Pub Date : 2026-01-07DOI: 10.1017/S0031182025101534
Teka Feyera, Brendan Sharpe, Isabelle Ruhnke, Stephen W Walkden-Brown
Ascaridia galli and Heterakis gallinarum, the most prevalent nematodes of chickens, inhabit the small intestine and caeca, respectively, and often co-occur. Current excreta egg count (EEC) methods do not differentiate between their eggs, and although chickens produce two distinct excreta types - intestinal excreta (IE) and caecal excreta (CE) - the distribution of eggs of these species across them remains poorly understood. Forty Hy-Line Brown laying hens (40 weeks, mean body weight (BW) 2·07 ± 0·02 kg), cleared of prior nematode infection and artificially infected with A. galli (n = 20) or H. gallinarum (n = 20) were housed in separate floor pens and monitored for 26 weeks. Assessments included clinical signs, EECs from IE, CE and mixed excreta (ME), and worm recovery from subsets of birds at 8, 14, 20 and 26 weeks. Neither infection resulted in clinical signs, but A. galli slightly reduced BW gain (0·5 g/week/hen) than H. gallinarum (2·8 g/week/hen). Egg detection aligned with worm predilection sites: A. galli eggs were predominantly found in IE, while H. gallinarum eggs were largely confined to CE. In ME samples, egg counts were reduced by 45% relative to IE for A. galli and 60% relative to CE for H. gallinarum. EECs showed a negative but non-significant association with excreta moisture content. Natural re-infection produced a stable adult worm population in both infections. These findings demonstrate that analysing IE and CE separately provides a practical, non-lethal approach for differentiating these infections, while ME appears to have limited diagnostic utility. Further studies should evaluate these patterns across broader conditions and individual variation.
{"title":"Differential detection of <i>Ascaridia galli</i> and <i>Heterakis gallinarum</i> eggs in intestinal and caecal excreta of floor-housed laying hens: a longitudinal study.","authors":"Teka Feyera, Brendan Sharpe, Isabelle Ruhnke, Stephen W Walkden-Brown","doi":"10.1017/S0031182025101534","DOIUrl":"10.1017/S0031182025101534","url":null,"abstract":"<p><p><i>Ascaridia galli</i> and <i>Heterakis gallinarum</i>, the most prevalent nematodes of chickens, inhabit the small intestine and caeca, respectively, and often co-occur. Current excreta egg count (EEC) methods do not differentiate between their eggs, and although chickens produce two distinct excreta types - intestinal excreta (IE) and caecal excreta (CE) - the distribution of eggs of these species across them remains poorly understood. Forty Hy-Line Brown laying hens (40 weeks, mean body weight (BW) 2·07 ± 0·02 kg), cleared of prior nematode infection and artificially infected with <i>A. galli</i> (n = 20) or <i>H. gallinarum</i> (n = 20) were housed in separate floor pens and monitored for 26 weeks. Assessments included clinical signs, EECs from IE, CE and mixed excreta (ME), and worm recovery from subsets of birds at 8, 14, 20 and 26 weeks. Neither infection resulted in clinical signs, but <i>A. galli</i> slightly reduced BW gain (0·5 g/week/hen) than <i>H. gallinarum</i> (2·8 g/week/hen). Egg detection aligned with worm predilection sites: <i>A. galli</i> eggs were predominantly found in IE, while <i>H. gallinarum</i> eggs were largely confined to CE. In ME samples, egg counts were reduced by 45% relative to IE for <i>A. galli</i> and 60% relative to CE for <i>H. gallinarum</i>. EECs showed a negative but non-significant association with excreta moisture content. Natural re-infection produced a stable adult worm population in both infections. These findings demonstrate that analysing IE and CE separately provides a practical, non-lethal approach for differentiating these infections, while ME appears to have limited diagnostic utility. Further studies should evaluate these patterns across broader conditions and individual variation.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"1-11"},"PeriodicalIF":2.4,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145912496","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-07DOI: 10.1017/S0031182025101522
Derya Topuz Ata, Anıl Ata, Chris Katharine C Carter
Leishmaniasis is a neglected parasitic disease responsible for significant morbidity and mortality. Currently, there is no vaccine approved for clinical use. Therefore, controlling infections in infected individuals depends on interventions to prevent infected female sand flies from biting humans, treatment of clinical infections or alternative treatment methods. This review focuses on the types of vaccine developed to control leishmaniasis and which vaccines have made it through to clinical trials. It also discusses the role CRISPR technology may play in improving vaccine candidates design.
{"title":"Leishmaniasis vaccine research: current status and new directions.","authors":"Derya Topuz Ata, Anıl Ata, Chris Katharine C Carter","doi":"10.1017/S0031182025101522","DOIUrl":"10.1017/S0031182025101522","url":null,"abstract":"<p><p>Leishmaniasis is a neglected parasitic disease responsible for significant morbidity and mortality. Currently, there is no vaccine approved for clinical use. Therefore, controlling infections in infected individuals depends on interventions to prevent infected female sand flies from biting humans, treatment of clinical infections or alternative treatment methods. This review focuses on the types of vaccine developed to control leishmaniasis and which vaccines have made it through to clinical trials. It also discusses the role CRISPR technology may play in improving vaccine candidates design.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"1-12"},"PeriodicalIF":2.4,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145912515","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-26DOI: 10.1017/S0031182025101479
David Minaya, Juan J Pellón, Carla Yauris, Kristhie Pillaca, Balder Choza, Jaime Pacheco, Gustavo Graciolli, José Iannacone
Hippoboscoidea flies exhibit highly specific ectoparasitic relationships with bats, shaped by both intrinsic factors (e.g. bat behaviour) and extrinsic factors (e.g. land use). Understanding the dynamics of these parasite-host interactions is essential for uncovering co-evolutionary patterns and informing conservation strategies. To this end, we studied bat-fly interactions across different elevations in a montane forest of Amazonas, northern Peru. The most abundant bats were Carollia brevicauda, C. perspicillata and Sturnira oporaphilum, while Paraeuctenodes similis and Trichobius joblingi were the most common flies. Most flies exhibited monoxenous host specificity. Bat-fly interaction networks revealed high modularity and specialization at both local and regional scales. Modules typically grouped bat species of the same genus or subfamily, suggesting that phylogenetic constraints and roosting behaviour may shape those interaction patterns. Nestedness within modules (compound structure) emerged in the aggregated regional network, aligning with the integrative hypothesis of specialization. Although network structures were broadly similar across sites, species turnover contributed to subtle differences in module composition and specialization. These differences were congruent with the changes in species roles of certain bats and flies. This study represents the first of its kind in Peru and addresses significant knowledge gaps in the ecology of bat-fly interactions in the Neotropics.
{"title":"Specialization of bat-fly interactions at different elevations in a montane forest of northern Peru.","authors":"David Minaya, Juan J Pellón, Carla Yauris, Kristhie Pillaca, Balder Choza, Jaime Pacheco, Gustavo Graciolli, José Iannacone","doi":"10.1017/S0031182025101479","DOIUrl":"10.1017/S0031182025101479","url":null,"abstract":"<p><p>Hippoboscoidea flies exhibit highly specific ectoparasitic relationships with bats, shaped by both intrinsic factors (e.g. bat behaviour) and extrinsic factors (e.g. land use). Understanding the dynamics of these parasite-host interactions is essential for uncovering co-evolutionary patterns and informing conservation strategies. To this end, we studied bat-fly interactions across different elevations in a montane forest of Amazonas, northern Peru. The most abundant bats were <i>Carollia brevicauda, C. perspicillata</i> and <i>Sturnira oporaphilum</i>, while <i>Paraeuctenodes similis</i> and <i>Trichobius joblingi</i> were the most common flies. Most flies exhibited monoxenous host specificity. Bat-fly interaction networks revealed high modularity and specialization at both local and regional scales. Modules typically grouped bat species of the same genus or subfamily, suggesting that phylogenetic constraints and roosting behaviour may shape those interaction patterns. Nestedness within modules (compound structure) emerged in the aggregated regional network, aligning with the integrative hypothesis of specialization. Although network structures were broadly similar across sites, species turnover contributed to subtle differences in module composition and specialization. These differences were congruent with the changes in species roles of certain bats and flies. This study represents the first of its kind in Peru and addresses significant knowledge gaps in the ecology of bat-fly interactions in the Neotropics.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"1-14"},"PeriodicalIF":2.4,"publicationDate":"2025-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145834681","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-26DOI: 10.1017/S0031182025101455
Ping He, Jehangir Khan, Kefeng Jiang, Peiying Peng, Wanxian Huang, Benjamin Sanogo, Du Gao, Zhong-Dao Wu, Song Liang, Xi Sun, Datao Lin
Biomphalaria straminea (Gastropoda: Planorbidae) and Physa acuta (Gastropoda: Physidae), both invasive species in southern China, are important vectors for zoonotic diseases. However, the lack of information on the infection dynamics of Angiostrongylus cantonensis in these snails leaves gaps in understanding the compatibility mechanisms between the snails and the parasite. This study aims to reveal differences in A. cantonensis infection between B. straminea and P. acuta from Guangdong, southern China, and to investigate the potential interaction mechanisms between A. cantonensis and P. acuta. We found that both phenotypic color variants of B. straminea snails were highly susceptible to A. cantonensis (100%). The load of the L3 larvae ranged from 243 to 765 per snail, and it was positively correlated with the infection dosage. Based on the comparison of third-stage larvae quantities, B. straminea is more suitable than P. acuta for establishing the life cycle of A. cantonensis in the laboratory. In contrast, geographic isolates of P. acuta exhibited variable susceptibility (13-91%) and markedly lower parasite loads, with 6-32 third-stage larvae per snail. Diverse strains of P. acuta exhibit distinct immune responses to A. cantonensis, characterized by varied expression patterns of immune-related genes such as TEP1, HSP70, FREP2, Cu-Zn_SOD1, Fe-Mn_SOD2, MIF and Galectin. Our findings establish B. straminea as both a high-risk vector and a laboratory model for studying the life cycle of A. cantonensis, while highlighting P. acuta as a model for investigating parasite-snail interactions, thereby enhancing our understanding of snail-parasite dynamics in southern China.
{"title":"Dynamics of <i>Angiostrongylus cantonensis</i> infection in invasive snails <i>Biomphalaria straminea</i> and <i>Physa acuta</i> from Guangdong, southern China.","authors":"Ping He, Jehangir Khan, Kefeng Jiang, Peiying Peng, Wanxian Huang, Benjamin Sanogo, Du Gao, Zhong-Dao Wu, Song Liang, Xi Sun, Datao Lin","doi":"10.1017/S0031182025101455","DOIUrl":"10.1017/S0031182025101455","url":null,"abstract":"<p><p><i>Biomphalaria straminea</i> (Gastropoda: Planorbidae) and <i>Physa acuta</i> (Gastropoda: Physidae), both invasive species in southern China, are important vectors for zoonotic diseases. However, the lack of information on the infection dynamics of <i>Angiostrongylus cantonensis</i> in these snails leaves gaps in understanding the compatibility mechanisms between the snails and the parasite. This study aims to reveal differences in <i>A. cantonensis</i> infection between <i>B. straminea</i> and <i>P. acuta</i> from Guangdong, southern China, and to investigate the potential interaction mechanisms between <i>A. cantonensis</i> and <i>P. acuta</i>. We found that both phenotypic color variants of <i>B. straminea</i> snails were highly susceptible to <i>A. cantonensis</i> (100%). The load of the L3 larvae ranged from 243 to 765 per snail, and it was positively correlated with the infection dosage. Based on the comparison of third-stage larvae quantities, <i>B. straminea</i> is more suitable than <i>P. acuta</i> for establishing the life cycle of <i>A. cantonensis</i> in the laboratory. In contrast, geographic isolates of <i>P. acuta</i> exhibited variable susceptibility (13-91%) and markedly lower parasite loads, with 6-32 third-stage larvae per snail. Diverse strains of <i>P. acuta</i> exhibit distinct immune responses to <i>A. cantonensis</i>, characterized by varied expression patterns of immune-related genes such as TEP1, HSP70, FREP2, Cu-Zn_SOD1, Fe-Mn_SOD2, MIF and Galectin. Our findings establish <i>B. straminea</i> as both a high-risk vector and a laboratory model for studying the life cycle of <i>A. cantonensis</i>, while highlighting <i>P. acuta</i> as a model for investigating parasite-snail interactions, thereby enhancing our understanding of snail-parasite dynamics in southern China.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"1-8"},"PeriodicalIF":2.4,"publicationDate":"2025-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145834692","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-26DOI: 10.1017/S0031182025101467
Jan Jarzabek, Paul William Denny
Recently, the WHO published a Target Product Profile for a diagnostic test for cutaneous leishmaniasis (CL) and a Roadmap to 2030 for Neglected Tropical Diseases. The documents highlight that existing diagnostic tools for CL are insufficient, whilst setting clear goals for improved sensitivity and reduced cost. The need for species typing in diagnostics is also becoming more pressing with the emergence of drug-resistance, especially of Leishmania tropica. Serological tests are unable to do this, while techniques that can, like PCR, require complex and expensive machinery. Isothermal assays like LAMP offer a promising solution, but more work also remains, as few species-specific LAMP assays have been developed thus far and CL in Ethiopia is particularly neglected. Additionally, since the COVID-19 pandemic, many cheap isothermal diagnostic devices have been produced, which have yet to be tested in the diagnosis of CL. Finally, artificial intelligence presents another avenue for rapid diagnosis by image analysis. In this comprehensive review, we examine the opportunities and challenges inherent to diagnostic development for CL, a priority undertaking that still faces many developmental hurdles.
{"title":"Molecular diagnostics for cutaneous leishmaniasis: progress towards fulfilling the WHO target product profile.","authors":"Jan Jarzabek, Paul William Denny","doi":"10.1017/S0031182025101467","DOIUrl":"10.1017/S0031182025101467","url":null,"abstract":"<p><p>Recently, the WHO published a Target Product Profile for a diagnostic test for cutaneous leishmaniasis (CL) and a Roadmap to 2030 for Neglected Tropical Diseases. The documents highlight that existing diagnostic tools for CL are insufficient, whilst setting clear goals for improved sensitivity and reduced cost. The need for species typing in diagnostics is also becoming more pressing with the emergence of drug-resistance, especially of <i>Leishmania tropica</i>. Serological tests are unable to do this, while techniques that can, like PCR, require complex and expensive machinery. Isothermal assays like LAMP offer a promising solution, but more work also remains, as few species-specific LAMP assays have been developed thus far and CL in Ethiopia is particularly neglected. Additionally, since the COVID-19 pandemic, many cheap isothermal diagnostic devices have been produced, which have yet to be tested in the diagnosis of CL. Finally, artificial intelligence presents another avenue for rapid diagnosis by image analysis. In this comprehensive review, we examine the opportunities and challenges inherent to diagnostic development for CL, a priority undertaking that still faces many developmental hurdles.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"1-19"},"PeriodicalIF":2.4,"publicationDate":"2025-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145834665","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-26DOI: 10.1017/S0031182025101510
Kerstin Junker, Boris R Krasnov
Both host identity and environmental factors are known to influence parasite species richness. Here, we analysed selected host traits and environmental variables associated with 3 aspects of helminth diversity in African ruminants. Based on the helminth faunas of 35 species of antelope and 1 species of giraffe, we studied drivers of species richness as well as taxonomic and functional diversity, combined for all helminths and separately for nematodes, cestodes and trematodes. A larger geographic host range and/or multiple habitats were associated with higher species richness in all helminths and each group individually as well as with functional diversity in all helminths, trematodes and cestodes. A wider host distribution range and larger relative brain size were both linked to higher taxonomic diversity in all helminths, and an increase in host longevity was linked to higher taxonomic diversity in nematodes. A higher level of climate moisture, relative humidity and primary production had a positive effect on trematode species richness and taxonomic diversity in all helminths, while trematode taxonomic diversity decreased in hosts from drier areas but increased in cestodes harboured by hosts from warmer areas. Our results highlight that patterns in parasite species richness and diversity emerge from an interplay of numerous factors, including host biology, environmental conditions and ecological traits of the parasites themselves. This points to the importance of carefully choosing the range of hosts considered for large-scale parasite diversity studies and underscores the need to avoid grouping too many types of parasites when looking for ecological patterns.
{"title":"Helminth faunas of wild African ruminants: effects of host traits and environmental variables on species richness and diversity.","authors":"Kerstin Junker, Boris R Krasnov","doi":"10.1017/S0031182025101510","DOIUrl":"10.1017/S0031182025101510","url":null,"abstract":"<p><p>Both host identity and environmental factors are known to influence parasite species richness. Here, we analysed selected host traits and environmental variables associated with 3 aspects of helminth diversity in African ruminants. Based on the helminth faunas of 35 species of antelope and 1 species of giraffe, we studied drivers of species richness as well as taxonomic and functional diversity, combined for all helminths and separately for nematodes, cestodes and trematodes. A larger geographic host range and/or multiple habitats were associated with higher species richness in all helminths and each group individually as well as with functional diversity in all helminths, trematodes and cestodes. A wider host distribution range and larger relative brain size were both linked to higher taxonomic diversity in all helminths, and an increase in host longevity was linked to higher taxonomic diversity in nematodes. A higher level of climate moisture, relative humidity and primary production had a positive effect on trematode species richness and taxonomic diversity in all helminths, while trematode taxonomic diversity decreased in hosts from drier areas but increased in cestodes harboured by hosts from warmer areas. Our results highlight that patterns in parasite species richness and diversity emerge from an interplay of numerous factors, including host biology, environmental conditions and ecological traits of the parasites themselves. This points to the importance of carefully choosing the range of hosts considered for large-scale parasite diversity studies and underscores the need to avoid grouping too many types of parasites when looking for ecological patterns.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"1-12"},"PeriodicalIF":2.4,"publicationDate":"2025-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145834656","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-19DOI: 10.1017/S0031182025101431
Wil Atencio, Shelby Ziegler, Stephen Greiman, John Carroll
Parasites can strongly influence host populations, particularly when the host is an ecosystem engineer. Oysters are ecosystem engineers that support estuarine communities and fisheries but are susceptible to 2 protozoan parasites, Perkinsus marinus (causing Dermo) and Haplosporidium nelsoni (causing MSX). Although both parasites are known to be influenced by environmental conditions, fine-scale temporal and spatial patterns remain underexplored in southeastern US estuaries. We examined parasite prevalence and intensity biweekly from April to October 2023 across 4 intertidal reefs on Sapelo Island, Georgia, and analysed concurrent water quality data (temperature, salinity, dissolved oxygen, pH) to identify potential environmental drivers of parasite prevalence and intensity. Parasite prevalence was high overall, 88% of oysters were infected with at least 1 parasite, and 34% were co-infected. Haplosporidium nelsoni prevalence was consistently high across sites, while P. marinus prevalence showed greater spatiotemporal variability, increasing through late summer and fall. Models indicated a time-lagged effect of environmental conditions on P. marinus prevalence, specifically with temperature and dissolved oxygen. Prevalence of H. nelsoni remained high throughout the year among sites and was best explained by temperature variability, salinity, and dissolved oxygen. Intensity levels did not differ among sites for either parasite. Our results demonstrate that even at small spatial scales and over time, oyster-parasite dynamics are shaped by multiple, interacting environmental factors, with time-lagged responses particularly evident for P. marinus. Understanding these dynamics is essential for predicting disease impacts under changing environmental conditions and informing management, restoration, and aquaculture strategies.
{"title":"Drivers of <i>Perkinsus marinus</i> and <i>Haplosporidium nelsoni</i> prevalence and intensity in oyster reefs around Sapelo Island, Georgia.","authors":"Wil Atencio, Shelby Ziegler, Stephen Greiman, John Carroll","doi":"10.1017/S0031182025101431","DOIUrl":"10.1017/S0031182025101431","url":null,"abstract":"<p><p>Parasites can strongly influence host populations, particularly when the host is an ecosystem engineer. Oysters are ecosystem engineers that support estuarine communities and fisheries but are susceptible to 2 protozoan parasites, <i>Perkinsus marinus</i> (causing Dermo) and <i>Haplosporidium nelsoni</i> (causing MSX). Although both parasites are known to be influenced by environmental conditions, fine-scale temporal and spatial patterns remain underexplored in southeastern US estuaries. We examined parasite prevalence and intensity biweekly from April to October 2023 across 4 intertidal reefs on Sapelo Island, Georgia, and analysed concurrent water quality data (temperature, salinity, dissolved oxygen, pH) to identify potential environmental drivers of parasite prevalence and intensity. Parasite prevalence was high overall, 88% of oysters were infected with at least 1 parasite, and 34% were co-infected. <i>Haplosporidium nelsoni</i> prevalence was consistently high across sites, while <i>P. marinus</i> prevalence showed greater spatiotemporal variability, increasing through late summer and fall. Models indicated a time-lagged effect of environmental conditions on <i>P. marinus</i> prevalence, specifically with temperature and dissolved oxygen. Prevalence of <i>H. nelsoni</i> remained high throughout the year among sites and was best explained by temperature variability, salinity, and dissolved oxygen. Intensity levels did not differ among sites for either parasite. Our results demonstrate that even at small spatial scales and over time, oyster-parasite dynamics are shaped by multiple, interacting environmental factors, with time-lagged responses particularly evident for <i>P. marinus</i>. Understanding these dynamics is essential for predicting disease impacts under changing environmental conditions and informing management, restoration, and aquaculture strategies.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"1-12"},"PeriodicalIF":2.4,"publicationDate":"2025-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145782369","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-19DOI: 10.1017/S0031182025101418
Md Haydar Ali, Ayna Begum, Md Shahadat Hossain, Sharmin Shahid Labony, Umme Razia Islam, Romana Parvin, Muhammad Mehedi Hasan, Anita Rani Dey, Md Abdul Alim, Anisuzzaman
Freshwater snails are important intermediate hosts for several parasitic diseases, including fascioliosis and schistosomiosis, with significant impacts on human and animal health. In Bangladesh, vector snails have been identified only by morphology. Here, we validate the species of freshwater snails acting as intermediate hosts for Fasciola and Schistosoma spp. using molecular and bioinformatics tools. Following morphology and morphometrics, we identified 9 species of snails: Lymnaea auricularia, Lymnaea luteola, Indoplanorbis exustus, Physa acuta, Viviparus bengalensis, Brotia spp., Thiara spp. and Pila globosa. Cercarial shedding tests revealed that L. auricularia (0.72%, 7 out of 977) and L. luteola (0.36%, 8 out of 2240) shed fasciolid cercariae, which polymerase chain reaction (PCR) confirmed. But I. exustus (5.43% 19 out of 350), L. auricularia (9.42%, 92 out of 977), L. luteola 10.09% (226 out of 2240), P. acuta (2.4%, 11 out of 450) and V. bengalensis (0.14%, 7 out of 500) shed schistosomatid cercariae. The same snail did not shed both fasciolid and schistosomatid cercariae simultaneously. PCR and sequencing of the Cox1 gene confirmed the species of the intermediate hosts. The sequences of L. auricularia, L. luteola, I. exustus, P. acuta and V. bengalensis were identical (99-99.7%) to reported sequences of these species. Phylogenetic analysis revealed that sequences of the present study for each species formed well-separated clusters with the corresponding reference sequences. Taken together, the results of this study highlight the importance of molecular tools for confirming snail species and will help target specific vector snails in the particular habitat when designing snail-borne trematode control programs.
{"title":"Ecology and molecular validation of species of vector snails of fascioliosis and schistosomiosis in Bangladesh.","authors":"Md Haydar Ali, Ayna Begum, Md Shahadat Hossain, Sharmin Shahid Labony, Umme Razia Islam, Romana Parvin, Muhammad Mehedi Hasan, Anita Rani Dey, Md Abdul Alim, Anisuzzaman","doi":"10.1017/S0031182025101418","DOIUrl":"10.1017/S0031182025101418","url":null,"abstract":"<p><p>Freshwater snails are important intermediate hosts for several parasitic diseases, including fascioliosis and schistosomiosis, with significant impacts on human and animal health. In Bangladesh, vector snails have been identified only by morphology. Here, we validate the species of freshwater snails acting as intermediate hosts for <i>Fasciola</i> and <i>Schistosoma</i> spp. using molecular and bioinformatics tools. Following morphology and morphometrics, we identified 9 species of snails: <i>Lymnaea auricularia, Lymnaea luteola, Indoplanorbis exustus, Physa acuta, Viviparus bengalensis, Brotia</i> spp., <i>Thiara</i> spp. and <i>Pila globosa</i>. Cercarial shedding tests revealed that <i>L. auricularia</i> (0.72%, 7 out of 977) and <i>L. luteola</i> (0.36%, 8 out of 2240) shed fasciolid cercariae, which polymerase chain reaction (PCR) confirmed. But <i>I. exustus</i> (5.43% 19 out of 350), <i>L. auricularia</i> (9.42%, 92 out of 977), <i>L. luteola</i> 10.09% (226 out of 2240), <i>P. acuta</i> (2.4%, 11 out of 450) and <i>V. bengalensis</i> (0.14%, 7 out of 500) shed schistosomatid cercariae. The same snail did not shed both fasciolid and schistosomatid cercariae simultaneously. PCR and sequencing of the <i>Cox1</i> gene confirmed the species of the intermediate hosts. The sequences of <i>L. auricularia, L. luteola, I. exustus, P. acuta</i> and <i>V. bengalensis</i> were identical (99-99.7%) to reported sequences of these species. Phylogenetic analysis revealed that sequences of the present study for each species formed well-separated clusters with the corresponding reference sequences. Taken together, the results of this study highlight the importance of molecular tools for confirming snail species and will help target specific vector snails in the particular habitat when designing snail-borne trematode control programs.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"1-11"},"PeriodicalIF":2.4,"publicationDate":"2025-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145782413","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Haemonchus contortus, a highly pathogenic gastrointestinal nematode, significantly impacts small ruminant production, causing substantial economic losses in sheep and goat farming. This study examined the genetic diversity and population structure of 171 H. contortus isolates collected from the abomasa of sheep slaughtered across 8 distinct regions in Xinjiang, China. Using sequence analysis, phylogenetic reconstruction and population genetic analyses of the mitochondrial nad4 gene, we identified 163 haplotypes, with haplotype diversity ranging from 0.995 to 1.000 and nucleotide diversity from 0.02007 to 0.03145. The Tacheng population displayed the highest nucleotide diversity. Analysis of molecular variance revealed that 91.83% of genetic variation occurred within populations, with minimal differentiation among them (Fst: -0.01296 to 0.04274). Neutrality tests (Tajima's D and Fu's Fs) indicated no recent population bottlenecks. Phylogenetic and haplotype network analyses showed no distinct geographic clustering, suggesting extensive gene flow, likely facilitated by host movement. These findings provide critical insights into the genetic structure of H. contortus in Xinjiang, informing strategies for managing anthelmintic resistance and controlling this economically significant parasite.
{"title":"Genetic diversity and population structure of <i>Haemonchus contortus</i> isolates from sheep across Xinjiang, China.","authors":"Waresi Tuersong, Reyilanmu Tuerhong, Abudusaimaiti Tuoheti, Ailixire Maimaiti, Dilare Xuekelaiti, Lianxi Xin, Aiheda Aideli, Yan Xiao, Min Hu, Saifuding Abula, Chahan Bayin, Qingyong Guo, Wei Zhang","doi":"10.1017/S0031182025101352","DOIUrl":"10.1017/S0031182025101352","url":null,"abstract":"<p><p><i>Haemonchus contortus</i>, a highly pathogenic gastrointestinal nematode, significantly impacts small ruminant production, causing substantial economic losses in sheep and goat farming. This study examined the genetic diversity and population structure of 171 <i>H. contortus</i> isolates collected from the abomasa of sheep slaughtered across 8 distinct regions in Xinjiang, China. Using sequence analysis, phylogenetic reconstruction and population genetic analyses of the mitochondrial <i>nad4</i> gene, we identified 163 haplotypes, with haplotype diversity ranging from 0.995 to 1.000 and nucleotide diversity from 0.02007 to 0.03145. The Tacheng population displayed the highest nucleotide diversity. Analysis of molecular variance revealed that 91.83% of genetic variation occurred within populations, with minimal differentiation among them (Fst: -0.01296 to 0.04274). Neutrality tests (Tajima's D and Fu's Fs) indicated no recent population bottlenecks. Phylogenetic and haplotype network analyses showed no distinct geographic clustering, suggesting extensive gene flow, likely facilitated by host movement. These findings provide critical insights into the genetic structure of <i>H. contortus</i> in Xinjiang, informing strategies for managing anthelmintic resistance and controlling this economically significant parasite.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"1-10"},"PeriodicalIF":2.4,"publicationDate":"2025-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145782442","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}