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Non-model organism research in the changing genomic landscape. 不断变化的基因组景观中的非模式生物研究。
IF 0.4 Q4 PARASITOLOGY Pub Date : 2019-04-01 DOI: 10.21608/puj.2019.6449.1026
Monika Gulia-Nuss

It is estimated that the planet earth is host to approximately ten million species of plants and animals with only approximately 1.5 million documented in the Catalogue of Life. However, our knowledge of biochemical, molecular, genetics, and cellular processes comes from the studies of fewer than a dozen organisms. Although focusing our research on these "model" organisms has paid off, the downside is that we know very little about the biology of the vast majority of organisms, the non-model organisms. Non-model organisms are organisms that have not been selected by the research community for extensive study mostly because they lack the features that make model organisms easy to investigate e.g. they cannot grow in the laboratory, have a long life cycle, low fecundity or poor genetics.

据估计,地球上大约有1000万种植物和动物,而只有大约150万种被记录在《生命目录》中。然而,我们对生物化学、分子、遗传学和细胞过程的知识来自于对不到12种生物体的研究。虽然我们对这些“模式”生物的研究取得了成效,但缺点是我们对绝大多数生物的生物学知之甚少,非模式生物。非模式生物是没有被研究界选择进行广泛研究的生物,主要是因为它们缺乏使模式生物易于研究的特征,例如它们不能在实验室中生长,生命周期长,繁殖力低或遗传不良。
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引用次数: 2
The Outcomes of Mesenchymal Stem Cells Therapy for Experimental Toxoplasmosis 间充质干细胞治疗实验性弓形虫病的结果
IF 0.4 Q4 PARASITOLOGY Pub Date : 2019-04-01 DOI: 10.21608/PUJ.2019.7541.1030
S. Etewa, A. Al-Hoot, S. Abdelmoaty, S. Mohammad, H. Moawad, M. Sarhan, Sara Ahmed Abd El-Rahman, M. El-Shafey, Eman Zakaria Abd El-Monem
Background: Toxoplasmosis is considered of the widest spread parasitic infections that affects approximately one third of human population. The formation of resident tissue cysts in chronically infected hosts is a challenge; none of the available drugs is capable of eradicating encysted forms of the parasite. It could be disastrous in immunosuppression due to reactivation of the dormant infection. The application of stem cells as promising therapy was tried in some parasitic diseases. Objective: In this work, stem cells therapy was investigated as a therapeutic line in treatment of murine toxoplasmosis. Materials and Methods: Parasitological, histopathological and immunohistochemical studies were performed to investigate the curable role of Bone Marrow Mesenchymal Stem Cells (BM MSCs).Results: The outcomes revealed high significant decrease of the number and size of brain tissue cysts on combining BM MSCs with spiramycin, pyrimethamine and folinic acid. The tested group by BM MSCs as mono-theraputic line of treatment showed poor curable role, as cleared by the results of liver, spleen, eye and brain tissues studies; some improvement was noticed by the recruitment of CD8+ that was cleared by the immunohistochemical study of brain and spleen sections.Conclusion: BM MSCs alone have a poor therapeutic role, otherwise combined with spiramycin, pyrimethamine and folinic acid for treatment of toxoplasmosis.
背景:弓形虫病被认为是传播最广泛的寄生虫感染,影响了大约三分之一的人口。在慢性感染的宿主中形成常驻组织囊肿是一个挑战;没有一种可用的药物能够根除寄生虫的囊状形式。由于潜伏感染的重新激活,免疫抑制可能是灾难性的。干细胞作为一种有前景的治疗方法在一些寄生虫病的治疗中进行了尝试。目的:研究干细胞治疗小鼠弓形虫病的治疗方法。材料与方法:采用寄生虫学、组织病理学和免疫组织化学方法研究骨髓间充质干细胞(bmmscs)的治疗作用。结果:骨髓间充质干细胞联合螺旋霉素、乙胺嘧啶和亚叶酸可显著减少脑组织囊肿的数量和大小。肝、脾、眼、脑组织的研究结果表明,以骨髓间充质干细胞作为单一治疗线的实验组,其治愈率较差;脑和脾切片的免疫组化研究表明,CD8+的募集有所改善。结论:骨髓间质干细胞单独治疗弓形虫病的疗效较差,否则联合螺旋霉素、乙胺嘧啶和亚叶酸治疗。
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引用次数: 6
Immunomodulating effect of Schistosoma mansoni soluble egg antigen on course of induced diabetes mellitus in experimental mice 曼氏血吸虫可溶性卵抗原对实验性小鼠糖尿病病程的免疫调节作用
IF 0.4 Q4 PARASITOLOGY Pub Date : 2019-04-01 DOI: 10.21608/PUJ.10929.1036
Naglaa S. M. El-Gebaly, M. Rehan, D. Abdelfattah
Background: Helminth infections, particularly S.mansoni, are known to induce a protective role against various forms of autoimmune diseases, including type 1diabetes (TID). The observed S.mansoni significant inhibition or delay of diabetes development in non-obese diabetic mice (NOD), appeared to be due to a modulation of the diabetes-associated th1response towards protective th2 responses through IL-10 production. Objective: To study the effect of S. mansoni SEA on the immune response in induced TIDmouse moduel.  Material and Methods: In this study, 90 male Swiss Albino mice of 6 weeks old, weighing between 90 and 100g were divided into 5 groups; control group (I): Streptozontocin (STZ)-treated group (II); soluble egg antigen (SEA)-immunized group (III); (STZ+SEA) group (IV); (SEA+STZ) group (V). Mice were subjected to measurement of blood glucose levels at two and four weeks by colorimetric method, and measurement of IL-10 by enzyme linked immunosorbent assay (ELISA). Histopathological examination of pancreatic sections of the five groups investigated signs suggesting presence or absence of pancreatic inflammation.   Results: Significant lowering of blood glucose level occurred at 2-weeks in groups III and V compared to group II and at 4-weeks in groups III, IV and V compared to group II, and in group V compared to group IV. Significant higher IL-10 level occurred at 2-weeks in groups IV and V compared to group II, and in groups IV and V compared to group III and in group V compared to group IV. In 4-weeks, significant increase in IL-10 level occurred in groups II, IV, V compared to group I, and in group V compared to group IV. No significant difference between groups III and I was recorded. Histopathological changes of pancreatic sections of groups I and III showed normal architecture of pancreatic cells; While groups II and IV coinciding with STZ treatment showed vacuolation and necrosis of islets of Langerhans at 2-weeks the inflammation subsided in group IV. In group V there was dilation of blood vessels with inflammatory cells at both weeks. Conclusion: S.mansoni derived SEA proved to be protective against TID leading to improvement of blood sugar control and indicating the protective role of S.mansoni infection.
背景:众所周知,蠕虫感染,特别是S.mansoni,可诱导对多种自身免疫性疾病的保护作用,包括1型糖尿病(TID)。在非肥胖糖尿病小鼠(NOD)中观察到的S.mansoni对糖尿病发展的显著抑制或延迟,似乎是由于通过IL-10的产生调节糖尿病相关的th1反应对保护性th2反应。目的:研究曼梭菌SEA对诱导的tid小鼠免疫应答的影响。材料与方法:选取体重90 ~ 100g的6周龄雄性瑞士白化小鼠90只,分为5组;对照组(I):链脲佐菌素(STZ)治疗组(II);可溶性蛋抗原(SEA)免疫组(III);(STZ+SEA)组(IV);(SEA+STZ)组(V)。用比色法测定小鼠在第2周和第4周的血糖水平,用酶联免疫吸附试验(ELISA)测定IL-10。五组胰腺切片的组织病理学检查显示胰腺炎症的存在或不存在迹象。结果:显著降低血糖水平分别发生在两组相比组II和III和V在4周组III, IV和V组II相比,第四组V相比组。显著更高的il - 10水平分别发生在两组第四章和第五章与第二组相比,在团体IV和V相比,第三组和第四组V相比组。在4周,显著增加il - 10水平发生在第二组,IV, V组相比,与IV组比较,III组和I组之间无显著差异。ⅰ组和ⅲ组胰腺切片的组织病理学改变显示胰腺细胞结构正常;与STZ同时治疗的II组和IV组在2周时出现朗格汉斯岛空泡化和坏死,IV组炎症消退。V组在两周均出现血管扩张和炎症细胞。结论:mansoni来源的SEA对TID具有保护作用,可改善血糖控制,提示mansoni感染具有保护作用。
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引用次数: 2
Potent lethal effect of Syzygium aromaticum essential oil on Blastocystis spp.: An in vitro study 香薷精油对囊虫的强致死作用:体外研究
IF 0.4 Q4 PARASITOLOGY Pub Date : 2019-04-01 DOI: 10.21608/PUJ.2019.10650.1035
E. Eldin, M Hayam
ABSTRACT Background: Blastocystis spp. Are protozoan parasites that cause a wide range of gastrointestinal manifestations and in is incriminated of being a possible element in the development of irritable bowel diseases as well as colorectal carcinoma. Metronidazole (MTZ) is commonly prescribed for treatment of blastocystosis. However, the reported increase in MTZ resistance parasites and undesirable side effects make the search for an alternative a priority. Syzygium aromaticum-eugenol rich  essential oil has been wiedly investigated for its medicinal properties. Objective: The present study was carried out to investigated the vitro effects of S.aromaticum-eugeonl rich essential oil on Blastocystis spp.in vitro. Material and Methods:  Stool samples were collected from patients complaining of diarrhea, referred for stool examination to the research and diagnostic laboratory unit of the parasitology department, Faculty of Medicine, Ain Shams University. Microscopically, positive stool samples for Blastocystis spp.  Were cultured. Compared with MTZ, the effects of different concentrations of S.aromaticum essential oil on the viability of Blastocystis spp., tested essential oil, MTZand untreated parasite control was measured. Results: The minimal lethal concentrations for S.aromaticum were 300 μg/ml at 24h, 200 μg/ml at 48h, 100 μg/ml at 72h and 50 μg/ml at 96h, as compared to MTZ 1mg/ml that did not induce complete inhibition till the end of the studied intervals. Notable shrinkage in the size of Blastocystis-treated with S.aromaticum, was significantly smaller than that of parasite control. Conclusion: These results highly suggest that S.aromaticum essential oil may be a promising and safe agent for treatment of blastocystis.
摘要背景:芽囊原虫是一种原生动物寄生虫,可引起广泛的胃肠道症状,被认为是肠易激综合征和结直肠癌发展的可能因素。甲硝唑(MTZ)通常用于治疗胚泡病。然而,据报道,MTZ耐药性寄生虫的增加和不良副作用使寻找替代品成为当务之急。对富含丁香酚的丁香精油的药用性能进行了初步研究。目的:研究富含芳构烯的精油对芽囊藻的体外作用。材料和方法:从抱怨腹泻的患者身上采集粪便样本,将其送往艾因沙姆斯大学医学院寄生虫学系的研究和诊断实验室进行粪便检查。显微镜下,培养了芽囊原虫属阳性粪便样本。与MTZ相比,测定了不同浓度的香茅精油、受试精油、MTZ和未经处理的寄生虫对照对芽囊原虫生存能力的影响。结果:香茅的最小致死浓度分别为24小时300μg/ml、48小时200μg/ml、72小时100μg/ml和96小时50μg/ml,而MTZ 1mg/ml直到研究间隔结束时才引起完全抑制。用S.aromicum处理的芽囊原虫的大小显著缩小,显著小于寄生虫对照。结论:香茅精油可能是一种安全有效的治疗胚泡病的药物。
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引用次数: 0
CD14 promotor polymorphisms associated with different allergic phenotypes and modulated with house dust mite allergy CD14启动子多态性与不同过敏表型相关并与屋尘螨过敏相关
IF 0.4 Q4 PARASITOLOGY Pub Date : 2019-02-23 DOI: 10.21608/PUJ.2019.7917.1031
Wafaa M. Zaki, H. Salem, H. M. Elazizy, Maryam Ebido Ajeeby
Background: House dust mite (HDM) constitutes a major cause of allergic disease all over the world; meanwhile interaction between genetic control, environmental factors in the context of allergen exposure may affect allergic phenotype. Cluster of Differentiation 14 (CD14) polymorphisms play a major role in genetic control of allergic phenotype.Objective: We aimed to assess the role of CD14 genetic polymorphisms at two loci A(-1,145)G, and G(-1,359)T in expression of atopic asthma and allergic rhinitis in the context of HDM exposure in Jazan, KSA.Subjects and Methods: Through a case control study, 160 subjects served as 60 atopic asthmatic patients, 40 allergic rhinitis patients and 60 healthy non-allergic controls. Clinical and immunological parameters for the studied subjects were assessed. Then, genotyping of two single nucleotide polymorphisms (SNPs) at A(-1,145)G, and G(-1,359)T, in the promoter region of the CD14 gene was conducted using restriction fragment length polymorphisms (RFLP-PCR).Results: The present study showed that in HDM sensitive subjects there was a significant association between GG genotype variant at A(-1,145)G with atopic asthma patients and another significant association between TT genotype variant at G(-1,359)T with allergic rhinitis patients.Conclusion: The impact of allergy induced by HDMs may be enhanced in individuals with specific CD14 gene variants resulting in exaggerated allergic phenotype.
背景:屋尘螨(HDM)是世界各地过敏性疾病的主要原因;同时,在过敏原暴露的背景下,遗传控制、环境因素之间的相互作用可能影响过敏表型。CD14多态性在过敏表型的遗传控制中起重要作用。目的:我们旨在评估两个基因座A(- 1145)G和G(- 1359)T在沙特阿拉伯吉赞市HDM暴露背景下特应性哮喘和变应性鼻炎表达中的CD14遗传多态性的作用。对象与方法:通过病例对照研究,160名受试者作为特应性哮喘患者60例,变应性鼻炎患者40例,健康非过敏对照60例。评估研究对象的临床和免疫学参数。然后,利用限制性片段长度多态性(RFLP-PCR)对CD14基因启动子区域A(- 1145)G和G(- 1359)T处的两个单核苷酸多态性(snp)进行基因分型。结果:本研究显示,在HDM敏感人群中,GG基因型变异a (-1,145)G与特应性哮喘患者显著相关,TT基因型变异G(-1,359)T与变应性鼻炎患者显著相关。结论:CD14基因特异变异个体对HDMs过敏的影响可能会增强,从而导致过敏表型的夸大。
{"title":"CD14 promotor polymorphisms associated with different allergic phenotypes and modulated with house dust mite allergy","authors":"Wafaa M. Zaki, H. Salem, H. M. Elazizy, Maryam Ebido Ajeeby","doi":"10.21608/PUJ.2019.7917.1031","DOIUrl":"https://doi.org/10.21608/PUJ.2019.7917.1031","url":null,"abstract":"Background: House dust mite (HDM) constitutes a major cause of allergic disease all over the world; meanwhile interaction between genetic control, environmental factors in the context of allergen exposure may affect allergic phenotype. Cluster of Differentiation 14 (CD14) polymorphisms play a major role in genetic control of allergic phenotype.Objective: We aimed to assess the role of CD14 genetic polymorphisms at two loci A(-1,145)G, and G(-1,359)T in expression of atopic asthma and allergic rhinitis in the context of HDM exposure in Jazan, KSA.Subjects and Methods: Through a case control study, 160 subjects served as 60 atopic asthmatic patients, 40 allergic rhinitis patients and 60 healthy non-allergic controls. Clinical and immunological parameters for the studied subjects were assessed. Then, genotyping of two single nucleotide polymorphisms (SNPs) at A(-1,145)G, and G(-1,359)T, in the promoter region of the CD14 gene was conducted using restriction fragment length polymorphisms (RFLP-PCR).Results: The present study showed that in HDM sensitive subjects there was a significant association between GG genotype variant at A(-1,145)G with atopic asthma patients and another significant association between TT genotype variant at G(-1,359)T with allergic rhinitis patients.Conclusion: The impact of allergy induced by HDMs may be enhanced in individuals with specific CD14 gene variants resulting in exaggerated allergic phenotype.","PeriodicalId":41408,"journal":{"name":"Parasitologists United Journal","volume":" ","pages":""},"PeriodicalIF":0.4,"publicationDate":"2019-02-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48544608","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Expression of cysteine proteinases and cystatins in parasites and use of cysteine proteinase inhibitors in parasitic diseases. Part III: Protozoa (2): Plasmodium spp. 寄生虫半胱氨酸蛋白酶和半胱氨酸抑素的表达及半胱氨酸蛋白酶抑制剂在寄生虫病中的应用第三部分:原生动物(2):疟原虫。
IF 0.4 Q4 PARASITOLOGY Pub Date : 2019-01-01 DOI: 10.21608/puj.2019.14599.1049
S. Abaza
Genomic analysis of P. falciparum revealed more than thirty cysteine proteases (CPs). However, the most studied CPs are four falcipains (FPs), three dipeptidyl peptidases, a calpain and a metacaspase. Beside the main function of hemoglobin degradation, CPs are not only essential for protein trafficking, but they are also involved in egress cascade, i.e. rupture of infected erythrocytes as well as de novo RBCs invasion. In addition, studies showed their essential role in exo-erythrocytic hepatic stages, as well as oocyst production and gamete egress in mosquitoes. Accordingly, CPs inhibitors (CPIs) are of great interest in development of novel anti-malarial drugs as well as a new strategy to eliminate malaria transmission. Several compounds were investigated as CPIs including herbal extracts, known proteases with reported inhibitory potency against papain-like family, chemical compounds and synthesized derivatives as well as commercially available drugs approved for human use for other diseases. However, no commercial drug-targeting FPs has been developed yet. On the other hand, endogenous parasites cystatins (CYSs) regulate CPs and prevent inappropriate effects of host enzymes. The present review will discuss the role of essential plasmodial CPs and the importance of search for or development of potent specific selective CPI as a novel anti-marital drug. Hopefully the rapid development of highly efficient technology promises advances of expression systems using genetic tools for metabolic regulation of protein expression. This is in addition to recent technology for advanced screening directed with molecular modeling using three-dimensional construction of the target CP. Abbreviations: ADMET: Computational tool to evaluate drug absorption, distribution, metabolism, excretion and toxicity; CALP: Calpain; CP: Cysteine proteinase; CPI: Cysteine proteinase inhibitor; CSP: Circumsporozoite protein; CYS: Cystatin; DPAP: Dipeptidyl aminopeptidase; E-64: A broad spectrum CPI; FP: Falcipain; HTS: High throughput screening; MCA: Metacaspase; MSP: Merozoite surface protein; PV: Parasitophorus vacuole; SAR: Structure activity relationship; SERA: Serine-repeat antigen; VP: Vivapain; VS: Virtual screening. CPs, CYSs, CPIs and Plasmodium spp. Abaza 73 [I] Cysteine proteinases (CPs) In three review articles published by Rosenthal[1-3], the important roles of malarial proteases in the erythrocytic life cycle stages were designated. These stages account for malarial clinical manifestations, passing from merozoites invasion to mature schizonts, rupture of infected RBCs and release of numerous invasive merozoites. The reviewer discussed all types of proteases, including CPs, required for hemoglobin degradation in the trophozoite stag and for synthesis in subsequent stages, as well as their roles in rupture and subsequent reinvasion of new RBCs. He also claimed that knockout gene encoding falcipain 2 (FP-2) led to a transient block in hemoglobin breakdown with signif
恶性疟原虫基因组分析揭示了30多种半胱氨酸蛋白酶(CPs)。然而,研究最多的CPs是四种镰状蛋白酶(FPs),三种二肽基肽酶,一种钙蛋白酶和一种metacaspase。除了血红蛋白降解的主要功能外,CPs不仅对蛋白质运输至关重要,而且还参与出口级联反应,即感染红细胞的破裂以及新生红细胞的入侵。此外,研究表明它们在蚊子的红细胞外肝期以及卵囊产生和配子排出中起重要作用。因此,CPs抑制剂(cpi)在开发新型抗疟疾药物以及消除疟疾传播的新策略方面具有重要意义。几种化合物作为cpi进行了研究,包括草药提取物,已知的蛋白酶,据报道对木瓜蛋白酶类家族具有抑制作用,化合物和合成衍生物以及批准用于人类治疗其他疾病的市售药物。然而,尚未开发出商业化的药物靶向FPs。另一方面,内源性寄生虫胱抑素(cystins, CYSs)调节CPs,防止宿主酶的不适当作用。本文将讨论基本疟原虫CPs的作用,以及寻找或开发有效的特异性选择性CPI作为一种新型抗婚姻药物的重要性。希望高效技术的快速发展带来了利用遗传工具对蛋白质表达进行代谢调节的表达系统的进步。ADMET:用于评估药物吸收、分布、代谢、排泄和毒性的计算工具;CALP: Calpain;CP:半胱氨酸蛋白酶;CPI:半胱氨酸蛋白酶抑制剂;环孢子子蛋白;半胱氨酸:半胱氨酸蛋白酶抑制物;DPAP:二肽基氨基肽酶;E-64:广谱CPI;FP: Falcipain;HTS:高通量筛选;MCA: Metacaspase;MSP:分裂子表面蛋白;PV:寄生物液泡;SAR:结构活性关系;血清:丝氨酸重复抗原;副总裁:Vivapain;VS:虚拟筛选。CPs、CYSs、CPIs和Plasmodium spp. Abaza 73[1]半胱氨酸蛋白酶(Cysteine proteinases, CPs)。Rosenthal[1-3]发表的三篇综述文章指出了疟原虫蛋白酶在红细胞生命周期各阶段的重要作用。这些阶段解释了疟疾的临床表现,从分裂子侵入到成熟分裂,感染红细胞破裂和释放大量侵入性分裂子。审稿人讨论了所有类型的蛋白酶,包括CPs,在滋养体阶段血红蛋白降解和随后阶段的合成所需的蛋白酶,以及它们在破裂和随后的新红细胞再入侵中的作用。他还声称,敲除编码恶性蛋白2 (FP-2)的基因导致血红蛋白分解的短暂阻断,并显著增加寄生虫对cpi的敏感性。相反,编码FP-1基因的破坏显示其在蚊子卵囊产生中起重要作用。除了FPs,恶性疟原虫基因组还发现了三种二肽基氨基肽酶(dpap),以前被认为是钙蛋白酶(calpain)的同源物,以及三种具有半胱氨酸基序的丝氨酸重复抗原(SERAs)。由于DPAP1仅局限于食物液泡中,除了dpap3和SERA-5在输出级联中的作用外,审稿人还讨论了DPAP1在血红蛋白分解中的作用。因此,他认为FP-2、DPAPs 1和3以及SERA-5是潜在的抗疟疾药物靶点。在试图表征恶性疟原虫推定的蛋白酶时,一组美国研究人员使用比较基因组分析预测了92种蛋白酶。进一步的系统发育分析证实了他们的预测。其中88个蛋白酶通过微阵列分析和反转录PCR鉴定了其指定的转录蛋白。对转录酶进行分类,发现最高的(36%)属于CPs。除了当时已确定和表征的CPs外,调查人员仅确定了两种新的潜在重要CPs;CALP和metacaspase (MCA)。第一个是钙活化的CP,被认为是分裂子侵入的必要催化酶。它作为抗疟疾药物靶点的有用性有两个原因。首先,在恶性疟原虫基因组中发现了一种典型的内源性CALP底物(蛋白激酶C, PKC),它对影响生物学和宿主-寄生虫相互作用的信号转导途径至关重要。第二,它与宿主calp不相似,因此使用抑制剂对宿主的影响最小。虽然以前的研究没有报道P。 恶性疟原虫基因组分析揭示了30多种半胱氨酸蛋白酶(CPs)。然而,研究最多的CPs是四种镰状蛋白酶(FPs),三种二肽基肽酶,一种钙蛋白酶和一种metacaspase。除了血红蛋白降解的主要功能外,CPs不仅对蛋白质运输至关重要,而且还参与出口级联反应,即感染红细胞的破裂以及新生红细胞的入侵。此外,研究表明它们在蚊子的红细胞外肝期以及卵囊产生和配子排出中起重要作用。因此,CPs抑制剂(cpi)在开发新型抗疟疾药物以及消除疟疾传播的新策略方面具有重要意义。几种化合物作为cpi进行了研究,包括草药提取物,已知的蛋白酶,据报道对木瓜蛋白酶类家族具有抑制作用,化合物和合成衍生物以及批准用于人类治疗其他疾病的市售药物。然而,尚未开发出商业化的药物靶向FPs。另一方面,内源性寄生虫胱抑素(cystins, CYSs)调节CPs,防止宿主酶的不适当作用。本文将讨论基本疟原虫CPs的作用,以及寻找或开发有效的特异性选择性CPI作为一种新型抗婚姻药物的重要性。希望高效技术的快速发展带来了利用遗传工具对蛋白质表达进行代谢调节的表达系统的进步。ADMET:用于评估药物吸收、分布、代谢、排泄和毒性的计算工具;CALP: Calpain;CP:半胱氨酸蛋白酶;CPI:半胱氨酸蛋白酶抑制剂;环孢子子蛋白;半胱氨酸:半胱氨酸蛋白酶抑制物;DPAP:二肽基氨基肽酶;E-64:广谱CPI;FP: Falcipain;HTS:高通量筛选;MCA: Metacaspase;MSP:分裂子表面蛋白;PV:寄生物液泡;SAR:结构活性关系;血清:丝氨酸重复抗原;副总裁:Vivapain;VS:虚拟筛选。CPs、CYSs、CPIs和Plasmodium spp. Abaza 73[1]半胱氨酸蛋白酶(Cysteine proteinases, CPs)。Rosenthal[1-3]发表的三篇综述文章指出了疟原虫蛋白酶在红细胞生命周期各阶段的重要作用。这些阶段解释了疟疾的临床表现,从分裂子侵入到成熟分裂,感染红细胞破裂和释放大量侵入性分裂子。审稿人讨论了所有类型的蛋白酶,包括CPs,在滋养体阶段血红蛋白降解和随后阶段的合成所需的蛋白酶,以及它们在破裂和随后的新红细胞再入侵中的作用。他还声称,敲除编码恶性蛋白2 (FP-2)的基因导致血红蛋白分解的短暂阻断,并显著增加寄生虫对cpi的敏感性。相反,编码FP-1基因的破坏显示其在蚊子卵囊产生中起重要作用。除了FPs,恶性疟原虫基因组还发现了三种二肽基氨基肽酶(dpap),以前被认为是钙蛋白酶(calpain)的同源物,以及三种具有半胱氨酸基序的丝氨酸重复抗原(SERAs)。由于DPAP1仅局限于食物液泡中,除了dpap3和SERA-5在输出级联中的作用外,审稿人还讨论了DPAP1在血红蛋白分解中的作用。因此,他认为FP-2、DPAPs 1和3以及SERA-5是潜在的抗疟疾药物靶点。在试图表征恶性疟原虫推定的蛋白酶时,一组美国研究人员使用比较基因组分析预测了92种蛋白酶。进一步的系统发育分析证实了他们的预测。其中88个蛋白酶通过微阵列分析和反转录PCR鉴定了其指定的转录蛋白。对转录酶进行分类,发现最高的(36%)属于CPs。除了当时已确定和表征的CPs外,调查人员仅确定了两种新的潜在重要CPs;CALP和metacaspase (MCA)。第一个是钙活化的CP,被认为是分裂子侵入的必要催化酶。它作为抗疟疾药物靶点的有用性有两个原因。
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引用次数: 3
Expression of cysteine proteinases and cystatins in parasites and use of cysteine proteinase inhibitors in parasitic diseases. Part III: Protozoa (1) 寄生虫半胱氨酸蛋白酶和半胱氨酸抑素的表达及半胱氨酸蛋白酶抑制剂在寄生虫病中的应用第三部分:原生动物(1)
IF 0.4 Q4 PARASITOLOGY Pub Date : 2019-01-01 DOI: 10.21608/puj.2019.11168.1037
S. Abaza
Out of five classes of proteases (cysteine, serine, threonine, aspartate and glutamate), cysteine proteases (CPs) are responsible for hydrolysis of peptide bonds essential in several biological activities. In protozoa, as with helminths, not only do CPs play the major role in nutrients digestion, but they also have several functions for parasite survival such as differentiation of life cycle stages, immunomodulation of host immune response, and autophagy. Most wellcharacterized CPs in protozoa that were investigated in the last two decades belong to papain-family enzymes (clan CA, family C1). The present review highlights, in general, several aspects of CPs functions in protozoal survival and different strategies utilized in development of potent CPIs. The review also includes detailed data regarding T. gondii CPs, and their inhibitors wether exogenous (CPIs) or endogenous cystatins (CYSs). Abbreviations CALP: calpain; CATH: Cathepsin; CP: Cysteine proteinase; CPB: Cathepsin B; CPC: Cathepsin C; CPI: Cysteine proteinase inhibitor; CPL: Cathepsin L; CYS: Cystatin; MCA: Metacaspase; MIC: Microneme; PCD: Programmed cell death; PV: Parasitophorous vacuole; ROP: Rhoptry; VAC: Vacuolar compartment. CPs, CYSs, CPIs and T. gondii Abaza 9 succeeded to define 27, 24 and 18 genes, respectively. Amino acid sequences of the defined genes revealed high modular structure, suggesting the feasibility to utilize specific primers as diagnostic markers[5]. Recently, Siqueira-Neto et al.,[6] reviewed the proposed functions of the most characterized 29 CPs only in seven protozoa; E. histolytica (six), Leishmania spp. (six), Plasmodium spp. (five), T. gondii (five), T. cruzi (three), T. brucei (two), and Cryptosporidium spp. (two). It is evident that the most common proposed character of these CPs is a virulence factor to facilitate parasite survival and invasion. For each CP, the reviewers presented the mechanism(s) to achieve parasite invasion including induction of macrophage pro-inflammatory response, degradation of extracellular matrix, differentiation of life cycle stages, modulation of parasite metabolism, and autophagy. Mechanisms involved in immunoevasion and immunomodulation of host immune response are also proposed in all reviewed protozoa. There are other proposed mechanisms specified for some protozoa such as encystation-excystation transformation, and degradation of host IgA and IgG (E. histolytica), crossing blood brain barrier (T. brucei), hemoglobin degradation, enhancement of oocysts production, sporozoites invasion of hepatocytes, and apicoplast development and homeostasis (Plasmodium spp.), and high expression in tachyzoites for digestion of cytosolic proteins (T. gondii). Beside their role in parasite invasion, CPs of apicomplexan protozoa are required for pathogen exit from the infected cells to invade other cells and continue the infection. In Plasmodium spp. and T. gondii, being obligate intracellular pathogens, schizogony or endodyogeny, involv
在五类蛋白酶(半胱氨酸、丝氨酸、苏氨酸、天冬氨酸和谷氨酸)中,半胱氨酸蛋白酶(CPs)负责水解多种生物活性中必需的肽键。在原生动物中,如蠕虫,CPs不仅在营养物质消化中起主要作用,而且对寄生虫的生存也有多种功能,如生命周期阶段的分化、宿主免疫反应的免疫调节和自噬。近二十年来研究的原生动物中特征最明显的cp属于木瓜蛋白酶家族酶(CA族,C1族)。总的来说,本综述强调了CPs在原生动物生存中的几个方面的功能,以及开发有效CPs的不同策略。该综述还包括关于弓形虫CPs及其抑制剂(外源性CPIs或内源性cy抑素CYSs)的详细数据。缩写CALP: calpain;导管:组织蛋白酶;CP:半胱氨酸蛋白酶;CPB:组织蛋白酶B;CPC:组织蛋白酶C;CPI:半胱氨酸蛋白酶抑制剂;CPL:组织蛋白酶L;半胱氨酸:半胱氨酸蛋白酶抑制物;MCA: Metacaspase;麦克风:Microneme;PCD:程序性细胞死亡;PV:寄生液泡;罗普:Rhoptry;真空室。CPs、CYSs、CPIs和弓形虫Abaza 9分别成功定义了27、24和18个基因。所定义基因的氨基酸序列显示高度模块化结构,表明利用特异性引物作为诊断标记[5]的可行性。最近,Siqueira-Neto等人回顾了最具特征的29种CPs仅在7种原生动物中的功能;溶组织芽胞杆菌(6),利什曼原虫(6),疟原虫(5),刚地弓形虫(5),克氏弓形虫(3),布鲁氏弓形虫(2),隐孢子虫(2)。很明显,这些CPs最常见的特征是促进寄生虫生存和入侵的毒力因子。对于每个CP,审稿人提出了实现寄生虫入侵的机制,包括诱导巨噬细胞的促炎反应、细胞外基质的降解、生命周期阶段的分化、寄生虫代谢的调节和自噬。在所有综述的原生动物中也提出了免疫逃避和免疫调节宿主免疫反应的机制。对于一些原生动物,还有其他被提出的机制,如囊胞转化和宿主IgA和IgG的降解(溶组织绦虫),穿过血脑屏障(布鲁氏绦虫),血红蛋白降解,卵囊生成增强,孢子虫入侵肝细胞,顶质体发育和稳态(疟原虫),以及用于消化胞质蛋白的速殖子的高表达(弓形虫)。顶复合体原生动物的CPs除了在寄生虫入侵中起作用外,还需要病原体从被感染的细胞中出来侵入其他细胞并继续感染。在疟原虫和弓形虫中,作为专性细胞内病原体,分裂或内生作用涉及在一个专门的寄生液泡(PV)内复制,分别产生多个分裂子或速殖子。宿主钙和CALP-1都与感染细胞的破裂有关,而顶复合体calp则通过其蛋白水解依赖机制[7]参与分裂子和速殖子从PV中逃逸。在2009年发表的另一份报告中,研究人员讨论了顶复体疟原虫和弓形虫的CALP在寄生虫出口中的作用。他们发现,在体外将DCG04(一种非特异性木瓜蛋白酶家族抑制剂E64的衍生物)添加到疟原虫感染的红细胞中,发现分裂期的阻断和完整红细胞膜内PV的分裂子被捕获。用皂素处理感染的红细胞溶解PV膜,然后离心去除寄生细胞,制成颗粒,得到纯化的可溶性部分。质谱分析仅鉴定出宿主CALP-1,证实其参与红细胞破裂。当用DCG04处理CALP-1缺失的红细胞时,寄生虫动力学在一定程度上得到改善,这表明顶复体calp在寄生虫出口中的重要性。研究人员得出结论,疟原虫和弓形虫的calp都利用宿主细胞的calp来促进PV或宿主质膜的逃逸,但他们未能探索其确切的机制[8]。细胞凋亡是促进先天和获得性免疫应答的重要途径。它可以通过内在或外在途径诱导。第一种是由细胞应激信号刺激的,如DNA损伤、缺乏必要的生长因子或感染。细胞毒性细胞(T细胞、自然杀伤细胞和非淋巴样细胞)通过死亡受体连接机制激活外部通路,诱导细胞死亡[9]。据报道,一些细胞毒性细胞可通过穿孔依赖的颗粒胞吐途径[10]诱导细胞死亡。 在五类蛋白酶(半胱氨酸、丝氨酸、苏氨酸、天冬氨酸和谷氨酸)中,半胱氨酸蛋白酶(CPs)负责水解多种生物活性中必需的肽键。在原生动物中,如蠕虫,CPs不仅在营养物质消化中起主要作用,而且对寄生虫的生存也有多种功能,如生命周期阶段的分化、宿主免疫反应的免疫调节和自噬。近二十年来研究的原生动物中特征最明显的cp属于木瓜蛋白酶家族酶(CA族,C1族)。总的来说,本综述强调了CPs在原生动物生存中的几个方面的功能,以及开发有效CPs的不同策略。该综述还包括关于弓形虫CPs及其抑制剂(外源性CPIs或内源性cy抑素CYSs)的详细数据。缩写CALP: calpain;导管:组织蛋白酶;CP:半胱氨酸蛋白酶;CPB:组织蛋白酶B;CPC:组织蛋白酶C;CPI:半胱氨酸蛋白酶抑制剂;CPL:组织蛋白酶L;半胱氨酸:半胱氨酸蛋白酶抑制物;MCA: Metacaspase;麦克风:Microneme;PCD:程序性细胞死亡;PV:寄生液泡;罗普:Rhoptry;真空室。CPs、CYSs、CPIs和弓形虫Abaza 9分别成功定义了27、24和18个基因。所定义基因的氨基酸序列显示高度模块化结构,表明利用特异性引物作为诊断标记[5]的可行性。最近,Siqueira-Neto等人回顾了最具特征的29种CPs仅在7种原生动物中的功能;溶组织芽胞杆菌(6),利什曼原虫(6),疟原虫(5),刚地弓形虫(5),克氏弓形虫(3),布鲁氏弓形虫(2),隐孢子虫(2)。很明显,这些CPs最常见的特征是促进寄生虫生存和入侵的毒力因子。对于每个CP,审稿人提出了实现寄生虫入侵的机制,包括诱导巨噬细胞的促炎反应、细胞外基质的降解、生命周期阶段的分化、寄生虫代谢的调节和自噬。在所有综述的原生动物中也提出了免疫逃避和免疫调节宿主免疫反应的机制。对于一些原生动物,还有其他被提出的机制,如囊胞转化和宿主IgA和IgG的降解(溶组织绦虫),穿过血脑屏障(布鲁氏绦虫),血红蛋白降解,卵囊生成增强,孢子虫入侵肝细胞,顶质体发育和稳态(疟原虫),以及用于消化胞质蛋白的速殖子的高表达(弓形虫)。顶复合体原生动物的CPs除了在寄生虫入侵中起作用外,还需要病原体从被感染的细胞中出来侵入其他细胞并继续感染。在疟原虫和弓形虫中,作为专性细胞内病原体,分裂或内生作用涉及在一个专门的寄生液泡(PV)内复制,分别产生多个分裂子或速殖子。宿主钙和CALP-1都与感染细胞的破裂有关,而顶复合体calp则通过其蛋白水解依赖机制[7]参与分裂子和速殖子从PV中逃逸。在2009年发表的另一份报告中,研究人员讨论了顶复体疟原虫和弓形虫的CALP在寄生虫出口中的作用。他们发现,在体外将DCG04(一种非特异性木瓜蛋白酶家族抑制剂E64的衍生物)添加到疟原虫感染的红细胞中,发现分裂期的阻断和完整红细胞膜内PV的分裂子被捕获。用皂素处理感染的红细胞溶解PV膜,然后离心去除寄生细胞,制成颗粒,得到纯化的可溶性部分。质谱分析仅鉴定出宿主CALP-1,证实其参与红细胞破裂。当用DCG04处理CALP-1缺失的红细胞时,寄生虫动力学在一定程度上得到改善,这表明顶复体calp在寄生虫出口中的重要性。研究人员得出结论,疟原虫和弓形虫的calp都利用宿主细胞的calp来促进PV或宿主质膜的逃逸,但他们未能探索其确切的机制[8]。细胞凋亡是促进先天和获得性免疫应答的重要途径。它可以通过内在或外在途径诱导。第一种是由细胞应激信号刺激的,如DNA损伤、缺乏必要的
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引用次数: 0
Guppy (Poecilia) Poeciliidae fish naturally infected with Lernaea cyprinacea parasites (Linnaeus 1758) in KSA 孔雀鱼:孔雀鱼科鱼类自然感染cyprinacea Lernaea寄生虫(Linnaeus 1758)
IF 0.4 Q4 PARASITOLOGY Pub Date : 2018-12-01 DOI: 10.21608/puj.2018.5257.1019
M. Ghobashy, Hewaydah E. Abou Shafeey, A. Taeleb
Background: The ornamental fish guppy (Poecilia reticulata) is a small colorful tropical cyprinid teleost fish. Lernaea cyprinacea (Anchor worm) are worldwide, crustacean copepod parasites that cause disease and mortality in several fish species of cultured or natural populations, especially wild-caught and pond-raised species of Poecilia. This study may be considered as a novel report from Kingdom of Saudi Arabia (KSA). Objective: The present study is an investigation of Lernaea isolates infecting apparently healthy Poecilia reticulate from KSA. Material and Methods: Guppy fish (Poecilia reticulata) were purchased two weeks prior to experiments. They were examined for parasitic infection and allowed to breed in the laboratory. They were observed for 15 days for appearance of infection by Lernaea spp. larva and adult parasites. The copepod specimens were removed by forceps, from different parts of the infected fish. Specimens were fixed in 70% alcohol, cleared in 90% lactic acid, mounted, and microscopically examined to identify the morphological features of L. cyprinacea. Results: After 15 days, L. cyprinacea were detected in the ventral, anal and caudal fins of several P. reticulata. Intense focal inflammation and hemorrhage was easily observed at the attachment site, which appeared red and ulcerated. Total prevalence of infection was 68.1% (32/47). The prevalence of infection in females (29/38; 76.3%) was greater than in males (3/9; 33.3%). Conclusion: P. reticulata may be considered as a newly recorded host of L. cyprinacea from KSA. PARASITOLOGISTS UNITED JOURNAL 142 Guppy (P. reticulata) is a small and colorful tropical ornamental teleost. It is a member of the family Poeciliidae(15) that undergo internal fertilization(16). Guppies, whose natural habitat is in northeast South America, were introduced to many countries and are now found all over the world. They are highly adaptable and thrive in many different environmental and ecological conditions(15). Male guppies, which are smaller than females, have ornamental caudal and dorsal fins, while females are duller in color. In several tropical countries they were used for biological control of mosquito larvae, the vectors of infectious malaria disease(17,18) and filariasis(19-21). The guppy became a model for biological studies because of its short generation interval, ease of breeding in laboratories, and the availability of many different strains(22-24). Although L. cyprinacea parasites infect a wide range of both fish culture and natural populations fishes, few species of Lernaea were described especially those infecting ornamental fishes that still require further research. This study investigates Lernaea infections in guppy (P. reticulata), the ornamental, small and colorful fish, in a sample from KSA. MAtEriAl And MEtHodS The present study was carried out in the laboratory of Zoological Research, Biology Department, Faculty of Science, Taif University, KSA. From a local breeder in El-Ta
背景:观赏鱼孔雀鱼(Poecilia reticulata)是一种小型的彩色热带鲤科硬骨鱼。Lernaea cyprinacea(锚虫)是世界范围内的甲壳类桡足类寄生虫,可导致几种养殖或自然种群的鱼类患病和死亡,特别是野生捕获和池塘饲养的Poecilia。本研究可视为沙特阿拉伯王国(KSA)的一项新报告。目的:研究勒纳菌感染表面健康的KSA网状纤毛的情况。材料与方法:实验前两周购买孔雀鱼(Poecilia reticulata)。对它们进行了寄生虫感染检查,并允许它们在实验室繁殖。观察15 d,观察勒氏杆菌幼虫和成虫感染情况。桡足类标本是用镊子从受感染的鱼的不同部位取出的。标本在70%酒精中固定,在90%乳酸中清除,挂载,显微镜检查以确定L. cyprinacea的形态特征。结果:15 d后,在几只网纹鲟的腹、肛、尾鳍中均检测到鲤科植物。附著部位容易出现强烈的局灶性炎症和出血,呈红色和溃疡。总感染率为68.1%(32/47)。女性感染率(29/38;76.3%)大于男性(3/9;33.3%)。结论:网纹假单胞菌可能是KSA地区新记录的cyprinacea寄主。孔雀鱼(P. reticulata)是一种小而多彩的热带观赏硬骨鱼。它是水蛭科(15)的一员,经过内部受精(16)。孔雀鱼的自然栖息地在南美洲东北部,被引入许多国家,现在在世界各地都有发现。它们具有很强的适应性,在许多不同的环境和生态条件下都能茁壮成长(15)。雄孔雀鱼比雌孔雀鱼小,有装饰性的尾鳍和背鳍,而雌孔雀鱼的颜色较暗。在一些热带国家,它们被用来生物控制蚊子幼虫、传染性疟疾病媒(17,18)和丝虫病(19-21)。孔雀鱼成为生物学研究的模型,因为它的世代间隔短,易于在实验室中繁殖,并且有许多不同的品种(22-24)。虽然L. cyprinacea寄生虫在养殖鱼类和自然种群中广泛感染,但Lernaea的种类很少,特别是侵染观赏鱼的种类还有待进一步研究。本研究调查了孔雀鱼(P. reticulata)的Lernaea感染,孔雀鱼是一种观赏的小而多彩的鱼。材料与方法本研究在台湾台湾大学理学院生物学系动物研究实验室进行。从沙特阿拉伯El-Taif的当地饲养员处购买了47条孔雀鱼(38条雌性和9条雄性)标本(只有彩色、活跃、健康和性成熟的雄性和雌性)(图1),并在检查前两周转移到水族馆。他们被允许在实验室里繁殖。每天对鱼进行外部桡足类寄生虫感染检查。所有水族箱均配有100 W的恒温器、温度计、气泵、空气管道和砾石清洗机或浸管(图2)。水族箱中的水来自一个集水箱,水箱中装有由去离子水与当地自来水混合(5:1)组成的持续曝气(脱氯)水。对自来水进行分析,其指标为:pH值8.46;总溶解盐水2.52 ppm;导电率0.0054 mS/cm。15 d后观察桡足类寄生虫幼虫和成虫的感染情况。用钳子从感染鱼的不同部位取出成年桡足类标本;皮肤和胸鳍、腹鳍和背鳍。在70%酒精中固定的标本在90%乳酚中清除,并在邻苯二甲酸二丁酯聚苯二甲苯(DPX)中固定。使用蔡司光学显微镜检查和拍摄安装的标本(25)。根据Robinson(26)对L. cyprinacea标本进行形态学鉴定。动物使用遵循机构动物护理和使用委员会(IACUC)批准和授权的协议。统计分析:记录桡足动物对寄主附着部位的偏好。采用QP3.0 (Quantitative Parasitology 3.0)软件计算侵染参数、流行率和强度。这个寄生虫学软件提供了统计正确的中位数来分析寄生虫表现出的高度聚集(右倾斜)频率分布。QP3.0描述宿主样本内的寄生虫感染,并比较不同宿主样本间的寄生虫感染。 采用mann - whitney检验,SPSS统计软件检验寄生虫数量差异的显著性(≤0.05)。
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引用次数: 2
Parasites and microbiota: A complex relationship 寄生虫和微生物群:一种复杂的关系
IF 0.4 Q4 PARASITOLOGY Pub Date : 2018-12-01 DOI: 10.21608/PUJ.2018.6308.1025
H. Elwakil
Helminth infection modifies intestinal microflora: The changes in the composition of the gut microbiota that associate helminths infection may be due to the secretion of anti-microbial components by the parasite, the disruption of the epithelial barrier by the parasite that alters the intestinal environment or the stimulation of specific immune responses(2). Indeed, alterations in composition of bacterial communities were found in stool samples of school children with nematodes infection living in rural Ecuador(3). This study found decreased abundance of Clostridia, with reduction in overall bacterial diversity in stool samples of children co-infected with T. trichiura and A. lumbricoides. In a comparative study between fecal stool samples from helminthinfected or non-infected individuals living in rural Malaysia, Lee et al.,(4) reported a significant increase in bacterial diversity among individuals infected with any helminth species, and an increased abundance of Paraprevotellaceae family in those individuals infected only with T. trichiura.
寄生虫感染改变肠道菌群:与寄生虫感染相关的肠道菌群组成的变化可能是由于寄生虫分泌抗微生物成分,寄生虫破坏上皮屏障从而改变肠道环境或刺激特异性免疫反应(2)。事实上,在厄瓜多尔农村感染线虫的学龄儿童的粪便样本中发现了细菌群落组成的变化(3)。本研究发现梭状芽胞杆菌丰度降低,同时感染毛状芽胞杆菌和蚓状芽胞杆菌的儿童粪便样本中细菌多样性总体减少。Lee等人(4)对马来西亚农村地区感染或未感染蠕虫的个体的粪便样本进行了比较研究,报告了感染任何一种蠕虫的个体中细菌多样性的显著增加,并且在仅感染毛状绦虫的个体中,拟虫科的丰度增加。
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引用次数: 1
Seroprevalence of Toxoplasma gondii infection in mentally retarded children in Egypt 埃及弱智儿童弓形虫感染的血清流行率
IF 0.4 Q4 PARASITOLOGY Pub Date : 2018-12-01 DOI: 10.21608/PUJ.2018.5929.1022
Alshaimaa Hamed, N. El-Gebaly, Azza Abdel megeid, E. Elsebaei
Background:Toxoplasmosis is one of the most common causes of latent infections in humans and animals. Its important clinical aspect is the probable danger of congenital transmission and its severe effects on the fetus. Infection is typically asymptomatic at birth, or is associated with serious neurological or ocular sequelae later in life with a broad spectrum of clinical presentations. Serologic screening detects acute infection in pregnant women which if unrecognized may be transmitted to the unborn. Objective:To investigateserologically the prevalence of toxoplasmosis as a hidden cause of mental retardation (MR) in a sample of children from urban and surrounding rural areas attending the New Children Hospital of Cairo University (Abu Reesh Hospital), Cairo. Materials and Methods: The present study was conducted on 200 children diagnosed as MR attending neurology outpatient clinics as a case group; and 200 samples as a control group fromnon-MR children attending other outpatient clinics with minor complaints like skin manifestations in dermatology clinic, upper respiratory infections and minor gastrointestinal complaints.Venous blood samples from the two groups of children were serologically tested for specific IgG by indirect hemagglutination test (IHAT). Relevant sociodemographic and clinical data related to the children and their mothers was collected using a designed sheet. Results: Our results showedthat the prevalence of toxoplasmosis in the MR children was significantly positive in 84/200 (42.0%) of the case group (P<0.001).The number of positive sera was 35/200 (17.5%) among control group. Associated clinical manifestations in the case group (MR) included convulsions in 53.5%, eye problems in 22.5%, splenomegaly in 16.5% and hepatomegaly in 9.5% of cases. There was no significant difference between urban and rural residences; and relevant risk factors in mothers included history of previous Toxoplasma infection (13.5%), history of abortion and still birth (each 36.5%) and premature deliveries (19.5%). History of contact with cats and consumption of undercooked meat rated 58% and 77.7% respectively. Conclusion: Screening females who are at risk for acquired toxoplasmosis is essential, before and during pregnancy to detect Toxoplasma seroconversion. Conversion from negative to positive testing would indicate exposure to infection, requiring the implementation of early treatment of infection to protect the unborn fetuses from trans-placental transmission.
背景:弓形虫病是人类和动物潜伏感染的最常见原因之一。其重要的临床方面是先天性传播的可能危险及其对胎儿的严重影响。感染通常在出生时无症状,或在以后的生活中伴有严重的神经或眼部后遗症,具有广泛的临床表现。血清学筛查检测急性感染的孕妇,如果不识别可能会传播到未出生的。目的:从血清学角度调查开罗大学新儿童医院(Abu Reesh医院)城市及周边农村儿童中弓形虫病作为智力迟钝(MR)隐性病因的流行情况。材料与方法:本研究以200名在神经内科门诊诊断为MR的儿童为病例组;另200个样本作为对照组,来自于在其他门诊就诊的非mr儿童,他们有轻微的主诉,如皮肤科诊所的皮肤表现、上呼吸道感染和轻微的胃肠道主诉。采用间接血凝试验(IHAT)对两组患儿静脉血进行特异性IgG血清学检测。使用设计的表格收集与儿童及其母亲有关的相关社会人口学和临床数据。结果:MR患儿弓形虫病阳性率为84/200(42.0%),差异有统计学意义(P<0.001)。对照组血清阳性率为35/200(17.5%)。病例组(MR)的相关临床表现包括53.5%的惊厥、22.5%的眼疾、16.5%的脾肿大和9.5%的肝肿大。城乡居民间无显著性差异;相关危险因素包括既往弓形虫感染史(13.5%)、流产和死产史(各36.5%)和早产史(19.5%)。与猫接触史和食用未煮熟肉类的比例分别为58%和77.7%。结论:筛查有获得性弓形虫病危险的女性在妊娠前和妊娠期检测弓形虫血清转化是必要的。检测结果由阴性变为阳性,表明胎儿暴露于感染,需要对感染进行早期治疗,以保护未出生胎儿免受经胎盘传播。
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引用次数: 7
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Parasitologists United Journal
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