El metaneumovirus humano es un nuevo patógeno asociado a infecciones respiratorias, principalmente en niños, que produce cuadros clínicos que van desde leves hasta graves, los cuales pueden incluso requerir tratamiento en unidades de cuidados intensivos. Hasta el momento, la reacción en cadena de la polimerasa con transcripción inversa y el cultivo celular son los métodos más usados para su diagnóstico. Se presentan los seis primeros casos de metapneumovirus humano en niños de Medellín, Colombia.

Human metapneumovirus is a newly discovered pathogen associated with respiratory disease and occurring mainly in children. It produces an acute viral respiratory disease picture that varies from mild disease to severe, and which can require strict surveillance in intensive care units. Currently, reverse transcriptase polymerase chain reaction and cell culture are the most common methods for its diagnosis. The first six cases of human metapneumovirus in Colombia are presented from Medellín.

We describe an acute febrile respiratory infection outbreak in a military unit in Trujillo, Peru. Cases were identified using the influenza like illness (ILI) definition of the Ministry of Health. Nasal swab samples used for a rapid influenza test (RIT) and pharyngeal swab samples for viral isolation were taken. For influenza A, genotyping of a partial sequence of the hemagglutinin region was performed. The rate attack was 82.9%. Fifty-nine cases appeared between April 1 and 8, 2008; 58 came from the military unit (MU) #1 and one from the MU #2. The RIT identified 40 cases of influenza A and 43 cases were confirmed through cell culture. Isolations were genetically similar to the A H1N1 Brisbane strain. Early detection of outbreaks in confined locations such as military bases permits immediate action in preventing disease propagation.

Se describe un brote de infección respiratoria febril aguda en una unidad militar de Trujillo, Perú. Se usó la definición de caso de síndrome gripal del Ministerio de Salud, se tomó hisopado nasal para prueba rápida de influenza (PRI) e hisopado faríngeo para aislamiento viral en cultivo celular. La genotipificación de influenza A fue por secuenciamiento genético de una región del gen de hemaglutinina teniendo como base la cepa vacunal de 2008. Se presentaron 59 casos entre el 01 y 08 de abril de 2008, la tasa de ataque fue de 82,9%. La PRI identificó a 40 casos positivos de influenza A y 43 casos fueron confirmados mediante cultivo celular. Los aislamientos fueron genéticamente similares con la cepa A H1N1 Brisbane. La detección precoz de un brote en lugares cerrados como las bases militares permite actuar de manera inmediata para prevenir su diseminación.

We describe an acute febrile respiratory infection outbreak in a military unit in Trujillo, Peru. Cases were identified using the influenza like illness (ILI) definition of the Ministry of Health. Nasal swab samples used for a rapid influenza test (RIT) and pharyngeal swab samples for viral isolation were taken. For influenza A, genotyping of a partial sequence of the hemagglutinin region was performed. The rate attack was 82.9%. Fifty-nine cases appeared between April 1 and 8, 2008; 58 came from the military unit (MU) #1 and one from the MU #2. The RIT identified 40 cases of influenza A and 43 cases were confirmed through cell culture. Isolations were genetically similar to the A H1N1 Brisbane strain. Early detection of outbreaks in confined locations such as military bases permits immediate action in preventing disease propagation.

Se describe un brote de infección respiratoria febril aguda en una unidad militar de Trujillo, Perú. Se usó la definición de caso de síndrome gripal del Ministerio de Salud, se tomó hisopado nasal para prueba rápida de influenza (PRI) e hisopado faríngeo para aislamiento viral en cultivo celular. La genotipificación de influenza A fue por secuenciamiento genético de una región del gen de hemaglutinina teniendo como base la cepa vacunal de 2008. Se presentaron 59 casos entre el 01 y 08 de abril de 2008, la tasa de ataque fue de 82,9%. La PRI identificó a 40 casos positivos de influenza A y 43 casos fueron confirmados mediante cultivo celular. Los aislamientos fueron genéticamente similares con la cepa A H1N1 Brisbane. La detección precoz de un brote en lugares cerrados como las bases militares permite actuar de manera inmediata para prevenir su diseminación.

Objective. To describe an Influenza outbreak in two military bases in Tumbes, department located in northern Peru. Material and methods. In patients within 5 days of symptoms the Ministry of Health case definition of Influenza-like illness was used. Nasal swabs were taken for Rapid Influenza Test (RIT) and throat swab for viral isolation, three cell lines (MDCK, VERO, LLCMK2) were used. For Influenza B genotypification we made a partial sequencing of hemaglutinine region of 898 pair bases, having 2007 vaccine strain B/Florida/4/2006 as a model. For Influenza A genotypification we analysed 958 pair bases, having 2007 vaccine strain A/Brisbane/10/2007 (H3N2) as a model. Results. We took 124 samples, 20 from military base (MB) # 1 and 104 from MB # 2. RIT promptly identified 41 positive cases: Flu B: 27, Flu A: 02, Flu: 12, with 62% of sensibility and specificity 100%. Finally, 66 cases were confirmed by virus isolation, 54 Flu B and 12 Flu A. Genotypification showed that isolates were genetically similar to Influenza B/Texas/4/2006 (n=34) and A/Texas/91/2007 (H3N2) (n=7). Most common symptoms found were fever, headache, malaise, cough, sore throat, myalgias and rinorrheae. Control strategies consisted to identify probable cases and to isolate them in a special room and to wear facemasks. Conclusions. We confirmed 66 cases by cellular culture. Isolates were genetically similar to Influenza B/Texas/4/2006 and A/Texas/91/2007 (H3N2).

Objetivo. Describir un brote de Influenza en dos bases militares en Tumbes, Perú. Material y métodos. Se utilizó la definición de caso de síndrome gripal del Ministerio de Salud en casos con menos de cinco días de inicio de síntomas. Se tomó hisopado nasal para la prueba rápida de Influenza (PRI) e hisopado faríngeo para aislamiento viral en tres líneas celulares (MDCK, VERO, LLCMK2). Para la genotipificación de Influenza B se usó un secuenciamiento parcial de la región de hemaglutinina de 898 pares de bases teniendo como base la cepa de la vacuna del 2007 (B/Florida/4/2006) y para el tipo A se analizó 958 pares de bases teniendo como referencia la cepa vacunal del 2007 (A/Brisbane/10/2007 (H3N2). Resultados. Se tomó 124 hisopados, 20 de la base militar (BM) # 1 y 104 de la BM # 2. La PRI identificó a 41 casos positivos: Flu B: 27, Flu A: 02, Flu: 12, con 62% de sensibilidad y 100% de especificidad. Finalmente, 66 casos fueron confirmados por cultivo celular, 54 Flu B y 12 Flu A. Los aislamientos de Tumbes fueron genéticamente similares con la cepa B/Texas/4/ 2006 (n=34) y A/Texas/91/2007 (H3N2)/ (n=7). Los síntomas más comunes fueron fiebre, cefalea, malestar general, tos, dolor de garganta, mialgias y rinorrea. Las medidas de control consistieron en el aislamiento de los casos identificados y el uso de mascarillas. Conclusiones. Se confirmó 66 casos de Influenza por cultivo celular. Los aislamientos tuvieron la mayor similitud genética con las cepas denominadas B/Texas/4/2006 y A/Texas/91/2007 (H3N2).

Objectives: To determine human immunodeficiency virus type 1 (HIV-1) subtype distribution, and the presence of recombinant strains in Argentina, Bolivia, Colombia, Chile, Ecuador, Paraguay, Peru, Uruguay, and Venezuela using epidemiological and genotyping studies. Materials and Methods: Participants in the studies performed in nine countries were included, amongst them female sex workers, men who have sex with men (MSM), HIV-positive individuals, pregnant women, and patients with tuberculosis (TB) were included. Envelope-base heteroduplex mobility assay (env HMA) testing was used, as well as ProRT, complete sequencing, or both for determining HIV-1 subtypes. Results: 3081 HIV positive individuals were identified (out of 42 290 volunteers), prevalences from less than 1% to 29% in the different populations studied, and it was higher among MSM. 1654 samples (54%) underwent genotyping. B subtype was found in 1380 (83%) samples, F subtype was found in 218 (13%) samples, and A and C subtypes were found in 0,1% and 0,4%, respectively. BF recombinant serotypes were found in 39 samples (2%), and CRF01_AE (0,1%), CRF17_BF (0,4%), and CRF02_AG (0,1%) were also found. In Venezuela, Colombia, Ecuador, Peru, Bolivia, and Chile (Andean countries) subtype B predominated, while in Argentina, Uruguay, and Paraguay there was a high frequency of F subtype. Conclusions: In most Andean countries, HIV-1 epidemic concentrated among MSM, who are predominantly infected with B subtype. F subtype is more frequent among female sex workers in Argentina and Uruguay. This is useful information in order to implement prevention plans and future vaccine tests in this region.

Objetivo: Determinar la distribución de los subtipos del virus de la inmunodeficiencia humana (VIH-1) y las presencia de cepas recombinantes en Argentina, Bolivia, Colombia, Chile, Ecuador, Paraguay, Perú, Uruguay y Venezuela a través de estudios epidemiológicos y de genotipificación. Materiales y Métodos: Se incluyeron a los participantes de los protocolos realizados en los nueve paises, incluyendo poblaciones de trabajadoras sexuales (TS), hombres que tienen sexo con hombres (HSH), individuos VIH positivos, gestantes y paciente con tuberculosis (TB). Se utilizó la prueba de movilidad heteroduplex de envoltura (env HMA), ProRT, secuenciamiento completo o ambas para determinar los subtipos de VIH 1. Resultados: Se identificaron 3081 individuos positivos al VIH (de un total de 42 290 voluntarios), las prevalencias oscilaban entre menos de 1% a 29% según población estudiada, siendo mayor en los HSH. Un total de 1654 muestras (54%) fueron genotipificadas. Se encontró el subtipo B en 1380 (83%) muestras, el subtipo F en 218 (13%), así como los subtipos A y C en 0,1% y 0,4% respectivamente. Se hallaron subtipos recombinantes BF en 39 muestras (2%) y formas recombinantes CRF01_AE(0,1%), CRF17_BF(0,4%) y CRF02_AG(0,1%). En Venezuela, Colombia, Ecuador, Perú, Bolivia y Chile (paises andinos) predominó el subtipo B, mientras en Argentina, Uruguay y Paraguay hubo un alto porcentaje del subtipo F. Conclusiones: En la mayoría de países andinos la epidemia de VIH-1 se concentró en los HSH con un predominio del subtipo B. El subtipo F es más frecuente en las TS en Argentina y Uruguay. Esta información es útil para implementar planes de prevención y futuros ensayos de vacunas en esta región.

O objetivo deste trabalho foi avaliar a eficácia da mefloquina numa região endêmica de leishmaniose cutânea por Leishmania (Viannia) braziliensis, considerando que esta droga de administração oral, eficaz no tratamento da malária, com meia vida prolongada e efeitos colaterais pouco freqüentes poderia ser menos tóxica e de mais fácil administração, quando comparada com os antimoniais pentavalentes. Em Corte de Pedra, no litoral sul do Estado da Bahia, foram tratados, aleatoriamente, dez pacientes portadores de lesões leishmanióticas, subdivididos em dois grupos. O primeiro grupo recebeu mefloquina pela via oral, dose de 250mg/dia, durante seis dias, repetindo-se o mesmo esquema após intervalo de três semanas. O segundo grupo recebeu antimoniato de meglumina (Glucantime®) diariamente, pela via endovenosa, na dose de 20mg/kg por 20 dias. Do grupo da mefloquina só um paciente apresentou cicatrização depois do segundo ciclo. Um desses, com quatro lesões apresentou nova lesão durante o primeiro ciclo de tratamento. A evolução dos outros três foi lenta sendo que em nove semanas nenhum deles tinha cicatrizado as úlceras que permaneciam com grande infiltração e sinais evidentes de atividade. O grupo tratado com Glucantime® apresentou evidente melhora.

The aim of this study was to evaluate the efficacy of mefloquine in the treatment of skin leishmaniasis in patients infected with Leishmania (Viannia) braziliensis at an endemic region. Mefloquine is an oral drug effective against malaria with a prolonged half-life, less toxicity and easier administration than pentavalent antimonials. At Corte de Pedra in the Southern litoral of Bahia State, two randomized groups of ten patients with leishmaniasis were treated. The first group was treated with oral mefloquine, 250mg per day in a single dose for six days and repeated three weeks later. The second group received meglumine antimoniate (Glucantime®), 20mg/kg daily administered intravenously for 20 days. Only one patient in the group treated with mefloquine showed evidence of clinical success. During treatment, one patient with four lesions developed a new lesion. The other three patients with clinical leismaniasis did not show evidence of clinical success after nine weeks of treatment. The group treated with Glucantime® showed evident clinical improvement of the skin lesions.