Kokila Sivabalakrishnan, Andrew Hemphill, S H P Parakrama Karunaratne, Arunasalam Naguleswaran, Isabel Roditi, Sinnathamby N Surendran, Ranjan Ramasamy
Aedes aegypti L. and Aedes albopictus Skuse mosquitoes (Diptera: Culicidae), the principal vectors of many human arboviral diseases, lay eggs and undergo preimaginal development in fresh water. They have recently been shown to also develop in brackish water in coastal areas. Previous findings showed that Ae. aegypti larvae developing in brackish water possessed thicker cuticles and greater larvicide resistance than larvae developing in fresh water. The present study compared cuticle ultrastructure, resistance to adulticides, and the activities of adulticide detoxifying enzymes in female mosquitoes emerging from fresh and brackish water-developing Ae. aegypti preimaginal stages. The results showed that brackish water-derived females possessed significantly thicker tarsal and abdominal cuticles compared to fresh water-derived females. Brackish water-derived Ae. aegypti females were also significantly more resistant to three different types of pyrethroids and malathion compared to fresh water-derived females. Corresponding reversal of cuticle changes and adulticide resistance when preimaginal salinity was reversed showed that preimaginal salinity determined both procuticle structure and adulticide resistance in brackish water-derived females. Compared with fresh water-derived Ae. aegypti females, brackish water-derived females had similar activities of the adulticide-detoxifying enzyme families of esterases and glutathione S-transferases and a modest increase in the activity of monooxygenases, all of which were lower than the threshold values attributed to resistance in field populations of Ae. aegypti. Reduced permeability of the thicker and remodelled cuticles in brackish water-derived Ae. aegypti females to adulticides is proposed to be mainly responsible for their greater resistance to different types of adulticides. Greater salinity tolerance of preimaginal stages, adult cuticle changes and higher larvicide and adulticide resistance are inherited properties of brackish water-developing Ae. aegypti that reverse in a few generations after transfer to fresh water. This is compatible with a role for epigenetic changes in the adaptation of Ae. aegypti to brackish water. Greater resistance of salinity-tolerant Ae. aegypti to adulticides and larvicides poses a hitherto unappreciated problem for controlling arboviral diseases, with attendant implications also for other mosquito-borne diseases.
{"title":"Preimaginal development of Aedes aegypti L. (Diptera: Culicidae) in brackish water gives rise to adult mosquitoes with thicker cuticles and greater insecticide resistance.","authors":"Kokila Sivabalakrishnan, Andrew Hemphill, S H P Parakrama Karunaratne, Arunasalam Naguleswaran, Isabel Roditi, Sinnathamby N Surendran, Ranjan Ramasamy","doi":"10.1111/mve.12799","DOIUrl":"https://doi.org/10.1111/mve.12799","url":null,"abstract":"<p><p>Aedes aegypti L. and Aedes albopictus Skuse mosquitoes (Diptera: Culicidae), the principal vectors of many human arboviral diseases, lay eggs and undergo preimaginal development in fresh water. They have recently been shown to also develop in brackish water in coastal areas. Previous findings showed that Ae. aegypti larvae developing in brackish water possessed thicker cuticles and greater larvicide resistance than larvae developing in fresh water. The present study compared cuticle ultrastructure, resistance to adulticides, and the activities of adulticide detoxifying enzymes in female mosquitoes emerging from fresh and brackish water-developing Ae. aegypti preimaginal stages. The results showed that brackish water-derived females possessed significantly thicker tarsal and abdominal cuticles compared to fresh water-derived females. Brackish water-derived Ae. aegypti females were also significantly more resistant to three different types of pyrethroids and malathion compared to fresh water-derived females. Corresponding reversal of cuticle changes and adulticide resistance when preimaginal salinity was reversed showed that preimaginal salinity determined both procuticle structure and adulticide resistance in brackish water-derived females. Compared with fresh water-derived Ae. aegypti females, brackish water-derived females had similar activities of the adulticide-detoxifying enzyme families of esterases and glutathione S-transferases and a modest increase in the activity of monooxygenases, all of which were lower than the threshold values attributed to resistance in field populations of Ae. aegypti. Reduced permeability of the thicker and remodelled cuticles in brackish water-derived Ae. aegypti females to adulticides is proposed to be mainly responsible for their greater resistance to different types of adulticides. Greater salinity tolerance of preimaginal stages, adult cuticle changes and higher larvicide and adulticide resistance are inherited properties of brackish water-developing Ae. aegypti that reverse in a few generations after transfer to fresh water. This is compatible with a role for epigenetic changes in the adaptation of Ae. aegypti to brackish water. Greater resistance of salinity-tolerant Ae. aegypti to adulticides and larvicides poses a hitherto unappreciated problem for controlling arboviral diseases, with attendant implications also for other mosquito-borne diseases.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143573155","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Karelly Melgarejo-Colmenares, Darío Vezzani, Marlene Kliger, María V. Cardo
Blood meal patterns of mosquitoes (Diptera: Culicidae) are strongly influenced by host availability. However, the role of community composition and abundance of vertebrate hosts in determining such patterns is still unclear. Here, we analysed the blood meal sources of field-collected mosquitoes in settings with a permanent overabundance of a specific vertebrate species. Mosquitoes were collected using a battery-powered handheld aspirator every 2 months between November 2021 and April 2022 in temperate Argentina. Blood-engorged mosquitoes were collected at 11 sites corresponding to five types of settings: two cattle fields, one rabbit breeding farm, three chicken farms, two dog boarding facilities, and three geriatric hospitals, characterised by the permanent overabundance of cows, rabbits, chickens, dogs, and humans, respectively. Blood meal analysis was performed via polymerase chain reaction (PCR) and sequencing. A principal component analysis (PCA) was performed in which variables were pairs comprising an engorged mosquito species and the host species it fed on. A total of 242 blood meals from Aedes (3 species), Culex (4), Isostomyia (1) and Psorophora (1) were identified. Among these, five mammals and 12 avian species were identified as hosts. Overall, 79% of the blood meals were taken from the overabundant host, ranging from 67% to 99% in all settings except for geriatric hospitals (7%). The proportion of feeds taken on the overabundant host was lowest for Culex quinquefasciatus Say (0.67, N = 119), Cx. pipiens molestus Forskal (0.5, N = 18) and the hybrid between the two (0.5, N = 2), and highest for Aedes aegypti Linnaeus (1, N = 2), Ae. albifasciatus Macquart (1, N = 3), Ae. crinifer Theobald (1, N = 46), Cx. eduardoi Casal & García (0.9, N = 10), Isostomyia paranensis Brèthes (1, N = 20) and Psorophora ferox Humboldt (1, N = 21). By fixing host abundance in preselected settings, we propose a field design that overcomes the difficulties of estimating host community composition. This approach aids in achieving a clearer understanding of mosquito feeding patterns and their implications for arbovirus disease transmission.
蚊子(双翅目:Culicidae)的血餐模式受宿主可用性的影响很大。然而,脊椎动物宿主的群落组成和丰度在决定这种模式中的作用仍不清楚。在此,我们分析了在特定脊椎动物物种长期过量的环境中野外采集的蚊子的血餐来源。2021 年 11 月至 2022 年 4 月期间,我们每两个月在阿根廷温带地区使用电池供电的手持吸蚊器收集蚊子。在 11 个地点收集了血吸蚊,这些地点分别对应五种类型的环境:两个养牛场、一个养兔场、三个养鸡场、两个养狗场和三个老年病医院,其特点是牛、兔、鸡、狗和人长期过量繁殖。血粉分析是通过聚合酶链反应(PCR)和测序进行的。进行了主成分分析(PCA),其中的变量是由吞食的蚊子种类和它吸食的宿主种类组成的对。共鉴定出 242 份血餐,分别来自伊蚊(3 种)、库蚊(4 种)、异刺蚊(1 种)和疟蚊(1 种)。其中,5 种哺乳动物和 12 种鸟类被确定为宿主。总体而言,79%的血餐取自过量宿主,除老年病医院(7%)外,其他环境中的比例从 67% 到 99% 不等。在过多宿主身上取食的比例最低的是 Culex quinquefasciatus Say (0.67, N = 119)、Cx. pipiens molestus Forskal (0.5, N = 18) 和两者的杂交种 (0.5, N = 2),最高的是埃及伊蚊 Aedes aegypti Linnaeus (1, N = 2)、白纹伊蚊 Ae. albifasciatus Macqual (0.5, N = 1)和白纹伊蚊 Ae. albifasciatus Macqual (0.5, N = 2)。cinifer Theobald (1, N = 46)、Cx. eduardoi Casal & García (0.9, N = 10)、Isostomyia paranensis Brèthes (1, N = 20) 和 Psorophora ferox Humboldt (1, N = 21)。通过固定预选环境中的寄主丰度,我们提出了一种野外设计方法,克服了估计寄主群落组成的困难。这种方法有助于更清楚地了解蚊子的觅食模式及其对虫媒病毒疾病传播的影响。
{"title":"Overabundant single-host settings as field labs to assess blood meal patterns of mosquitoes","authors":"Karelly Melgarejo-Colmenares, Darío Vezzani, Marlene Kliger, María V. Cardo","doi":"10.1111/mve.12798","DOIUrl":"10.1111/mve.12798","url":null,"abstract":"<p>Blood meal patterns of mosquitoes (Diptera: Culicidae) are strongly influenced by host availability. However, the role of community composition and abundance of vertebrate hosts in determining such patterns is still unclear. Here, we analysed the blood meal sources of field-collected mosquitoes in settings with a permanent overabundance of a specific vertebrate species. Mosquitoes were collected using a battery-powered handheld aspirator every 2 months between November 2021 and April 2022 in temperate Argentina. Blood-engorged mosquitoes were collected at 11 sites corresponding to five types of settings: two cattle fields, one rabbit breeding farm, three chicken farms, two dog boarding facilities, and three geriatric hospitals, characterised by the permanent overabundance of cows, rabbits, chickens, dogs, and humans, respectively. Blood meal analysis was performed via polymerase chain reaction (PCR) and sequencing. A principal component analysis (PCA) was performed in which variables were pairs comprising an engorged mosquito species and the host species it fed on. A total of 242 blood meals from <i>Aedes</i> (3 species), <i>Culex</i> (4), <i>Isostomyia</i> (1) and <i>Psorophora</i> (1) were identified. Among these, five mammals and 12 avian species were identified as hosts. Overall, 79% of the blood meals were taken from the overabundant host, ranging from 67% to 99% in all settings except for geriatric hospitals (7%). The proportion of feeds taken on the overabundant host was lowest for <i>Culex quinquefasciatus</i> Say (0.67, <i>N</i> = 119), <i>Cx. pipiens molestus</i> Forskal (0.5, <i>N</i> = 18) and the hybrid between the two (0.5, <i>N</i> = 2), and highest for <i>Aedes aegypti</i> Linnaeus (1, <i>N</i> = 2), <i>Ae. albifasciatus</i> Macquart (1, <i>N</i> = 3), <i>Ae. crinifer</i> Theobald (1, <i>N</i> = 46), <i>Cx. eduardoi</i> Casal & García (0.9, <i>N</i> = 10), <i>Isostomyia paranensis</i> Brèthes (1, <i>N</i> = 20) and <i>Psorophora ferox</i> Humboldt (1, <i>N</i> = 21). By fixing host abundance in preselected settings, we propose a field design that overcomes the difficulties of estimating host community composition. This approach aids in achieving a clearer understanding of mosquito feeding patterns and their implications for arbovirus disease transmission.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 3","pages":"576-591"},"PeriodicalIF":1.9,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143537230","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Melanie Ruiz, Rodrigo J. Alonso, Malena Rospide, Diana B. Acosta, Regino Cavia, Juliana P. Sanchez
Many ectoparasite species serve as vectors for bacteria that are significant to both public and animal health, with wild, domestic and synanthropic mammals acting as reservoirs. However, limited information exists on the circulation and incidence of these vectors in Argentina. We examined the diversity, prevalence and abundance of ectoparasites, along with the presence of Rickettsia spp., of Didelphis albiventris Lund (Didelphimorphia, Didelphidae) within a rural landscape of the Pampas region, Argentina. We also analysed variations in ectoparasite populations concerning seasonality, livestock farm type and farmers' management practices. Seven species of hematophagous ectoparasites were collected, including mites (Mesostigmata, Laelapidae: Laelaps echidninus Berlese); ticks (Ixodida, Ixodidae: Ixodes loricatus Neumann); fleas (Siphonaptera, Rhopalopsyllidae: Polygenis platensis Jordan and Rothschild and Polygenis rimatus Jordan); Stephanocircidae: Craneopsylla minerva wolffhuegeli (Rothschild, Pulicidae: Ctenocephalides felis Bouché); and lice (Phthiraptera, Polyplacidae: Polyplax spinulosa Burmeister). Additionally, two bacteria were detected: Rickettsia felis Bouyer et al. (Rickettsiales, Rickettsiaceae) and Rickettsia sp. (Rickettsiales, Rickettsiaceae) were closely related to Rickettsia bellii Philip et al. (Rickettsiales, Rickettsiaceae). Fleas were the most prevalent and abundant group, with C. felis showing the highest values of mean abundance and prevalence. Parasitological comparisons between dairy farms and feedlots revealed similar results, with comparable densities of D. albiventris in both farm types. Ectoparasite abundance varied seasonally, peaking during the colder season. Regression analysis indicated higher ectoparasite infestation levels on farms with more dogs. The detection of pathogenic bacteria, coupled with the high prevalence and abundance of vectors, such as C. felis, suggests a significant epidemiological risk in the region. The commensal behaviour of D. albiventris facilitates it to thrive in areas modified by anthropogenic activity, positioning this species as a potential nexus between wild and domestic epidemiological cycles of parasites and emerging pathogens. Therefore, our findings suggest that D. albiventris plays a key role in the transmission and maintenance of ectoparasites and ectoparasite-borne bacteria within these ecosystems.
{"title":"Diversity and eco-epidemiology of ectoparasites and Rickettsia spp. associated with the opossums Didelphis albiventris Lund in livestock farms from Argentinian Pampas region\u0000 Diversidad y eco-epidemiología de ectoparásitos y Rickettsia spp. asociados a la zarigüeya Didelphis albiventris Lund en explotaciones ganaderas de la región pampeana argentina","authors":"Melanie Ruiz, Rodrigo J. Alonso, Malena Rospide, Diana B. Acosta, Regino Cavia, Juliana P. Sanchez","doi":"10.1111/mve.12796","DOIUrl":"10.1111/mve.12796","url":null,"abstract":"<p>Many ectoparasite species serve as vectors for bacteria that are significant to both public and animal health, with wild, domestic and synanthropic mammals acting as reservoirs. However, limited information exists on the circulation and incidence of these vectors in Argentina. We examined the diversity, prevalence and abundance of ectoparasites, along with the presence of <i>Rickettsia</i> spp., of <i>Didelphis albiventris</i> Lund (Didelphimorphia, Didelphidae) within a rural landscape of the Pampas region, Argentina. We also analysed variations in ectoparasite populations concerning seasonality, livestock farm type and farmers' management practices. Seven species of hematophagous ectoparasites were collected, including mites (Mesostigmata, Laelapidae: <i>Laelaps echidninus</i> Berlese); ticks (Ixodida, Ixodidae: <i>Ixodes loricatus</i> Neumann); fleas (Siphonaptera, Rhopalopsyllidae: <i>Polygenis platensis</i> Jordan and Rothschild and <i>Polygenis rimatus</i> Jordan); Stephanocircidae: <i>Craneopsylla minerva wolffhuegeli</i> (Rothschild, Pulicidae: <i>Ctenocephalides felis</i> Bouché); and lice (Phthiraptera, Polyplacidae: <i>Polyplax spinulosa</i> Burmeister). Additionally, two bacteria were detected: <i>Rickettsia felis</i> Bouyer et al. (Rickettsiales, Rickettsiaceae) and <i>Rickettsia</i> sp. (Rickettsiales, Rickettsiaceae) were closely related to <i>Rickettsia bellii</i> Philip et al. (Rickettsiales, Rickettsiaceae). Fleas were the most prevalent and abundant group, with <i>C. felis</i> showing the highest values of mean abundance and prevalence. Parasitological comparisons between dairy farms and feedlots revealed similar results, with comparable densities of <i>D. albiventris</i> in both farm types. Ectoparasite abundance varied seasonally, peaking during the colder season. Regression analysis indicated higher ectoparasite infestation levels on farms with more dogs. The detection of pathogenic bacteria, coupled with the high prevalence and abundance of vectors, such as <i>C. felis</i>, suggests a significant epidemiological risk in the region. The commensal behaviour of <i>D. albiventris</i> facilitates it to thrive in areas modified by anthropogenic activity, positioning this species as a potential nexus between wild and domestic epidemiological cycles of parasites and emerging pathogens. Therefore, our findings suggest that <i>D. albiventris</i> plays a key role in the transmission and maintenance of ectoparasites and ectoparasite-borne bacteria within these ecosystems.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 3","pages":"431-444"},"PeriodicalIF":1.9,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143441306","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}