105 research outputs found
Notes on Phlebotomine sand flies of Michoacán, Mexico, with a key
Four species of phlebotomine sand flies were collected in the Municipality of Sahuayo, on the High Plateau of Michoacán, representing the first records of phlebotomine sand flies in this region. Two of them, Micropygomyia (Coquillettimyia) vindicator (Dampf) and Psathyromyia (Forattiniella) texana (Dampf), are new records for Michoacán. A total of ten phlebotomine species are now known to occur in this state, and we present a key for their identification
Determinación de virus del oeste del Nilo (von) en los años 2006 y 2007 en el estado de Nuevo León, México
Respuesta conductual de Aedes aegypti (Linneaus, 1762) frente adulticidas piretroides de uso frecuente en Salud Pública
Objetivos. Evaluar la respuesta conductual de la generación F1 de Aedes aegyti (L) colectados en el área metropolitana de Monterrey (Nuevo León, México) frente a tres adulticidas piretroides de uso frecuente en salud pública. Materiales y métodos. Se utilizó un sistema modular novedoso denominado HITSS (High-Throughput Screening System), para evaluar dos respuestas de comportamiento (irritación de contacto y repelencia espacial), así como la toxicidad de tres insecticidas DDT, permetrina y bifentrina a diferentes concentraciones (0,025, 0,25, 25 y 250 nmol/cm2). Resultados. En la concentración 2,5 nmol/cm2, el DDT (4,3 ± 2,4) y la permetrina (8,0 ± 1,4) son los insecticidas que tienen mayor efecto irritante (p<0,05); la bifentrina requiere dosis 20 veces más alta para lograr efectos similares. En repelencia espacial, los tres insecticidas evaluados producen respuestas similares en todas las concentraciones; para DDT de 7 a 14%; permetrina de 9 a 15% y bifentrina de 19 a 27%. La permetrina y bifentrina a concentraciones 0,025 nmol/cm2, producen efectos knockdown superiores a 34%, con una mortalidad 19%, el DDT requiere concentraciones diez veces más alta para lograr efectos similares. Conclusiones. El sistema HITTS puede ser usado para evaluar la respuesta conductual frente a insecticidas
Universal primers for the amplification and sequence analysis pf actin-1 from diverse mosquito species
We report the development of universal primers for the reverse-transcription polymerase chain reaction (RT-PCR) amplification and nucleotide sequence analysis of actin cDNAs from taxonomically diverse mosquito species. Primers specific to conserved regions of the invertebrate actin-1 gene were designed after actin cDNA sequences of Anopheles gambiae, Bombyx mori, Drosophila melanogaster, and Caenorhabditis elegans. The efficacy of these primers was determined by RT-PCR with the use of total RNA from mosquitoes belonging to 30 species and 8 genera (Aedes, Anopheles, Culex, Deinocerites, Mansonia, Psorophora, Toxorhynchites, and Wyeomyia). The RT-PCR products were sequenced, and sequence data were used to design additional primers. One primer pair, denoted as Act-2F (5′-ATGGTCGGYATGGGNCAGAAGGACTC-3′) and Act-8R (5′-GATTCCATACCCAGGAAG-GADGG-3′), successfully amplified an RT-PCR product of the expected size (683-nt) in all mosquito spp. tested. We propose that this primer pair can be used as an internal control to test the quality of RNA from mosquitoes collected in vector surveillance studies. These primers can also be used in molecular experiments in which the detection, amplification or silencing of a ubiquitously expressed mosquito housekeeping gene is necessary. Sequence and phylogenetic data are also presented in this report
Plan de Negocio - Sitio web de comercio electr?nico para la venta de juegos de mesa modernos utilizando CRM en el Per?
La presente tesis es un plan de negocios sobre el desarrollo de un sitio web para la venta de juegos de mesa modernos. As? mismo, se tendr? como factor clave la segmentaci?n por comportamiento de los clientes a trav?s del CRM BITRIX24, de manera que se puedan plantear promociones, comunicaci?n y ofertas de productos dirigidos a los consumidores, sustentados en los resultados que el programa nos pueda brindar. Como parte de este plan de negocios, se realizaron entrevistas a profundidad a los principales proveedores del sector, como tambi?n a los usuarios de juego de mesa modernos. Realizada la investigaci?n, destacan los principales resultados como: Las marcas no manejan ning?n tipo de Customer Relationship Management, lo que no les permite entender a cabalidad el comportamiento de los diferentes segmentos de clientes. Importante resultado de la investigaci?n fue conocer, de primera mano, que el sector viene en un constante crecimiento, sobre todo a ra?z de la pandemia que gatill? un incremento muy importante en las ventas desde el a?o 2020
Detection of West Nile virus-specific antibodies and nucleic acid in horses and mosquitoes, respectively, in Nuevo Leon State, northern Mexico, 2006–2007
Abstract. In the last 5 years, there has been only one reported human case of West Nile virus (WNV) disease in northern Mexico. To determine if the virus was still circulating in this region, equine and entomological surveillance for WNV was conducted in the state of Nuevo Leon in northern Mexico in 2006 and 2007. A total of 203 horses were serologically assayed for antibodies to WNV using an epitope-blocking enzyme-linked immunosorbent assay (bELISA). Seroprevalences for WNV in horses sampled in 2006 and 2007 were 26% and 45%, respectively.
Mosquito collections in 2007 produced 7365 specimens representing 15 species. Culex mosquitoes were screened for WNV RNA and other genera (Mansonia, Anopheles,
Aedes, Psorophora and Uranotaenia) were screened for flaviviruses using reversetranscription (RT)-PCR. Two pools consisting of Culex spp. mosquitoes contained
WNV RNA. Molecular species identification revealed that neither pool included Culex quinquefasciatus (Say) (Diptera:Culicidae) complex mosquitoes. No evidence
of flaviviruses was found in the other mosquito genera examined. These data provide evidence that WNV is currently circulating in northern Mexico and that non-Cx.
quinquefasciatus spp. mosquitoes may be participating in the WNV transmission cycle in this region
Detection of aedes aegypti mosquitoes infected with dengue virus as a complementary method for increasing the sensitivity of surveillance: identification of serotypes 1, 2, and 4 by rt-pcr in Quintana Roo, Mexico
Abstract. Sensitivity of monitoring Aedes aegypti (L.) populations was determined to identify the distribution of dengue virus (DENV) during epidemics in Quintana
Roo. From September to November 2012, we used a motorized aspirator to collect 2,144 female Ae. aegypti from 569 homes. These were grouped into 220 to use
semi-nested RT-PCR for DENV, and positive groups were analyzed individually. Five groups (2.27%) were positive for DENV. Individual analysis yielded eight
groups that tested positive, six with DENV-2, one DENV-1, and one DENV-4. The latter was not reported by the surveillance system that year. The mean number of female mosquitoes per household was 3.77 ± 5.71, and the rate of viral infection of Ae. aegypti was 0.4%. Most infected mosquitoes (49%) were concentrated in 10% of the houses. Monitoring Ae. aegypti infected with DENV has the potential to complement the current system of clinical and entomological surveillance
West Nile Virus Survey of Birds, Horses, and Mosquitoes of the Pacific Coast, Southern Mexico
Abstract. Serology of West Nile virus vectors and non-human reservoirs was surveyed at Acapulco, Jose Azueta, and Ometepec, three Pacific Coast localities of
Guerrero State, Mexico. The objectives of this study were to use enzyme-linked immnosorbent assay (ELISA) to assess West Nile virus antibodies of bird and equine serum samples and use reverse transcription of polymerase chain reaction (RT-PCR) to detect the virus in field-collected resting mosquitoes. Forty birds trapped using mist nets yielded 10% seroprevalence. Similarly, 18.6% of 102
equine blood samples had West Nile virus. In addition, 4,854 mosquitoes were caught using motorized backpack aspirators and grouped into 116 pools. Of the 16 species and seven genera, no mosquito was positive for West Nile virus. Our study demonstrated West Nile virus seroprevalence on resident birds and equines in Guerrero State, Mexico
Deriva de células epiteliales de tejido de piel descongelado de Ovis canadensis mexicana para la formación de un banco de germoplasma
En nuestro país existen diversas especies de mamíferos de interés ecológico que ostentan alguna categoría de riesgo o peligro de extinción. Con la finalidad de resguardar la información genética de estas especies se han desarrollado técnicas de conservación ex situ, las cuales son componentes fundamentales de programas de conservación global que contemplan operaciones de almacenamiento del genoma. El almacenamiento se lleva a cabo mediante las colecciones de células y tejidos incorporados a bancos de germoplasma, que son una alternativa eficaz y próxima para hacerle frente al panorama crítico que sufre la fauna silvestre amenazada. En el presente trabajo se derivaron por vez primera en México, células epiteliales (queratinocitos) y de tejido conectivo (fibroblastos) a los 28 días de cultivo, a partir de piel de Ovis canadensis mexicana post-congelación de 54 días, para la formación de bancos de germoplasma
Detection of dengue virus serotype 2 in aedes aegypti in Quintana Roo, Mexico, 2011
Abstract. In October 2011, the State Health Department announced that several laboratory-confirmed cases of dengue had occurred among residents in two neighborhoods of Benito Juarez, Quintana Roo State, Mexico. To identify the dengue virus serotype(s) temporally and spatially associated with the cases, entomologic-based virus surveillance was initiated in October 2011 in both
neighborhoods. Adult mosquitoes were collected from 88 houses by CDCbackpack aspirator, and all female Aedes aegypti L. (n = 419) were individually homogenized and assayed in pools of as many as 10 by reverse transcriptionpolymerase chain reaction (RT-PCR) using dengue virus-specific primers. Five (12%) of 41 pools were positive for dengue virus RNA. The individual mosquitoes that comprised the pools were analyzed separately by RT-PCR using dengue virus serotype-specific primers. Six mosquitoes were positive for dengue virus serotype-2 (DENV-2) RNA, three of which were collected in the same house. The mean number of female Ae. aegypti collected in each house was 4.76 ± 6.19. The overall
dengue virus-infection rate in female Ae. aegypti was 1.4%. Interestingly, most (60%) of mosquito females were collected only from 15 (17%) houses. In summary,
we provide evidence of recent DENV-2 transmission in Quintana Roo State
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