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"Mohammad Hossein Motazedian"

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"Mohammad Hossein Motazedian"

Case Report

Cutaneous Leishmaniasis of the Eyelids: A Case Series with Molecular Identification and Literature Review
Iraj Mohammadpour, Mohammad Hossein Motazedian, Farhad Handjani, Gholam Reza Hatam
Korean J Parasitol 2016;54(6):787-792.
Published online December 31, 2016
DOI: https://doi.org/10.3347/kjp.2016.54.6.787
Cutaneous leishmaniasis (CL) is a protozoan disease which is endemic in Iran. It is transmitted by the Phlebotomus sand fly. The eyelid is rarely involved possibly because the movement of the lids impedes the sand fly from biting the skin in this region. Here, we report 6 rare cases of eyelid CL. The patients were diagnosed by skin scraping, culture, and PCR from the lesions. Skin scraping examination showed Leishmania spp. amastigotes in the cytoplasm of macrophages. Culture examination was positive for Leishmania spp. PCR was positive for Leishmania major and Leishmania tropica. The lesions were disguised as basal cell carcinoma, chalazion, hordeolum, and impetigo. The patients were treated with intramuscular meglumine antimoniate (20 mg/kg/day) for at least 3 weeks. They showed a dramatic response, and the lesions almost completely disappeared. We emphasized the importance of clinical and diagnostic features of lesions, characterized the phylogenetic relationship of isolated parasites, and reviewed the literature on ocular leishmaniasis.

Citations

Citations to this article as recorded by  Crossref logo
  • Management strategies for chalazia in pediatric patients: A scoping review
    Tom Kornhauser, Abdelrahman M. Elhusseiny, John D. Pemberton
    European Journal of Ophthalmology.2025; 35(4): 1481.     CrossRef
  • Self-administration of herbal treatment for periocular cutaneous leishmaniasis: A case report and systematic review
    Rawan N. AlThaqib, Faisal A. Altahan, Hamad M. Alsulaiman, Diego Strianese, Azza Maktabi
    Saudi Journal of Ophthalmology.2025; 39(2): 174.     CrossRef
  • Atypical Manifestations of Old World Cutaneous Leishmaniasis: A Systematic Review and Clinical Atlas of Unusual Clinical and Specific Anatomical Presentations
    Bahareh Abtahi‐Naeini, Seyed Naser Emadi, Zabihollah Shahmoradi, Mahsa Pourmahdi‐Boroujeni, Ali Saffaei, Fereshte Rastegarnasab
    Health Science Reports.2025;[Epub]     CrossRef
  • Unilateral erythematous nodule over eyelid
    Farzana Ansari, Akriti Agrawal, Anupama Bains, Poonam Elhence
    Indian Journal of Dermatology, Venereology and Leprology.2023; 89: 928.     CrossRef
  • Ocular Leishmaniasis - A systematic review
    Guillaume Mignot, Yagnaseni Bhattacharya, Aravind Reddy
    Indian Journal of Ophthalmology.2021; 69(5): 1052.     CrossRef
  • The Geographical Distribution of Human Cutaneous and Visceral Leishmania Species Identified by Molecular Methods in Iran: A Systematic Review With Meta-Analysis
    Homa Hajjaran, Reza Saberi, Alireza Borjian, Mahdi Fakhar, Seyed Abdollah Hosseini, Sajjad Ghodrati, Mehdi Mohebali
    Frontiers in Public Health.2021;[Epub]     CrossRef
  • Dermatoses infectieuses des paupières
    A. Hamerstehl, M. Verstappen, P. del Giudice
    Annales de Dermatologie et de Vénéréologie - FMC.2021; 1(8): 542.     CrossRef
  • Noninvasive Biological Samples to Detect and Diagnose Infections due to Trypanosomatidae Parasites: A Systematic Review and Meta-Analysis
    Denis Sereno, Mohammad Akhoundi, Kourosh Sayehmri, Asad Mirzaei, Philippe Holzmuller, Veerle Lejon, Etienne Waleckx
    International Journal of Molecular Sciences.2020; 21(5): 1684.     CrossRef
  • Leishmania cytochrome b gene sequence polymorphisms in southern Iran: relationships with different cutaneous clinical manifestations
    Iraj Mohammadpour, Gholam Reza Hatam, Farhad Handjani, Farzaneh Bozorg-Ghalati, Daniel PourKamal, Mohammad Hossein Motazedian
    BMC Infectious Diseases.2019;[Epub]     CrossRef
  • Case Report: Mucocutaneous Leishmaniasis Masquerading as Idiopathic Midline Granulomatous Disease
    Nilesh Tejura, Eunjung Kim, Lisa L. Dever, Debra Chew
    The American Journal of Tropical Medicine and Hygiene.2019; 101(5): 1107.     CrossRef
  • Efficacy of cryotherapy plus topical Juniperus excelsa M. Bieb cream versus cryotherapy plus placebo in the treatment of Old World cutaneous leishmaniasis: A triple-blind randomized controlled clinical trial
    Mohammad Mahdi Parvizi, Farhad Handjani, Mahmoodreza Moein, Gholamreza Hatam, Majid Nimrouzi, Jafar Hassanzadeh, Nasrin Hamidizadeh, Hamid Reza Khorrami, Mohammad Mehdi Zarshenas, Waleed Saleh Al-Salem
    PLOS Neglected Tropical Diseases.2017; 11(10): e0005957.     CrossRef
  • 9,921 View
  • 207 Download
  • 11 Web of Science
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Brief Communication

Prevalence of Enteric Protozoan Oocysts with Special Reference to Sarcocystis cruzi among Fecal Samples of Diarrheic Immunodeficient Patients in Iran
Mahmoud Agholi, Shahrbanou Naderi Shahabadi, Mohammad Hossein Motazedian, Gholam Reza Hatam
Korean J Parasitol 2016;54(3):339-344.
Published online June 30, 2016
DOI: https://doi.org/10.3347/kjp.2016.54.3.339
The genus Sarcocystis is not usually considered as an important enteric pathogen in immune compromised patients. It might be expected that species for which humans are the final host (Sarcocystis hominis and Sarcocystis suihominis as well as possibly others) would be encountered increasingly often in immunodeficient persons. This study aimed to address how to detect and differentiate Sarcocystis oocysts and/or sporocysts from enteric protozoans in the diarrheal samples of immunodeficient patients in Shiraz, Iran. Diarrheal samples of 741 immunodeficient patients with recurrent persistent or chronic diarrhea were examined by microscopy and molecular biological analysis. Oocysts-positive samples were 68 Cryptosporidium spp., 9 Cystoisospora belli (syn. Isospora belli), 2 Cyclospora cayetanensis, and 15 microsporidia (Enterocytozoon bieneusi). Sarcocystis-like sporocysts found from a woman were identified as Sarcocystis cruzi through 18S rDNA amplification and phylogenetic analysis. To the best of our knowledge, this is the first report of S. cruzi from a human.

Citations

Citations to this article as recorded by  Crossref logo
  • Simultaneous Detection of Sarcocystis hominis, S. heydorni, and S. sigmoideus in Human Intestinal Sarcocystosis, France, 2021–2024
    Maxime Moniot, Patricia Combes, Damien Costa, Nicolas Argy, Marie-Fleur Durieux, Thomas Nicol, Céline Nourrisson, Philippe Poirier
    Emerging Infectious Diseases.2025;[Epub]     CrossRef
  • Unveiling the hidden threat: prevalence of Enterocytozoon bieneusi and other intestinal parasitic infections among organ transplant recipients in Southern Iran
    Mohammad Hossein Motazedian, Leila Morabi, Shahrokh Ezzatzadegan Jahromi, Mojtaba Shafiekhani, Saeed Shahabi, Hamed Nikoupour Dailami, Siavash Gholami, Bahador Sarkari
    Gut Pathogens.2025;[Epub]     CrossRef
  • Molecular characterisation of sarcosporidiosis in cattle of Duhok governorate in Kurdistan region of Iraq
    S. N. Hussein, M. S. Shukur, A. A. Ibrahim
    BULGARIAN JOURNAL OF VETERINARY MEDICINE.2025; 28(2): 210.     CrossRef
  • Worldwide Epidemiology of Cyclospora cayetanensis in HIV/AIDS Patients: A Systematic Review and Meta-Analysis
    Farzad Mahdavi, Ali Pouryousef, Mohammad Reza Mohammadi, Kambiz Karimi, Asma Mousivand, Farajolah Maleki, Ali Asghari, Mina Mamizadeh
    Acta Parasitologica.2025;[Epub]     CrossRef
  • Prevalence and Associated Risk Factors of Cyclospora cayetanensis in Immunocompromised Patients: A Systematic Review and Meta‐Analysis
    Ali Ghorbani, Rostam Menati, Farshad Kakian, Ali Pouryousef, Asma Mousivand, Kambiz Karimi, Farajolah Maleki, Ali Asghari, Jalil Feizi, Panagiotis Karanis
    Canadian Journal of Infectious Diseases and Medical Microbiology.2025;[Epub]     CrossRef
  • Infectious etiologies of persistent and chronic diarrhea in Asian developing countries: A systematic review and meta‐analysis
    Matthew Chung Yi Koh, Shi Ni Tan, Jinghao Nicholas Ngiam, Paul Anantharajah Tambyah, Kewin Tien Ho Siah
    Journal of Gastroenterology and Hepatology.2024; 39(9): 1760.     CrossRef
  • Microscopic and Molecular Identification of Cyclospora cayetanensis and Cystoisospora belli in HIV-Infected People in Tabriz, Northwest of Iran
    Saba Ramezanzadeh, Gholamreza Barzegar, Hamid Owaysee Osquee, Majid Pirestani, Mahmoud Mahami-Oskouei, Maryam Hajizadeh, Seyed Abdollah Hosseini, Sonia M. Rodrigues Oliveira, Mahmoud Agholi, Maria de Lourdes Pereira, Ehsan Ahmadpour
    Tropical Medicine and Infectious Disease.2023; 8(7): 368.     CrossRef
  • Prevalence of Intestinal Parasitic Diseases in HIV Patients in Tabriz(Original article)
    Saba Ramezanzadeh, Golam Reza Barzegar, Hamid Oveisi Oskouei, Majid Pirestani, Mahmoud Mahami-Oskouei, Farzaneh Jafarian, Ehsan Ahmadpour, Seyed Abdollah Hosseini
    Journal of Ardabil University of Medical Sciences.2023; 23(4): 352.     CrossRef
  • Global Burden of Cyclospora cayetanensis Infection and Associated Risk Factors in People Living with HIV and/or AIDS
    Saba Ramezanzadeh, Apostolos Beloukas, Abdol Sattar Pagheh, Mohammad Taghi Rahimi, Seyed Abdollah Hosseini, Sonia M. Rodrigues Oliveira, Maria de Lourdes Pereira, Ehsan Ahmadpour
    Viruses.2022; 14(6): 1279.     CrossRef
  • Investigation of Sarcocystis spp. in slaughtered cattle and sheep by peptic digestion and histological examination in Sulaimani Province, Iraq
    Shadan Hassan Abdullah
    Veterinary World.2021; 14(2): 468.     CrossRef
  • Prevalence of intestinal microsporidiosis by morphological and molecular methods in eastern Iran
    Mahmoodreza Behravan, Mustapha Ahmed Yusuf, Rahmat Solgi, Ali Haghighi
    Gene Reports.2021; 24: 101296.     CrossRef
  • Comparison of Two Real-Time PCR Assays Targeting Ribosomal Sequences for the Identification of Cystoisospora belli in Human Stool Samples
    Martin Blohm, Andreas Hahn, Ralf Matthias Hagen, Kirsten Alexandra Eberhardt, Holger Rohde, Gérard Leboulle, Torsten Feldt, Fred Stephen Sarfo, Veronica Di Cristanziano, Hagen Frickmann, Ulrike Loderstädt
    Pathogens.2021; 10(8): 1053.     CrossRef
  • Molecular differentiation of cattle Sarcocystis spp. by multiplex PCR targeting 18S and COI genes following identification of Sarcocystis hominis in human stool samples
    S. Rubiola, T. Civera, E. Ferroglio, S. Zanet, T. Zaccaria, S. Brossa, R. Cipriani, F. Chiesa
    Food and Waterborne Parasitology.2020; 18: e00074.     CrossRef
  • Sarcocystosis in Ruminants of Iran, as Neglected Food-Borne Disease: A Systematic Review and Meta-analysis
    Davood Anvari, Elahe Narouei, Mona Hosseini, Mohammad Reza Narouei, Ahmad Daryani, Seyyed Ali Shariatzadeh, Abdol Sattar Pagheh, Shirzad Gholami, Shahabeddin Sarvi, Dariush Sargazi, Reza Saberi, Seyed Abdollah Hosseini, Abolghasem Siyadatpanah
    Acta Parasitologica.2020; 65(3): 555.     CrossRef
  • Cystoisospora belliinfections in humans: the past 100 years
    J. P. Dubey, S. Almeria
    Parasitology.2019; 146(12): 1490.     CrossRef
  • Sarcocystis spp. in Romanian Slaughtered Cattle: Molecular Characterization and Epidemiological Significance of the Findings
    Kálmán Imre, Gheorghe Dărăbuș, Emil Tîrziu, Sorin Morariu, Mirela Imre, Judit Plutzer, Marius V. Boldea, Adriana Morar
    BioMed Research International.2019; 2019: 1.     CrossRef
  • First molecular characterization of Sarcocystis spp. in cattle in Qena Governorate, Upper Egypt
    Asmaa M. El-kady, Nermean M. Hussein, Amal A. Hassan
    Journal of Parasitic Diseases.2018; 42(1): 114.     CrossRef
  • Simultaneous Molecular Detection of Cryptosporidium and Cyclospora from Raw Vegetables in Korea
    Seobo Sim, Jua Won, Jae-Whan Kim, Kyungjin Kim, Woo-Yoon Park, Jae-Ran Yu
    The Korean Journal of Parasitology.2017; 55(2): 137.     CrossRef
  • Molecular Identification of Sarcocystis spp. in Sheep and Cattle by PCR-RFLP from Southwest of Iran
    Mahmoud Rahdar, Tahereh Kardooni
    Jundishapur Journal of Microbiology.2017;[Epub]     CrossRef
  • Human intestinal sarcocystosis in Iran: there but not seen
    Mahmoud Agholi, Zahra Taghadosi, Davood Mehrabani, Farzaneh Zahabiun, Zahra Sharafi, Mohammad Hossein Motazedian, Gholam Reza Hatam, Shahrbanou Naderi Shahabadi
    Parasitology Research.2016; 115(12): 4527.     CrossRef
  • 12,327 View
  • 149 Download
  • 20 Web of Science
  • Crossref
Original Article
Evaluation of Recombinant SAG1, SAG2, and SAG3 Antigens for Serodiagnosis of Toxoplasmosis
Khadijeh Khanaliha, Mohammad Hossein Motazedian, Bahram Kazemi, Bahador Shahriari, Mojgan Bandehpour, Zarin Sharifniya
Korean J Parasitol 2014;52(2):137-142.
Published online April 18, 2014
DOI: https://doi.org/10.3347/kjp.2014.52.2.137

Serologic tests are widely accepted for diagnosing Toxoplasma gondii but purification and standardization of antigen needs to be improved. Recently, surface tachyzoite and bradyzoite antigens have become more attractive for this purpose. In this study, diagnostic usefulness of 3 recombinant antigens (SAG1, SAG2, and SAG3) were evaluated, and their efficacy was compared with the available commercial ELISA. The recombinant plasmids were transformed to JM109 strain of Escherichia coli, and the recombinants were expressed and purified. Recombinant SAG1, SAG2, and SAG3 antigens were evaluated using different groups of sera in an ELISA system, and the results were compared to those of a commercial IgG and IgM ELISA kit. The sensitivity and specificity of recombinant surface antigens for detection of anti-Toxoplasma IgG in comparison with commercially available ELISA were as follows: SAG1 (93.6% and 92.9%), SAG2 (100.0% and 89.4%), and SAG3 (95.4% and 91.2%), respectively. A high degree of agreement (96.9%) was observed between recombinant SAG2 and commercial ELISA in terms of detecting IgG anti-Toxoplasma antibodies. P22 had the best performance in detecting anti-Toxoplasma IgM in comparison with the other 2 recombinant antigens. Recombinant SAG1, SAG2, and SAG3 could all be used for diagnosis of IgG-specific antibodies against T. gondii.

Citations

Citations to this article as recorded by  Crossref logo
  • IgM Antibody Detection as a Diagnostic Marker for Acute Toxoplasmosis: Current Status of Studies and Main Limitations
    Karolina Sołowińska, Lucyna Holec-Gąsior
    Antibodies.2025; 14(2): 44.     CrossRef
  • Analysis of the Correlation Between Toxoplasma gondii Seropositivity and Alzheimer’s Disease
    Jianjun Wang, Ping Lin, Dan Li, Biyu Yang, Jiaqi Wang, Meng Feng, Xunjia Cheng
    Pathogens.2024; 13(11): 1021.     CrossRef
  • Seroprevalence and Epidemiology of Toxoplasma gondii in Animals in the Qinghai-Tibetan Plateau Area, China
    Guojing Li, Wangli Zheng, Jinfang Yang, Tongsheng Qi, Yongcai He, Wangkai Chen, Hejia Ma, Yali Sun, Ying Li, Ming Kang, Jixu Li
    Pathogens.2021; 10(4): 432.     CrossRef
  • Detection of Toxoplasma gondii Infections using Virus-Like Particles Displaying T. gondii ROP4 Antigen
    Min-Ju Kim, Jie Mao, Hae-Ji Kang, Ki-Back Chu, Fu-Shi Quan
    The Korean Journal of Parasitology.2021; 59(6): 565.     CrossRef
  • Prevalence of Toxoplasma gondii parasite in captive Mexican jaguars determined by recombinant surface antigens (SAG1) and dense granular antigens (GRA1 and GRA7) in ELISA-based serodiagnosis
    Alejandro Reynoso-Palomar, Dulce Moreno-Gálvez, Abel Villa-Mancera
    Experimental Parasitology.2020; 208: 107791.     CrossRef
  • Evaluation of a PCR assay for diagnosis of toxoplasmosis in serum and peripheral blood mononuclear cell among HIV/AIDS patients
    Farah Bokharaei-Salim, Abdoulreza Esteghamati, Khadijeh Khanaliha, Saeed Kalantari, Shirin Sayyahfar, Tahereh Donyavi, Saba Garshasbi, Qasem Asgari, Borna Salemi
    Journal of Parasitic Diseases.2020; 44(1): 159.     CrossRef
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    PLOS Neglected Tropical Diseases.2020; 14(10): e0008733.     CrossRef
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    Leonardo Manuel, Gabriela Santos-Gomes, Emilia V. Noormahomed
    Parasites & Vectors.2020;[Epub]     CrossRef
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    Marcos Alexandre Bezerra, Luiz Miguel Pereira, Luciana Baroni, Ana Patrícia Yatsuda
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    晓敬 孙
    Open Journal of Natural Science.2019; 07(06): 585.     CrossRef
  • Toxoplasma gondii-positive human sera recognise intracellular tachyzoites and bradyzoites with diverse patterns of immunoreactivity
    Marijo S. Roiko, Kaice LaFavers, Diane Leland, Gustavo Arrizabalaga
    International Journal for Parasitology.2018; 48(3-4): 225.     CrossRef
  • Development of an immunochromatographic test based on monoclonal antibodies against surface antigen 3 (TgSAG3) for rapid detection of Toxoplasma gondii
    Jiaqing Luo, Hongchao Sun, Xianfeng Zhao, Suhua Wang, Xunhui Zhuo, Yi Yang, Xueqiu Chen, Chaoqun Yao, Aifang Du
    Veterinary Parasitology.2018; 252: 52.     CrossRef
  • Antigens to Detect the Acute Phase of Toxoplasmosis in Pregnant Women: Standardized Comparison
    Juan Gabriel Costa, María Julia Vilariño
    Biomarkers in Medicine.2018; 12(5): 517.     CrossRef
  • P35 and P22 Toxoplasma gondii antigens abbreviate regions to diagnose acquired toxoplasmosis during pregnancy: toward single-sample assays
    Juan G. Costa, Leandro E. Peretti, Valeria S. García, Luz Peverengo, Verónica D.G. González, Luis M. Gugliotta, Maria L. Dalla Fontana, Claudia M. Lagier, Iván S. Marcipar
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  • Cloning and Sequencing of Truncated Toxoplasma gondii Subtilisin-Like 1 Antigen
    Ahmad Rouhizadeh, Ata A Ghadiri, Mohammad Razi Jalali, Masoud Ghorbanpour, Mohammad Hossein Razi Jalali
    Zahedan Journal of Research in Medical Sciences.2016;[Epub]     CrossRef
  • Evaluation of Recombinant SRS3 Antigen for Diagnosis of Toxoplasmosis by Enzyme-Linked Immunosorbent Assay
    Seyedeh Mahya Marashiyan, Fatemeh Moradian, Geita Saadatnia, Majid Golkar
    Archives of Clinical Infectious Diseases.2016;[Epub]     CrossRef
  • Cloning and Expression of Major Surface Antigen 1 Gene of Toxoplasma gondii RH Strain Using the Expression Vector pVAX1 in Chinese Hamster Ovary Cells
    Rahman Abdizadeh, Sharif Maraghi, Ata A. Ghadiri, Mehdi Tavalla, Saeedeh Shojaee
    Jundishapur Journal of Microbiology.2015;[Epub]     CrossRef
  • 11,487 View
  • 109 Download
  • 17 Web of Science
  • Crossref