Literature DB >> 19961705

Oropouche fever outbreak, Manaus, Brazil, 2007-2008.

Maria Paula G Mourãão, Michelle S Bastos, João Boscoe L Gimaqu, Bruno Rafaelle Mota, Giselle S Souza, Gustavo Henrique N Grimmer, Elizabeth S Galusso, Eurico Arruda, Luiz Tadeu M Figueiredo.   

Abstract

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Year:  2009        PMID: 19961705      PMCID: PMC3044544          DOI: 10.3201/eid1512.090917

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


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To the Editor: Oropouche virus (OROV) is an arbovirus, Orthobunyavirus, transmitted among sloths, marsupials, primates, and birds by the mosquitoes Aedes serratus and Culex quinquefasciatus. Notably, this virus has adapted to an urban cycle involving man, with midges (Culicoides paraensis) as the main vector (). Oropouche fever is the second most frequent arboviral disease in Brazil, surpassed only by dengue. OROV causes large, explosive outbreaks of acute febrile illness in cities and villages in the Amazon and central regions of Brazil. An estimated 500,000 cases of OROV infection have occurred in Brazil in the past 48 years. In addition to outbreaks, OROV can also cause sporadic human infections (). The Tropical Medicine Foundation of Amazonas State (TMF-AM) is a tertiary care center specializing in tropical and infectious diseases and is located in the city of Manaus. Syndromic surveillance for acute febrile illness has been conducted by TMF-AM since 1998. During January 2007 through November 2008, we obtained blood samples from 631 patients who had acute febrile illness for ≥5 days but who had negative results at initial screening for malaria (thick blood smear) and dengue (MAC-ELISA). Blood samples were tested for OROV immunoglobulin (Ig) M antibodies by an indirect enzyme immune assay using infected cells as antigen, as previously reported for dengue (). For the indirect enzyme immune assay using infected cells as antigen, C6/36 A. albopictus cells were grown in 96 well microplates; these cells were infected with OROV (BeAn 1991 strain). After 4 days, the cells were fixed in the wells with 7% formalin buffered at pH 7.0. The microplate was blocked with 5% skim milk and, after washing the wells, 100 µL of serum diluted 1:400 was added into infected and uninfected wells. After incubation and washing the wells, a peroxidase-conjugated goat anti-human IgM was added; finally, the ABTS substrate (KPL, Inc., Gaithersburg, MD, USA) was added into the wells. The plates were incubated and read on a spectrophotometer at 405 nm. The cutoff for the test was determined to be the mean of optical densities read in all wells containing uninfected cells plus 3 standard deviations. Of the 631 patients in the study, 128 (20.3%) had IgM antibodies to OROV. The age range was 2–81 years (mean 29.5 ± 14 years), and 77 (60.2%) were women or girls. Most of the cases occurred November through March during the rainy season. In addition to fever, the patients had headache (93 [72.7%]), myalgia (90 [70.3%]), and arthralgia (74 [57.8%]). Rash was observed in 54 patients (42.2%), and hemorrhagic phenomena (petechiae, epistaxis, and gingival bleeding) were observed in 20 patients (15.5%). All patients recovered without sequelae and were not hospitalized. Despite the knowledge of the occurrence of several arboviruses in the Amazon region, most cases of arboviral diseases remain undiagnosed, probably because of their generally mild and self-limited clinical manifestations. Patients usually recover completely after a couple of days. However, even more severe cases may remain undiagnosed, especially because of long distances to health care facilities, difficulties in sample transportation, and lack of laboratory facilities capable of conducting the diagnostic assays. With regard to OROV infections, diagnosis of OROV may be easily confused with other acute febrile illness, including malaria and dengue, both of which are highly endemic in Manaus. In the present study, an inhouse enzyme immune assay for IgM using infected cell culture as antigen was found suitable for the diagnosis of OROV infections in the acute phase. Thus, a combination of a systematic surveillance for acute febrile illnesses and efficient laboratory diagnosis for OROV resulted in the discovery of an outbreak, which would probably have been overlooked if it had occurred in any region simultaneously with large dengue outbreaks or in the absence of laboratory diagnosis. The cases of OROV fever reported here likely represent a small portion of the cases; a much higher number of cases probably occurred in Manaus during the study period. The clinical characteristics of most cases of OROV fever in this outbreak were similar to previously reported descriptions of the illness. Notably, however, 20 (15.5%) patients from Manaus had spontaneous hemorrhagic phenomena (petecchiae, epistaxis, and gingival bleeding) that had not previously been described in OROV fever (–). Moreover, symptoms of involvement of the central nervous system were not observed. In recent years, the area of circulation and the epidemic potential of OROV have increased, and this virus has emerged as a public health problem in Brazil and other countries in the Americas. Presently, OROV is the most common of the Brazilian zoonotic arboviruses infecting humans (). Further evidence of the spread of OROV was its isolation in 2003 from a small primate, a marmoset (Callithrix), in the state of Minas Gerais in southeast Brazil, far from the Amazon region (). Considering that midges (Culicoides paraensis) occur in most low altitude areas of the Americas, it is conceivable that environmental destruction and climate changes could result in OROV outbreaks in the large cities of Brazil, as well as in other parts of the Western Hemisphere ().
  9 in total

1.  Emergent arboviruses in Brazil.

Authors:  Luiz Tadeu Moraes Figueiredo
Journal:  Rev Soc Bras Med Trop       Date:  2007 Mar-Apr       Impact factor: 1.581

2.  Oropouche virus. I. A review of clinical, epidemiological, and ecological findings.

Authors:  F P Pinheiro; A P Travassos da Rosa; J F Travassos da Rosa; R Ishak; R B Freitas; M L Gomes; J W LeDuc; O F Oliva
Journal:  Am J Trop Med Hyg       Date:  1981-01       Impact factor: 2.345

3.  Venezuelan equine encephalitis and Oropouche virus infections among Peruvian army troops in the Amazon region of Peru.

Authors:  D M Watts; V Lavera; J Callahan; C Rossi; M S Oberste; J T Roehrig; C B Cropp; N Karabatsos; J F Smith; D J Gubler; M T Wooster; W M Nelson; C G Hayes
Journal:  Am J Trop Med Hyg       Date:  1997-06       Impact factor: 2.345

4.  An enzyme immunoassay for dengue antibody using infected cultured mosquito cells as antigen.

Authors:  L T Figueiredo; R E Shope
Journal:  J Virol Methods       Date:  1987-09       Impact factor: 2.014

5.  Oropouche virus. IV. Laboratory transmission by Culicoides paraensis.

Authors:  F P Pinheiro; A L Hoch; M L Gomes; D R Roberts
Journal:  Am J Trop Med Hyg       Date:  1981-01       Impact factor: 2.345

6.  Oropouche fever epidemic in Northern Brazil: epidemiology and molecular characterization of isolates.

Authors:  Helena B Vasconcelos; Raimunda S S Azevedo; Samir M Casseb; Joaquim P Nunes-Neto; Jannifer O Chiang; Patrick C Cantuária; Maria N O Segura; Lívia C Martins; Hamilton A O Monteiro; Sueli G Rodrigues; Márcio R T Nunes; Pedro F C Vasconcelos
Journal:  J Clin Virol       Date:  2008-12-30       Impact factor: 3.168

7.  Two new Culicoides of the paraensis species group (Diptera: Ceratopogonidae) from the Amazonian region of Peru.

Authors:  Maria Luiza Felippe-Bauer; Abraham G Cáceres; Cristiane S Silva; William Valderrama-Bazan; Antero Gonzales-Perez
Journal:  Mem Inst Oswaldo Cruz       Date:  2004-03-09       Impact factor: 2.743

8.  Oropouche virus isolation, southeast Brazil.

Authors:  Márcio Roberto Teixeira Nunes; Lívia Carício Martins; Sueli Guerreiro Rodrigues; Jannifer Oliveira Chiang; Raimunda do Socorro da Silva Azevedo; Amelia P A Travassos da Rosa; Pedro Fernando da Costa Vasconcelos
Journal:  Emerg Infect Dis       Date:  2005-10       Impact factor: 6.883

9.  Sporadic oropouche virus infection, acre, Brazil.

Authors:  Ana Carolina Bernardes-Terzian; Roberta Vieira de-Moraes-Bronzoni; Betânia Paiva Drumond; Mônica Da Silva-Nunes; Natal Santos da-Silva; Marcelo Urbano-Ferreira; Márcia Aparecida Sperança; Maurício Lacerda Nogueira
Journal:  Emerg Infect Dis       Date:  2009-02       Impact factor: 6.883

  9 in total
  24 in total

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Authors:  Scott C Weaver; Caroline Charlier; Nikos Vasilakis; Marc Lecuit
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2.  Mayaro fever in the city of Manaus, Brazil, 2007-2008.

Authors:  Maria Paula Gomes Mourão; Michele de Souza Bastos; Regina Pinto de Figueiredo; João Bosco Lima Gimaque; Elizabeth dos Santos Galusso; Valéria Munique Kramer; Cintia Mara Costa de Oliveira; Felipe Gomes Naveca; Luiz Tadeu Moraes Figueiredo
Journal:  Vector Borne Zoonotic Dis       Date:  2011-09-16       Impact factor: 2.133

3.  Generation of Recombinant Oropouche Viruses Lacking the Nonstructural Protein NSm or NSs.

Authors:  Natasha L Tilston-Lunel; Gustavo Olszanski Acrani; Richard E Randall; Richard M Elliott
Journal:  J Virol       Date:  2015-12-23       Impact factor: 5.103

4.  Oropouche virus infection and pathogenesis are restricted by MAVS, IRF-3, IRF-7, and type I interferon signaling pathways in nonmyeloid cells.

Authors:  Jose Luiz Proenca-Modena; Renata Sesti-Costa; Amelia K Pinto; Justin M Richner; Helen M Lazear; Tiffany Lucas; Jennifer L Hyde; Michael S Diamond
Journal:  J Virol       Date:  2015-02-25       Impact factor: 5.103

5.  Identification of Oropouche Orthobunyavirus in the cerebrospinal fluid of three patients in the Amazonas, Brazil.

Authors:  Michele de Souza Bastos; Luiz Tadeu Moraes Figueiredo; Felipe Gomes Naveca; Rossicleia Lins Monte; Natália Lessa; Regina Maria Pinto de Figueiredo; João Bosco de Lima Gimaque; Guilherme Pivoto João; Rajendranath Ramasawmy; Maria Paula Gomes Mourão
Journal:  Am J Trop Med Hyg       Date:  2012-04       Impact factor: 2.345

Review 6.  Presence and Multi-Species Spatial Distribution of Oropouche Virus in Brazil within the One Health Framework.

Authors:  Sofia Sciancalepore; Maria Cristina Schneider; Jisoo Kim; Deise I Galan; Ana Riviere-Cinnamond
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7.  Evaluation of Aedes aegypti, Aedes albopictus, and Culex quinquefasciatus Mosquitoes Competence to Oropouche virus Infection.

Authors:  Silvana F de Mendonça; Marcele N Rocha; Flávia V Ferreira; Thiago H J F Leite; Siad C G Amadou; Pedro H F Sucupira; João T Marques; Alvaro G A Ferreira; Luciano A Moreira
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8.  Iquitos virus: a novel reassortant Orthobunyavirus associated with human illness in Peru.

Authors:  Patricia V Aguilar; Alan D Barrett; Mohammad F Saeed; Douglas M Watts; Kevin Russell; Carolina Guevara; Julia S Ampuero; Luis Suarez; Manuel Cespedes; Joel M Montgomery; Eric S Halsey; Tadeusz J Kochel
Journal:  PLoS Negl Trop Dis       Date:  2011-09-20

Review 9.  Apoptosis, autophagy and unfolded protein response pathways in Arbovirus replication and pathogenesis.

Authors:  Mahmoud Iranpour; Adel Rezaei Moghadam; Mina Yazdi; Sudharsana R Ande; Javad Alizadeh; Emilia Wiechec; Robbin Lindsay; Michael Drebot; Kevin M Coombs; Saeid Ghavami
Journal:  Expert Rev Mol Med       Date:  2016-01-19       Impact factor: 5.600

10.  The salivary secretome of the biting midge, Culicoides sonorensis.

Authors:  Christopher J Lehiy; Barbara S Drolet
Journal:  PeerJ       Date:  2014-06-05       Impact factor: 2.984

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