavirus (BKV) and lymphotropic polyomavirus (LPV). MCV antibodies were detected in 77% of the general population, with no variations according to age.
    MeSH term(s) Adolescent ; Adult ; Aged ; Aged, 80 and over ; Animals ; Antibodies, Viral/blood ; Antigens, Viral/genetics ; Antigens, Viral/isolation & purification ; BK Virus/immunology ; Baculoviridae/genetics ; Carcinoma, Merkel Cell/virology ; Cell Line ; Cross Reactions ; Female ; Gene Expression ; Genetic Vectors ; Humans ; Insecta ; Male ; Merkel Cells/virology ; Mice ; Microscopy, Electron, Transmission ; Polyomavirus/genetics ; Polyomavirus/immunology ; Polyomavirus Infections/diagnosis ; Sensitivity and Specificity ; Virosomes/genetics ; Virosomes/isolation & purification ; Virosomes/ultrastructure ; Young Adult
    Chemical Substances Antibodies, Viral ; Antigens, Viral ; Virosomes
    Language English
    Publishing date 2010-02-24
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 390499-4
    ISSN 1098-660X ; 0095-1137
    ISSN (online) 1098-660X
    ISSN 0095-1137
    DOI 10.1128/JCM.01691-09
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Generation of Merkel Cell Polyomavirus (MCV)-Like Particles and Their Application to Detection of MCV Antibodies

    Touzé, Antoine / Gaitan, Julien / Arnold, Françoise / Cazal, Raphaël / Fleury, Maxime J / Combelas, Nicolas / Sizaret, Pierre-Yves / Guyetant, Serge / Maruani, Annabel / Baay, Marc / Tognon, Mauro / Coursaget, Pierre

    Journal of clinical microbiology JCM. 2010 May, v. 48, no. 5

    2010  

    Abstract: The genome of a new human polyomavirus, known as Merkel cell polyomavirus (MCV), has recently been reported to be integrated within the cellular DNA of Merkel cell carcinoma (MCC), a rare human skin cancer. To investigate MCV seroprevalence in the ... ...

    Abstract The genome of a new human polyomavirus, known as Merkel cell polyomavirus (MCV), has recently been reported to be integrated within the cellular DNA of Merkel cell carcinoma (MCC), a rare human skin cancer. To investigate MCV seroprevalence in the general population, we expressed three different MCV VP1 in insect cells using recombinant baculoviruses. Viruslike particles (VLPs) were obtained with only one of the three VP1 genes. High-titer antibodies against VP1 VLPs were detected in mice immunized with MCV VLPs, and limited cross-reactivity was observed with BK polyomavirus (BKV) and lymphotropic polyomavirus (LPV). MCV antibodies were detected in 77% of the general population, with no variations according to age.
    Language English
    Dates of publication 2010-05
    Size p. 1767-1770.
    Publishing place American Society for Microbiology
    Document type Article
    ZDB-ID 390499-4
    ISSN 1098-660X ; 0095-1137
    ISSN (online) 1098-660X
    ISSN 0095-1137
    Database NAL-Catalogue (AGRICOLA)

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  10. Article: Identification of the neutralizing epitopes of Merkel cell polyomavirus major capsid protein within the BC and EF surface loops

    Fleury, Maxime J J / Nicol, Jérôme T.J. / Samimi, Mahtab / Arnold, Françoise / Cazal, Raphael / Ballaire, Raphaelle / Mercey, Olivier / Gonneville, Hélène / Combelas, Nicolas / Vautherot, Jean-François / Moreau, Thierry / Lorette, Gérard / Coursaget, Pierre / Touzé, Antoine

    Plos One 3 (10), 1-13. (2015)

    Abstract: Merkel cell polyomavirus (MCPyV) is the first polyomavirus clearly associated with a human cancer, i.e. the Merkel cell carcinoma (MCC). Polyomaviruses are small naked DNA viruses that induce a robust polyclonal antibody response against the major capsid ...

    Abstract Merkel cell polyomavirus (MCPyV) is the first polyomavirus clearly associated with a human cancer, i.e. the Merkel cell carcinoma (MCC). Polyomaviruses are small naked DNA viruses that induce a robust polyclonal antibody response against the major capsid protein (VP1). However, the polyomavirus VP1 capsid protein epitopes have not been identified to date. The aim of this study was to identify the neutralizing epitopes of the MCPyV capsid. For this goal, four VP1 mutants were generated by insertional mutagenesis in the BC, DE, EF and HI loops between amino acids 88-89, 150-151, 189-190, and 296-297, respectively. The reactivity of these mutants and wild-type VLPs was then investigated with anti-VP1 monoclonal antibodies and anti-MCPyV positive human sera. The findings together suggest that immunodominant conformational neutralizing epitopes are present at the surface of the MCPyV VLPs and are clustered within BC and EF loops.
    Language English
    Document type Article
    Database AGRIS - International Information System for the Agricultural Sciences and Technology

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