Changes in climate may cause changes in the ranges, phenology and interactions of insects with other species and lead parasites to switch host species. A study of louse (flat) flies in the United Kingdom, Republic of Ireland and Isle of Man, in which licensed bird ringers acting as citizen scientists collected ectoparasites that left birds during ringing, showed recent range shifts of several species. The Common or Bird Louse Fly Ornithomya avicularia (Linnaeus, 1758), a vector of Haemoproteus sp. and trypanosomes, has undergone a major northwards range expansion of over 300 km in the United Kingdom (UK) since the 1960s. The Finch Louse Fly Ornithomya fringillina (Curtis, 1836) has also expanded its range over 300 km northwards and 400 km westwards into the Island of Ireland, and the Swallow Louse Fly Ornithomya biloba (Dufour, 1827) is now established in Wales and Southern England. The Grouse Louse Fly Ornithomya chloropus (Bergroth, 1901) has undergone a range contraction at lower altitudes and on the southern edge of its range. Other species of louse fly were detected: Crataerina pallida (Latreille, 1812), Stenepteryx hirundinis (Linnaeus, 1758), Pseudolynchia garzettae (Rondani, 1879) and Icosta minor (Bigot, 1858). Some generalist species have shifted their phenology, whereas the more specialist nest parasites of migrant birds have not, as the arrival and breeding dates of their hosts have not changed. The range changes of the generalist species of these ectoparasites may have implications for bird health, especially if they switch to new host species as their ranges shift.
{"title":"Citizen scientists mapping the United Kingdom's and Republic of Ireland's flat flies (louse flies) (Diptera: Hippoboscidae) reveal a vector's range shift","authors":"Denise C. Wawman","doi":"10.1111/mve.12795","DOIUrl":"10.1111/mve.12795","url":null,"abstract":"<p>Changes in climate may cause changes in the ranges, phenology and interactions of insects with other species and lead parasites to switch host species. A study of louse (flat) flies in the United Kingdom, Republic of Ireland and Isle of Man, in which licensed bird ringers acting as citizen scientists collected ectoparasites that left birds during ringing, showed recent range shifts of several species. The Common or Bird Louse Fly <i>Ornithomya avicularia</i> (Linnaeus, 1758), a vector of <i>Haemoproteus</i> sp. and trypanosomes, has undergone a major northwards range expansion of over 300 km in the United Kingdom (UK) since the 1960s. The Finch Louse Fly <i>Ornithomya fringillina</i> (Curtis, 1836) has also expanded its range over 300 km northwards and 400 km westwards into the Island of Ireland, and the Swallow Louse Fly <i>Ornithomya biloba</i> (Dufour, 1827) is now established in Wales and Southern England. The Grouse Louse Fly <i>Ornithomya chloropus</i> (Bergroth, 1901) has undergone a range contraction at lower altitudes and on the southern edge of its range. Other species of louse fly were detected: <i>Crataerina pallida</i> (Latreille, 1812), <i>Stenepteryx hirundinis</i> (Linnaeus, 1758), <i>Pseudolynchia garzettae</i> (Rondani, 1879) and <i>Icosta minor</i> (Bigot, 1858). Some generalist species have shifted their phenology, whereas the more specialist nest parasites of migrant birds have not, as the arrival and breeding dates of their hosts have not changed. The range changes of the generalist species of these ectoparasites may have implications for bird health, especially if they switch to new host species as their ranges shift.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 3","pages":"559-575"},"PeriodicalIF":1.9,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mve.12795","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143374419","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}
<p>Advancements in technology have meant that there have been significant developments in the field of forensic entomology, allow researchers to develop tools to more accurately identify entomological evidence, as well as provide more accurate estimates of postmortem interval (PMI).</p><p>Since its inception in the early thirteenth century (Benecke, <span>2001</span>), the use of insects in medico-legal investigations has often been met with trepidation. However, over time the reluctance of legal professionals to allow entomological evidence into a court of law has waned, and currently, entomological evidence is accepted in many countries as part of criminal proceedings (Du Plessis & Meintjes-Van der Walt, <span>2004</span>; Hall, <span>2021</span>). With the advancement of scientific techniques and technologies, and the introduction of artificial intelligence (AI) tools, it is paramount that the scientific community is constantly evolving and developing novel methods to analyse entomological samples.</p><p>The development of forensic entomology accelerated in the twentieth century with advancements in biology and technology. Researchers began to catalogue the predictable patterns of insect colonization on corpses (Anderson & VanLaerhoven, <span>1996</span>; Eberhardt & Elliot, <span>2008</span>), noting how environmental factors such as temperature influence insect activity and development. Studying the influence of temperature on the developmental rates of necrophagous insect species is pivotal for enabling their reliable use as forensic indicators (Amendt et al., <span>2010</span>); however, the effect of suboptimal temperatures and their potential casework implications remain as relevant topics that deserve further investigation (López-García & Martín-Vega, <span>2025</span>). The potential effect of other abiotic factors on insect biology is another aspect that needs further study in order to strengthen the reliability of the interpretation of entomological evidence in forensic investigations (Ferreira et al., <span>2025</span>).</p><p>In recent decades, forensic entomology has embraced cutting-edge technologies and interdisciplinary approaches. DNA barcoding and similar molecular techniques allow rapid and precise identification of insect species (Durango-Manrique et al., <span>2025</span>), which is essential for a reliable analysis and interpretation of entomological evidence. Nonetheless, morphological descriptions of the different life stages can also provide powerful tools for the unequivocal identification of forensically relevant species (Grella et al., <span>2025</span>; Martínez-Sánchez et al., <span>2024</span>). Additionally, advances in stable isotope analysis enable investigators to trace the geographic origin of insects (Owings et al., <span>2021</span>), further narrowing the location of death or body transport. High-resolution imaging and AI also have enhanced the accuracy and efficiency of insect identificat
技术的进步意味着法医昆虫学领域有了重大发展,使研究人员能够开发出更准确地识别昆虫学证据的工具,并提供更准确的死后间隔(PMI)估计。自13世纪初开始使用昆虫以来(Benecke, 2001年),在医学-法律调查中使用昆虫常常受到恐惧。然而,随着时间的推移,法律专业人员不愿允许昆虫学证据进入法庭的情况已经减弱,目前,昆虫学证据在许多国家被接受为刑事诉讼的一部分(杜普莱西斯&;meintje - van der Walt, 2004;大厅,2021)。随着科学技术和技术的进步,以及人工智能(AI)工具的引入,科学界不断发展和开发分析昆虫学样本的新方法至关重要。随着生物学和技术的进步,法医昆虫学的发展在20世纪加速了。研究人员开始对昆虫在尸体上定居的可预测模式进行编目(安德森&;VanLaerhoven, 1996;爱伯哈,Elliot, 2008),指出温度等环境因素如何影响昆虫的活动和发育。研究温度对尸食性昆虫物种发育速率的影响对于将其可靠地用作法医指标至关重要(amend等,2010);然而,次优温度的影响及其潜在的个案影响仍然是值得进一步调查的相关主题(López-García &;Martin-Vega, 2025)。其他非生物因素对昆虫生物学的潜在影响是另一个需要进一步研究的方面,以加强法医调查中昆虫学证据解释的可靠性(Ferreira et al., 2025)。近几十年来,法医昆虫学采用了尖端技术和跨学科方法。DNA条形码和类似的分子技术可以快速和精确地识别昆虫物种(Durango-Manrique等人,2025),这对于昆虫学证据的可靠分析和解释至关重要。尽管如此,不同生命阶段的形态学描述也可以为法医相关物种的明确鉴定提供强大的工具(Grella等人,2025;Martínez-Sánchez et al., 2024)。此外,稳定同位素分析的进步使调查人员能够追踪昆虫的地理来源(Owings等人,2021年),进一步缩小死亡或尸体运输的位置。高分辨率成像和AI也提高了昆虫识别和生命阶段分析的准确性和效率(Gao et al., 2024)。探索最先进技术适用性的创新方法为法医昆虫学研究中高度相关的主题提供了新的见解,例如尸食性吹蝇幼虫的摄食后行为(Mactaggart等人,2025)或吹蝇蛹内阶段的年龄估计(th mmel等人,2025)。法医昆虫学与其他领域,如法医微生物学和环境科学的结合,开辟了新的调查途径(Benbow &;Pechal, 2019)。例如,对微生物群落和昆虫活动之间相互作用的研究改进了PMI估算(Benbow &;Pechal, 2019)。人们正在探索无人机等遥感技术在大范围内探测昆虫活动的潜力,特别是在大规模伤亡事件中(Syed Mohd Daud et al., 2024)。此外,法医昆虫学研究的进步不仅有利于调查可疑的人类死亡,而且有利于调查虐待和忽视弱势群体(Eremeeva等人,2025年)或野生动物偷猎调查(Pienaar &;Dadour, 2025)。该学科也已扩展到死后间隔估计之外,包括应用,例如通过分析昆虫幼虫来检测组织中的药物存在(growth等人,2024年),以及根据特定地区特有的昆虫物种确定死亡地点。尽管如上所述存在一定的局限性和挑战(amend et al., 2010;Wang et al., 2021),法医昆虫学在技术进步和跨学科合作的推动下继续发展。它在破案和提供证据方面的关键作用强调了这一领域正在进行的研究和创新的重要性。zanth kotz:写作-原稿;写作——审阅和编辑。Daniel Martín-Vega:写作-原稿;写作——审阅和编辑。
{"title":"Keeping up with the times: The application of innovative techniques in forensic entomology","authors":"Zanthé Kotzé, Daniel Martín-Vega","doi":"10.1111/mve.12792","DOIUrl":"10.1111/mve.12792","url":null,"abstract":"<p>Advancements in technology have meant that there have been significant developments in the field of forensic entomology, allow researchers to develop tools to more accurately identify entomological evidence, as well as provide more accurate estimates of postmortem interval (PMI).</p><p>Since its inception in the early thirteenth century (Benecke, <span>2001</span>), the use of insects in medico-legal investigations has often been met with trepidation. However, over time the reluctance of legal professionals to allow entomological evidence into a court of law has waned, and currently, entomological evidence is accepted in many countries as part of criminal proceedings (Du Plessis & Meintjes-Van der Walt, <span>2004</span>; Hall, <span>2021</span>). With the advancement of scientific techniques and technologies, and the introduction of artificial intelligence (AI) tools, it is paramount that the scientific community is constantly evolving and developing novel methods to analyse entomological samples.</p><p>The development of forensic entomology accelerated in the twentieth century with advancements in biology and technology. Researchers began to catalogue the predictable patterns of insect colonization on corpses (Anderson & VanLaerhoven, <span>1996</span>; Eberhardt & Elliot, <span>2008</span>), noting how environmental factors such as temperature influence insect activity and development. Studying the influence of temperature on the developmental rates of necrophagous insect species is pivotal for enabling their reliable use as forensic indicators (Amendt et al., <span>2010</span>); however, the effect of suboptimal temperatures and their potential casework implications remain as relevant topics that deserve further investigation (López-García & Martín-Vega, <span>2025</span>). The potential effect of other abiotic factors on insect biology is another aspect that needs further study in order to strengthen the reliability of the interpretation of entomological evidence in forensic investigations (Ferreira et al., <span>2025</span>).</p><p>In recent decades, forensic entomology has embraced cutting-edge technologies and interdisciplinary approaches. DNA barcoding and similar molecular techniques allow rapid and precise identification of insect species (Durango-Manrique et al., <span>2025</span>), which is essential for a reliable analysis and interpretation of entomological evidence. Nonetheless, morphological descriptions of the different life stages can also provide powerful tools for the unequivocal identification of forensically relevant species (Grella et al., <span>2025</span>; Martínez-Sánchez et al., <span>2024</span>). Additionally, advances in stable isotope analysis enable investigators to trace the geographic origin of insects (Owings et al., <span>2021</span>), further narrowing the location of death or body transport. High-resolution imaging and AI also have enhanced the accuracy and efficiency of insect identificat","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 1","pages":"1-2"},"PeriodicalIF":1.9,"publicationDate":"2025-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mve.12792","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143111762","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}
Mustafa M. Soliman, Magdi S. A. El-Hawagry, Abdallah M. Samy
Aedes aegypti, the primary vector of several medically significant arboviruses—including dengue fever, yellow fever, chikungunya and Zika—was successfully eradicated from Egypt in 1963. However, since 2011, there have been increasing reports of its re-emergence, alongside dengue outbreaks in southern Egyptian governorates, raising significant public health concerns. This study aimed to model the current and future distribution of Ae. aegypti in Egypt. Local occurrence data were integrated with bioclimatic, anthropogenic and biological environmental variables to identify key factors influencing the distribution of Ae. aegypti. Maximum entropy (MaxEnt) modelling demonstrated strong predictive performance (area under the receiver operating characteristic curve [AUC] mean = 0.975; true skill statistic [TSS] mean = 0.789). The key determinants of habitat suitability were identified as human population density, annual precipitation and the normalised difference vegetation index (NDVI). Current predictions indicate that suitable habitats for Ae. aegypti are concentrated in the Nile Valley, Nile Delta, Fayoum Basin, Red Sea coast and South Sinai. Projections under future climate change scenarios suggest an expansion of suitable habitats, particularly in the Nile Delta region. By 2050, the model predicts a 61%–68% increase in suitable habitat area, with a further 64%–69% increase by 2070, depending on the future climate scenarios. These findings are crucial for informing vector control and disease prevention strategies, particularly considering Egypt's status as one of the world's leading tourist destinations.
{"title":"Re-emergence of Aedes aegypti (Linnaeus) in Egypt: Predicting distribution shifts under climate changes","authors":"Mustafa M. Soliman, Magdi S. A. El-Hawagry, Abdallah M. Samy","doi":"10.1111/mve.12794","DOIUrl":"10.1111/mve.12794","url":null,"abstract":"<p><i>Aedes aegypti</i>, the primary vector of several medically significant arboviruses—including dengue fever, yellow fever, chikungunya and Zika—was successfully eradicated from Egypt in 1963. However, since 2011, there have been increasing reports of its re-emergence, alongside dengue outbreaks in southern Egyptian governorates, raising significant public health concerns. This study aimed to model the current and future distribution of <i>Ae. aegypti</i> in Egypt. Local occurrence data were integrated with bioclimatic, anthropogenic and biological environmental variables to identify key factors influencing the distribution of <i>Ae. aegypti</i>. Maximum entropy (MaxEnt) modelling demonstrated strong predictive performance (area under the receiver operating characteristic curve [AUC] mean = 0.975; true skill statistic [TSS] mean = 0.789). The key determinants of habitat suitability were identified as human population density, annual precipitation and the normalised difference vegetation index (NDVI). Current predictions indicate that suitable habitats for <i>Ae. aegypti</i> are concentrated in the Nile Valley, Nile Delta, Fayoum Basin, Red Sea coast and South Sinai. Projections under future climate change scenarios suggest an expansion of suitable habitats, particularly in the Nile Delta region. By 2050, the model predicts a 61%–68% increase in suitable habitat area, with a further 64%–69% increase by 2070, depending on the future climate scenarios. These findings are crucial for informing vector control and disease prevention strategies, particularly considering Egypt's status as one of the world's leading tourist destinations.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 3","pages":"548-558"},"PeriodicalIF":1.9,"publicationDate":"2025-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143066470","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}
Culicoides oxystoma Kieffer (Diptera: Ceratopogonidae) transmits many pathogens, including seven viruses, four protozoa and one nematode. This species has a wide distribution range across northern Afro-tropical, Palearctic, Australian, Indo-Malayan realms with a broad host spectrum, including cattle, buffaloes, sheep, pigs, dogs, horses and even humans. The heterogeneous nature of Culicoides' blood-feeding patterns is well documented, but the influence of various host blood meal sources on gut bacterial composition remains scant. Adult midges were collected during April (2023) by operating UV light traps in cattle, buffalo sheds and poultry farm in Purulia (India). Besides C. oxystoma, eleven Culicoides species were collected across the sheds and farm, seven of which are vectors. Culicoides liui Wirth and Hubert and C. thurmanae Wirth and Hubert are reported from India for the first time. In all the sheds, engorged females of C. oxystoma were ubiquitous. Identification of culturable gut bacteria and the host blood meal of C. oxystoma were done through the polymerase chain reaction (PCR)-based method. Blood meal analysis confirmed the following hosts: cattle, buffaloes and humans. Identification of blood meal of engorged C. oxystoma caught from poultry farm showed positive results for humans but not for birds. Among bacteria, Bacillus cereus was abundant in all of the engorged females. Bacillus paramycoides and Enterococcus faecium were identified from females feeding on cattle and buffaloes' blood, while Alcaligenes faecalis was found in the gut contents of females that fed on cattle and human blood. The gut bacteria Alcaligenes faecalis exhibited alpha haemolytic activity. In contrast, Bacillus sp., B. cereus, B. flexus, B. licheniformis, B. thuringiensis, B. paramycoides, E. faecium, Paenibacillus sp. and Pseudomonas sp. exhibited beta haemolysis. This is the first report on the composition of gut bacteria, with particular emphasis on the haemolytic bacteria of C. oxystoma with different host blood meals. The pathogenic bacteria B. cereus, B. licheniformis and A. faecalis within the females could potentially impact pathogen acquisition and increase the probability of their zoonotic transmissibility.
库蠓(双翅目:蠓科)传播多种病原体,包括7种病毒、4种原生动物和1种线虫。该物种分布广泛,横跨非洲热带北部、古北、澳大利亚、印度-马来亚地区,宿主范围广泛,包括牛、水牛、羊、猪、狗、马甚至人类。库蠓的血液摄食模式的异质性已被充分记录,但各种宿主血粉来源对肠道细菌组成的影响仍然很少。2023年4月,在印度普鲁里亚(Purulia)的牛棚、水牛棚和家禽养殖场采用紫外灯诱捕法采集成蚊。除库蠓外,棚舍和农场共捕获库蠓11种,其中媒介库蠓7种。库蠓(Culicoides liui Wirth and Hubert)和库蠓(C. thurmanae Wirth and Hubert)为印度首次报道。在所有的棚内,都有大量的雌蜂。采用基于聚合酶链反应(PCR)的方法对可培养肠道细菌和氧口梭菌宿主血粉进行鉴定。血粉分析证实了以下宿主:牛、水牛和人类。血液鉴定吃饭狼吞虎咽的c . oxystoma家禽养殖场被显示为人类而不是鸟类积极的结果。细菌中蜡样芽孢杆菌含量丰富。从取食牛和水牛血液的雌虫中鉴定出副芽孢杆菌和粪肠球菌,在取食牛和人血液的雌虫肠道内容物中鉴定出粪碱性杆菌。肠道细菌粪碱性菌表现出α溶血活性。相比之下,芽孢杆菌、蜡样芽孢杆菌、弯曲芽孢杆菌、地衣芽孢杆菌、苏云金芽孢杆菌、副芽孢杆菌、粪芽孢杆菌、Paenibacillus sp.和假单胞菌sp.表现出β溶血。这是关于肠道细菌组成的第一份报告,特别强调了C. oxystoma的溶血细菌与不同宿主血餐的关系。雌性体内的蜡样芽孢杆菌、地衣芽孢杆菌和粪芽孢杆菌可能影响病原体的获取,增加其人畜共患传播的可能性。
{"title":"Investigating the influence of blood meal sources on the composition of culturable haemolytic gut bacteria of a wild-caught BTV vector Culicoides oxystoma Kieffer (Diptera: Ceratopogonidae)","authors":"Ankita Sarkar, Paramita Banerjee, Surajit Kar, Arjun Pal, Abhijit Mazumdar","doi":"10.1111/mve.12793","DOIUrl":"10.1111/mve.12793","url":null,"abstract":"<p><i>Culicoides oxystoma</i> Kieffer (Diptera: Ceratopogonidae) transmits many pathogens, including seven viruses, four protozoa and one nematode. This species has a wide distribution range across northern Afro-tropical, Palearctic, Australian, Indo-Malayan realms with a broad host spectrum, including cattle, buffaloes, sheep, pigs, dogs, horses and even humans. The heterogeneous nature of <i>Culicoides</i>' blood-feeding patterns is well documented, but the influence of various host blood meal sources on gut bacterial composition remains scant. Adult midges were collected during April (2023) by operating UV light traps in cattle, buffalo sheds and poultry farm in Purulia (India). Besides <i>C. oxystoma</i>, eleven <i>Culicoides</i> species were collected across the sheds and farm, seven of which are vectors. <i>Culicoides liui</i> Wirth and Hubert and <i>C. thurmanae</i> Wirth and Hubert are reported from India for the first time. In all the sheds, engorged females of <i>C. oxystoma</i> were ubiquitous. Identification of culturable gut bacteria and the host blood meal of <i>C. oxystoma</i> were done through the polymerase chain reaction (PCR)-based method. Blood meal analysis confirmed the following hosts: cattle, buffaloes and humans. Identification of blood meal of engorged <i>C. oxystoma</i> caught from poultry farm showed positive results for humans but not for birds. Among bacteria, <i>Bacillus cereus</i> was abundant in all of the engorged females. <i>Bacillus paramycoides</i> and <i>Enterococcus faecium</i> were identified from females feeding on cattle and buffaloes' blood, while <i>Alcaligenes faecalis</i> was found in the gut contents of females that fed on cattle and human blood. The gut bacteria <i>Alcaligenes faecalis</i> exhibited alpha haemolytic activity. In contrast, <i>Bacillus</i> sp., <i>B. cereus</i>, <i>B. flexus</i>, <i>B. licheniformis</i>, <i>B. thuringiensis</i>, <i>B. paramycoides</i>, <i>E</i>. <i>faecium</i>, <i>Paenibacillus</i> sp. and <i>Pseudomonas</i> sp. exhibited beta haemolysis. This is the first report on the composition of gut bacteria, with particular emphasis on the haemolytic bacteria of <i>C. oxystoma</i> with different host blood meals. The pathogenic bacteria <i>B. cereus</i>, <i>B. licheniformis</i> and <i>A. faecalis</i> within the females could potentially impact pathogen acquisition and increase the probability of their zoonotic transmissibility.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 3","pages":"538-547"},"PeriodicalIF":1.9,"publicationDate":"2025-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143053000","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}
Stephen R. Fricker, Gunnar Keppel, Craig R. Williams
We investigated the mosquito community along 315 km of the Murray River, where we identified three assemblages (upper, middle, and lower river) that exhibited different patterns of species richness and diversity over 20 years. In the lower reaches (i.e., more southern latitudes), species richness and community diversity declined over time, while there was no significant change in either the middle or upper reaches. While the overall mean abundance of the common, pathogen-carrying mosquito (Diptera: Culicidae) species Aedes camptorhynchus Thomson, increased in the lower river but declined in the upper river. These results provide important information on the diversity and abundance of mosquito communities adjacent to the Murray River and highlight the importance of considering spatial and temporal variation when assessing the risk of mosquito-borne diseases. Furthermore, data presented here illustrate that there the common public narrative around increasing mosquito abundance and geographic expansion under climate change is not universally true.
{"title":"Characterisation of riverine mosquito (Diptera: Culicidae) community structure in southern Australia and the impact of a major flood based on analysis of a 20-year dataset","authors":"Stephen R. Fricker, Gunnar Keppel, Craig R. Williams","doi":"10.1111/mve.12787","DOIUrl":"10.1111/mve.12787","url":null,"abstract":"<p>We investigated the mosquito community along 315 km of the Murray River, where we identified three assemblages (upper, middle, and lower river) that exhibited different patterns of species richness and diversity over 20 years. In the lower reaches (i.e., more southern latitudes), species richness and community diversity declined over time, while there was no significant change in either the middle or upper reaches. While the overall mean abundance of the common, pathogen-carrying mosquito (Diptera: Culicidae) species <i>Aedes camptorhynchus</i> Thomson, increased in the lower river but declined in the upper river. These results provide important information on the diversity and abundance of mosquito communities adjacent to the Murray River and highlight the importance of considering spatial and temporal variation when assessing the risk of mosquito-borne diseases. Furthermore, data presented here illustrate that there the common public narrative around increasing mosquito abundance and geographic expansion under climate change is not universally true.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 2","pages":"335-350"},"PeriodicalIF":1.9,"publicationDate":"2025-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mve.12787","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143047219","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}
Grace K. Nichol, J. Scott Weese, Shaun J. Dergousoff, Amy L. Greer, Katie M. Clow
Dermacentor variabilis (Say) (Acari: Ixodidae) is a vector for pathogens that can impact human and animal health. The geographic range of this species is expanding, but there are some areas with limited up-to-date information on the distribution of D. variabilis. Therefore, the objective of this study was to describe the spatial and temporal patterns of adult D. variabilis activity in central and eastern Canada. Ticks were collected from companion animals by veterinary clinic staff. Suspected locations of tick acquisition were spatially projected, and a spatial scan statistic was used to identify statistically significant clusters of frequent submissions from veterinary clinics. Submissions were categorised by calendar week to evaluate temporal trends. In total, 1198 adult D. variabilis, one nymphal D. variabilis and one Dermacentor albipictus (Packard) were collected from the provinces of Manitoba, Ontario, Quebec, New Brunswick, Nova Scotia and Prince Edward Island from April 2019 through March 2020. Peaks in adult D. variabilis submissions occurred in May and June. Most of the submissions were received from south-eastern Manitoba, eastern Ontario and central and western Nova Scotia. A statistically significant cluster of frequent submissions that included seven veterinary clinics was identified in Nova Scotia. These findings can be used to determine the locations and times at which humans and their companion animals should be considered at an increased risk of exposure to D. variabilis and the pathogens they carry.
{"title":"Spatial and temporal analyses of Dermacentor variabilis (Say) (Acari: Ixodidae) in central and eastern Canada","authors":"Grace K. Nichol, J. Scott Weese, Shaun J. Dergousoff, Amy L. Greer, Katie M. Clow","doi":"10.1111/mve.12790","DOIUrl":"10.1111/mve.12790","url":null,"abstract":"<p><i>Dermacentor variabilis</i> (Say) (Acari: Ixodidae) is a vector for pathogens that can impact human and animal health. The geographic range of this species is expanding, but there are some areas with limited up-to-date information on the distribution of <i>D. variabilis</i>. Therefore, the objective of this study was to describe the spatial and temporal patterns of adult <i>D. variabilis</i> activity in central and eastern Canada. Ticks were collected from companion animals by veterinary clinic staff. Suspected locations of tick acquisition were spatially projected, and a spatial scan statistic was used to identify statistically significant clusters of frequent submissions from veterinary clinics. Submissions were categorised by calendar week to evaluate temporal trends. In total, 1198 adult <i>D. variabilis</i>, one nymphal <i>D. variabilis</i> and one <i>Dermacentor albipictus</i> (Packard) were collected from the provinces of Manitoba, Ontario, Quebec, New Brunswick, Nova Scotia and Prince Edward Island from April 2019 through March 2020. Peaks in adult <i>D. variabilis</i> submissions occurred in May and June. Most of the submissions were received from south-eastern Manitoba, eastern Ontario and central and western Nova Scotia. A statistically significant cluster of frequent submissions that included seven veterinary clinics was identified in Nova Scotia. These findings can be used to determine the locations and times at which humans and their companion animals should be considered at an increased risk of exposure to <i>D. variabilis</i> and the pathogens they carry.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 3","pages":"515-524"},"PeriodicalIF":1.9,"publicationDate":"2025-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mve.12790","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143047231","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}
Thitipong Hongsuwong, Pattarapon Khemrattrakool, Theerawit Phanphoowong, Patchara Sriwichai, Kittiyod Poovorawan, Joel Tarning, Kevin C. Kobylinski
Mass ivermectin (IVM) treatment of livestock (MITL) is under consideration as a malaria control tool as IVM-treated livestock are lethal to blood-feeding Anopheles mosquitoes. MITL is routinely used as a prophylaxis in livestock to reduce the burden and transmission of helminth infections. Recently, there has been a shift in the veterinary IVM market in Southeast Asia wherein nearly all standard IVM formulations are now co-formulated with clorsulon (CLO). CLO is used to treat the trematode liver fluke, Fasciola hepatica. Thus, the co-administration of IVM and CLO simultaneously targets multiple livestock infections. Additionally, F. hepatica frequently afflicts human populations in endemic areas, making control of F. hepatica in livestock beneficial for One Health. CLO interrupts glycolysis in F. hepatica, but its potential effect against Anopheles mosquitoes has never been evaluated. Anopheles dirus mosquitoes were blood-fed CLO across a range of concentrations (1–10,000 nM; 0.38–3807 ng/mL), and mosquito survival was monitored for 10 days. Co-feeding experiments were also performed with An. dirus blood-fed on IVM at two concentrations (4 and 6 ng/mL) without and with CLO corresponding to peak concentration in cattle (Cmax) (2700 ng/mL) and five times the Cmax (13,500 ng/mL), and mosquito survival was monitored for 10 days. CLO had no mosquito-lethal effect on An. dirus. The IVM and CLO co-feed experiment did not indicate any altered effect of IVM on mosquito survival when co-fed with CLO. IVM-CLO livestock co-formulations would not likely alter the Anopheles mosquito-lethal effect of MITL. The use of MITL-CLO for malaria control would have health benefits for livestock, treating helminth and liver fluke infections, and additional One Health benefits by reducing transmission risk of liver flukes to humans.
{"title":"Potential interaction between clorsulon and ivermectin for malaria vector control","authors":"Thitipong Hongsuwong, Pattarapon Khemrattrakool, Theerawit Phanphoowong, Patchara Sriwichai, Kittiyod Poovorawan, Joel Tarning, Kevin C. Kobylinski","doi":"10.1111/mve.12788","DOIUrl":"10.1111/mve.12788","url":null,"abstract":"<p>Mass ivermectin (IVM) treatment of livestock (MITL) is under consideration as a malaria control tool as IVM-treated livestock are lethal to blood-feeding <i>Anopheles</i> mosquitoes. MITL is routinely used as a prophylaxis in livestock to reduce the burden and transmission of helminth infections. Recently, there has been a shift in the veterinary IVM market in Southeast Asia wherein nearly all standard IVM formulations are now co-formulated with clorsulon (CLO). CLO is used to treat the trematode liver fluke, <i>Fasciola hepatica.</i> Thus, the co-administration of IVM and CLO simultaneously targets multiple livestock infections. Additionally, <i>F. hepatica</i> frequently afflicts human populations in endemic areas, making control of <i>F. hepatica</i> in livestock beneficial for One Health. CLO interrupts glycolysis in <i>F. hepatica</i>, but its potential effect against <i>Anopheles</i> mosquitoes has never been evaluated. <i>Anopheles dirus</i> mosquitoes were blood-fed CLO across a range of concentrations (1–10,000 nM; 0.38–3807 ng/mL), and mosquito survival was monitored for 10 days. Co-feeding experiments were also performed with <i>An. dirus</i> blood-fed on IVM at two concentrations (4 and 6 ng/mL) without and with CLO corresponding to peak concentration in cattle (<i>C</i><sub>max</sub>) (2700 ng/mL) and five times the <i>C</i><sub>max</sub> (13,500 ng/mL), and mosquito survival was monitored for 10 days. CLO had no mosquito-lethal effect on <i>An. dirus</i>. The IVM and CLO co-feed experiment did not indicate any altered effect of IVM on mosquito survival when co-fed with CLO. IVM-CLO livestock co-formulations would not likely alter the <i>Anopheles</i> mosquito-lethal effect of MITL. The use of MITL-CLO for malaria control would have health benefits for livestock, treating helminth and liver fluke infections, and additional One Health benefits by reducing transmission risk of liver flukes to humans.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 2","pages":"393-397"},"PeriodicalIF":1.9,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143008117","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}
Maxcilene da Silva de Oliveira, Rosa Cristina Ribeiro da Silva, Antonia Suely Guimarães e Silva, Judson Chaves Rodrigues, Ronayce Conceição de Jesus Serrão Pimenta, Francisco Santos Leonardo, José Manuel Macário Rebêlo, Valéria Cristina Soares Pinheiro
Land use and cover changes lead to fragmentation of the natural habitats of sand flies and modify the epidemiological profile of leishmaniasis. This process contributes to the infestation of adjacent rural settlements by vector sand fly species with different degrees of adaptation, promoting leishmaniasis outbreaks. This study aimed to assess land use and cover changes over a 12-year period and investigate the diversity and abundance of sand fly assemblages in the rural area of Codó, Maranhão State, Brazil. Temporal analysis of land use and cover changes was conducted using Sentinel-2 satellite imagery treated in QGIS software (free version 3.10) and classified using Orfeo Toolbox. Sand flies were sampled in alternate months between August 2022 and June 2023 using Centers for Disease Control and Prevention (CDC) light traps and white and black Shannon traps installed in peridomestic and extradomestic environments. Map images showed that the predominant land covers in 2012 and 2014 were dense and sparse vegetation, with few buildings. In 2021 and 2023, areas of sparse and dense vegetation were fragmented as new settlements were established. The entomological survey resulted in the capture of 3375 sand flies (CDC = 856, white Shannon = 650, black Shannon = 1969) belonging to 20 species. The most abundant species were Psychodopygus wellcomei Fraiha, Shaw & Lainson, 1971 (78.19%), followed by Nyssomyia whitmani (Antunes & Coutinho, 1939) (7.53%). Additionally, Ny. whitmani was the most abundant species (84.97%) in peridomestic environments, whereas Ps. wellcomei was the most abundant species (96.51%) in extradomestic environments. The sand fly assemblage was highly diverse, with a high abundance of competent vectors of Leishmania spp. These findings can promote community participation in surveillance and control efforts to prevent leishmaniasis cases.
{"title":"Land use and cover changes and sand fly (Diptera: Psychodidae) assemblages in an emerging focus of leishmaniasis\u0000 Mudança no uso e ocupação do solo e assembleias de flebotomíneos (Diptera, Psychodidae) em um foco emergente de leishmanioses","authors":"Maxcilene da Silva de Oliveira, Rosa Cristina Ribeiro da Silva, Antonia Suely Guimarães e Silva, Judson Chaves Rodrigues, Ronayce Conceição de Jesus Serrão Pimenta, Francisco Santos Leonardo, José Manuel Macário Rebêlo, Valéria Cristina Soares Pinheiro","doi":"10.1111/mve.12791","DOIUrl":"10.1111/mve.12791","url":null,"abstract":"<p>Land use and cover changes lead to fragmentation of the natural habitats of sand flies and modify the epidemiological profile of leishmaniasis. This process contributes to the infestation of adjacent rural settlements by vector sand fly species with different degrees of adaptation, promoting leishmaniasis outbreaks. This study aimed to assess land use and cover changes over a 12-year period and investigate the diversity and abundance of sand fly assemblages in the rural area of Codó, Maranhão State, Brazil. Temporal analysis of land use and cover changes was conducted using Sentinel-2 satellite imagery treated in QGIS software (free version 3.10) and classified using Orfeo Toolbox. Sand flies were sampled in alternate months between August 2022 and June 2023 using Centers for Disease Control and Prevention (CDC) light traps and white and black Shannon traps installed in peridomestic and extradomestic environments. Map images showed that the predominant land covers in 2012 and 2014 were dense and sparse vegetation, with few buildings. In 2021 and 2023, areas of sparse and dense vegetation were fragmented as new settlements were established. The entomological survey resulted in the capture of 3375 sand flies (CDC = 856, white Shannon = 650, black Shannon = 1969) belonging to 20 species. The most abundant species were <i>Psychodopygus wellcomei</i> Fraiha, Shaw & Lainson, 1971 (78.19%), followed by <i>Nyssomyia whitmani</i> (Antunes & Coutinho, 1939) (7.53%). Additionally, <i>Ny. whitmani</i> was the most abundant species (84.97%) in peridomestic environments, whereas <i>Ps. wellcomei</i> was the most abundant species (96.51%) in extradomestic environments. The sand fly assemblage was highly diverse, with a high abundance of competent vectors of <i>Leishmania</i> spp. These findings can promote community participation in surveillance and control efforts to prevent leishmaniasis cases.</p>","PeriodicalId":18350,"journal":{"name":"Medical and Veterinary Entomology","volume":"39 3","pages":"525-537"},"PeriodicalIF":1.9,"publicationDate":"2025-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143008113","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}