Pub Date : 2025-10-31DOI: 10.1016/j.exppara.2025.109043
Thainá de Melo , Isadora do Monte Silveira Bruno , Luciana Brandão-Bezerra , Christiane Leal Corrêa , Silvia Amaral G da Silva , Luciana Silva Rodrigues , Alba Cristina Miranda de Barros Alencar , José Roberto Machado-Silva , Renata Heisler Neves
Schistosomiasis is a neglected disease that affects millions of people in endemic areas and it is heavily influenced by changes in the host's metabolic profile. This study investigated liver tissue remodeling in acute experimental schistosomiasis and diet-induced dyslipidemia in female Swiss Webster mice. The mice were fed either a high-fat diet (HFD) or a standard diet (SD) for 29 weeks. At week 20, the animals were subcutaneously infected with 100 cercariae of Schistosoma mansoni (BH strain). After 9 weeks of infection, the mice were euthanized, and blood samples were collected for biochemical analysis. Additionally, peritoneal lavage was performed to evaluate cytokine profiles. Liver was collected, processed, and stained using Hematoxylin and Eosin, Gomori's Reticulin, and Picrosirius Red for histopathological, stereological, morphometric, and collagen granuloma analyses. Biochemical tests confirmed dyslipidemia in the HFD-fed mice. Peritoneal cells exhibited a proinflammatory immune response, and liver displayed a highly inflamed architectural morphology. Morphometric analysis of centrilobular and hepatic veins revealed that both HFD and schistosomiasis altered vessel morphology. The findings suggest that diet-induced dyslipidemia interferes with certain aspects of acute experimental schistosomiasis, contributing to immune cytokine profile remodeling by macrophages, liver disorganization, and modulation of the morphometric parameters of centrilobular and hepatic veins.
{"title":"Remodeling of liver tissue and the inflammatory profile in a dyslipidemic mice model infected with acute schistosomiasis","authors":"Thainá de Melo , Isadora do Monte Silveira Bruno , Luciana Brandão-Bezerra , Christiane Leal Corrêa , Silvia Amaral G da Silva , Luciana Silva Rodrigues , Alba Cristina Miranda de Barros Alencar , José Roberto Machado-Silva , Renata Heisler Neves","doi":"10.1016/j.exppara.2025.109043","DOIUrl":"10.1016/j.exppara.2025.109043","url":null,"abstract":"<div><div>Schistosomiasis is a neglected disease that affects millions of people in endemic areas and it is heavily influenced by changes in the host's metabolic profile. This study investigated liver tissue remodeling in acute experimental schistosomiasis and diet-induced dyslipidemia in female Swiss Webster mice. The mice were fed either a high-fat diet (HFD) or a standard diet (SD) for 29 weeks. At week 20, the animals were subcutaneously infected with 100 cercariae of <em>Schistosoma mansoni</em> (BH strain). After 9 weeks of infection, the mice were euthanized, and blood samples were collected for biochemical analysis. Additionally, peritoneal lavage was performed to evaluate cytokine profiles. Liver was collected, processed, and stained using Hematoxylin and Eosin, Gomori's Reticulin, and Picrosirius Red for histopathological, stereological, morphometric, and collagen granuloma analyses. Biochemical tests confirmed dyslipidemia in the HFD-fed mice. Peritoneal cells exhibited a proinflammatory immune response, and liver displayed a highly inflamed architectural morphology. Morphometric analysis of centrilobular and hepatic veins revealed that both HFD and schistosomiasis altered vessel morphology. The findings suggest that diet-induced dyslipidemia interferes with certain aspects of acute experimental schistosomiasis, contributing to immune cytokine profile remodeling by macrophages, liver disorganization, and modulation of the morphometric parameters of centrilobular and hepatic veins.</div></div>","PeriodicalId":12117,"journal":{"name":"Experimental parasitology","volume":"279 ","pages":"Article 109043"},"PeriodicalIF":1.6,"publicationDate":"2025-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145426716","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-28DOI: 10.1016/j.exppara.2025.109042
Eli Vanlal , Oumsalama Elhelu , Olayemi G. Fagunloye , Matty Knight
Sialic acid-binding immunoglobulin-like lectins (siglecs) are cell surface receptors involved in immune signaling. When Schistosoma mansoni infects its intermediate host, the Biomphalaria glabrata snail, early stress responses such as upregulation of heat shock protein 70 (Hsp70) are observed. We hypothesized that stress-induced Hsp70 translocates to the cell membrane and interacts with siglec homologs to modulate immune response in the snail. Utilizing in-silico approaches, we identified B. glabrata transcripts homologous to human and molluscan siglecs, followed by homology modeling and molecular docking, which predicted a salt bridge between glutamic acid 479 on Hsp70 and lysine 47 on a siglec homolog, (BgPrx), suggesting a plausible binding interface.
To validate this, we performed real-time qPCR from infected BB02 snails, revealing significant upregulation of siglec homolog transcripts shortly after infection. Additionally, protein fractionation and immunocytochemistry confirmed Hsp70 localization to the membrane post infection. These results support a model in which siglec–Hsp70 interactions dampen stress signaling and may suppress host immune defenses. Concurrently, S. mansoni employs glycan mimicry, presenting host-like sialylated structures that likely engage siglecs and further misdirect the immune response.
Together, our findings suggest that BgHsp70–siglec interactions, in combination with parasite glycan mimicry, constitute a potential immune evasion mechanism enabling schistosome establishment in susceptible B. glabrata snails.
{"title":"Siglec homologs interact with membrane-bound Heat Shock Protein 70 (Hsp70) during early infection of the Schistosoma mansoni susceptible (BB02) Biomphalaria glabrata snail host","authors":"Eli Vanlal , Oumsalama Elhelu , Olayemi G. Fagunloye , Matty Knight","doi":"10.1016/j.exppara.2025.109042","DOIUrl":"10.1016/j.exppara.2025.109042","url":null,"abstract":"<div><div>Sialic acid-binding immunoglobulin-like lectins (siglecs) are cell surface receptors involved in immune signaling. When <em>Schistosoma mansoni</em> infects its intermediate host, the <em>Biomphalaria glabrata</em> snail, early stress responses such as upregulation of heat shock protein 70 (Hsp70) are observed. We hypothesized that stress-induced Hsp70 translocates to the cell membrane and interacts with siglec homologs to modulate immune response in the snail. Utilizing in-silico approaches, we identified <em>B. glabrata</em> transcripts homologous to human and molluscan siglecs, followed by homology modeling and molecular docking, which predicted a salt bridge between glutamic acid 479 on Hsp70 and lysine 47 on a siglec homolog, (<em>BgPrx</em>), suggesting a plausible binding interface.</div><div>To validate this, we performed real-time qPCR from infected BB02 snails, revealing significant upregulation of siglec homolog transcripts shortly after infection. Additionally, protein fractionation and immunocytochemistry confirmed Hsp70 localization to the membrane post infection. These results support a model in which siglec–Hsp70 interactions dampen stress signaling and may suppress host immune defenses. Concurrently, <em>S. mansoni</em> employs glycan mimicry, presenting host-like sialylated structures that likely engage siglecs and further misdirect the immune response.</div><div>Together, our findings suggest that <em>Bg</em>Hsp70–siglec interactions, in combination with parasite glycan mimicry, constitute a potential immune evasion mechanism enabling schistosome establishment in susceptible <em>B. glabrata</em> snails.</div></div>","PeriodicalId":12117,"journal":{"name":"Experimental parasitology","volume":"279 ","pages":"Article 109042"},"PeriodicalIF":1.6,"publicationDate":"2025-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145399567","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-24DOI: 10.1016/j.exppara.2025.109044
Alex Yagoo , M.C. John Milton , Jelin Vilvest , Mariya Vaishnika A
Background
Mosquito-borne diseases transmitted by Aedes aegypti and Culex quinquefasciatus pose major public health challenges worldwide. The emergence of resistance to synthetic insecticides, along with concerns about their ecological and health impacts, highlights the urgent need for novel, eco-friendly alternatives. This study investigates the larvicidal and growth-disrupting effects of β-isocostic acid, a sesquiterpene isolated from Sphaeranthus indicus, while considering its relevance for non-target safety and integrated vector control.
Methods
Larvae of Ae. aegypti and Cx. quinquefasciatus were exposed to β-isocostic acid at concentrations of 0.5, 1.0, and 1.5 mg/L. Developmental parameters—including larval, pupal, and adult durations were monitored. Growth index was calculated to assess developmental progression. Histopathological analysis of third-instar larvae was performed using hematoxylin-eosin staining to examine midgut alterations. Emergence quality and behavioural abnormalities in adults were also recorded.
Results
β-Isocostic acid significantly delayed larval and pupal development in both mosquito species. At 0.5 mg/L, Ae. aegypti larvae developed in 8.4 ± 1.0 days versus 6.0 ± 0.0 days in controls, while Cx. quinquefasciatus larvae required 7.5 ± 1.0 days compared to 6.2 ± 0.2 days. Growth index values confirmed reduced developmental rates. Histopathological changes included epithelial vacuolization, disruption of microvilli, and peritrophic membrane rupture. Deformities such as crumpled wings and sluggish behaviour were observed in emerging adults, indicating compromised viability.
Conclusion
β-Isocostic acid exerts potent, multi-stage developmental disruption in mosquito vectors through growth retardation and midgut damage. These findings support its potential as a botanical larvicide; however, further studies are warranted to evaluate non-target toxicity and feasibility for use in sustainable mosquito control strategies.
{"title":"Developmental disruption and midgut histopathology induced by β-isocostic acid in Aedes aegypti and Culex quinquefasciatus (Diptera: Culicidae)","authors":"Alex Yagoo , M.C. John Milton , Jelin Vilvest , Mariya Vaishnika A","doi":"10.1016/j.exppara.2025.109044","DOIUrl":"10.1016/j.exppara.2025.109044","url":null,"abstract":"<div><h3>Background</h3><div>Mosquito-borne diseases transmitted by <em>Aedes aegypti</em> and <em>Culex quinquefasciatus</em> pose major public health challenges worldwide. The emergence of resistance to synthetic insecticides, along with concerns about their ecological and health impacts, highlights the urgent need for novel, eco-friendly alternatives. This study investigates the larvicidal and growth-disrupting effects of β-isocostic acid, a sesquiterpene isolated from <em>Sphaeranthus indicus</em>, while considering its relevance for non-target safety and integrated vector control.</div></div><div><h3>Methods</h3><div>Larvae of <em>Ae. aegypti</em> and <em>Cx. quinquefasciatus</em> were exposed to β-isocostic acid at concentrations of 0.5, 1.0, and 1.5 mg/L. Developmental parameters—including larval, pupal, and adult durations were monitored. Growth index was calculated to assess developmental progression. Histopathological analysis of third-instar larvae was performed using hematoxylin-eosin staining to examine midgut alterations. Emergence quality and behavioural abnormalities in adults were also recorded.</div></div><div><h3>Results</h3><div>β-Isocostic acid significantly delayed larval and pupal development in both mosquito species. At 0.5 mg/L, <em>Ae. aegypti</em> larvae developed in 8.4 ± 1.0 days versus 6.0 ± 0.0 days in controls, while <em>Cx. quinquefasciatus</em> larvae required 7.5 ± 1.0 days compared to 6.2 ± 0.2 days. Growth index values confirmed reduced developmental rates. Histopathological changes included epithelial vacuolization, disruption of microvilli, and peritrophic membrane rupture. Deformities such as crumpled wings and sluggish behaviour were observed in emerging adults, indicating compromised viability.</div></div><div><h3>Conclusion</h3><div>β-Isocostic acid exerts potent, multi-stage developmental disruption in mosquito vectors through growth retardation and midgut damage. These findings support its potential as a botanical larvicide; however, further studies are warranted to evaluate non-target toxicity and feasibility for use in sustainable mosquito control strategies.</div></div>","PeriodicalId":12117,"journal":{"name":"Experimental parasitology","volume":"278 ","pages":"Article 109044"},"PeriodicalIF":1.6,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145359794","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-08DOI: 10.1016/j.exppara.2025.109032
Laura Machín , Rachel Nápoles , Beatriz Tamargo , Arianna Yglesias-Rivera , Lars Gille , William N. Setzer , Lianet Monzote
Previous studies have demonstrated the antileishmanial potentialities of endoperoxide (EP) compounds, including artemisinin (ART). In the design of pharmaceutical formulations, the lipid-based delivery systems based on cochleates has attracted attention due to their stability, versatility, biocompatibility and biodegradability. The aim of the present study was to compare the in vitro and in vivo antileishmanial activity of ART with their nanocochleates formulations (ART-C) and reference drug Glucantime®. The antileishmanial and cytotoxic activities were evaluated on intracellular amastigotes of Leishmania (Leishmania) amazonensis and peritoneal macrophages from BALB/c mice, respectively. In vivo assessment was also performed on cutaneous leishmaniasis induced in BALB/c mice using a treatment protocol of 5 doses at 30 mg/kg every 4 days by intralesional route. The ART-C maintained its in vitro activity with an IC50 of 16.3 ± 3.6 μM, which was similar to ART (14.9 ± 2.4 μM). In both cases, no cytotoxicity on peritoneal macrophages was observed at maximum concentration tested (170 μM). In ART-C treated mice, the disease development was prevented (p < 0.05) with respect to animals treated with empty cochleates (EC), treated with ART, and untreated mice, under enhanced of IL-12 formation. Our results demonstrate the benefit of ART-C as a promising antileishmanial therapeutic formulation.
{"title":"In vitro and in vivo activity of a lipid-based artemisinin formulation against Leishmania (Leishmania) amazonensis","authors":"Laura Machín , Rachel Nápoles , Beatriz Tamargo , Arianna Yglesias-Rivera , Lars Gille , William N. Setzer , Lianet Monzote","doi":"10.1016/j.exppara.2025.109032","DOIUrl":"10.1016/j.exppara.2025.109032","url":null,"abstract":"<div><div>Previous studies have demonstrated the antileishmanial potentialities of endoperoxide (EP) compounds, including artemisinin (ART). In the design of pharmaceutical formulations, the lipid-based delivery systems based on cochleates has attracted attention due to their stability, versatility, biocompatibility and biodegradability. The aim of the present study was to compare the <em>in vitro</em> and <em>in vivo</em> antileishmanial activity of ART with their nanocochleates formulations (ART-C) and reference drug Glucantime®. The antileishmanial and cytotoxic activities were evaluated on intracellular amastigotes of <em>Leishmania</em> (<em>Leishmania</em>) <em>amazonensis</em> and peritoneal macrophages from BALB/c mice, respectively. <em>In vivo</em> assessment was also performed on cutaneous leishmaniasis induced in BALB/c mice using a treatment protocol of 5 doses at 30 mg/kg every 4 days by intralesional route. The ART-C maintained its <em>in vitro</em> activity with an IC<sub>50</sub> of 16.3 ± 3.6 μM, which was similar to ART (14.9 ± 2.4 μM). In both cases, no cytotoxicity on peritoneal macrophages was observed at maximum concentration tested (170 μM). In ART-C treated mice, the disease development was prevented (<em>p</em> < 0.05) with respect to animals treated with empty cochleates (EC), treated with ART, and untreated mice, under enhanced of IL-12 formation. Our results demonstrate the benefit of ART-C as a promising antileishmanial therapeutic formulation.</div></div>","PeriodicalId":12117,"journal":{"name":"Experimental parasitology","volume":"278 ","pages":"Article 109032"},"PeriodicalIF":1.6,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145274187","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-03DOI: 10.1016/j.exppara.2025.109033
Ayesha Malik , Kiran Afshan , Min-Kuang Lee , Abdul Razzaq , Munib Hussain , Sabika Firasat , Muhammad Morshed
Background
Theileria spp. are economically important tick-borne hemoprotozoan parasites that threaten livestock health and productivity, particularly in tropical and subtropical regions. In this study, we developed and validated a qPCR-based diagnostic panel for the sensitive and specific detection of Theileria infections in ruminants from Khyber Pakhtunkhwa (KP), Pakistan. The panel included a broad-range Pan-Theileria assay as well as four species-specific assays for Theileria annulata, T. parva, T. lestoquardi, and T. ovis, the main species infecting domestic ruminants in the region.
Methods
A total of 1026 tick-infested animals were examined, including sheep (n = 514), goats (n = 462), and cattle (n = 50). Blood was collected from symptomatic animals, and 51 microscopically confirmed Theileria-positive samples were selected for further analysis. DNA was extracted using the phenol-chloroform method for clinical validation. Primers and hydrolysis probes were designed to target the hypervariable V4 region of the 18S rRNA gene, allowing high-resolution species identification.
Results
Analytical validation using synthetic gBlock™ gene fragments showed strong assay performance, with excellent linearity (R2 = 0.982–0.9965), high PCR efficiency (86.2 %–105.2 %), and detection limits of 10–100 copies per reaction. Reproducibility was confirmed with coefficients of variation ≤5 %. The Pan-Theileria assay detected 47 positives. Sequencing of the 18S rRNA gene confirmed these results and additionally identified three cases of T. orientalis, two of which were also detected by qPCR. One sample tested positive for T. ovis. Overall, the assay achieved 100 % clinical sensitivity and specificity within this validation set, though larger multi-site field evaluations are needed to confirm these findings.
Conclusion
This is the first comprehensive qPCR-based diagnostic platform for simultaneous detection and speciation of Theileria spp. in Pakistan. The tool provides a powerful approach for large-scale surveillance, timely diagnosis, and improved control of tropical theileriosis in endemic areas.
{"title":"Molecular diagnosis of tropical theileriosis: Development and validation of species-specific qPCR assays in Pakistan","authors":"Ayesha Malik , Kiran Afshan , Min-Kuang Lee , Abdul Razzaq , Munib Hussain , Sabika Firasat , Muhammad Morshed","doi":"10.1016/j.exppara.2025.109033","DOIUrl":"10.1016/j.exppara.2025.109033","url":null,"abstract":"<div><h3>Background</h3><div><em>Theileria</em> spp. are economically important tick-borne hemoprotozoan parasites that threaten livestock health and productivity, particularly in tropical and subtropical regions. In this study, we developed and validated a qPCR-based diagnostic panel for the sensitive and specific detection of <em>Theileria</em> infections in ruminants from Khyber Pakhtunkhwa (KP), Pakistan. The panel included a broad-range Pan-<em>Theileria</em> assay as well as four species-specific assays for <em>Theileria annulata</em>, <em>T. parva</em>, <em>T. lestoquardi</em>, and <em>T. ovis</em>, the main species infecting domestic ruminants in the region.</div></div><div><h3>Methods</h3><div>A total of 1026 tick-infested animals were examined, including sheep (n = 514), goats (n = 462), and cattle (n = 50). Blood was collected from symptomatic animals, and 51 microscopically confirmed <em>Theileria</em>-positive samples were selected for further analysis. DNA was extracted using the phenol-chloroform method for clinical validation. Primers and hydrolysis probes were designed to target the hypervariable V4 region of the 18S rRNA gene, allowing high-resolution species identification.</div></div><div><h3>Results</h3><div>Analytical validation using synthetic gBlock™ gene fragments showed strong assay performance, with excellent linearity (R<sup>2</sup> = 0.982–0.9965), high PCR efficiency (86.2 %–105.2 %), and detection limits of 10–100 copies per reaction. Reproducibility was confirmed with coefficients of variation ≤5 %. The Pan-<em>Theileria</em> assay detected 47 positives. Sequencing of the 18S rRNA gene confirmed these results and additionally identified three cases of <em>T. orientalis</em>, two of which were also detected by qPCR. One sample tested positive for <em>T. ovis.</em> Overall, the assay achieved 100 % clinical sensitivity and specificity within this validation set, though larger multi-site field evaluations are needed to confirm these findings.</div></div><div><h3>Conclusion</h3><div>This is the first comprehensive qPCR-based diagnostic platform for simultaneous detection and speciation of <em>Theileria</em> spp. in Pakistan. The tool provides a powerful approach for large-scale surveillance, timely diagnosis, and improved control of tropical theileriosis in endemic areas.</div></div>","PeriodicalId":12117,"journal":{"name":"Experimental parasitology","volume":"278 ","pages":"Article 109033"},"PeriodicalIF":1.6,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145229824","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-02DOI: 10.1016/j.exppara.2025.109031
Maria Victoria Solana , Pizzarello Gimena , Galante Martina , Solana Hugo
Fasciolosis is a zoonotic disease caused by Fasciola hepatica, and poses significant public health and economic challenges, particularly in regions where livestock farming is predominant. This study evaluates the effect of table vinegar on F. hepatica metacercariae viability and infectivity through an innovative In vitro excystment assay, in order to test the effectiveness of common household sanitization practices. Metacercariae were exposed to different concentrations of vinegar solutions at varying durations, and viability and excystment capacity were subsequently assessed, simulating gastrointestinal conditions. Both vinegar concentration and exposure time significantly influenced excystment rates, with higher vinegar concentrations resulting in decreased metacercariae viability, however, conditions equivalent to commonly promoted household practices were found to be inefficient at eliminating infection risk. This is the first study to employ an in vitro excystment assay to evaluate the infectivity of F. hepatica metacercariae after exposure to vinegar. Our findings highlight that typical household practices, such as briefly soaking vegetables in diluted vinegar, are inadequate for effectively eliminating parasite viability and thus could favor infection, affecting public health.
{"title":"In vitro evaluation of the efficacy of acetic acid at 6 % (table vinegar) on inhibiting Fasciola hepatica metacercariae","authors":"Maria Victoria Solana , Pizzarello Gimena , Galante Martina , Solana Hugo","doi":"10.1016/j.exppara.2025.109031","DOIUrl":"10.1016/j.exppara.2025.109031","url":null,"abstract":"<div><div>Fasciolosis is a zoonotic disease caused by <em>Fasciola hepatica</em>, and poses significant public health and economic challenges, particularly in regions where livestock farming is predominant. This study evaluates the effect of table vinegar on <em>F. hepatica</em> metacercariae viability and infectivity through an innovative <em>In vitro</em> excystment assay, in order to test the effectiveness of common household sanitization practices. Metacercariae were exposed to different concentrations of vinegar solutions at varying durations, and viability and excystment capacity were subsequently assessed, simulating gastrointestinal conditions. Both vinegar concentration and exposure time significantly influenced excystment rates, with higher vinegar concentrations resulting in decreased metacercariae viability, however, conditions equivalent to commonly promoted household practices were found to be inefficient at eliminating infection risk. This is the first study to employ an in vitro excystment assay to evaluate the infectivity of <em>F. hepatica</em> metacercariae after exposure to vinegar. Our findings highlight that typical household practices, such as briefly soaking vegetables in diluted vinegar, are inadequate for effectively eliminating parasite viability and thus could favor infection, affecting public health.</div></div>","PeriodicalId":12117,"journal":{"name":"Experimental parasitology","volume":"278 ","pages":"Article 109031"},"PeriodicalIF":1.6,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145228344","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-01DOI: 10.1016/j.exppara.2025.109030
Shabbir Hussain , Aqleemul Islam , Zeenat Islam , Fayaz Ahmad , Kamal Jaiswal , Suman Mishra
Gastrointestinal nematodes (GINs) are the major constraint to the production of small ruminants worldwide, causing significant losses in growth, productivity, and overall health. Clinical infections may linked to anaemia, diarrhoea, anorexia, oedema, and even mortality, whereas subclinical infections result in hidden production losses. Synthetic drugs are the primary means of control; however, their indiscriminate use has led to the emergence of parasite strains resistant to multiple classes of anthelmintics, this has created strong need for sustainable alternatives. Ethnomedicinal plants have emerged as promising alternative, with Artemisia brevifolia Wall ex Dc. is used as an anthelmintic remedy in small ruminants. The current study aimed to appraise the phytochemical characterization and in vitro anthelmintic activity of crude ethanolic extract (CEE) and crude aqueous extract (CAE) of A. brevifolia. CEE exhibited higher phenolic and flavonoid contents than CAE, with FTIR showing more distinct absorption peaks. HPLC-UV confirmed the presence of key phenolics (gallic acid, quercetin, ferulic acid, vanillic acid, and kaempferol), while LC-MS identified 33 compounds. Anthelmintic activity, assessed through egg hatch test (EHT), larval motility test (LMT), and adult worm motility inhibition assay (AWMIA), revealed that CEE exhibited 87.5 % egg hatch inhibition at 50 mg/mL and complete (100 %) adult worm motility inhibition after 8h post exposure (PE) at 25 mg/mL, while CAE showed 82.7 % and 63.3 % inhibition, respectively. Both extract exhibit dose dependent larvicidal activity. The findings of the present study divulged the remarkable phytochemical characterization and anthelmintic properties of A. brevifolia, and it could be a promising anthelmintic agent in veterinary medicine.
{"title":"Phytochemical characterization and insight into the in vitro anthelmintic activity of Artemisia brevifolia Wall ex Dc. against the different life stages of the gastrointestinal nematode of sheep","authors":"Shabbir Hussain , Aqleemul Islam , Zeenat Islam , Fayaz Ahmad , Kamal Jaiswal , Suman Mishra","doi":"10.1016/j.exppara.2025.109030","DOIUrl":"10.1016/j.exppara.2025.109030","url":null,"abstract":"<div><div>Gastrointestinal nematodes (GINs) are the major constraint to the production of small ruminants worldwide, causing significant losses in growth, productivity, and overall health. Clinical infections may linked to anaemia, diarrhoea, anorexia, oedema, and even mortality, whereas subclinical infections result in hidden production losses. Synthetic drugs are the primary means of control; however, their indiscriminate use has led to the emergence of parasite strains resistant to multiple classes of anthelmintics, this has created strong need for sustainable alternatives. Ethnomedicinal plants have emerged as promising alternative, with <em>Artemisia brevifolia</em> Wall ex Dc. is used as an anthelmintic remedy in small ruminants. The current study aimed to appraise the phytochemical characterization and <em>in vitro</em> anthelmintic activity of crude ethanolic extract (CEE) and crude aqueous extract (CAE) of <em>A. brevifolia.</em> CEE exhibited higher phenolic and flavonoid contents than CAE, with FTIR showing more distinct absorption peaks. HPLC-UV confirmed the presence of key phenolics (gallic acid, quercetin, ferulic acid, vanillic acid, and kaempferol), while LC-MS identified 33 compounds. Anthelmintic activity, assessed through egg hatch test (EHT), larval motility test (LMT), and adult worm motility inhibition assay (AWMIA), revealed that CEE exhibited 87.5 % egg hatch inhibition at 50 mg/mL and complete (100 %) adult worm motility inhibition after 8h post exposure (PE) at 25 mg/mL, while CAE showed 82.7 % and 63.3 % inhibition, respectively. Both extract exhibit dose dependent larvicidal activity. The findings of the present study divulged the remarkable phytochemical characterization and anthelmintic properties of <em>A. brevifolia</em>, and it could be a promising anthelmintic agent in veterinary medicine.</div></div>","PeriodicalId":12117,"journal":{"name":"Experimental parasitology","volume":"277 ","pages":"Article 109030"},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145185109","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-23DOI: 10.1016/j.exppara.2025.109029
Zeenat Islam , Aqleemul Islam , Khurshid Ahmad Tariq , Jasmeena Syed , Shabbir Hussain , Fayaz Ahmad
Haemonchus contortus –the barber's pole worm poses a critical threat to ruminant health and productivity worldwide. This is due to its high host pathogenicity and poor susceptibility to chemical anthelmintics. To address this threat, sustainable and natural solutions are needed to control its infections. This study evaluated the anthelmintic efficacy of Salvia sclarea extracts against H. contortus in comparison to reference drug – the Albendazole. The extracts were obtained in ethyl acetate, ethanol, and petroleum ether, analyzed phytochemically and subjected to in-vitro testing at different concentrations using the Adult Motility Inhibition Assay (AMIA) and Egg Hatch Inhibition Assay (EHIA). The most effective extract was ethyl acetate in terms of its 100 % worm mortality at all tested concentrations 6 h post treatment and 87.38 % inhibition of egg hatching at 2 mg/mL. The ethyl acetate extract demonstrated the greatest potency, with an LC50 of 0.22 mg/mL, compared to ethanol (LC50 = 0.55 mg/mL) and petroleum ether (LC50 = 3.66 mg/mL), confirming its superior ovicidal efficacy against H. contortus. Terpenoids, coumarins, and phenolics were the main bioactive agents present in the extract. Using complementary GC-MS profiling, prominent anti-parasitic components including Sclareol and Geranylgeraniol were identified. These findings demonstrate potential of S. sclarea as a natural substitute for synthetic anthelmintics; however, in vivo studies are needed to validate the efficacy and safety of the bio-active constituents of S. sclarea against the target parasite in host animals.
{"title":"In-vitro anthelmintic activity and phytochemistry of Salvia sclarea extracts against Haemonchus contortus","authors":"Zeenat Islam , Aqleemul Islam , Khurshid Ahmad Tariq , Jasmeena Syed , Shabbir Hussain , Fayaz Ahmad","doi":"10.1016/j.exppara.2025.109029","DOIUrl":"10.1016/j.exppara.2025.109029","url":null,"abstract":"<div><div><em>Haemonchus contortus</em> –the barber's pole worm poses a critical threat to ruminant health and productivity worldwide. This is due to its high host pathogenicity and poor susceptibility to chemical anthelmintics. To address this threat, sustainable and natural solutions are needed to control its infections. This study evaluated the anthelmintic efficacy of <em>Salvia sclarea</em> extracts against <em>H. contortus</em> in comparison to reference drug – the Albendazole. The extracts were obtained in ethyl acetate, ethanol, and petroleum ether, analyzed phytochemically and subjected to <em>in-vitro</em> testing at different concentrations using the Adult Motility Inhibition Assay (AMIA) and Egg Hatch Inhibition Assay (EHIA). The most effective extract was ethyl acetate in terms of its 100 % worm mortality at all tested concentrations 6 h post treatment and 87.38 % inhibition of egg hatching at 2 mg/mL. The ethyl acetate extract demonstrated the greatest potency, with an LC<sub>50</sub> of 0.22 mg/mL, compared to ethanol (LC<sub>50</sub> = 0.55 mg/mL) and petroleum ether (LC<sub>50</sub> = 3.66 mg/mL), confirming its superior ovicidal efficacy against <em>H. contortus.</em> Terpenoids, coumarins, and phenolics were the main bioactive agents present in the extract. Using complementary GC-MS profiling, prominent anti-parasitic components including Sclareol and Geranylgeraniol were identified. These findings demonstrate potential of <em>S. sclarea</em> as a natural substitute for synthetic anthelmintics; however, <em>in vivo</em> studies are needed to validate the efficacy and safety of the bio-active constituents of <em>S. sclarea</em> against the target parasite in host animals.</div></div>","PeriodicalId":12117,"journal":{"name":"Experimental parasitology","volume":"277 ","pages":"Article 109029"},"PeriodicalIF":1.6,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145148384","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-17DOI: 10.1016/j.exppara.2025.109028
Nayer Mehdizad Bakhtiar , Mahmoud Mahami-Oskouei , Ehsan Ahmadpour , Mohammad Hasan Kohansal , Adel Spotin
Recurrent cystic echinococcosis (RCE) occurs by the spillage of live protoscoleces during unsuccessful surgery or spontaneous rupturing of fertile hydatid cyst. Currently, RCE presents a significant concern within surgical community. Managing RCE cases is challenging due to limitations in diagnostic follow-up, therapeutic pitfalls, emerging drug resistance, and innate immunological responses between host-parasite cross-talk. Recent advances suggest that parasite-derived microRNAs hold promise as biomarkers for early detection and monitoring of RCE. Additionally, combining benzimidazoles (parasito-static) with praziquantel (parasiticidal) in nano-formulation derivatives has demonstrated potential pharmacokinetic synergism, highlighting the need for personalized treatment plans. Optimizing surgical methods and ensuring regular chemotherapy following both conservative and radical surgeries are crucial for minimizing RCE. Furthermore, identifying β-tubulin codons in albendazole-resistant hydatid cyst and the role of toll-like receptor polymorphisms are critical for developing targeted therapies. The insights presented here aim to support specialists in developing effective interventions and preventive measures to reduce and improve patient outcomes in.
{"title":"Current challenges and future prospects in patients with recurrent cystic echinococcosis; an updated mini review","authors":"Nayer Mehdizad Bakhtiar , Mahmoud Mahami-Oskouei , Ehsan Ahmadpour , Mohammad Hasan Kohansal , Adel Spotin","doi":"10.1016/j.exppara.2025.109028","DOIUrl":"10.1016/j.exppara.2025.109028","url":null,"abstract":"<div><div>Recurrent cystic echinococcosis (RCE) occurs by the spillage of live protoscoleces during unsuccessful surgery or spontaneous rupturing of fertile hydatid cyst<em>.</em> Currently, RCE presents a significant concern within surgical community. Managing RCE cases is challenging due to limitations in diagnostic follow-up, therapeutic pitfalls, emerging drug resistance, and innate immunological responses between host-parasite cross-talk. Recent advances suggest that parasite-derived microRNAs hold promise as biomarkers for early detection and monitoring of RCE. Additionally, combining benzimidazoles (parasito-static) with praziquantel (parasiticidal) in nano-formulation derivatives has demonstrated potential pharmacokinetic synergism, highlighting the need for personalized treatment plans. Optimizing surgical methods and ensuring regular chemotherapy following both conservative and radical surgeries are crucial for minimizing RCE. Furthermore, identifying β-tubulin codons in albendazole-resistant hydatid cyst and the role of toll-like receptor polymorphisms are critical for developing targeted therapies. The insights presented here aim to support specialists in developing effective interventions and preventive measures to reduce and improve patient outcomes in.</div></div>","PeriodicalId":12117,"journal":{"name":"Experimental parasitology","volume":"277 ","pages":"Article 109028"},"PeriodicalIF":1.6,"publicationDate":"2025-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145091704","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-16DOI: 10.1016/j.exppara.2025.109027
Pinaki Prasad Sengupta, Siju Susan Jacob, Samer Shamshad, S. Sudhagar, A.G.S. Chandu, S.S. Patil, S Madhaba Maharana
Porcine cysticercosis caused by the metacestode stage of Taenia solium is an economically challenging disease having public health importance. Being one of the neglected tropical diseases, surveillance of porcine cysticercosis is essentially warranted in endemic countries to detect the transmission foci of infection to humans. Keeping this as background, in the present study, the genes encoding for two cystic fluid antigens (Ag2 and Ag2V1) of metacestode of T.solium were amplified, ligated into cloning vector, transformed into E.coli Top 10 cells and sequenced. After analysis and confirmation of nucleotide sequence of Ag2 and Ag2V1 genes, the purified and restriction enzyme digested PCR products were cloned. The confirmed positive clones were induced for expression of recombinant proteins and the proteins were purified by Ni-NTA affinity chromatography. The hyperimmune sera raised against native antigens of metacestode of T.solium were employed to characterize the purified recombinant proteins by Western blotting. After confirming the recombinant proteins, indirect enzyme linked immuno sorbent assays (iELISA) using recombinant Ag2 and Ag2V1 antigens were standardized. The iELISA employing recombinant Ag2 and Ag2V1 antigens revealed sensitivity of 98.1 % and 93.4 % and specificity of 91.2 % and 97.5 %, respectively. The weighted Cohen's kappa was calculated as 0.89 (95 % CI 0.804 to 0.975) for Ag2 and 0.857 (95 % CI 0.755 to 0.959) for Ag2V1. The assays developed in the present study can be employed for the surveillance of porcine cysticercosis to help in clean pork production. However, further studies involving larger sample sizes, particularly from scavenging pigs, are warranted to validate these findings.
猪带绦虫甲壳期引起的猪囊虫病是一种具有经济挑战性的疾病,具有公共卫生重要性。猪囊虫病是一种被忽视的热带病,在流行国家监测猪囊虫病是必要的,以发现人类感染的传播焦点。在此背景下,本研究扩增了猪梭菌囊液抗原Ag2和Ag2V1的编码基因,并将其连接到克隆载体上,转化到大肠杆菌Top 10细胞中进行测序。对Ag2和Ag2V1基因的核苷酸序列进行分析和确认后,对纯化后的限制性内切酶酶切PCR产物进行克隆。将确定的阳性克隆诱导表达重组蛋白,并用Ni-NTA亲和层析纯化重组蛋白。采用免疫印迹法(Western blotting)对猪绦虫metacestode天然抗原培养的高免疫血清进行鉴定。确认重组蛋白后,采用重组Ag2和Ag2V1抗原进行间接酶联免疫吸附试验(iELISA)。采用重组Ag2和Ag2V1抗原的iELISA检测结果显示,灵敏度分别为98.1%和93.4%,特异性分别为91.2%和97.5%。Ag2的加权Cohen's kappa为0.89 (95% CI 0.804至0.975),Ag2V1的加权Cohen's kappa为0.857 (95% CI 0.755至0.959)。本研究建立的检测方法可用于猪囊虫病的监测,为清洁猪肉生产提供帮助。然而,涉及更大样本量的进一步研究,特别是来自食腐猪的研究,有必要验证这些发现。
{"title":"Exploring the diagnostic utility of recombinant low molecular weight cystic fluid proteins, Ag2 and Ag2V1, for serosurveillance of porcine cysticercosis","authors":"Pinaki Prasad Sengupta, Siju Susan Jacob, Samer Shamshad, S. Sudhagar, A.G.S. Chandu, S.S. Patil, S Madhaba Maharana","doi":"10.1016/j.exppara.2025.109027","DOIUrl":"10.1016/j.exppara.2025.109027","url":null,"abstract":"<div><div>Porcine cysticercosis caused by the metacestode stage of <em>Taenia solium</em> is an economically challenging disease having public health importance. Being one of the neglected tropical diseases, surveillance of porcine cysticercosis is essentially warranted in endemic countries to detect the transmission foci of infection to humans. Keeping this as background, in the present study, the genes encoding for two cystic fluid antigens (Ag2 and Ag2V1) of metacestode of <em>T.solium</em> were amplified, ligated into cloning vector, transformed into <em>E.coli</em> Top 10 cells and sequenced. After analysis and confirmation of nucleotide sequence of Ag2 and Ag2V1 genes, the purified and restriction enzyme digested PCR products were cloned. The confirmed positive clones were induced for expression of recombinant proteins and the proteins were purified by Ni-NTA affinity chromatography. The hyperimmune sera raised against native antigens of metacestode of <em>T.solium</em> were employed to characterize the purified recombinant proteins by Western blotting. After confirming the recombinant proteins, indirect enzyme linked immuno sorbent assays (iELISA) using recombinant Ag2 and Ag2V1 antigens were standardized. The iELISA employing recombinant Ag2 and Ag2V1 antigens revealed sensitivity of 98.1 % and 93.4 % and specificity of 91.2 % and 97.5 %, respectively. The weighted Cohen's kappa was calculated as 0.89 (95 % CI 0.804 to 0.975) for Ag2 and 0.857 (95 % CI 0.755 to 0.959) for Ag2V1. The assays developed in the present study can be employed for the surveillance of porcine cysticercosis to help in clean pork production. However, further studies involving larger sample sizes, particularly from scavenging pigs, are warranted to validate these findings.</div></div>","PeriodicalId":12117,"journal":{"name":"Experimental parasitology","volume":"277 ","pages":"Article 109027"},"PeriodicalIF":1.6,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145085251","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}