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      Nuevos registros de distribución para Uranotaenia sapphirina (Osten Sacken, 1868) (Diptera: Culicidae) en Quintana Roo, México Translated title: New distributional records of Uranotaenia sapphirina (Osten Sacken, 1868) (Díptera: Culicidae) in Quintana Roo, Mexico

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          Abstract

          Resumen Se realizaron colectas de larvas de culícidos en tres localidades del estado de Quintana Roo, México (Leona Vicario, Cacao y Ramonal) durante los meses de abril y mayo de 2021. Se identificó la especie Uranotaenia sapphirina, con lo cual se aportan nuevas localidades y se actualiza la lista de culícidos presentes en Quintana Roo a 87 especies.

          Translated abstract

          Abstract Culicidae larvae collections were carried out in three localities in the state of Quintana Roo, Mexico (Leona Vicario, Cacao and Ramonal) during the months of April and May 2021. The species Uranotaenia sapphirina, was identified, with this records new locations are provided and updating the list of Culicidae present in Quintana Roo to 87 species.

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          Most cited references22

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          Epidemiology of West Nile Virus in Connecticut: A Five-Year Analysis of Mosquito Data 1999–2003

          Two hundred and ten isolations of West Nile virus (WNV) were obtained from 17 mosquito species in six genera in statewide surveillance conducted in Connecticut from June through October, 1999-2003. Culex pipiens (86), Culex salinarius (32), Culex restuans (26), Culiseta melanura (32), and Aedes vexans (12) were implicated as the most likely vectors of WNV in the region based on virus isolation data. Culex pipiens was abundant from July through September and is likely involved in early season enzootic transmission and late season epizootic amplification of the virus in wild bird populations. Epidemic transmission of WNV to humans in urban locales is probable. The abundance of Cx. restuans in June and July and isolations of WNV in early July suggest that this species may play an important role as an enzootic vector involved in early amplification of WNV virus among wild birds. Its involvement as a bridge vector to humans is unlikely. Culex salinarius was the most frequently captured Culex species and was abundant in August and September when virus activity was at its height. Frequent isolations of WNV from this species in September when the majority of human cases were reported in union with its abundance at this time of the year, demonstrated vector competence, and broad feeding habits, make Cx. salinarius a likely bridge vector to humans, horses and other mammals. Multiple isolations WNV from Cs. melanura collected in more rural locales in late August and September, provide supportive evidence to suggest that this predominant avian feeder may play a significant role in epizootic amplification of the virus among wild bird populations in these environs. Aedes vexans was the only species of Aedes or Ochlerotatus from which multiple isolations of WNV were made in more than one year and was among the most frequently trapped and abundant species throughout the season. Since Ae. vexans predominately feeds on mammals it is unlikely to play a significant role in epizootic amplification of WNV, however, because of its abundance and aggressive mammalian and human biting behavior it must receive strong consideration as a bridge vector to humans and horses. The occasional virus isolations obtained from Aedes cinereus (4), Uranotaenia sapphirina (3), Ochlerotatus canadensis (2), Ochlerotatus trivittatus (2), Ochlerotatus sollicitans (2), Ochlerotatus sticticus (2), Psorophora ferox (2), Anopheles punctipennis, Anopheles walkeri, Ochlerotatus cantator, Ochlerotatus taeniorhynchus, and Ochlerotatus triseriatus in conjunction with their inefficient vector competency and host feeding preferences indicate that these species likely play a very minor role in either the enzootic maintenance or epizootic transmission of WNV in this region. The principal foci of WNV activity in Connecticut were identified as densely populated (>3,000 people/mi2) residential communities in coastal Fairfield and New Haven Counties, and in the case of 2002, similar locales in proximity of the city of Hartford in central Hartford County. In almost all instances we observed a correlation both temporally and spatially between the isolation of WNV from field-collected mosquitoes and subsequent human cases in these locales. In most years the incidence of human cases closely paralleled the number of virus isolations made from mosquitoes with both peaks falling in early September. We conclude that the isolation of WNV from field-collected mosquitoes is a sensitive indicator of virus activity that is associated with the risk of human infection that habitually extends from early August through the end of October in Connecticut.
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            Identification of Uranotaenia sapphirina as a specialist of annelids broadens known mosquito host use patterns

            Feeding upon vertebrate blood by mosquitoes permits transmission of diverse pathogens, including viruses, protozoa, and nematodes. Despite over a century of intensive study, no mosquito species is known to specialize on non-vertebrate hosts. Using molecular analyses and field observations, we provide the first evidence, to our knowledge, that a mosquito, Uranotaenia sapphirina, specializes on annelid hosts (earthworms and leeches) while its sympatric congener, Uranotaenia lowii, feeds only on anurans (frogs and toads). Our results demonstrate that Ur. sapphirina feeds on annelid hosts (100% of identified blood meals; n = 72; collected throughout Florida), findings that are supported by field observations of these mosquitoes feeding on Sparganophilus worms and freshwater leeches. These findings indicate that adult mosquitoes utilize a much broader range of host taxa than previously recognized, with implications for epidemiology and the evolution of host use patterns in mosquitoes.
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              Diversity of mosquitoes and the aquatic insects associated with their oviposition sites along the Pacific coast of Mexico

              Background The abundance, richness and diversity of mosquitoes and aquatic insects associated with their oviposition sites were surveyed along eight states of the Pacific coast of Mexico. Diversity was estimated using the Shannon index (H’), similarity measures and cluster analysis. Methods Oviposition sites were sampled during 2–3 months per year, over a three year period. Field collected larvae and pupae were reared and identified to species following adult emergence. Aquatic insects present at oviposition sites were also collected, counted and identified to species or genus. Results In total, 15 genera and 74 species of mosquitoes were identified: Anopheles pseudopunctipennis, An. albimanus and Aedes aegypti were the most abundant and widely-distributed species, representing 47% of total mosquito individuals sampled. New species records for certain states are reported. Anopheline diversity was lowest in Sinaloa state (H’ = 0.54) and highest in Chiapas (H’ = 1.61) and Michoacán (H’ = 1.56), whereas culicid diversity was lowest in Michoacán (H’ = 1.93), Colima (H’ = 1.95), Sinaloa (H’ = 1.99) and Jalisco (H’ = 2.01) and highest in Chiapas (H’ = 2.66). In total, 10 orders, 57 families, 166 genera and 247 species of aquatic insects were identified in samples. Aquatic insect diversity was highest in Chiapas, Oaxaca and Michoacán (H’ = 3.60-3.75). Mosquito larval/pupal abundance was not correlated with that of predatory Coleoptera and Hemiptera. Conclusion This represents the first update on the diversity and geographic distribution of the mosquitoes and aquatic insects of Mexico in over five decades. This information has been cataloged in Mexico’s National Biodiversity Information System (SNIB-CONABIO) for public inspection.
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                Author and article information

                Journal
                rche
                Revista chilena de entomología
                Rev. chil. entomol.
                Sociedad Chilena de Entomología (Santiago, , Chile )
                0034-740X
                0718-8994
                September 2021
                : 47
                : 3
                : 613-617
                Affiliations
                [1] Chetumal Quintana Roo orgnameServicios Estatales de Salud de Quintana Roo México karla.miis94@ 123456gmail.com
                [3] Chetumal Quintana Roo orgnameLaboratorio Estatal de Salud Pública de Quintana Roo México xinia81@ 123456hotmail.com
                [4] Ciudad de México orgnameCentro Nacional de Programas Preventivos y Control de Enfermedades México cgonzalez_vectores@ 123456hotmail.com
                [2] Ejido Juan Sarabia Quintana Roo orgnameTecnológico Nacional de México orgdiv1Instituto Tecnológico de la Zona Maya México
                Article
                S0718-89942021000300613 S0718-8994(21)04700300613
                10.35249/rche.47.3.21.19
                5dfe18a3-62d0-4262-a813-c90b2eace88f

                This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

                History
                : 13 August 2021
                : 08 September 2021
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 22, Pages: 5
                Product

                SciELO Chile

                Categories
                Nota Científica

                mosquitos,Distribution,mosquitoes,Uranotaeniini,Distribución

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