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Featured researches published by Iray Maria Rocco.


The Lancet | 2001

Serious adverse events associated with yellow fever 17DD vaccine in Brazil: a report of two cases.

Pedro Fc Vasconcelos; Expedito Jose de Albuquerque Luna; Ricardo Galler; Luiz J. da Silva; Terezinha Lisieux Moraes Coimbra; Vera Lrs Barros; Thomas P. Monath; Sueli G Rodigues; Cristina Laval; Zouraide G Costa; Maria Fg Vilela; Cecília Ls Santos; Cristina Mo Papaiordanou; Venancio Af Alves; Liliana D Andrade; Helena Keico Sato; Elisabeth St Rosa; Gustavo B Froguas; Ethel Lacava; Leda Mr Almeida; Ana Cr Cruz; Iray Maria Rocco; Raimunda Tm Santos; Otavio Oliva; Brazilian Yellow

BACKGROUND The yellow fever vaccine is regarded as one of the safest attenuated virus vaccines, with few side-effects or adverse events. We report the occurrence of two fatal cases of haemorrhagic fever associated with yellow fever 17DD substrain vaccine in Brazil. METHODS We obtained epidemiological, serological, virological, pathological, immunocytochemical, and molecular biological data on the two cases to determine the cause of the illnesses. FINDINGS The first case, in a 5-year-old white girl, was characterised by sudden onset of fever accompanied by headache, malaise, and vomiting 3 days after receiving yellow fever and measles-mumps-rubella vaccines. Afterwards she decompensated with icterus and haemorrhagic signs and died after a 5-day illness. The second patient-a 22-year-old black woman-developed a sore throat and fever accompanied by headache, myalgia, nausea, and vomiting 4 days after yellow fever vaccination. She then developed icterus, renal failure, and haemorrhagic diathesis, and died after 6 days of illness. Yellow fever virus was recovered in suckling mice and C6/36 cells from blood in both cases, as well as from fragments of liver, spleen, skin, and heart from the first case and from these and other viscera fragments in case 2. RNA of yellow fever virus was identical to that previously described for 17D genomic sequences. IgM ELISA tests for yellow fever virus were negative in case 1 and positive in case 2; similar tests for dengue, hantaviruses, arenaviruses, Leptospira, and hepatitis viruses A-D were negative. Tissue injuries from both patients were typical of wild-type yellow fever. INTERPRETATION These serious and hitherto unknown complications of yellow fever vaccination are extremely rare, but the safety of yellow fever 17DD vaccine needs to be reviewed. Host factors, probably idiosyncratic reactions, might have had a substantial contributed to the unexpected outcome.


The Lancet | 1994

New arenavirus isolated in Brazil

Terezinha Lisieux Moraes Coimbra; Elza da Silva Nassar; L. T M de Souza; Ivani Bisordi Ferreira; Iray Maria Rocco; M. N. Burattini; A. P A Travassos da Rosa; Pedro Fernando da Costa Vasconcelos; F. P. Pinheiro; J. W. LeDuc; Rebeca Rico-Hesse; Jean-Paul Gonzalez; Robert B. Tesh; Peter B. Jahrling

A new arenavirus, called Sabiá, was isolated in Brazil from a fatal case of haemorrhagic fever initially thought to be yellow fever. Antigenic and molecular characterisation indicated that Sabiá virus is a new member of the Tacaribe complex. A laboratory technician working with the agent was also infected and developed a prolonged, non-fatal influenza-like illness. Sabiá virus is yet another arenavirus causing human disease in South America.


Transfusion | 2016

Probable transfusion-transmitted Zika virus in Brazil

Maria Lourdes Barjas-Castro; Rodrigo Nogueira Angerami; Mariana Sequetin Cunha; Akemi Suzuki; Juliana S. Nogueira; Iray Maria Rocco; Adriana Yurika Maeda; Fernanda G.S. Vasami; Gizelda Katz; I.F.S.F. Boin; R.S.B. Stucchi; Mariângela Ribeiro Resende; Danillo Lucas Alves Espósito; Renato Pereira de Souza; Benedito A. da Fonseca; Marcelo Addas-Carvalho

Zika virus (ZIKV) is an emerging arthropod‐borne flavivirus transmitted by Aedes mosquitoes. Recent commentaries regarding ZIKV routes of transmission describe a potential transmission by transfusion. Herein, we report a probable case of transfusion‐transmitted ZIKV infection through a platelet transfusion that was detected from postdonation information.


Antiviral Research | 2003

In vitro and in vivo antiviral properties of sulfated galactomannans against yellow fever virus (BeH111 strain) and dengue 1 virus (Hawaii strain).

Lucy Ono; Wagner Wollinger; Iray Maria Rocco; Terezinha Lisieux Moraes Coimbra; Philip A.J. Gorin; Maria-Rita Sierakowski

Two galactomannans, one extracted from seeds of Mimosa scabrella, having a mannose to galactose ratio of 1.1, and another with a 1.4 ratio from seeds of Leucaena leucocephala, were sulfated. The products from M. scabrella (BRS) and L. leucocephala (LLS) had a degree of sulfation of 0.62 and 0.50, and an average molecular weight of 620x10(3) and 574x10(3) gmol(-1), respectively. Their activities against yellow fever virus (YFV; BeH111 strain) and dengue 1 virus (DEN-1; Hawaii strain) were evaluated. This was carried out in young mice following intraperitoneal infection with YFV. At a dose of 49 mgkg(-1), BRS and LLS gave protection against death in 87.7 and 96.5% of the mice, respectively. When challenged with 37.5 LD50 of YFV, mice previously inoculated with BRS+virus or LLS+virus, showed 93.3 and 100% resistance, respectively, with neutralization titers similar to mice injected with 25 LD50 of formaldehyde-inactivated YFV. In vitro experiments with YFV and DEN-1 in C6/36 cell culture assays in 24-well microplates showed that concentrations that produced a 100-fold decrease in virus titer of YFV were 586 and 385 mgl(-1) for BRS and LLS, respectively. For DEN-1 they were 347 and 37 mgl(-1), respectively. Sulfated galactomannans, thus demonstrate in vitro and in vivo activity against flaviviruses.


Revista Do Instituto De Medicina Tropical De Sao Paulo | 2005

St. Louis encephalitis vírus: first isolation from a human in São Paulo state, Brasil

Iray Maria Rocco; Cecília Luiza Simões Santos; Ivani Bisordi; Selma Petrella; Luiz Eloy Pereira; Renato Pereira de Souza; Terezinha Lisieux Moraes Coimbra; Thirsa Álvares Franco Bessa; Fabíola Maiumi Oshiro; Luciana B.Q. Lima; Matheus de Paula Cerroni; Antonia T. Marti; Vera M. Barbosa; Gizelda Katz; Akemi Suzuki

This paper reports the isolation of St. Louis encephalitis virus (SLEV) from a febrile human case suspected to be dengue, in Sao Pedro, Sao Paulo State. A MAC-ELISA done on the patients acute and convalescent sera was inconclusive and hemagglutination inhibition test detected IgG antibody for flaviviruses. An indirect immunofluorescent assay done on the C6/36 cell culture inoculated with the acute serum was positive for flaviviruses but negative when tested with dengue monoclonal antibodies. RNA extracted from the infected cell culture supernatant was amplified by RT-PCR in the presence of NS5 universal flavivirus primers and directly sequenced. Results of BLAST search indicated that this sequence shares 93% nucleotide similarity with the sequence of SLEV (strain-MSI.7), confirmed by RT-PCR performed with SLEV specific primers. Since SLEV was identified as the cause of human disease, it is necessary to improve surveillance in order to achieve early detection of this agent in the state of Sao Paulo and in Brazil. This finding is also an alert to health professionals about the need for more complete clinical and epidemiological investigations of febrile illnesses as in the reported case. SLEV infections can be unrecognized or confused with other ones caused by an arbovirus, such as dengue.


Journal of Medical Virology | 2010

Detection of a new yellow fever virus lineage within the South American genotype I in Brazil.

Renato Pereira de Souza; Peter G. Foster; Maria Anice Mureb Sallum; Terezinha Lisieux Moraes Coimbra; Adriana Yurika Maeda; Vivian Regina Silveira; Eduardo Stramandinoli Moreno; Fernanda Giselle da Silva; Iray Maria Rocco; Ivani Bisordi Ferreira; Akemi Suzuki; Fabíola M. Oshiro; Selma Petrella; Luiz Eloy Pereira; Giselda Katz; Ciléa H Tengan; Melissa Mascheratti Siciliano; Cecília L.S. dos Santos

Nucleotide sequences of two regions of the genomes of 11 yellow fever virus (YFV) samples isolated from monkeys or humans with symptomatic yellow fever (YF) in Brazil in 2000, 2004, and 2008 were determined with the objective of establishing the genotypes and studying the genetic variation. Results of the Bayesian phylogenetic analysis showed that sequences generated from strains from 2004 and 2008 formed a new subclade within the clade 1 of the South American genotype I. The new subgroup is here designated as 1E. Sequences of YFV strains recovered in 2000 belong to the subclade 1D, which comprises previously characterized YFV strains from Brazil. Molecular dating analyses suggested that the new subclade 1E started diversifying from 1D about 1975 and that the most recent 2004–2008 isolates arose about 1985. J. Med. Virol. 82:175–185, 2010.


PLOS Neglected Tropical Diseases | 2011

Dengue Virus Type 4 Phylogenetics in Brazil 2011: Looking beyond the Veil

Renato Pereira de Souza; Iray Maria Rocco; Adriana Yurika Maeda; Carine Spenassatto; Ivani Bisordi; Akemi Suzuki; Vivian Regina Silveira; Sarai Joaquim dos Santos Silva; Roberta M. Azevedo; Fernanda Modesto Tolentino; Jaqueline C. Assis; Margarida Georgina Bassi; Bibiana Paula Dambros; Gabriela Luchiari Tumioto; Tatiana Schäffer Gregianini; Luiza Terezinha Madia de Souza; Maria do Carmo Sampaio Tavares Timenetsky; Cecília Luiza Simões Santos

Dengue Fever and Dengue Hemorrhagic Fever are diseases affecting approximately 100 million people/year and are a major concern in developing countries. In the present study, the phylogenetic relationship of six strains of the first autochthonous cases of DENV-4 infection occurred in Sao Paulo State, Parana State and Rio Grande do Sul State, Brazil, 2011 were studied. Nucleotide sequences of the envelope gene were determined and compared with sequences representative of the genotypes I, II, III and Sylvatic for DEN4 retrieved from GenBank. We employed a Bayesian phylogenetic approach to reconstruct the phylogenetic relationships of Brazilian DENV-4 and we estimated evolutionary rates and dates of divergence for DENV-4 found in Brazil in 2011. All samples sequenced in this study were located in Genotype II. The studied strains are monophyletic and our data suggest that they have been evolving separately for at least 4 to 6 years. Our data suggest that the virus might have been present in the region for some time, without being noticed by Health Surveillance Services due to a low level of circulation and a higher prevalence of DENV-1 and DENV- 2.


Revista Do Instituto De Medicina Tropical De Sao Paulo | 2001

First isolation of dengue 3 in Brazil from an imported case

Iray Maria Rocco; Berenice Bustamanti Kavakama; Cecília Luiza Simões Santos

The authors report the isolation of dengue 3 virus for the first time in Brazil. The patient, resident in Limeira-SP, traveled to Nicaragua on May 16th, 1998, where he stayed for two months. Starting on August 14 th he had fever, headache, myalgia, arthralgia, retro-orbital pain and diarrhea. He returned to Brazil on August 16th and was hospitalized in the next day. The patient had full recovery and was discharged on August 20th. The virus was isolated in C6/36 cell culture inoculated with serum collected on the 6th day after the onset of the symptoms. The serotype 3 was identified by indirect immunofluorescence assays performed with type-specific monoclonal antibodies. This serotype was further confirmed by polymerase chain reaction analysis. The introduction of a new dengue serotype in a susceptible population is a real threat for the occurrence of severe forms of the disease. The isolation and identification of dengue virus are important in order to monitoring the serotypes circulating in Brazil and to take the measures necessary to prevent and control an epidemic.


Revista Do Instituto De Medicina Tropical De Sao Paulo | 1994

Surveillance of arbovirus infections in the atlantic forest region, State of São Paulo, Brazil: I. detection of hemagglutination-inhibition antibodies in wild birds between 1978 and 1990

Ivani Bisordi Ferreira; Luiz Eloy Pereira; Iray Maria Rocco; Antonia T. Marti; Luiza Terezinha Madia de Souza; Lygia Busch Iversson

We report data related to arbovirus antibodies detected in wild birds periodically captured from January 1978 to December 1990 in the counties of Salesópolis (Casa Grande Station), Itapetininga and Ribeira Valley, considering the different capture environments. Plasmas were examined using hemagglutination-inhibition (HI) tests. Only monotypic reactions were considered, except for two heterotypic reactions in which a significant difference in titer was observed for a determined virus of the same antigenic group. Among a total of 39,911 birds, 269 birds (0.7%) belonging to 66 species and 22 families were found to have a monotypic reaction for Eastern equine encephalitis (EEE), Venezuelan equine encephalitis (VEE), Western equine encephalitis (WEE), Ilheus (ILH), Rocio (ROC), St. Louis encephalitis (SLE), SP An 71686, or Caraparu (CAR) viruses. Analysis of the data provided information of epidemiologic interest with respect to these agents. Birds with positive serology were distributed among different habitats, with a predominance of unforested habitats. The greatest diversity of positive reactions was observed among species which concentrate in culture fields.


Revista Do Instituto De Medicina Tropical De Sao Paulo | 2007

Mayaro virus: imported cases of human infection in São Paulo State, Brazil

Terezinha Lisieux Moraes Coimbra; Cecília Luiza Simões Santos; Akemi Suzuki; Selma Petrella; Ivani Bisordi; Adélia Hiroko Nagamori; Antonia T. Marti; Raimundo N. Santos; Danya M. Fialho; Shirlene Lavigne; Marcia R. Buzzar; Iray Maria Rocco

Mayaro virus (MAYV) is an arbovirus (Togaviridae: Alphavirus) enzootic in tropical South America and maintained in a sylvan cycle involving wild vertebrates and Haemagogus mosquitoes. MAYV cases occur sporadically in persons with a history of recent activities inside or around forests. This paper reports three cases of MAYV fever detected in men infected in Camapuã, MS, Brazil. Serum samples collected at four days and two months after the onset of the symptoms and examined by hemagglutination inhibition test, revealed monotypic seroconversion to MAYV. Isolation of the virus was obtained from one of the samples by inoculation of the first blood samples into newborn mice. A suspension of the infected mouse brain was inoculated into C6/36 cells culture and the virus was identified by indirect immunofluorescent assay with alphavirus polyclonal antibodies. RT-PCR, performed with RNA extracted from the supernatant of C6/36 infected cells in the presence of alphavirus generic primers as well as specific MAYV primers, confirmed these results. The reported cases illustrate the importance of laboratory confirmation in establishing a correct diagnosis. Clinical symptoms are not always indicative of a disease caused by an arbovirus. Also MAYV causes febrile illness, which may be mistaken for dengue.

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