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Brief Communication

Seropositivity of Toxoplasma gondii and Toxocara spp. in Children with Cryptogenic Epilepsy, Benha, Egypt
Maysa Ahmad Eraky, Soha Abdel-Hady, Karim Fetouh Abdallah
Korean J Parasitol 2016;54(3):335-338.
Published online June 30, 2016
DOI: https://doi.org/10.3347/kjp.2016.54.3.335
The present study aimed to investigate the possible association of Toxoplasma gondii and Toxocara spp. infections with cryptogenic epilepsy in children. The study was carried out between June 2014 and March 2015. T otal 90 children (40 with cryptogenic epilepsy, 30 with non-cryptogenic epilepsy, and 20 healthy control children) were evaluated to determine the anti-Toxocara and anti-T . gondii IgG seropositivity using ELISA kits. Epileptic cases were selected from those attending the pediatrics outpatient clinic of Benha University Hospital, Pediatrics Neurology Unit, and from Benha Specialized Hospital of children. The results showed that the level of anti-T . gondii IgG seropositivity was significantly higher among children with cryptogenic epilepsy (20%) than among children with non-cryptogenic children (0%). In healthy controls (10%), there was no association between toxocariasis seropositivity and cryptogenic epilepsy (only 5.7%; 4 out of 70 cases) among cases and 10% (2 out of 20) among controls. Among toxocariasis IgG positive cases, 3 (7.5%) were cryptogenic, and only 1 (3.3%) was non-cryptogenic. These statistically significant results support the association between T . gondii infection and cryptogenic epilepsy while deny this association with toxocariasis.

Citations

Citations to this article as recorded by  Crossref logo
  • Evaluation of Toxoplasma gondii in the Etiology of Cryptogenic Epilepsy: A Case-control Study
    Selahattin Aydemir, Milad Torkamanian Afshar, Özlem Sarı Torkamanian Afshar, Zeynep Taş Cengiz, Mustafa Kiraz, Caner Baydar, Hasan Yılmaz
    Archives Of Epilepsy.2024; : 39.     CrossRef
  • Effects of diet and ovariectomy on Toxoplasma gondii brain infection: functional alterations and neuronal loss in rats
    Nene Ahidjo, Paul F Seke Etet, Leonard Ngarka, Frederic Maidawa Yaya, Ethel W Ndianteng, Aude L Eyenga Nna, Luc Yvan Meka’a Zang, Christelle Kemmo, Caroline N C Nwasike, Floriane G Yonkeu Tatchou, Wepnyu Y Njamnshi, Leonard N Nfor, Patrick V Tsouh Fokou,
    Brain Communications.2024;[Epub]     CrossRef
  • Common infectious and parasitic diseases as a cause of seizures: geographic distribution and contribution to the burden of epilepsy
    Elza Márcia T. Yacubian, Angelina Kakooza‐Mwesige, Gagandeep Singh, Arturo Carpio, Nathália V. de Figueiredo, Ricardo Lutzky Saute, Tissiana Marques de Haes
    Epileptic Disorders.2022; 24(6): 994.     CrossRef
  • Seroprevalence and Genetic Characterization of Toxoplasma gondii among Children with Neurodevelopmental Disorders in Egypt
    Sara M. Elzeky, Nairmen Nabih, Aida A. Abdel-Magied, Dina S. Abdelmagid, Aya E. Handoussa, Marwa M. Hamouda, Wei Wang
    Journal of Tropical Medicine.2022; 2022: 1.     CrossRef
  • Exposure to Toxocara Canis is not Associated with New-Onset Epilepsy
    Vivek Rishi, Rajveer Singh, Manoj Kumar Goyal, Manish Modi, Vivek Garg, J. S. Thakur, R. K. Sehgal, N. Khandelwal, Gourav Jain, Amith S. Kumar, Aditya Choudhary, Sudesh Prabhakar, Vivek Lal
    Neurology India.2022; 70(6): 2383.     CrossRef
  • Cerebral Toxocariasis as a Cause of Epilepsy: A Pediatric Case
    Grazia Bossi, Raffaele Bruno, Stefano Novati, Roberta Maserati, Georgia Mussati, Mariasole Prevedoni Gorone, Edoardo Vecchio Nepita, Corrado Regalbuto, Gioia Gola, Anna Maria Simoncelli, Antonella Bruno, Paola Musso, Edoardo Clerici, Gian Luigi Marseglia
    Neuropediatrics.2021; 52(02): 142.     CrossRef
  • Case-Control Study to Assess the Association between Epilepsy and Toxocara Infection/Exposure
    Ali Alizadeh Khatir, Mahdi Sepidarkish, Mohammad Reza Rajabalizadeh, Solmaz Alizadeh Moghaddam, Saeed Aghapour, Saeed Mehravar, Peter J. Hotez, Robin B. Gasser, Ali Rostami
    Microorganisms.2021; 9(10): 2091.     CrossRef
  • Neurological and Neurobehavioral Disorders Associated with Toxoplasma gondii Infection in Humans
    Maxwell A. Virus, Evie G. Ehrhorn, LeeAnna M. Lui, Paul H. Davis, Hassen Mamo
    Journal of Parasitology Research.2021; 2021: 1.     CrossRef
  • Toxoplasma infection and risk of epilepsy: A case-control study of incident patients
    Ali Alizadeh Khatir, Solmaz Alizadeh Moghaddam, Mustafa Almukhtar, Hossein Ghorbani, Arefeh Babazadeh, Saeed Mehravar, Ali Rostami
    Microbial Pathogenesis.2021; 161: 105302.     CrossRef
  • Frequency ofToxocara canisantibodies in Mexican paediatric patients with epilepsy
    M.d.L. Caballero-García, J. Simón-Salvador, J.C. Hernández-Aguilar, A. Reyes-Lopez, B. Nogueda-Torres, E. Jiménez-Cardoso
    Journal of Helminthology.2020;[Epub]     CrossRef
  • A review on toxoplasmosis in humans and animals from Egypt
    I. E. Abbas, I. Villena, J. P. Dubey
    Parasitology.2020; 147(2): 135.     CrossRef
  • Zoonotic and vector-borne parasites and epilepsy in low-income and middle-income countries
    Gagandeep Singh, Samuel A. Angwafor, Alfred K. Njamnshi, Henry Fraimow, Josemir W. Sander
    Nature Reviews Neurology.2020; 16(6): 333.     CrossRef
  • Effects of Toxoplasma gondii infection and schizophrenia comorbidity on serum lipid profile: A population retrospective study from Eastern China
    Fei Xu, Xinyu Ma, Yuwei Zhu, Arjen Sutterland, Ruitang Cheng, Sunhan Miao, Jialu Chen, Liying Qiu, Yonghua Zhou
    Microbial Pathogenesis.2020; 149: 104587.     CrossRef
  • An updated meta-analysis of the association between Toxoplasma gondii infection and risk of epilepsy
    Maryam Sadeghi, Seyed Mohammad Riahi, Mona Mohammadi, Vafa Saber, Somayeh Aghamolaie, Solmaz Alizadeh Moghaddam, Shima Aghaei, Mostafa Javanian, H Ray Gamble, Ali Rostami
    Transactions of The Royal Society of Tropical Medicine and Hygiene.2019; 113(8): 453.     CrossRef
  • Updated evidence of the association between toxocariasis and epilepsy: Systematic review and meta-analysis
    Jaime Luna, Calogero Edoardo Cicero, Guillaume Rateau, Graziella Quattrocchi, Benoit Marin, Elisa Bruno, François Dalmay, Michel Druet-Cabanac, Alessandra Nicoletti, Pierre-Marie Preux, Agnes Fleury
    PLOS Neglected Tropical Diseases.2018; 12(7): e0006665.     CrossRef
  • Seroprevalence of Toxoplasma gondii infection in children with central nervous system disorders in Mansoura, Egypt: a case–control study
    Samar N El-Beshbishi, Nora L El-Tantawy, Sara M Elzeky, Khalid F Abdalaziz, Raefa A Atia
    Transactions of The Royal Society of Tropical Medicine and Hygiene.2018;[Epub]     CrossRef
  • Toxocariasis in humans in Africa – A systematic review
    Felix Lötsch, Rieke Vingerling, Rene Spijker, Martin Peter Grobusch
    Travel Medicine and Infectious Disease.2017; 20: 15.     CrossRef
  • 10,061 View
  • 129 Download
  • 24 Web of Science
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Original Articles
Xenomonitoring of Different Filarial Nematodes Using Single and Multiplex PCR in Mosquitoes from Assiut Governorate, Egypt
Ahmed Kamal Dyab, Lamia Ahmed Galal, Abeer El-Sayed Mahmoud, Yasser Mokhtar
Korean J Parasitol 2015;53(1):77-83.
Published online February 27, 2015
DOI: https://doi.org/10.3347/kjp.2015.53.1.77

Dirofilaria immitis, Dirofilaria immitis, and Dirofilaria repens are filarial nematodes transmitted by mosquitoes belonging to Culex, Aedes, and Anopheles genera. Screening by vector dissection is a tiresome technique. We aimed to screen filarial parasites in their vectors by single and multiplex PCR and evaluate the usefulness of multiplex PCR as a rapid xenomonitoring and simultaneous differentiation tool, in area where 3 filarial parasites are coexisting. Female mosquitoes were collected from 7 localities in Assiut Governorate, were microscopically identified and divided into pools according to their species and collection site. Detection of W. bancrofti, D. immitis, and D. repens using single PCR was reached followed by multiplex PCR. Usefulness of multiplex PCR was evaluated by testing mosquito pools to know which genera and species are used by filarial parasites as a vector. An overall estimated rate of infection (ERI) in mosquitoes was 0.6%; the highest was Culex spp. (0.47%). W. bancrofti, D. immitis, and D. repens could be simultaneously and differentially detected in infected vectors by using multiplex PCR. Out of 100 mosquito pools, 8 were positive for W. bancrofti (ERI of 0.33%) and 3 pools each were positive for D. immitis and D. repens (ERI 0.12%). The technique showed 100% sensitivity and 98% specificity. El-Nikhila, El-Matiaa villages, and Sahel Seleem district in Assiut Governorate, Egypt are still endemic foci for filarial parasites. Multiplex PCR offers a reliable procedure for molecular xenomonitoring of filariasis within their respective vectors in endemic areas. Therefore, it is recommended for evaluation of mosquito infection after lymphatic filariasis eradication programs.

Citations

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  • Current Gaps in Survey Design and Analysis for Molecular Xenomonitoring of Vector‐Borne Neglected Tropical Diseases: A Systematic Review
    Angus McLure, Tilahun Alamnia, Zhiwei Xu, Colleen L. Lau, Helen J. Mayfield
    Tropical Medicine & International Health.2025; 30(9): 893.     CrossRef
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    Mahmoud K.F. El-Sayed, Manal M. El-Shahawi, Yasmeen M. Ali, Doaa R. Abdel-Haleem, Fatma S.M. Abu El-Azm
    Bioorganic Chemistry.2023; 130: 106258.     CrossRef
  • Mosquito Vectors (Diptera: Culicidae) and Mosquito-Borne Diseases in North Africa
    Amira Nebbak, Lionel Almeras, Philippe Parola, Idir Bitam
    Insects.2022; 13(10): 962.     CrossRef
  • The use of molecular xenomonitoring for surveillance of mosquito-borne diseases
    Mary M. Cameron, Anita Ramesh
    Philosophical Transactions of the Royal Society B: Biological Sciences.2021; 376(1818): 20190816.     CrossRef
  • Bancroftian Filariasis Still Endemic in Some Foci in Sohag Governorate, Upper Egypt
    Refaat MA Khalifa, Amal M Ahmed, Mohamed AA Taha, Nasr Eldeen MM Ali, Haitham KA Abd El Samea, Dabbu Jaijyan
    Journal of Parasite Research.2019; 1(1): 1.     CrossRef
  • Comparative evaluation of dry and liquid RIME LAMP in detecting trypanosomes in dead tsetse flies
    Peter Nambala, Janelisa Musaya, Kyoko Hayashida, Emmanuel Maganga, Edward Senga, Kelita Kamoto, John Chisi, Chihiro Sugimoto
    Onderstepoort Journal of Veterinary Research.2018;[Epub]     CrossRef
  • Implementing a community vector collection strategy using xenomonitoring for the endgame of lymphatic filariasis elimination
    Sellase Pi-Bansa, Joseph Harold Nyarko Osei, Joannitta Joannides, Maame Esi Woode, David Agyemang, Elizabeth Elhassan, Samuel Kweku Dadzie, Maxwell Alexander Appawu, Michael David Wilson, Benjamin Guibehi Koudou, Dziedzom Komi de Souza, Jürg Utzinger, Dan
    Parasites & Vectors.2018;[Epub]     CrossRef
  • Finding Wolbachia in Filarial larvae and Culicidae Mosquitoes in Upper Egypt Governorate
    Ahmed K. Dyab, Lamia A. Galal, Abeer E. Mahmoud, Yasser Mokhtar
    The Korean Journal of Parasitology.2016; 54(3): 265.     CrossRef
  • Trypanosome infection rates in tsetse flies in the “silent” sleeping sickness focus of Bafia in the Centre Region in Cameroon
    Gustave Simo, Pierre Fongho, Oumarou Farikou, Prosper Innocent Ndjeuto Ndjeuto-Tchouli, Judith Tchouomene-Labou, Flobert Njiokou, Tazoacha Asonganyi
    Parasites & Vectors.2015;[Epub]     CrossRef
  • 10,851 View
  • 163 Download
  • 13 Web of Science
  • Crossref
Opportunistic Parasites among Immunosuppressed Children in Minia District, Egypt
Ekhlas H. Abdel-Hafeez, Azza K. Ahmad, Basma A. Ali, Fadia A. Moslam
Korean J Parasitol 2012;50(1):57-62.
Published online March 6, 2012
DOI: https://doi.org/10.3347/kjp.2012.50.1.57

A total of 450 stool samples were collected from inpatient and outpatient clinics of Pediatric Department, Minia University Hospital, Minia District, Egypt. Two groups of patients were studied, including 200 immunosuppressed and 250 immunocompetent children. Stool samples were subjected to wet saline and iodine mounts. A concentration technique (formol-ether sedimentation method) was carried out for stool samples diagnosed negative by wet saline and iodine mounts. Samples were stained by 2 different methods; acid fast stain (modified Ziehl-Neelsen stain) and Giemsa stain. Total 188 cases (94%) were diagnosed positive for parasitic infections among immunosuppressed children, whereas 150 cases (60%) were positive in immunocompetent children (P<0.0001). The most common protozoan infection in immunosuppressed group was Cryptosporidium parvum (60.2%), followed by Blastocystis hominis (12.1%), Isospora belli (9.7%), and Cyclospora caytenensis (7.8%). On the other hand, Entamoeba histolytica (24.6%) and Giardia lamblia (17.6%) were more common than other protozoans in immunocompetent children.

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