Co-circulación viral de Dengue y Chikungunya en mosquitos Aedes aegypti infectados naturalmente en Venezuela / Dengue and Chikungunya viral co-circulation in naturally infected Aedes aegypti mosquitoes in Venezuela

Para detectar los arbovirus Dengue (DENV), Zika (ZIKV) y Chikungunya (CHIKV) en mosquitos Aedes aegypti (Ae. aegypti), se evaluaron dos municipios del estado Aragua, Francisco Linares Alcántara (FLA) y Mario Briceño Iragorry (MBI). Se capturaron 163 mosquitos en MBI y 105 en FLA con aspirador de espalda. Estos se agruparon (2-9 mosquitos) para la extracción de ARN y análisis mediante RT-PCR específica para cada virus. Se calcularon, Tasa Mínima de Infección (TMI) y Estimación de Máxima Verosimilitud (EMV). Los resultados evidenciaron co-infección de mosquitos por DENV-3 y CHIKV en FLA, y solo por CHIKV en MBI. Las TMI en MBI fueron para DENV (0%), CHIKV (0,61%), en FLA los valores para DENV y CHIKV, fueron 1,90% y 2,86%; respectivamente. Las EMV fueron en MBI igual a 0% para DENV y 0,63% para CHIKV, en FLA DENV (0,19%) y CHIKV (1,53%). Se comprobó la infección natural de Ae. aegypti con DENV y CHIKV, específicamente la co-circulación viral de DENV-3 y CHIKV en FLA, en MBI solo fue detectado CHIKV. La ausencia de detección de ZIKV probablemente se debió a interferencia viral. Los resultados indican la relevancia de incorporar a las prácticas convencionales de control vectorial, la detección específica de virus en zonas endemo-epidémicas durante todo el año, lo que favorecería las intervenciones y puesta en marcha de estrategias de control y prevención efectivas para limitar la permanente transmisión viral(AU)

To detect Dengue (DENV), Zika (ZIKV) and Chikungunya (CHIKV) in mosquitoes (Ae. aegypti) we evaluated two municipalities in Aragua State, Francisco Linares Alcántara (FLA) and Mario BriceñoIragorry (MBI). We captured 163 mosquitoes in MBI and 105 in FLA using Back Aspirator. The mosquitoes were grouped (2-9 mosquitoes per tube) for RNA extraction and typification by RT-PCR. We calculated Minimal Infection Rate (MIR) and Maximum Likelihood Estimation (MLE). The results showed co-infection by DENV-3 and CHIKV in FLA, and CHIKV in MBI. The MIR was to DENV 0% and 0.61% to CHIKV in MBI, whiles in FLA the values were 1.90% and 2.86% to DENV y CHIKV, respectively. The EMV were in MBI to DENV 0% and 0.63% to CHIKV, in the case of FLA DENV value was 0.19% and CHIKV 1.53%. We showed the natural infection of Ae. aegypti mosquitoes with DENV-3 and CHIKV in FLA and CHIKV in MBI. The absent of detection to ZIKV was probably due to viral interference. The results showed the relevance of incorporation of these techniques to conventional practices about vectorial control, specifically detection of viruses in endemic and epidemic regions during all year, because these practices could contribute to the effective interventions to control and prevention the viral transmission(AU)

Evidencia de Chlamydia no psittaci en psitácidos en cautiverio de Venezuela / Evidence of non-psittaci Chlamydia in parrots in captivity in Venezuela / Evidência de Chlamydia não psittaci em psitacídeos em cativeiro na Venezuela

Resumen Chlamydia psittaci (Cp) es una bacteria intracelular obligada causante de la clamidiosis aviar, capaz de infectar a más de 460 especies de aves. Sin embargo, desde 2008 han sido identificadas otras especies chlamydiales en aves de vida libre y en cautiverio. El presente estudio tuvo como objetivo la identificación de un segmento del gen 16s ADNr de Cp a través de la reacción en cadena de la polimerasa anidada en dos psitácidos del género Ara ararauna y Ara chloropterus de un parque zoológico de Venezuela. Los resultados revelaron que las aves no poseían ADN compatible con Cp, pero sí para la familia Chlamydiaceae. En este sentido se aporta evidencia de la presencia de otra posible especie chlamydial en las Ara muestreadas en estado portador asintomático. Dichas aves provenían de decomisos y se desconocía su origen. Estos factores favorecen la infección por otra especie de Chlamydia. Si bien los productos de reacción en cadena de la polimerasa (PCR) obtenidos no fueron secuenciados, existen altas probabilidades de ser una Chlamydia no psittaci debido a que un elevado número de reportes a escala mundial afirman la capacidad de transmisión del resto de las especies en aves. En este sentido es necesaria la notificación de los hallazgos chlamydiales para el estudio de su capacidad patogénica en nuevos reservorios, riesgo zoonótico y la protección de la fauna silvestre y en cautiverio, principalmente la que se encuentra en riesgo de extinción.

Abstract Chlamydia psittaci (Cp) is an obligate intracellular bacterium that causes avian chlamydiosis, capable of infecting more than 460 bird species. However, since 2008, other chlamydial species have been identified in free-living and captive birds. This study aimed to identify a segment of the 16s rDNA gene of Cp using nested polymerase chain reaction in two Psittacidae birds of the genus Ara ararauna and Ara chloropterus from a zoo in Venezuela. The results revealed that these birds did not have DNA compatible with Cp, but they did have for the Chlamydiaceae family. Thus, the paper evidences the presence of another possible chlamydial species in the sampled Ara in an asymptomatic carrier state. These birds were confiscated and their origin was unknown. These factors favor infection by another species of Chlamydia. Although the resulting polymerase chain reaction (PCR) products were not sequenced, there is a high probability of being a non-psittaci Chlamydia, because a large number of reports on a global scale affirm the transmission capacity of the rest of the species in birds. In this sense, it is necessary to report chlamydial findings in order to study their pathogenic capacity in new reservoirs, zoonotic risk, and the protection of wildlife and animals in captivity, mainly those at risk of extinction.

Resumo Chlamydia psittaci (Cp) é uma bactéria intracelular obrigada causadora da clamidiose aviar, capaz de infectar a mais de 460 espécies de aves. Entretanto, desde 2008 foram identificadas outras espécies chlamydiais em aves de vida livre e em cativeiro. O presente estudo teve como objetivo a identificação de um segmento do gene 16s ADNr de Cp através da reação em cadeia da polimerase aninhados em dois psitacídeos do género Ara ararauna e Ara chloropterus de um parque zoológico da Venezuela. Os resultados revelaram que as aves não possuíam DNA compatível com Cp, mas sim para a família Chlamydiaceae. Neste sentido se aponta evidência da presença de outra possível espécie chlamydial nas Ara amostradas em estado portador assintomático. Tais aves provinham de apreensões e se desconhecia sua origem. Estes fatores favorecem a infecção por outra espécie de Chlamydia. Ainda que os produtos de Reação em Cadeia da Polimerase (PCR) obtidos não foram sequenciados, existem altas probabilidades de ser uma Chlamydia não psittaci devido a que um elevado número de relatos em escala mundial afirma a capacidade de transmissão do resto das espécies em aves. Neste sentido é necessária a notificação das descobertas chlamydiais para o estudo de sua capacidade patogênica em novos reservatórios risco zoonótico e a proteção da fauna silvestre e em cativeiro, principalmente a que se encontra em risco de extinção.

Development and evaluation of a novel high-throughput image-based fluorescent neutralization test for detection of Zika virus infection.

Zika virus (ZIKV) is an emerging arbovirus belonging to the genus flavivirus that comprises other important public health viruses, such as dengue (DENV) and yellow fever (YFV). In general, ZIKV infection is a self-limiting disease, however cases of Guillain-Barré syndrome and congenital brain abnormalities in newborn infants have been reported. Diagnosing ZIKV infection remains a challenge, as viral RNA detection is only applicable until a few days after the onset of symptoms. After that, serological tests must be applied, and, as expected, high cross-reactivity between ZIKV and other flavivirus serology is observed. Plaque reduction neutralization test (PRNT) is indicated to confirm positive samples for being more specific, however it is laborious intensive and time consuming, representing a major bottleneck for patient diagnosis. To overcome this limitation, we developed a high-throughput image-based fluorescent neutralization test for ZIKV infection by serological detection. Using 226 human specimens, we showed that the new test presented higher throughput than traditional PRNT, maintaining the correlation between results. Furthermore, when tested with dengue virus samples, it showed 50.53% less cross reactivity than MAC-ELISA. This fluorescent neutralization test could be used for clinical diagnosis confirmation of ZIKV infection, as well as for vaccine clinical trials and seroprevalence studies.

Chlamydia psittaci EN AVES PSITACIDAS EN DOS PARQUES ZOOLÓGICOS DE VENEZUELA / Chlamydia psittaci in Psitacines Birds in Two Zoological Parks of Venezuela

RESUMEN La determinación de Chlamydia psittaci (Cp) en aves psitácidas en parques zoológicos de Venezuela representa una estrategia de conservación y preservación para este grupo de aves, donde múltiples especies se encuentran amenazadas de extinción y otras han perdido su capacidad de reincorporación a su hábitat natural. A través de la reacción en cadena de la polimerasa anidada (PCR) fue amplificada la subunidad 16S del ADNr de Cp en 50 muestras de hisopado cloacal de aves psitácidas, reportando una frecuencia de 62 %. El trabajo fue realizado en el Parque Zoológico Las Delicias (PZD) 8 % y el Aquarium de Valencia (AV) 54 %. La elevada frecuencia fue asociada a un genotipo de baja concentración y virulencia debido a la ausencia de signos clínicos de clamidiosis aviar. Estos resultados demuestran la necesidad de promover la detección de Cp, principalmente para el AV que actúa como centro de recepción de ejemplares de decomiso, y, al igual que el PZD, poseen otras especies vulnerables a la extinción con riesgo de infección a Cp.

ABSTRACT The determination of Chlamydia psittaci (Cp) in psittacida birds in zoological parks in Venezuela represents a strategy of conservation and preservation for this group of birds, where multiple species are threatened with extinction and others have lost their capacity of reincorporation to their natural habitat. Through the nested polymerase chain reaction (PCR) the 16S subunit of Cp DNAr was amplified in 50 cloacal swab samples from psittacine birds, reporting a frequency of 62 %. The work was carried out in the Zoo Park Las Delicias (PZD) 8% and the Aquarium of Valencia (AV) 54%. The high frequency was associated with a genotype of low concentration and virulence due to the absence of clinical signs of avian chlamydiosis. These results demonstrate the need to promote the detection of Cp, mainly for the AV that acts as a center of reception of specimens of confiscation, and, like the PZD, have other species vulnerable to extinction with risk of infection to Cp.

Asian genotype of Chikungunya virus circulating in Venezuela during 2014.

Chikungunya virus emerged on Saint-Martin Island in the Caribbean in late 2013. Since then in July of 2104 Venezuela reported autochthonous cases. This study reports the first phylogenetic characterization of CHIKV autochthonous cases in Venezuela, 2014. The phylogenetic analysis showed that the CHIKV circulating in Venezuela (Aragua state) belong to the Asian genotype (Caribbean clade) and it is related to viruses that circulated in the same year in the Caribbean.

[Cloning alphavirus and flavivirus sequences for use as positive controls in molecular diagnostics]. / Clonación de secuencias de alfavirus y flavivirus para su uso como controles positivos en el diagnóstico molecular.

The purpose of the study was to obtain a positive control to validate molecular techniques (reverse transcription- polymerase chain reaction [RT-PCR]) used in the diagnosis and research of viral infections. From strains of Chikungunya virus (CHIKV), Zika virus, and Dengue virus (DENV-1, DENV-2, DENV- 3, and DENV-4) viral RNAs were extracted to obtain complementary DNA using RT-PCR from the nsP4 (CHIKV), NS5 (Zika virus), C/prM-M, and 5'UTR-C (DENV-1, DENV-2, DENV-3, DENV-4) sequences, which were cloned into pGEM®-T Easy. Cloning was confirmed through colony PCR, from which plasmid DNA was extracted for fragment cloning verification. Cloning of cDNA corresponding to nsP4, NS5, C/prM-M, and 5'UTR-C of the different viral agents was achieved. In conclusion, recombinant plasmids were obtained with each of the sequences specified for further assessment as positive controls in molecular techniques in an effort to avoid the use of cell cultures, which can be costly, time-consuming, and potentially dangerous.

Clonación de secuencias de alfavirus y flavivirus para su uso como controles positivos en el diagnóstico molecular / Cloning alphavirus and flavivirus sequences for use as positive controls in molecular diagnostics

RESUMEN El objetivo de la investigación fue obtener controles positivos para la validación de técnicas moleculares (RT-PCR) utilizadas en diagnóstico e investigación de infecciones virales. A partir de cepas de CHIKV, Zika, DENV-1, DENV-2, DENV-3 y DENV-4, se extrajeron ARN virales para obtener por RT-PCR los ADN complementarios (ADNc) de las secuencias nsP4 (CHIKV), NS5 (virus Zika), C/prM-M y 5´UTR-C (DENV-1, DENV-2, DENV-3, DENV-4) que fueron clonados en pGEM®-T Easy. La clonación se confirmó mediante PCR de colonias, de las cuales se extrajo el ADN plasmídico para la verificación de la clonación de los fragmentos. Se logró la clonación de ADNc correspondientes a nsP4, NS5, C/prM-M y 5´UTR-C de los distintos agentes virales. En conclusión se obtuvieron los plásmidos recombinantes con cada una de las secuencias especificadas para su posterior valoración como controles positivos en técnicas moleculares, evitando el uso de cultivos celulares que pueden resultar costosos, laboriosos y potencialmente peligrosos.

ABSTRACT The purpose of the study was to obtain a positive control to validate molecular techniques (reverse transcription- polymerase chain reaction [RT-PCR]) used in the diagnosis and research of viral infections. From strains of Chikungunya virus (CHIKV), Zika virus, and Dengue virus (DENV-1, DENV-2, DENV- 3, and DENV-4) viral RNAs were extracted to obtain complementary DNA using RT-PCR from the nsP4 (CHIKV), NS5 (Zika virus), C/prM-M, and 5′UTR-C (DENV-1, DENV-2, DENV-3, DENV-4) sequences, which were cloned into pGEM®-T Easy. Cloning was confirmed through colony PCR, from which plasmid DNA was extracted for fragment cloning verification. Cloning of cDNA corresponding to nsP4, NS5, C/prM-M, and 5′UTR-C of the different viral agents was achieved. In conclusion, recombinant plasmids were obtained with each of the sequences specified for further assessment as positive controls in molecular techniques in an effort to avoid the use of cell cultures, which can be costly, time-consuming, and potentially dangerous.

Sequential waves of gene expression in patients with clinically defined dengue illnesses reveal subtle disease phases and predict disease severity.

BACKGROUND: Dengue virus (DENV) infection can range in severity from mild dengue fever (DF) to severe dengue hemorrhagic fever (DHF) or dengue shock syndrome (DSS). Changes in host gene expression, temporally through the progression of DENV infection, especially during the early days, remains poorly characterized. Early diagnostic markers for DHF are also lacking. METHODOLOGY/PRINCIPAL FINDINGS: In this study, we investigated host gene expression in a cohort of DENV-infected subjects clinically diagnosed as DF (n = 51) and DHF (n = 13) from Maracay, Venezuela. Blood specimens were collected daily from these subjects from enrollment to early defervescence and at one convalescent time-point. Using convalescent expression levels as baseline, two distinct groups of genes were identified: the "early" group, which included genes associated with innate immunity, type I interferon, cytokine-mediated signaling, chemotaxis, and complement activity peaked at day 0-1 and declined on day 3-4; the second "late" group, comprised of genes associated with cell cycle, emerged from day 4 and peaked at day 5-6. The up-regulation of innate immune response genes coincided with the down-regulation of genes associated with viral replication during day 0-3. Furthermore, DHF patients had lower expression of genes associated with antigen processing and presentation, MHC class II receptor, NK and T cell activities, compared to that of DF patients. These results suggested that the innate and adaptive immunity during the early days of the disease are vital in suppressing DENV replication and in affecting outcome of disease severity. Gene signatures of DHF were identified as early as day 1. CONCLUSIONS/SIGNIFICANCE: Our study reveals a broad and dynamic picture of host responses in DENV infected subjects. Host response to DENV infection can now be understood as two distinct phases with unique transcriptional markers. The DHF signatures identified during day 1-3 may have applications in developing early molecular diagnostics for DHF.

Sentinel surveillance of influenza-like illness in two hospitals in Maracay, Venezuela: 2006-2010.

BACKGROUND: Limited information exists on the epidemiology of acute febrile respiratory illnesses in tropical South American countries such as Venezuela. The objective of the present study was to examine the epidemiology of influenza-like illness (ILI) in two hospitals in Maracay, Venezuela. METHODOLOGY/PRINCIPAL FINDINGS: We performed a prospective surveillance study of persons with ILI who presented for care at two hospitals in Maracay, Venezuela, from October 2006 to December 2010. A respiratory specimen and clinical information were obtained from each participant. Viral isolation and identification with immunofluorescent antibodies and molecular methods were employed to detect respiratory viruses such as adenovirus, influenza A and B, parainfluenza, and respiratory sincytial virus, among others. There were 916 participants in the study (median age: 17 years; range: 1 month--86 years). Viruses were identified in 143 (15.6%) subjects, and one participant was found to have a co-infection with more than one virus. Influenza viruses, including pandemic H1N1 2009, were the most frequently detected pathogens, accounting for 67.4% (97/144) of the viruses detected. Adenovirus (15/144), parainfluenza virus (13/144), and respiratory syncytial virus (11/144) were also important causes of ILI in this study. Pandemic H1N1 2009 virus became the most commonly isolated influenza virus during its initial appearance in 2009. Two waves of the pandemic were observed: the first which peaked in August 2009 and the second--higher than the preceding - that peaked in October 2009. In 2010, influenza A/H3N2 re-emerged as the most predominant respiratory virus detected. CONCLUSIONS/SIGNIFICANCE: Influenza viruses were the most commonly detected viral organisms among patients with acute febrile respiratory illnesses presenting at two hospitals in Maracay, Venezuela. Pandemic H1N1 2009 influenza virus did not completely replace other circulating influenza viruses during its initial appearance in 2009. Seasonal influenza A/H3N2 was the most common influenza virus in the post-pandemic phase.

Evolution of dengue virus type 3 genotype III in Venezuela: diversification, rates and population dynamics.

BACKGROUND: Dengue virus (DENV) is a member of the genus Flavivirus of the family Flaviviridae. DENV are comprised of four distinct serotypes (DENV-1 through DENV-4) and each serotype can be divided in different genotypes. Currently, there is a dramatic emergence of DENV-3 genotype III in Latin America. Nevertheless, we still have an incomplete understanding of the evolutionary forces underlying the evolution of this genotype in this region of the world. In order to gain insight into the degree of genetic variability, rates and patterns of evolution of this genotype in Venezuela and the South American region, phylogenetic analysis, based on a large number (n = 119) of envelope gene sequences from DENV-3 genotype III strains isolated in Venezuela from 2001 to 2008, were performed. RESULTS: Phylogenetic analysis revealed an in situ evolution of DENV-3 genotype III following its introduction in the Latin American region, where three different genetic clusters (A to C) can be observed among the DENV-3 genotype III strains circulating in this region. Bayesian coalescent inference analyses revealed an evolutionary rate of 8.48 x 10⁻4 substitutions/site/year (s/s/y) for strains of cluster A, composed entirely of strains isolated in Venezuela. Amino acid substitution at position 329 of domain III of the E protein (A→V) was found in almost all E proteins from Cluster A strains. CONCLUSIONS: A significant evolutionary change between DENV-3 genotype III strains that circulated in the initial years of the introduction in the continent and strains isolated in the Latin American region in recent years was observed. The presence of DENV-3 genotype III strains belonging to different clusters was observed in Venezuela, revealing several introduction events into this country. The evolutionary rate found for Cluster A strains circulating in Venezuela is similar to the others previously established for this genotype in other regions of the world. This suggests a lack of correlation among DENV genotype III substitution rate and ecological pattern of virus spread.

Incidencia de infecciones sintomáticas y asintomáticas por virus dengue en Maracay, Venezuela: 2006-2007 / Incidence of symptomatic and asymptomatic dengue virus infections in Maracay, Venezuela: 2006-2007

Con el objetivo de estimar las tasas de incidencia de infecciones sintomáticas y asintomáticas por virus dengue (DENV) durante un año (octubre 2006-septiembre 2007) en cuatro barrios de Maracay (Venezuela) se realizó un estudio prospectivo consistente de visitas domiciliarias, tres veces por semana, para detectar casos de dengue y de encuestas serológicas semestrales para determinar infecciones asintomáticas probables por DENV. Los sujetos de estudio pertenecían a una cohorte de 2663 personas ≥5 años de edad. El diagnóstico confirmatorio de DENV se realizó mediante la reacción en cadena de la polimerasa con transcriptasa inversa (RT-PCR). Las pruebas serológicas se realizaron mediante el ensayo inmunoenzimático de captura de IgM anti-dengue (MAC-ELISA). Los resultados determinaron tasas de incidencia de 5,7 y 18,6 por 100 000 personas/día (p/d) para las infecciones sintomáticas y asintomáticas, respectivamente. La tasa de incidencia de las infecciones sintomáticas observada en las personas <15 años de edad fue significativamente mayor que la encontrada en los sujetos ≥15 años (15,8 versus 2,9 por 100 000 p/d). Por otro lado, las tasas de incidencia de las infecciones asintomáticas en ambos grupos de edad fueron similares (17,3 y 18,9 por 100 000 p/d, respectivamente). Se detectaron los cuatro serotipos del DENV en tres de los barrios estudiados. Se observó que la edad y la hiperendemicidad fueron probablemente los factores que más contribuyeron a la incidencia del dengue en los cuatro barrios investigados. Seguramente, las infecciones asintomáticas contribuyeron a incrementar la transmisión viral en el área de estudio.

The incidence rates of symptomatic and asymptomatic dengue virus (DENV) infections in four "barrios" of Maracay, Venezuela, during one-year (October 2006-September 2007) were estimated. A prospective study consisting of house visits three-times a week to detect dengue cases, and semiannual serological surveys to determine probable asymptomatic dengue virus (DENV) infections was conducted. The study subjects belonged to a cohort of 2,663 people ≥5 year-old. Confirmatory diagnosis of DENV infections was carried out by reverse-transcriptase polymerase chain reaction (RT-PCR). Serological surveys were performed by anti-dengue IgM-capture immunoassay (MAC-ELISA). The results showed that the incidence rates for symptomatic and asymptomatic infections were determined to be 5.7 and 18.6 per 100,000 persons/day (p/d), respectively. The incidence rate of symptomatic infections was significantly higher in persons <15 year-old than that found in subjects ≥15 years (15.8 versus 2.9 per 100,000 p/d). On the other hand, the incidence rates of asymptomatic infections in both age groups were similar (17.3 and 18.9 per 100,000 p/d, respectively). All four DENV serotypes were detected in three of the four "barrios" studied. Finally, age and hyperendemicity were probably the contributing factors to the incidence of dengue in the four "barrios" investigated. Surely, the asymptomatic infections contributed to increase the viral transmission in the study area.

Dengue virus serotype 4, northeastern Peru, 2008.

In 2008, dengue virus serotype 4 (DENV-4) emerged in northeastern Peru, causing a large outbreak and displacing DENV-3, which had predominated for the previous 6 years. Phylogenetic analysis of 2008 and 2009 isolates support their inclusion into DENV-4 genotype II, forming a lineage distinct from strains that had previously circulated in the region.

Dengue virus infections in a cohort of schoolchildren from Maracay, Venezuela: a 2-year prospective study.

In 2001, we began a prospective longitudinal study in a cohort of schoolchildren 5-13 years of age residing in Maracay, Venezuela, to determine the cumulative incidence of dengue virus (DENV) infections by virus serotype. This report presents serological data from 710 schoolchildren who were tested during the first 2 years of the study. Serological evaluations were conducted by plaque reduction neutralization test (PRNT). At study initiation, 51% of children had PRNT antibody titers against one (30.1% = 13.4% DENV-1, 14.2% DENV-2, 0.6% DENV-3, and 2% DENV-4) or multiple DENV serotypes (20.9%). By the end of the first year, 89 of 348 (25.6%) PRNT-negative children seroconverted, and 94 of 362 (26%) who were PRNT-positive in their baseline sera tested positive for additional serotypes, for an overall cumulative incidence of DENV infections of 25.8%. By serotype, the percentages found were 1.4% DENV-1, 1.4% DENV-2, 19% DENV-3, and 1.2% DENV-4. In the second year, 37 of 259 (14.3%) PRNT-negative children seroconverted, and 83 of 451 (18.4%) who had monotypic and multitypic PRNT patterns in their baseline sera exhibited additional serotype seroconversions, for an overall cumulative incidence of DENV infections of 16.9%. By serotype, the percentages found were 0.8% DENV-1, 1.5% DENV-2, 8.5% DENV-3, and 2.3% DENV-4. Overall, these results suggest a high cumulative incidence of DENV infections among 5-13-year-old school children in Maracay, Venezuela.

[Laboratory diagnosis of dengue virus infections in Aragua State, Venezuela: October 1997-December 1998]. / Diagnóstico de laboratorio de infecciones por el virus dengue en el estado Aragua; Venezuela: Octubre 1997-Diciembre 1998.

The efficacy of a proactive dengue surveillance system to predict epidemics depends on the laboratory diagnostic capacity for an early detection of virus circulation. This study shows the results of the dengue virologic and serologic surveillance accomplished in Aragua State (Venezuela) from October 1997 to December 1998. Five hundred and forty seven sera from suspected dengue patients were tested using the techniques of Virus Isolation and Immunofluorescence Serotyping (VIIS), Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR), Anti-dengue IgM Capture Enzyme Immunoassay (MAC-ELISA) and Haemagglutination Inhibition test (HI). Of the tested sera, 97.4% resulted positive to at least one technique; of these, 60.4% were classified as confirmed cases (virologically positives) and 39.6% as probable cases (virologically negatives/serologically positives). Though the majority of positive cases occurred during the 1997 and 1998 epidemic periods, the gradual increase of the seropositive rates between both periods suggested the incoming 1998 outbreak. Den-1 (51.2%), Den-2 (37.9%) and Den-4 (10.6%) infected patients were detected as well as one dual infection of Den-2 and Den-4 (0.3%). Dengue hyperendemicity (co-circulation of Den-1, Den-2 and Den-4) in Aragua State was confirmed together with the detection of few cases (6.5%) of Dengue Hemorrhagic Fever/Dengue Shock Syndrome cases (HF/DSS); 38.1% of these cases occurred in patients with secondary infections. The high percentage (85.7%) of DHF/DSS cases infected by Den-2 virus supports the reported virulence of this serotype.

Diagnóstico de laboratorio de infecciones por el virus dengue en el estado Aragua Venezuela: octubre 1997-diciembre 1998 / Laboratory diagnosis of dengue virus infections in Aragua state Venezuela: october 1997-december 1998

La eficacia de un sistema de vigilancia epidemiológica proactivo para predecir epidemias de dengue de la capacidad del laboratorio para detectar tempranamente la circulación viral. Este estudio muestra los resultados de la vigilancia virológica del dengue, realizada en el estado Aragua (Venezuela) desde octubre 1997 hasta diciembre 1998. Se evluaron 547 sueros de pacientes sospechosos de dengue mediante las técnicas de aislamiento viral y serotipicación por inmunofluorescencia (AVSI), reacción en cadena de la polimerasa con transcriptasa inversa (RT-PCR), inmunoensayo enzimático de captura de IgM anti-dengue (MAC-ELISA) e inhibición de la hemaglutinación (IHA). De los sueros examinados, 97,4 por ciento resultaron positivos a por lo menos una técnica; de estos, 60,4 por ciento fueron clasificados como casos confirmados (virológicamente positivos) y 39,6 por ciento como casos probables (virológicamente negativos, serológicamente positivos). Aunque la gran mayoría de los casos positivos ocurrieron en los períodos epidémicos de 1997 y 1998, el incremento paulatino de las tasas de serotipos entre ambos períodos sugería la llegada de la epidemia de 1998. Se detectaron pacientes infectados con virus Den-1 (51,2 por ciento), Den-2 (37,9 por ciento), Den-4 (10,6 por ciento), y una infección mixta por Den-2 y Den-4 (0,3 por ciento). Se confirma la hiperdemicidad del dengue (co-circulación de Den-1, Den-2 y Den-4) en el estado Aragua, conjuntamente con la detección de pocos pasos (6,5 por ciento) de fiebre hemorrágica de dengue/síndrome de choque por dengue (FHD/SCD); 38,1 por ciento de estos casos ocurrieron en pacientes con infecciones secundarias. El alto porcentaje (85,7 por ciento) de casos de FHD/SCD infectados con el virus Den-2 apoya la reportada virulencia de este serotipo

Comportamiento biológico de 3 cepas del virus dengue-2 en 2 líneas celulares de mosquitos / Biological behavior of 3 strains of the dengue-2 virus in 2 cell lines of mosquitoes

Strains A-15 (isolated in Cuba, 1981), Jamaica (isolated in Jamaica, 1981) and Nueva Guinea "C" (standard) from dengue-2 virus were compared according to the time of appearance of the cytopathic effect (CPE), to the time of appearance of specific fluorescence and to the kynetics of viral multiplication on being innoculated in the cell lines AP-61 (Aedes pseudoscutellaris) and C6/36 HT (Aedes albopictus). The results showed that the CPE of highest intensity and earliest appearance was for A-15, followed by Jamaica and Nueva Guinea "C" (NGC). AP-61 seems to favor the CPE of Jamaica with respect to that of the same strain in C6/36 HT. The fluorescence was earlier for Jamaica and A-15 and more intensive for the latter, whereas NGC manifested late. This behaviour was similar in the 2 cellular systems. The greatest titres during the kinetics of viral multiplication were obtained from A-15 in both lines, although in AP-61 they tend to be equal from the 4th day on. The strain A-15 showed a particular behaviour of these biological properties on comparing them with the other strains under study, which may be related to changes found in its neucleotide sequence.

Estudio de algunas propiedades biológicas de 3 cepas de dengue 2 con diferencias en sus secuencias nucleotídicas / Study of various biological properties of 3 strains of dengue 2 with differences in their nucleotide sequences

Some biological properties of Dengue-2 strains such as A-15 (isolated in Cuba in 1981); Jamaica (isolated in Jamaica in 1981) and New Guinea "C" (NG"C") standard strain differing in their nucleotide sequences were studied. The results showed that the cytopathic effect in C6/36 HT cell line occurred earlier in A-15 strain and that fluorescence was first detected in Jamaica and A-15 strains. This seems to indicate that rapid detection of strains does not have any relation to neither their history of passage nor the original isolation system. A-15 and NG"C" strains exhibited an heterogeneous pattern formed by big and small plaques but average size of plaques in NG"C" was lower whereas Jamaica showed only small plaques. The most neurovirulent strain in mice was NG"G" followed by A-15 whereas Jamaica was not neurovirulent at all. These results indicate that A-15 has a different biological behaviour which is probably due to intrinsic differences. It should be taken into account that 7 amino acid changes were found in the envelope protein which may have affected the expression of some biological properties.