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Aniba rosaeodora essential oil as a potent, eco-friendly larvicide against Aedes albopictus 蔷薇精油是一种高效、环保的杀蚊剂,可杀灭白纹伊蚊
IF 1.6 4区 医学 Q3 PARASITOLOGY Pub Date : 2025-11-01 Epub Date: 2025-10-30 DOI: 10.1016/j.exppara.2025.109047
Roselyn Manngaihsiam, Zothan Siama, Kiran R. Kharat
Mosquito-borne diseases pose a significant threat to global health, necessitating innovative and sustainable vector control strategies. Aedes albopictus, a key vector, requires effective larvicidal agents to mitigate its spread. Herein, we aimed to evaluate the larvicidal efficacy of Aniba rosaeodora essential oil (AREO) against A. albopictus larvae, assess its cytotoxic and neurotoxic mechanisms, and explore its potential as a sustainable alternative to conventional mosquito larvicides. The larvicidal activity of AREO was tested against A. albopictus larvae by measuring its concentration- and time-dependent toxicity. Histological analysis and scanning electron microscopy (SEM) were used to examine cytotoxic effects on larval tissues. Acetylcholinesterase (AChE) inhibition was assessed to determine neurotoxic mechanisms. AREO demonstrated significant larvicidal activity, with LC50 values of 40.225 and 10.382 ppm at 24 and 48 h, respectively. Histological analysis revealed midgut epithelial disintegration, whereas SEM confirmed structural damage to the cuticle. AREO exhibited potent AChE inhibition (78.8 % at 100 ppm compared with the control), indicating a neurotoxic mode of action. To the best of our knowledge, this is the first study to report AREO as an effective larvicidal agent against A. albopictus. Despite its limitations, such as the need for field trials and broader ecotoxicity studies, AREO shows promise as a sustainable alternative to conventional mosquito larvicides.
蚊媒疾病对全球健康构成重大威胁,需要创新和可持续的病媒控制战略。白纹伊蚊是一种重要的病媒,需要有效的杀幼虫剂来减轻其传播。本研究旨在评价蔷薇精油(AREO)对白纹伊蚊幼虫的杀幼虫效果,评估其细胞毒性和神经毒性机制,并探讨其作为常规杀幼虫剂的可持续替代品的潜力。通过浓度依赖性和时间依赖性的毒力测定,研究了AREO对白纹伊蚊幼虫的杀虫活性。采用组织学分析和扫描电镜(SEM)观察对幼虫组织的细胞毒作用。评估乙酰胆碱酯酶(AChE)抑制以确定神经毒性机制。在24 h和48 h杀灭幼虫的LC50分别为40.225和10.382 ppm。组织学分析显示中肠上皮解体,扫描电镜证实角质层结构损伤。AREO表现出强有力的AChE抑制作用(与对照组相比,100 ppm时为78.8%),表明其作用方式具有神经毒性。据我们所知,这是第一个报道AREO作为白纹伊蚊有效的杀幼虫剂的研究。尽管存在局限性,例如需要实地试验和更广泛的生态毒性研究,但AREO有望成为传统灭蚊幼虫剂的可持续替代品。
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引用次数: 0
In vitro evaluation of the efficacy of acetic acid at 6 % (table vinegar) on inhibiting Fasciola hepatica metacercariae 6%醋酸(食醋)对肝片形吸虫囊蚴抑制作用的体外评价。
IF 1.6 4区 医学 Q3 PARASITOLOGY Pub Date : 2025-11-01 Epub Date: 2025-10-02 DOI: 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.
片形吸虫病是一种由肝片形吸虫引起的人畜共患疾病,对公共卫生和经济构成重大挑战,特别是在畜牧业占主导地位的地区。本研究通过创新的体外排出试验,评估食醋对肝囊蚴活力和传染性的影响,以检验常见家庭卫生措施的有效性。将囊蚴在不同时间暴露于不同浓度的醋溶液中,随后模拟胃肠道状况评估其生存能力和排泄能力。醋浓度和暴露时间都显著影响排泄率,较高的醋浓度导致囊蚴活力降低,然而,通常提倡的家庭做法在消除感染风险方面效果不佳。这是第一个采用体外排出试验来评估接触醋后肝囊蚴感染的研究。我们的研究结果强调,典型的家庭做法,如在稀释的醋中短暂浸泡蔬菜,不足以有效消除寄生虫的生存能力,因此可能有利于感染,影响公众健康。
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引用次数: 0
In vitro and in vivo activity of a lipid-based artemisinin formulation against Leishmania (Leishmania) amazonensis 脂质青蒿素制剂抗亚马逊利什曼原虫的体内外活性研究。
IF 1.6 4区 医学 Q3 PARASITOLOGY Pub Date : 2025-11-01 Epub Date: 2025-10-08 DOI: 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.
以前的研究已经证明了内过氧化物(EP)化合物,包括青蒿素(ART)具有抗利什曼病的潜力。在药物配方设计中,以耳蜗酸酯为基础的脂质给药系统因其稳定性、通用性、生物相容性和可生物降解性而备受关注。本研究的目的是比较ART及其纳米酸盐制剂(ART- c)和参比药物葡聚糖®的体外和体内抗利什曼原虫活性。分别对BALB/c小鼠细胞内亚马逊利什曼原虫(Leishmania)和腹腔巨噬细胞的抗利什曼原虫和细胞毒活性进行了评价。本研究还对BALB/c小鼠皮肤利什曼病进行了体内评估,采用5次剂量,每4天30 mg/kg,局部给药。ART- c的IC50为16.3±3.6 μM,与ART的IC50(14.9±2.4 μM)相近。两组小鼠在最大浓度(170 μM)下均未观察到对腹腔巨噬细胞的细胞毒性。在增强IL-12形成的情况下,ART- c治疗的小鼠,与空耳蜗(EC)治疗、ART治疗和未治疗的小鼠相比,疾病的发展被阻止(p < 0.05)。我们的结果证明ART-C作为一种有前途的抗利什曼病治疗制剂的益处。
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引用次数: 0
Current challenges and future prospects in patients with recurrent cystic echinococcosis; an updated mini review 复发性囊性包虫病患者目前面临的挑战和未来前景更新的迷你评论。
IF 1.6 4区 医学 Q3 PARASITOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-17 DOI: 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.
复发性囊性包虫病(RCE)发生在手术失败或可育包虫囊自然破裂时的活原头节外溢。目前,RCE是外科医学界关注的一个重要问题。由于诊断随访、治疗陷阱、新出现的耐药性和宿主-寄生虫串扰之间的先天免疫反应的局限性,管理RCE病例具有挑战性。最近的进展表明,寄生虫衍生的microrna有望成为早期检测和监测RCE的生物标志物。此外,将苯并咪唑(防寄生虫)与吡喹酮(杀寄生虫)联合制成纳米制剂衍生物已显示出潜在的药代动力学协同作用,这突出了个性化治疗计划的必要性。优化手术方法并确保在保守和根治性手术后定期化疗是减少RCE的关键。此外,鉴定阿苯达唑耐药包虫病中β-微管蛋白密码子以及toll样受体多态性的作用对于开发靶向治疗至关重要。本文提出的见解旨在支持专家制定有效的干预措施和预防措施,以减少RCE并改善CE患者的预后。
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引用次数: 0
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 短叶蒿(Artemisia brevifolia Wall ex Dc)的植物化学特性及体外驱虫活性研究。针对绵羊胃肠道线虫的不同生命阶段。
IF 1.6 4区 医学 Q3 PARASITOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-26 DOI: 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.
胃肠道线虫(GINs)是全球小型反刍动物生产的主要制约因素,对生长、生产力和整体健康造成重大损失。临床感染可能与贫血、腹泻、厌食、水肿甚至死亡有关,而亚临床感染则导致隐性生产损失。合成药物是主要的管制手段;然而,它们的滥用导致寄生虫菌株对多种类型的驱虫药产生抗药性,这就产生了对可持续替代品的强烈需求。民族药用植物已成为有希望的替代选择,如短叶蒿。被用作小反刍动物的驱虫药。本研究旨在评价短叶蒿粗醇提物(CEE)和粗水提物(CAE)的植物化学特性和体外驱虫活性。CEE的酚类和类黄酮含量高于CAE, FTIR的吸收峰更明显。HPLC-UV确认了主要酚类物质(没食子酸、槲皮素、阿魏酸、香草酸和山奈酚)的存在,LC-MS鉴定了33个化合物。通过虫卵孵化试验(EHT)、幼虫运动试验(LMT)和成虫运动抑制试验(AWMIA)对虫卵活性进行评估,结果表明,在50 mg/ml浓度下,CEE对虫卵孵化的抑制率为87.5%,在25 mg/ml浓度下,暴露后8h (PE)对成虫运动的抑制率为100%,而CAE的抑制率分别为82.7%和63.3%。两种提取物均表现出剂量依赖性的杀幼虫活性。本研究结果揭示了短叶甲具有显著的植物化学特性和驱虫药特性,是一种很有发展前景的兽药驱虫剂。
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引用次数: 0
Targeting the zinc metalloprotease gp63 of Leishmania for vaccine design and new drug discovery using immunoinformatics, molecular docking and molecular dynamics simulation studies 基于免疫信息学、分子对接和分子动力学模拟研究的针对利什曼原虫锌金属蛋白酶gp63的疫苗设计和新药开发
IF 1.6 4区 医学 Q3 PARASITOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-02 DOI: 10.1016/j.exppara.2025.109009
Mohammad Tuhin Ali , Tania Rahman , Parag Palit , Muhammad Ikhtear Uddin , Veronique Seidel
Leishmaniasis is a vector-borne parasitic disease caused by Leishmania spp., for which there is no vaccine and an urgent need for better drugs. The zinc metalloprotease gp63 of Leishmania has been identified as an antigenic structure for vaccine design and a promising target for new antileishmanial agents. In this study, immunoinformatics was used to design a full vaccine construct with the cytotoxic T-lymphocyte (CTL) and helper T-lymphocyte (HTL) epitopes of gp63 from Old and New World Leishmania spp. The vaccine construct comprising of these epitopes, with suitable adjuvant and linker sequences, was found to be thermostable, highly antigenic and non-allergenic. A total of 13 linear B-cell epitopes, and 12 continuous and four discontinuous B-cell epitopes, were further identified using the BepiPred and ElliPro prediction programs, respectively. In addition, molecular docking and molecular dynamics simulation studies were performed to identify new antileishmanial molecules with the potential to target gp63. Nareline - a phytomolecule from the antileishmanial plant Alstonia scholaris - showed the best predictive binding affinity for gp63, forming stable interactions with key residues in the active site of this protein. This study highlights the promising role of gp63 in the search for new vaccines and therapeutic agents to combat leishmaniasis.
利什曼病是一种由利什曼原虫引起的媒介传播的寄生虫病,目前还没有疫苗,迫切需要更好的药物。利什曼原虫锌金属蛋白酶gp63已被确定为疫苗设计的抗原结构和新的抗利什曼原虫药物的有希望的靶点。本研究利用免疫信息学方法设计了含新旧利什曼原虫gp63细胞毒性t淋巴细胞(CTL)和辅助性t淋巴细胞(HTL)表位的完整疫苗结构,该疫苗结构包含合适的佐剂和连接序列,具有耐热性、高抗原性和非过敏性。使用BepiPred和ElliPro预测程序进一步鉴定了13个线性b细胞表位,12个连续b细胞表位和4个不连续b细胞表位。此外,我们还进行了分子对接和分子动力学模拟研究,以鉴定可能靶向gp63的新抗利什曼原虫分子。Nareline是一种来自抗利什曼病植物Alstonia scholaris的植物分子,对gp63表现出最好的预测结合亲和力,与gp63蛋白活性位点的关键残基形成稳定的相互作用。这项研究强调了gp63在寻找对抗利什曼病的新疫苗和治疗剂方面的有希望的作用。
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引用次数: 0
Formulation and testing of different infused attractive sugar baits (ASBs) in sodium alginate against laboratory strain Aedes aegypti 不同海藻酸钠诱导糖饵对埃及伊蚊的配制及试验研究。
IF 1.6 4区 医学 Q3 PARASITOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-14 DOI: 10.1016/j.exppara.2025.109026
Ranjitha Sambanthan , Nur Faeza Abu Kassim , Sara A. Abuelmaali , Wan Maryam Wan Ahmad Kamil , Sumiyyah Sabar , Kamarul Zaman Zarkasi , Wan Rosli Wan Ishak , Cameron E. Webb
Sugar-feeding is essential to mosquitoes with both sexes that often interacting with flowering plants to acquire sugar. Alginate Sugar Baits are made up of sodium alginate (ALG) which is a safe, natural, and biodegradable polymer. The Alginate Sugar Baits are infused with sugar variants making them Attractive Sugar Baits (ASBs) as a means of providing long-term efficacy to enhance mosquito attraction. However, fundamental gaps in understanding the characteristics of ASBs and the attraction of mosquitoes towards it limits the efficacy of utilizing such bait technology. Testing of non-choice and choice assay of different group of ASBs towards Aedes aegypti to demonstrate the effectiveness of ASBs as a potential baiting tool was performed using 30 % v/v of mango, 25 % v/v of Chrysanthemum, 30 % v/v of mix and sucrose ASBs. These formulations assessed using Field Emission Scanning Electron Microscope (FESEM), Energy Dispersive X-ray (EDX), Ultraviolet–Visible-Near Infrared Spectroscopy (UV–VIS–NIR), Fourier Transform Infrared Spectroscopy (FTIR) and X-ray Diffraction (XRD) analysis. Results indicated that the 30 % mango ASB achieved the highest mosquito attraction, with a mean attraction of (34.17 ± 7.94), optimal reflectance (8 %) and absorbance (3.1 units). These ASBs are recommended as highly promising candidates as an alternative for repellent insecticides, serving as baiting tools for mosquito attraction.
对于经常与开花植物相互作用以获取糖分的两性蚊子来说,食糖是必不可少的。海藻酸盐糖饵由海藻酸钠(ALG)组成,它是一种安全、天然、可生物降解的聚合物。海藻酸盐糖饵注入糖变体,使其成为有吸引力的糖饵(asb),作为一种长期有效的手段,以增强对蚊子的吸引力。然而,在了解asb的特性和蚊子对其的吸引力方面存在根本性的差距,限制了这种诱饵技术的使用效果。采用芒果30% v/v、菊花25% v/v、混合30% v/v、蔗糖30% v/v的抗菌素对埃及伊蚊进行非选择试验和选择试验,验证抗菌素作为潜在诱蚊工具的有效性。这些配方通过场发射扫描电子显微镜(FESEM)、能量色散x射线(EDX)、紫外-可见-近红外光谱(UV-VIS-NIR)、傅里叶变换红外光谱(FTIR)和x射线衍射(XRD)分析进行评估。结果表明,30%芒果ASB诱蚊率最高,平均诱蚊率为(34.17±7.94),最佳反射率为8%,吸光度为3.1单位。这些asb被推荐为极有前途的驱避杀虫剂替代品,作为吸引蚊子的诱饵工具。
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引用次数: 0
Ultrastructural characterization and pathogenicity of Allovohlkamfia spelaea in a murine model: Neuropulmonary infections and therapeutic potential of ellagic acid 小鼠神经肺部感染模型的超微结构特征和致病性:鞣花酸的治疗潜力。
IF 1.6 4区 医学 Q3 PARASITOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-02 DOI: 10.1016/j.exppara.2025.109008
Enas A.M. Huseein , Fatma A.S. Anwar , Gamal H. Abed , Hossam El-Din M. Omar , Tasneem M. Hassan , Haiam M.M. Farrag , Sary Kh Abdel-Gahfar , Mahmoud Soliman , Alzahraa Abdelraouf Ahmad

Background

Allovahlkampfia spelaea (A. spelaea) is a free-living amoeba that has recently been recognized to cause Acanthamoeba-like keratitis, the treatment of which is complex. The pathogenic potential of Allovahlkampfia spp. remains unexplored. This study characterized A. spelaea through ultrastructural morphological analysis and investigated the pathogenic potential of the A. spelaea strain KS1, which was isolated from a patient with keratitis, in a murine model, with a focus on neuro-pulmonary infections. Additionally, this study assessed the therapeutic effectiveness of ellagic acid (EA) against tissue damage caused by amoebic infections.

Methods

Immunosuppressed male Wister rats were intranasally inoculated with A. spelaea trophozoites (1 × 106/ml) and divided into control, infected untreated, and infected treated (50 mg/kg EA daily) groups. Histopathological and ultrastructural analyses of brain and lung tissues were conducted by scanning and transmission electron microscopy. Additionally, the therapeutic effects of EA were assessed via comparative tissue pathology.

Results

A. spelaea infection induced A. spelaea-induced neural lesions resembling granulomatous amoebic encephalitis (GAE) in the brain, which was characterized by gliosis, vasculitis, and necrosis, in addition to severe pulmonary damage, including suppurative bronchopneumonia and abscesses. Trophozoites presented with pseudopodia, acanthopodia, and amoebostomes, whereas cysts presented with double-layered walls. EA-treated rats presented nearly normal brain and lung histology, with reduced inflammation and gliosis, highlighting the anti-inflammatory and antioxidant properties of EA.

Conclusion

This study highlights the neurotropic and pulmonary pathogenicity of A. spelaea, with ultrastructures parallel to those of Vahlkampfia spp. and Acanthamoeba spp. Ellagic acid significantly reduces infection-induced damage, underscoring its potential as a therapeutic agent for infections caused by free-living amoebae.
背景:Allovahlkampfia spelaea (a . spelaea)是一种自由生活的变形虫,最近被认为是引起棘阿米巴样角膜炎,其治疗是复杂的。Allovahlkampfia spp.的致病潜力仍未探明。本研究通过超微结构形态学分析对spelaea进行了表征,并在小鼠模型中研究了从角膜炎患者中分离到的spelaea菌株KS1的致病潜力,重点研究了神经-肺部感染。此外,本研究评估了鞣花酸(EA)对阿米巴感染引起的组织损伤的治疗效果。方法:对免疫抑制的雄性Wister大鼠鼻内接种褐皮草滋养体(1×106/ml),分为对照组、感染未处理组和感染处理组(50 mg/kg EA每日)。采用扫描电镜和透射电镜对脑组织和肺组织进行组织病理学和超微结构分析。此外,通过比较组织病理学评估EA的治疗效果。结果:spelae感染可引起脑内类似肉芽肿性阿米巴脑炎(GAE)的神经病变,表现为神经胶质瘤、血管炎和坏死,并伴有严重的肺损害,包括化脓性支气管肺炎和脓肿。滋养体表现为假足、棘足和变形虫,而囊肿表现为双层壁。经ea处理的大鼠脑组织和肺组织基本正常,炎症和神经胶质瘤减少,显示了ea的抗炎和抗氧化作用。这项研究强调了a . spelaea的嗜神经性和肺致病性,其超微结构与Vahlkampfia spp.和棘阿米巴spp.相似。鞣花酸显著减少感染引起的损伤,强调了其作为治疗由自由生活的阿米巴引起的感染的药物的潜力。
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引用次数: 0
Olive oil and linoleic acid as potential acaricidal agents against Psoroptes cuniculi mites 橄榄油和亚油酸作为潜在的杀螨剂。
IF 1.6 4区 医学 Q3 PARASITOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-09 DOI: 10.1016/j.exppara.2025.109025
Montañez-Palma Lilia Francisca , Hallal-Calleros Claudia , Castañeda-Ramírez Gloria Sarahí , Hernández-Núñez Emanuel , Wong -Villarreal Arnoldo , Aguilar-Marcelino Liliana , Flores-Pérez Fernando Iván
Psoroptes cuniculi mite is an important ectoparasite in rabbit breeding. Extra virgin olive oil (EVOO) is a vegetable oil with anti-inflammatory and regenerative properties, and linoleic acid (LA) also has beneficial properties for health. The activity against P. cuniculi mites of EVOO was evaluated at concentrations of 1, 5, 10, 30, 60 and 100 %; LA was evaluated at 50, 100, 150, 200, 300 and 400 mg/mL. The effectiveness was evaluated by the immersion technique using 11 mites and four replicates, and post-treatment mortality was analyzed after 24 and 48 h. Also, the composition of EVOO was determined by gas chromatography-mass spectrometry; seven compounds were identified, with the major compounds being: 1) oleic acid (47.4 %), 2) glycidol oleate (34.2 %), 3) linoleic acid (7.0 %). Pure EVOO caused a mortality of 74.4 % after 24 h and 100 % after 48 h of treatment. LA caused 94.6 % and 98.4 % of mortality at 24 and 48 h, respectively, at a concentration of 400 mg/mL. Based on the results of the current investigation, EVOO and LA are proposed as potential effective treatments for the control of P. cuniculi mites.
兔恙螨是兔养殖中一种重要的体外寄生虫。特级初榨橄榄油(EVOO)是一种具有抗炎和再生特性的植物油,亚油酸(LA)也对健康有益。研究了EVOO在浓度为1、5、10、30、60和100%时对线虫螨的抑制作用;分别在50、100、150、200、300和400 mg/mL时测定LA。采用11只螨、4个重复的浸渍法评价效果,分析处理后24和48 h的死亡率,并采用气相色谱-质谱法测定EVOO的成分;共鉴定出7个化合物,主要化合物为油酸(47.4%)、油酸甘油醇(34.2%)、亚油酸(7.0%)。纯EVOO治疗24 h死亡率为74.4%,48 h死亡率为100%。浓度为400 mg/mL的LA在24 h和48 h的死亡率分别为94.6%和98.4%。根据目前的调查结果,EVOO和LA被认为是潜在的有效的防治虫螨的方法。
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引用次数: 0
β-sitosterol: A novel molluscicidal agent from Liagora farinosa against Biomphalaria alexandrina snails with computational insights into its interaction with the retinoid X Receptor β-谷甾醇:一种新型杀螺剂,利用计算方法研究其与类视黄醇X受体的相互作用。
IF 1.6 4区 医学 Q3 PARASITOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-09 DOI: 10.1016/j.exppara.2025.109023
Heba Abdel-Tawab , Shrouk E. Al-Sayed , Khaled N.M. Elsayed , Chuanyi Wang , Ebtesam Al-olayan , Enas I.A. Mohamed , Amina M. Ibrahim , Almahy M. El-Mallah
Schistosomiasis is a tropical parasitic disease that presents significant public health concerns, occurring in both acute and chronic forms. In Egypt, the freshwater snail Biomphalaria alexandrina is the intermediate host of Schistosoma mansoni. This study evaluated the molluscicidal potential of β-sitosterol, isolated from the marine red alga Liagora farinosa, along with its methanolic extract, against B. alexandrina. Bioassay results demonstrated potent molluscicidal activity, with the methanolic extract exhibiting LC50 and LC90 values of 187.5 mg/L and 231.8 mg/L, respectively, and β-sitosterol showing enhanced potency with LC50 and LC90 values of 36.1 mg/L and 41.7 mg/L after 48 h of exposure. Sublethal concentrations of β-sitosterol significantly reduced snail survival and reproductive rates. Biochemical analyses revealed a marked decrease in total antioxidant capacity and superoxide dismutase (SOD) activity, accompanied by increased levels of malondialdehyde (MDA) and reduced glutathione (GSH), indicating oxidative stress. Histopathological examination of treated snails showed extensive damage in the digestive and hermaphrodite glands, including vacuolation, cellular rupture, and degeneration of reproductive cells. Ultrastructural alterations such as nuclear disintegration, cytoplasmic vacuolation, residual body accumulation, and microvilli loss were also observed. Computational studies suggested retinoid X receptor to be a plausible target for β-sitosterol in its molluscicidal activity. These findings highlight the potential of L. farinosa extracts and β-sitosterol as bioactive agents for Schistosoma mansoni intermediate host. However, further research is required to assess their impact on non-target aquatic organisms.
血吸虫病是一种引起重大公共卫生关切的热带寄生虫病,有急性和慢性两种形式。在埃及,淡水蜗牛Biomphalaria alexandrina是曼氏血吸虫的中间宿主。本研究评价了从海洋红藻Liagora farinosa中分离得到的β-谷甾醇及其甲醇提取物对绿僵菌的杀软体动物潜能。生物测定结果表明,乙醇提取物的LC50和LC90分别为187.5 mg/L和231.8 mg/L, β-谷甾醇的LC50和LC90分别为36.1 mg/L和41.7 mg/L,具有较强的杀螺活性。亚致死浓度的β-谷甾醇显著降低了蜗牛的存活率和繁殖率。生化分析显示,总抗氧化能力和超氧化物歧化酶(SOD)活性显著降低,丙二醛(MDA)和谷胱甘肽(GSH)水平升高,表明氧化应激。处理过的蜗牛的组织病理学检查显示消化腺和雌雄同体腺的广泛损伤,包括空泡化、细胞破裂和生殖细胞变性。超微结构的改变,如核解体、细胞质空泡化、残体堆积和微绒毛丢失也被观察到。计算研究表明,类维甲酸X受体可能是β-谷甾醇灭螺活性的一个合理靶点。这些研究结果表明,糠草提取物和β-谷甾醇具有作为曼氏血吸虫中间宿主生物活性物质的潜力。然而,需要进一步的研究来评估它们对非目标水生生物的影响。
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Experimental parasitology
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