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1.
Nat Commun ; 11(1): 2842, 2020 06 05.
Article in English | MEDLINE | ID: mdl-32503971

ABSTRACT

Characterizing the circulation of Mayaro virus (MAYV), an emerging arbovirus threat, is essential for risk assessment but challenging due to cross-reactivity with other alphaviruses such as chikungunya virus (CHIKV). Here, we develop an analytical framework to jointly assess MAYV epidemiology and the extent of cross-reactivity with CHIKV from serological data collected throughout French Guiana (N = 2697). We find strong evidence of an important sylvatic cycle for MAYV with most infections occurring near the natural reservoir in rural areas and in individuals more likely to go to the forest (i.e., adult males) and with seroprevalences of up to 18% in some areas. These findings highlight the need to strengthen MAYV surveillance in the region and showcase how modeling can improve interpretation of cross-reacting assays.


Subject(s)
Alphavirus Infections/epidemiology , Arboviruses/isolation & purification , Chikungunya virus/immunology , Communicable Diseases, Emerging/epidemiology , Epidemiological Monitoring , Adolescent , Adult , Alphavirus Infections/blood , Alphavirus Infections/immunology , Alphavirus Infections/virology , Antibodies, Viral/blood , Antibodies, Viral/immunology , Arboviruses/immunology , Child , Child, Preschool , Communicable Diseases, Emerging/blood , Communicable Diseases, Emerging/immunology , Communicable Diseases, Emerging/virology , Cross Reactions/immunology , Cross-Sectional Studies , Female , French Guiana/epidemiology , Humans , Immunoglobulin G/blood , Immunoglobulin G/immunology , Infant , Male , Middle Aged , Rural Health/statistics & numerical data , Seroepidemiologic Studies , Young Adult
2.
Am J Trop Med Hyg ; 102(4): 880-883, 2020 04.
Article in English | MEDLINE | ID: mdl-32043455

ABSTRACT

Zika virus (ZIKV) caused a public health threat in the United States in 2016, leading to rapid development and implementation of blood screening assays for ZIKV RNA. Several ZIKV sequences from clinical cases have been reported, but none from asymptomatic/pre-symptomatic infections. We isolated and sequenced ZIKV from asymptomatic/pre-symptomatic blood donor (ABD-ZIKV) samples and compared with reported clinical sequences. Twelve ABD-ZIKV isolates were produced from 67 cultivated samples, and isolates were genetically similar among themselves. Most isolates shared mutations with the clinical isolate PRVABC59 2015, whereas two ABD-ZIKV isolates shared specific mutations with U.S. clinical isolates from 2016. The ABD-ZIKV strains clustered into two distinct subclades: one comprised mostly ABD-ZIKV from Puerto Rico, and another one comprised ABD-ZIKV from Florida and QTX-02 isolate (Puerto Rico). In this study, we showed the circulation of two slightly distinct virus strains among Puerto Rico blood donors, one of which was also reported in Florida.


Subject(s)
Blood Donors , Phylogeny , Zika Virus Infection/blood , Zika Virus/genetics , Zika Virus/isolation & purification , Adult , Communicable Diseases, Emerging/blood , Communicable Diseases, Emerging/epidemiology , Florida/epidemiology , Genomics , Humans , Puerto Rico/epidemiology , Zika Virus Infection/diagnosis , Zika Virus Infection/epidemiology
3.
Rev. argent. transfus ; 40(1): 19-32, 2014. tab
Article in Spanish | BINACIS | ID: bin-131224

ABSTRACT

Las infecciones emergentes juegan un papel importantísimo en medicina transfusional. La experiencia con HIV puso en evidencia la necesidad de actuar rápidamente. La lentitud en la respuesta de los Bancos de Sangre y la falta de un liderazgo en la adopción de medidas preventivas dieron lugar a una transmisión importante por vía transfusional. En cuanto a las hepatitis postransfusionales NANB, aprendimos las lecciones acerca de las pruebas subrogantes. Sin embargo, la respuesta para prevenir la transmisión de HCV fue lenta porque la comunidad científica estaba focalizada en la transmisión de HIV. En el caso del XMRV, la presión ejercida por la comunidad fue muy importante. Se formaron grupos multidisciplinarios de expertos que realizaron gran cantidad de estudios y la respuesta ocurrió rápidamente, aunque al poco tiempo se demostró que este patógeno no era relevante para la Medicina Transfusional. Con respecto al WNV, la familiaridad con los modelos desarrollados por el CDC para estimar los riesgos y las lecciones aprendidas por las experiencias con HIV y HCV facilitaron una respuesta rápida y se implementaron medidas rápidamente para minimizar el riesgo de transmisión por vía transfusional. Se abrió un nuevo paradigma: la importancia de considerar los riesgos de transfusión que pueden derivar de agentes que causan viremias breves, usualmente asintomáticas, pero con el potencial de generar brotes estacionales de alta incidencia. La respuesta a la amenaza con WNV fue rápida, apropiada y exitosa. Las nuevas herramientas de biología molecular han permitido el aislamiento de numerosos gérmenes emergentes y lo seguirán haciendo en el futuro. Estar alertas ante nuevos patógenos de potencial importancia es nuestra responsabilidad. (AU)


Emerging infections play an extremely important role in transfusion medicine. Experience with HIV highlighted the necessity to act quickly. The slow Blood Banks response and the lack of leadership in the adoption of preventive measures resulted in a significant transfusional transmission. Regarding the post-transfusion NANB hepatitis, we have learned the lessons about the surrogate tests. However, the response to prevent HCV transmission was slow given that the scientific community was focused on HIV transmission. In the case of XMRV, pressure from the community was extremely important. Multidisciplinary groups of experts who conducted many studies were formed and the answer came quickly, but soon it was proved that this pathogen was not relevant to Transfusion Medicine. With respect to WNV, familiarity with the models developed by the CDC to estimate the risks and lessons learned from experiences with HIV and HCV facilitated a quick response, and measures were quickly implemented to minimize the risk of transmission by transfusion. A new paradigm came up: the importance of con¡sidering the risks of transfusion that may result from agents that cause brief, usually asymptomatic viremia, but with the potential to generate high incidence seasonal outbreaks of viralloads. The response to the threat with WNV was rapid, appropriate and successful. The new tools of molecular biology have allowed the isolation of many emerging germs and will continue to do so in the future. Being alert to new pathogens of potential importance is our responsibility. (AU)


Subject(s)
Blood Safety , Communicable Diseases, Emerging/blood , Transfusion Medicine , Infection Control/methods , HIV Infections , Hepatitis C , Gammaretrovirus , Arboviruses , West Nile virus , Dengue Virus , Chikungunya virus , Yellow Fever , Public Health
4.
Rev. argent. transfus ; 40(1): 19-32, 2014. tab
Article in Spanish | LILACS | ID: lil-740615

ABSTRACT

Las infecciones emergentes juegan un papel importantísimo en medicina transfusional. La experiencia con HIV puso en evidencia la necesidad de actuar rápidamente. La lentitud en la respuesta de los Bancos de Sangre y la falta de un liderazgo en la adopción de medidas preventivas dieron lugar a una transmisión importante por vía transfusional. En cuanto a las hepatitis postransfusionales NANB, aprendimos las lecciones acerca de las pruebas subrogantes. Sin embargo, la respuesta para prevenir la transmisión de HCV fue lenta porque la comunidad científica estaba focalizada en la transmisión de HIV. En el caso del XMRV, la presión ejercida por la comunidad fue muy importante. Se formaron grupos multidisciplinarios de expertos que realizaron gran cantidad de estudios y la respuesta ocurrió rápidamente, aunque al poco tiempo se demostró que este patógeno no era relevante para la Medicina Transfusional. Con respecto al WNV, la familiaridad con los modelos desarrollados por el CDC para estimar los riesgos y las lecciones aprendidas por las experiencias con HIV y HCV facilitaron una respuesta rápida y se implementaron medidas rápidamente para minimizar el riesgo de transmisión por vía transfusional. Se abrió un nuevo paradigma: la importancia de considerar los riesgos de transfusión que pueden derivar de agentes que causan viremias breves, usualmente asintomáticas, pero con el potencial de generar brotes estacionales de alta incidencia. La respuesta a la amenaza con WNV fue rápida, apropiada y exitosa. Las nuevas herramientas de biología molecular han permitido el aislamiento de numerosos gérmenes emergentes y lo seguirán haciendo en el futuro. Estar alertas ante nuevos patógenos de potencial importancia es nuestra responsabilidad.


Emerging infections play an extremely important role in transfusion medicine. Experience with HIV highlighted the necessity to act quickly. The slow Blood Banks response and the lack of leadership in the adoption of preventive measures resulted in a significant transfusional transmission. Regarding the post-transfusion NANB hepatitis, we have learned the lessons about the surrogate tests. However, the response to prevent HCV transmission was slow given that the scientific community was focused on HIV transmission. In the case of XMRV, pressure from the community was extremely important. Multidisciplinary groups of experts who conducted many studies were formed and the answer came quickly, but soon it was proved that this pathogen was not relevant to Transfusion Medicine. With respect to WNV, familiarity with the models developed by the CDC to estimate the risks and lessons learned from experiences with HIV and HCV facilitated a quick response, and measures were quickly implemented to minimize the risk of transmission by transfusion. A new paradigm came up: the importance of con­sidering the risks of transfusion that may result from agents that cause brief, usually asymptomatic viremia, but with the potential to generate high incidence seasonal outbreaks of viralloads. The response to the threat with WNV was rapid, appropriate and successful. The new tools of molecular biology have allowed the isolation of many emerging germs and will continue to do so in the future. Being alert to new pathogens of potential importance is our responsibility.


Subject(s)
Infection Control/methods , Communicable Diseases, Emerging/blood , Transfusion Medicine , Blood Safety , Arboviruses , Yellow Fever , Gammaretrovirus , Hepatitis C , HIV Infections , Public Health , Chikungunya virus , Dengue Virus , West Nile virus
5.
Transfusion ; 46(1): 111-7, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16398739

ABSTRACT

BACKGROUND: West Nile virus (WNV) is the etiologic agent of an emerging disease in the Western Hemisphere that can be transmitted to humans by blood transfusion. WNV first appeared in the United States in 1999, in Canada in 2001, and in Mexico in 2002. The aim of this nationwide study was to determine the prevalence of WNV in blood donors in Mexico as a first step in preventing its transfusion-associated transmission. STUDY DESIGN AND METHODS: In July and August 2004, a total of 3856 fresh plasma specimens collected from each state's center for blood transfusion in 29 of 31 Mexican states were screened with an investigational WNV assay (Procleix,(R) Gen-Probe Inc. and Chiron Corp.), a nucleic acid test based on transcription-mediated amplification (TMA). Reactive specimens were confirmed with a second TMA-based test, the alternative WNV assay (Gen-Probe), and with WNV capture enzyme-linked immunosorbent assays (ELISAs) for detection of immunoglobulin M (IgM) and IgG antibodies. In addition, 3714 frozen plasma samples collected in 2002 and 2003 were similarly tested. RESULTS: One of 3856 fresh samples from an asymptomatic donor from Chihuahua was reactive by both TMA-based tests and IgM ELISA, suggesting a recently acquired infection. The observed percentage of viremic donors blood donors was 0.03 percent. Results from frozen samples were not included in the prevalence calculation and none were TMA-reactive for WNV. CONCLUSIONS: WNV is present in the Mexican blood supply and measures should be taken to reduce the risk of transfusion transmission.


Subject(s)
Antibodies, Viral/blood , Blood Banks , Blood Donors , Communicable Diseases, Emerging/blood , RNA, Viral/blood , West Nile Fever/blood , West Nile virus , Blood/virology , Blood Transfusion , Communicable Diseases, Emerging/prevention & control , Enzyme-Linked Immunosorbent Assay , Humans , Mexico , Reverse Transcriptase Polymerase Chain Reaction , West Nile Fever/prevention & control , West Nile Fever/transmission
6.
Cad Saude Publica ; 18(6): 1593-7, 2002.
Article in Portuguese | MEDLINE | ID: mdl-12488886

ABSTRACT

This article describes a serological survey for rickettsiosis in the county of Novo Cruzeiro, Minas Gerais State, Brazil, in 1998, testing schoolchildren and dogs. Sera included 331 samples from schoolchildren from an endemic area and 142 samples from schoolchildren from a non-endemic area in the county. All children examined were healthy and had not reported clinical symptoms of Brazilian spotted fever prior to the serological survey. Some 35 children in the endemic area were reactive to Rickettsia rickettsiiby indirect fluorescent antibody (IFA) with a titer of 1:64, corresponding to 10.6%. Sera from 73 dogs were tested, showing seroreactivity (IFA 1:64) to Rickettsia rickettsi, Ehrlichia chaffeensis, and Ehrlichia canisin 3 (4.11%), 11 (15.07%), and 13 (17.81%), respectively. The results in schoolchildren and the presence of canine seroreactivity to Ehrlichiaspecies that are potentially pathogenic to humans suggests the risk of transmission of other Rickettsiaein the study area.


Subject(s)
Antibodies, Bacterial/analysis , Communicable Diseases, Emerging/epidemiology , Endemic Diseases/statistics & numerical data , Rocky Mountain Spotted Fever/epidemiology , Animals , Brazil/epidemiology , Child , Communicable Diseases, Emerging/blood , Communicable Diseases, Emerging/veterinary , Dog Diseases/blood , Dog Diseases/epidemiology , Dogs , Fluorescent Antibody Technique, Indirect , Humans , Prevalence , Rickettsia rickettsii , Rocky Mountain Spotted Fever/blood , Rocky Mountain Spotted Fever/veterinary , Seroepidemiologic Studies , Siphonaptera , Ticks
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