Maria Fernanda López Berrizbeitia, Kordiyeh Hamidi
Rodents represent the most diverse mammalian group and are considered important hosts for different groups of parasites serving as vectors for some zoonotic agents. Although there have been numerous studies conducted on occurrence records of ectoparasites on rodents, there is a paucity of knowledge regarding the biogeographical patterns of ectoparasites on this group of small mammals. In this study, a quantitative approach was employed to identify patterns of distributional congruence (PDCs) of ectoparasites of rodents in Iran. A total of 121 occurrence records for 37 species of ectoparasites (ticks, mites, lice and fleas) in Iran were analysed using endemicity analysis NDM/VNDM. Twelve consensus areas, characterised by 30 species, were found which were grouped into three PDCs. The PDCs showed that the highest endemicity values were primarily linked to the Zagros Mountains and central Persian areas. The patterns as a whole showed a clear tendency of the Zagros Mountains, forest steppe and central Persian desert basins ecoregions to provide possible areas of endemism. The current study extends the knowledge on the distribution patterns of four main groups of ectoparasites in association with rodent species in Iran and emphasises the significance of endemic zones in controlling management of reservoirs and vectors and conservation efforts.
{"title":"Patterns of distributional congruence of rodent ectoparasites in Iran: A first approach","authors":"Maria Fernanda López Berrizbeitia, Kordiyeh Hamidi","doi":"10.1111/mve.70009","DOIUrl":"10.1111/mve.70009","url":null,"abstract":"<p>Rodents represent the most diverse mammalian group and are considered important hosts for different groups of parasites serving as vectors for some zoonotic agents. Although there have been numerous studies conducted on occurrence records of ectoparasites on rodents, there is a paucity of knowledge regarding the biogeographical patterns of ectoparasites on this group of small mammals. In this study, a quantitative approach was employed to identify patterns of distributional congruence (PDCs) of ectoparasites of rodents in Iran. A total of 121 occurrence records for 37 species of ectoparasites (ticks, mites, lice and fleas) in Iran were analysed using endemicity analysis NDM/VNDM. Twelve consensus areas, characterised by 30 species, were found which were grouped into three PDCs. The PDCs showed that the highest endemicity values were primarily linked to the Zagros Mountains and central Persian areas. The patterns as a whole showed a clear tendency of the Zagros Mountains, forest steppe and central Persian desert basins ecoregions to provide possible areas of endemism. The current study extends the knowledge on the distribution patterns of four main groups of ectoparasites in association with rodent species in Iran and emphasises the significance of endemic zones in controlling management of reservoirs and vectors and conservation efforts.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 4","pages":"643-652"},"PeriodicalIF":1.9,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144959808","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}
Gaia G. Mortier, Stuart Black, Andrew C. Kitchener, Georg Hantke, Luke A. Stevens, Lea J. Grayston-Smith, Phillip J. Baker, M. Alejandra Perotti
Climate change is expected to expand the geographic ranges of ectoparasites, increasing the transmission of vector-borne diseases and necessitating a better understanding of ectoparasite–host trophic dynamics. Haematophagous ectoparasites can serve as valuable subsamples of their hosts, retaining isotopic values that reflect dietary information in both their blood meals and tissues. However, differences in the life histories and feeding strategies of lice, fleas and ticks may influence how host isotopic composition is preserved. Here, stable isotope values of carbon (δ13C) and nitrogen (δ15N) were used to investigate trophic interactions between ectoparasites and their mammalian hosts in three pairings: lice (Anoplura: Polyplacidae; n = 101) from Eurasian red squirrels Sciurus vulgaris L. (Rodentia: Sciuridae), fleas (Siphonaptera: Ceratophyllidae; n = 92) from fat dormice Glis glis L. (Rodentia: Gliridae) and ticks (Ixodida: Ixodidae; n = 16) from European hedgehogs Erinaceus europaeus L. (Eulipotyphla: Erinaceidae). Our findings indicate that ectoparasites reflect the dietary patterns of their hosts, with lice exhibiting the closest isotopic values, followed by fleas and ticks. All parasites had significantly higher δ15N values than their hosts, indicative of trophic enrichment, but their δ13C values varied. Notably, we found that the presence of a blood meal did not significantly affect the isotopic values found in lice and fleas, while ticks showed a significant difference between exoskeleton and blood meal in δ13C values. This study highlights the importance of understanding how the life histories of parasite species influence the preservation of isotopic host signals in order to be able to utilise stable isotope analyses of ectoparasites to infer host dietary niches and preferences, with broader implications for understanding host–parasite dynamics and disease transmission pathways.
{"title":"Stable isotope analysis of ectoparasites as a tool for understanding trophic interactions with mammalian hosts","authors":"Gaia G. Mortier, Stuart Black, Andrew C. Kitchener, Georg Hantke, Luke A. Stevens, Lea J. Grayston-Smith, Phillip J. Baker, M. Alejandra Perotti","doi":"10.1111/mve.70008","DOIUrl":"10.1111/mve.70008","url":null,"abstract":"<p>Climate change is expected to expand the geographic ranges of ectoparasites, increasing the transmission of vector-borne diseases and necessitating a better understanding of ectoparasite–host trophic dynamics. Haematophagous ectoparasites can serve as valuable subsamples of their hosts, retaining isotopic values that reflect dietary information in both their blood meals and tissues. However, differences in the life histories and feeding strategies of lice, fleas and ticks may influence how host isotopic composition is preserved. Here, stable isotope values of carbon (<i>δ</i><sup>13</sup>C) and nitrogen (<i>δ</i><sup>15</sup>N) were used to investigate trophic interactions between ectoparasites and their mammalian hosts in three pairings: lice (Anoplura: Polyplacidae; <i>n</i> = 101) from Eurasian red squirrels <i>Sciurus vulgaris</i> L. (Rodentia: Sciuridae), fleas (Siphonaptera: Ceratophyllidae; <i>n</i> = 92) from fat dormice <i>Glis glis</i> L. (Rodentia: Gliridae) and ticks (Ixodida: Ixodidae; <i>n</i> = 16) from European hedgehogs <i>Erinaceus europaeus</i> L. (Eulipotyphla: Erinaceidae). Our findings indicate that ectoparasites reflect the dietary patterns of their hosts, with lice exhibiting the closest isotopic values, followed by fleas and ticks. All parasites had significantly higher <i>δ</i><sup>15</sup>N values than their hosts, indicative of trophic enrichment, but their <i>δ</i><sup>13</sup>C values varied. Notably, we found that the presence of a blood meal did not significantly affect the isotopic values found in lice and fleas, while ticks showed a significant difference between exoskeleton and blood meal in <i>δ</i><sup>13</sup>C values. This study highlights the importance of understanding how the life histories of parasite species influence the preservation of isotopic host signals in order to be able to utilise stable isotope analyses of ectoparasites to infer host dietary niches and preferences, with broader implications for understanding host–parasite dynamics and disease transmission pathways.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 4","pages":"664-674"},"PeriodicalIF":1.9,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://resjournals.onlinelibrary.wiley.com/doi/epdf/10.1111/mve.70008","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144959786","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Federica Usai, Filippo Maria Dini, Ilaria Guarniero, Enrica Bellinello, Laura Stancampiano
Species belonging to the genus Lipoptena have received limited attention and have historically been subject to misidentifications. Recent records of L. fortisetosa in Europe have rekindled interest in these hippoboscids, leading to the discovery of a new species in Spain in 2024, which has been named L. andaluciensis. During an opportunistic sampling conducted in March 2023 and October 2024 on the Italian red deer (Cervus elaphus italicus), an Italian endemic subspecies, within the ancient relict lowland forest of the Bosco della Mesola Nature Reserve, hippoboscids morphologically identical to L. andaluciensis were collected and examined. This represents the first record of this species in Italy. In total, 257 specimens of Lipoptena were collected and analysed (161 in 2023 and 94 in 2024), all identified as L. andaluciensis. Additionally, Lipoptena specimens collected from fallow deer in 2007 within the same nature reserve, which had remained unidentified until now, were re-examined. A total of 66 specimens were reassessed, of which 63 were morphologically identified as L. andaluciensis and 3 as L. cervi. Morphological identification of the 2023 and 2024 specimens was further confirmed through molecular analysis using COI as a barcode marker. Molecular analysis also revealed the presence of a nuclear copy of the COI gene (NUMTs) in the nuclear genome of L. andaluciensis. The discovery of L. andaluciensis in Spain and in Italy since 2007 raises the possibility that this species has a much broader distribution, particularly at lower altitudes and within a Mediterranean climatic zone. It is plausible that its presence has so far gone unnoticed or has been misidentified.
属于Lipoptena属的物种受到了有限的关注,并且在历史上受到了错误的识别。最近欧洲对L. fortisetosa的记录重新燃起了人们对这些海马的兴趣,导致2024年在西班牙发现了一个新物种,被命名为L. andaluciensis。在2023年3月和2024年10月对Bosco della Mesola自然保护区古遗址低地森林中的意大利特有亚种意大利马鹿(Cervus elaphus italicus)进行了机会性采样,收集并检查了与L. andaluciensis形态相同的马尾。这是该物种在意大利的首次记录。共采集和分析了257份Lipoptena标本(2023年161份,2024年94份),均鉴定为安达卢西亚l.a。此外,2007年在同一自然保护区从黇鹿身上采集的Lipoptena标本,直到现在仍未被确认,被重新检查。共鉴定66份标本,其中63份形态鉴定为安达卢西亚乳杆菌,3份形态鉴定为宫颈乳杆菌。利用COI作为条形码标记,通过分子分析进一步确认了2023和2024标本的形态鉴定。分子分析还揭示了L. andaluciensis核基因组中存在COI基因(NUMTs)的核拷贝。自2007年以来,在西班牙和意大利发现了L. andaluciensis,这提高了该物种分布范围更广的可能性,特别是在低海拔地区和地中海气候带。到目前为止,它的存在似乎没有被注意到,或者被错误地识别了。
{"title":"The enigmatic case of Lipoptena sp. in the Bosco della Mesola Nature Reserve (Italy)","authors":"Federica Usai, Filippo Maria Dini, Ilaria Guarniero, Enrica Bellinello, Laura Stancampiano","doi":"10.1111/mve.70002","DOIUrl":"10.1111/mve.70002","url":null,"abstract":"<p>Species belonging to the genus <i>Lipoptena</i> have received limited attention and have historically been subject to misidentifications. Recent records of <i>L. fortisetosa</i> in Europe have rekindled interest in these hippoboscids, leading to the discovery of a new species in Spain in 2024, which has been named <i>L. andaluciensis</i>. During an opportunistic sampling conducted in March 2023 and October 2024 on the Italian red deer (<i>Cervus elaphus italicus</i>), an Italian endemic subspecies, within the ancient relict lowland forest of the Bosco della Mesola Nature Reserve, hippoboscids morphologically identical to <i>L. andaluciensis</i> were collected and examined. This represents the first record of this species in Italy. In total, 257 specimens of <i>Lipoptena</i> were collected and analysed (161 in 2023 and 94 in 2024), all identified as <i>L. andaluciensis</i>. Additionally, <i>Lipoptena</i> specimens collected from fallow deer in 2007 within the same nature reserve, which had remained unidentified until now, were re-examined. A total of 66 specimens were reassessed, of which 63 were morphologically identified as <i>L. andaluciensis</i> and 3 as <i>L. cervi</i>. Morphological identification of the 2023 and 2024 specimens was further confirmed through molecular analysis using COI as a barcode marker. Molecular analysis also revealed the presence of a nuclear copy of the COI gene (NUMTs) in the nuclear genome of <i>L. andaluciensis</i>. The discovery of <i>L. andaluciensis</i> in Spain and in Italy since 2007 raises the possibility that this species has a much broader distribution, particularly at lower altitudes and within a Mediterranean climatic zone. It is plausible that its presence has so far gone unnoticed or has been misidentified.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"40 1","pages":"82-90"},"PeriodicalIF":1.9,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12865754/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144883152","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Alpha Kargbo, Aamir M. Osman, Edrisa Jawo, Lamin K. M. Fatty, Flavia C. M. Collere, Marcos R. André, Ahmed A. Hassan-Kadle, Thállitha S. W. J. Vieira, Rosangela Z. Machado, Rafael F. C. Vieira
Ticks are significant vectors of pathogens affecting both animals and humans, with the climate and environment of Sub-Saharan Africa providing ideal conditions for their growth. However, there are limited data on ticks and tick-borne pathogens (T&TBPs) in cattle in The Gambia. This study aimed to identify tick species on cattle and conduct molecular screening for T&TBPs. A total of 92 ticks were collected from 306 indigenous cattle. Ticks were first identified morphologically using taxonomic keys and then confirmed molecularly through DNA sequencing. DNA was extracted from the right fourth leg of six representative ticks for species confirmation, while 77 whole adult ticks were used for screening T&TBPs. Screening polymerase chain reaction (PCR) assays targeted Anaplasma marginale msp1β gene, Ehrlichia spp. dsb gene and hemotropic Mycoplasma spp. 16S rRNA gene. Ehrlichia-positive samples underwent additional assays targeting the sodB, 16S rRNA and groEL genes, followed by Sanger sequencing and phylogenetic analyses. A total of 92 (53 M, 37 F and two nymphs) ticks were collected from 30/306 (9.8%; 95% confidence interval [CI]: 5.6%–12.2%) cattle. Adult ticks were identified as Hyalomma marginatum (73/92; 79.3%; 45 M and 28 F), Amblyomma variegatum (8/92; 8.7%; 8 M), Hyalomma rufipes (4/92; 4.3%; 4 F) and Rhipicephalus evertsi (1/92; 1.1%; one F). The 16S rRNA sequences of six (four engorged female and two nymphs) ticks showed 98.6–100% identity with reference sequences from Rhipicephalus geigyi. Twelve out of 77 (15.6%) ticks tested positive for at least one TBP. Eight H. marginatum (six M and two F) (10.4%) were positive for Ehrlichia spp. dsb gene, three H. marginatum (two M and one F) (3.9%) for A. marginale and two (one H. marginatum F and one A. variegatum M) (2.6%) for hemotropic Mycoplasma spp. All Ehrlichia-positive samples showed 100% detection for the 16S rRNA gene and 62.5% for the sodB gene. BLASTn analysis revealed 99.3%–99.7% identity with Ehrlichia sp. from Brazil and 98.2%–99.3% identity with E. minasensis from Panama and Pakistan. Phylogenetic analysis grouped the sequences from this study with Ehrlichia spp. and E. minasensis from ticks in the Czech Republic and Brazil. This study identified various tick species and pathogens in cattle from The Gambia, including the first report of E. minasensis, A. marginale and hemotropic Mycoplasma spp. in the country. These findings highlight the importance of ongoing surveillance and research on tick-borne diseases in the region.
{"title":"Ticks and tick-borne bacterial pathogens found on hard ticks (Acari: Ixodidae) on cattle in the Central River region of The Gambia","authors":"Alpha Kargbo, Aamir M. Osman, Edrisa Jawo, Lamin K. M. Fatty, Flavia C. M. Collere, Marcos R. André, Ahmed A. Hassan-Kadle, Thállitha S. W. J. Vieira, Rosangela Z. Machado, Rafael F. C. Vieira","doi":"10.1111/mve.70004","DOIUrl":"10.1111/mve.70004","url":null,"abstract":"<p>Ticks are significant vectors of pathogens affecting both animals and humans, with the climate and environment of Sub-Saharan Africa providing ideal conditions for their growth. However, there are limited data on ticks and tick-borne pathogens (T&TBPs) in cattle in The Gambia. This study aimed to identify tick species on cattle and conduct molecular screening for T&TBPs. A total of 92 ticks were collected from 306 indigenous cattle. Ticks were first identified morphologically using taxonomic keys and then confirmed molecularly through DNA sequencing. DNA was extracted from the right fourth leg of six representative ticks for species confirmation, while 77 whole adult ticks were used for screening T&TBPs. Screening polymerase chain reaction (PCR) assays targeted <i>Anaplasma marginale msp1β</i> gene, <i>Ehrlichia</i> spp. <i>dsb</i> gene and hemotropic <i>Mycoplasma</i> spp. 16S rRNA gene. <i>Ehrlichia</i>-positive samples underwent additional assays targeting the <i>sodB</i>, 16S rRNA and <i>groEL</i> genes, followed by Sanger sequencing and phylogenetic analyses. A total of 92 (53 M, 37 F and two nymphs) ticks were collected from 30/306 (9.8%; 95% confidence interval [CI]: 5.6%–12.2%) cattle. Adult ticks were identified as <i>Hyalomma marginatum</i> (73/92; 79.3%; 45 M and 28 F), <i>Amblyomma variegatum</i> (8/92; 8.7%; 8 M), <i>Hyalomma rufipes</i> (4/92; 4.3%; 4 F) and <i>Rhipicephalus evertsi</i> (1/92; 1.1%; one F). The 16S rRNA sequences of six (four engorged female and two nymphs) ticks showed 98.6–100% identity with reference sequences from <i>Rhipicephalus geigyi</i>. Twelve out of 77 (15.6%) ticks tested positive for at least one TBP. Eight <i>H. marginatum</i> (six M and two F) (10.4%) were positive for <i>Ehrlichia</i> spp. <i>dsb</i> gene, three <i>H. marginatum</i> (two M and one F) (3.9%) for <i>A. marginale</i> and two (one <i>H. marginatum</i> F and one <i>A. variegatum</i> M) (2.6%) for hemotropic <i>Mycoplasma</i> spp. All <i>Ehrlichia</i>-positive samples showed 100% detection for the 16S rRNA gene and 62.5% for the <i>sodB</i> gene. BLASTn analysis revealed 99.3%–99.7% identity with <i>Ehrlichia</i> sp. from Brazil and 98.2%–99.3% identity with <i>E. minasensis</i> from Panama and Pakistan. Phylogenetic analysis grouped the sequences from this study with <i>Ehrlichia</i> spp. and <i>E. minasensis</i> from ticks in the Czech Republic and Brazil. This study identified various tick species and pathogens in cattle from The Gambia, including the first report of <i>E. minasensis</i>, <i>A. marginale</i> and hemotropic <i>Mycoplasma</i> spp. in the country. These findings highlight the importance of ongoing surveillance and research on tick-borne diseases in the region.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"40 1","pages":"91-100"},"PeriodicalIF":1.9,"publicationDate":"2025-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12865750/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144859356","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mathilde Uiterwijk, Frans Jacobs, Karst de Boer, Arno-Jan Feddema, Rianka P. M. Vloet, Marian Dik, José L. Gonzales, Piet A. van Rijn, Armin R. W. Elbers, Melle Holwerda
Bluetongue virus (BTV) is an arthropod-borne virus that is transmitted between ruminants by Culicoides (Order Diptera, Family Ceratopogonidae) midges. In September 2023, BTV serotype 3 (BTV-3/NET2023) emerged in the Netherlands, causing a devastating epidemic in sheep and cattle. The aim of this study was to determine which midge species contributed to the spread of BTV-3 and to what extent the virus is present in local midge populations. Midges were collected using Onderstepoort UV-light suction traps on BTV-affected farms in the centre of the Netherlands, from October 2023 till March 2024. Species, sex and parity of the midges were morphologically determined. Pooled female parous and gravid midges were subjected to pan-BTV and BTV-3 real-time polymerase chain reaction (PCR) testing. Pool prevalence, minimum infection rate (MIR) and infection rate (IR) were calculated. In total, 33,093 midges were morphologically identified, all being indigenous Culicoides species. Of these, 10,835 parous or gravid female midges were selected and pooled in 383 pools (mean 28.3 midges per pool, range 1–115). A total of 155 pools (40.5%) tested BTV positive, with a mean MIR/100 of 1.4 and an IR of 2.2 (95% confidence interval: 1.9–2.6). All positive pools were from batches that were collected in October 2023 (week 40 and 41). BTV-RNA was detected in the Culicoides species C. obsoletus Meigen, C. scoticus Downes and Kettle, C. chiopterus Meigen, C. dewulfi Goetghebuer and C. punctatus Meigen. The high proportion of BTV-PCR positive midge pools is indicative of a high vector competence for BTV-3/NET2023 of Dutch indigenous midges present on farms; it could potentially partly explain the rapid spread of the virus throughout the Netherlands.
{"title":"Culicoides species involved in the BTV-3 epidemic, the Netherlands, 2023–2024","authors":"Mathilde Uiterwijk, Frans Jacobs, Karst de Boer, Arno-Jan Feddema, Rianka P. M. Vloet, Marian Dik, José L. Gonzales, Piet A. van Rijn, Armin R. W. Elbers, Melle Holwerda","doi":"10.1111/mve.70007","DOIUrl":"10.1111/mve.70007","url":null,"abstract":"<p>Bluetongue virus (BTV) is an arthropod-borne virus that is transmitted between ruminants by <i>Culicoides</i> (Order Diptera, Family Ceratopogonidae) midges. In September 2023, BTV serotype 3 (BTV-3/NET2023) emerged in the Netherlands, causing a devastating epidemic in sheep and cattle. The aim of this study was to determine which midge species contributed to the spread of BTV-3 and to what extent the virus is present in local midge populations. Midges were collected using Onderstepoort UV-light suction traps on BTV-affected farms in the centre of the Netherlands, from October 2023 till March 2024. Species, sex and parity of the midges were morphologically determined. Pooled female parous and gravid midges were subjected to pan-BTV and BTV-3 real-time polymerase chain reaction (PCR) testing. Pool prevalence, minimum infection rate (MIR) and infection rate (IR) were calculated. In total, 33,093 midges were morphologically identified, all being indigenous <i>Culicoides</i> species. Of these, 10,835 parous or gravid female midges were selected and pooled in 383 pools (mean 28.3 midges per pool, range 1–115). A total of 155 pools (40.5%) tested BTV positive, with a mean MIR/100 of 1.4 and an IR of 2.2 (95% confidence interval: 1.9–2.6). All positive pools were from batches that were collected in October 2023 (week 40 and 41). BTV-RNA was detected in the <i>Culicoides</i> species <i>C. obsoletus</i> Meigen, <i>C. scoticus</i> Downes and Kettle, <i>C. chiopterus</i> Meigen, <i>C. dewulfi</i> Goetghebuer and <i>C. punctatus</i> Meigen. The high proportion of BTV-PCR positive midge pools is indicative of a high vector competence for BTV-3/NET2023 of Dutch indigenous midges present on farms; it could potentially partly explain the rapid spread of the virus throughout the Netherlands.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"40 1","pages":"111-122"},"PeriodicalIF":1.9,"publicationDate":"2025-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12865740/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144855758","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Supipi H. Wijesundara, Sanduni R. Piumali, Thilini C. Weeraratne, Faseeha Noordeen, Priyanka P. de Silva W.A.
The critical impact of mosquito-borne diseases on public health, along with the failure of current control strategies, highlights the need for novel mosquito control approaches mainly in tropical countries. This study explored the larvicidal properties of bacterial isolates from the egg surfaces of Aedes aegypti L. and Aedes albopictus Skuse (Diptera: Culicidae), the primary and secondary dengue vector mosquitoes in Sri Lanka. Among 30 bacterial isolates, a local strain of Pseudomonas mosselii Quesnel isolated from the egg surfaces of the dengue vectors demonstrated strong larvicidal activity against Ae. aegypti. Larvicidal assays using the bacterial supernatant (OD 1.7) and freeze-dried products were performed across concentrations ranging from 80 to 2.1 mg/mL. The LC50 values for the supernatant were 55, 54 and 52 mg/mL at 24, 48 and 72 h, respectively, with corresponding LC90 values of 91, 89 and 86 mg/mL. Freeze-dried supernatant showed LC50 values of 2.73, 2.64 and 2.63 mg/mL, while freeze-dried bacterial culture showed higher toxicity with LC50 values of 2.57, 2.51 and 2.44 mg/mL. Strong larvicidal activity was observed against Culex quinquefasciatus Say (Diptera: Culicidae), a primary vector of filariasis. The freeze-dried products retained their efficacy for up to 2 months. Ovicidal and adulticidal assays indicated no significant effects on mosquito eggs or adults. However, the active components of bacterial metabolites significantly impacted the development of Aedes larvae. Toxicity effects were observed in non-target organisms, including zooplankton and tadpoles. These findings suggest the local Ps. mosselii strain as a potential bio-larvicide against dengue vectors while underscoring the need for further environmental assessment.
{"title":"Larvicidal potential of Pseudomonas mosselii isolated from Aedes (Diptera: Culicidae) egg surfaces against dengue vector mosquitoes and its impact on non-target organisms","authors":"Supipi H. Wijesundara, Sanduni R. Piumali, Thilini C. Weeraratne, Faseeha Noordeen, Priyanka P. de Silva W.A.","doi":"10.1111/mve.70006","DOIUrl":"10.1111/mve.70006","url":null,"abstract":"<p>The critical impact of mosquito-borne diseases on public health, along with the failure of current control strategies, highlights the need for novel mosquito control approaches mainly in tropical countries. This study explored the larvicidal properties of bacterial isolates from the egg surfaces of <i>Aedes aegypti</i> L. and <i>Aedes albopictus</i> Skuse (Diptera: Culicidae), the primary and secondary dengue vector mosquitoes in Sri Lanka. Among 30 bacterial isolates, a local strain of <i>Pseudomonas mosselii</i> Quesnel isolated from the egg surfaces of the dengue vectors demonstrated strong larvicidal activity against <i>Ae. aegypti</i>. Larvicidal assays using the bacterial supernatant (OD 1.7) and freeze-dried products were performed across concentrations ranging from 80 to 2.1 mg/mL. The LC<sub>50</sub> values for the supernatant were 55, 54 and 52 mg/mL at 24, 48 and 72 h, respectively, with corresponding LC<sub>90</sub> values of 91, 89 and 86 mg/mL. Freeze-dried supernatant showed LC<sub>50</sub> values of 2.73, 2.64 and 2.63 mg/mL, while freeze-dried bacterial culture showed higher toxicity with LC<sub>50</sub> values of 2.57, 2.51 and 2.44 mg/mL. Strong larvicidal activity was observed against <i>Culex quinquefasciatus</i> Say (Diptera: Culicidae), a primary vector of filariasis. The freeze-dried products retained their efficacy for up to 2 months. Ovicidal and adulticidal assays indicated no significant effects on mosquito eggs or adults. However, the active components of bacterial metabolites significantly impacted the development of <i>Aedes</i> larvae. Toxicity effects were observed in non-target organisms, including zooplankton and tadpoles. These findings suggest the local <i>Ps. mosselii</i> strain as a potential bio-larvicide against dengue vectors while underscoring the need for further environmental assessment.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 4","pages":"875-888"},"PeriodicalIF":1.9,"publicationDate":"2025-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144804420","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}