Detection of Toxoplasma gondii bradyzoite genes in the peripheral blood mononuclear cells among patients with toxoplasmic chorioretinitis

Author:

Khanaliha Khadijeh1ORCID,Hedayatfar Alireza23,Minaeian Sara4,Bokharaei-Salim Farah5,Alemzadeh Sayyed Amirpooya2,Garshasbi Saba6,Fagheei Aghmiyuni Zeinab4,Salemi Borna7

Affiliation:

1. Research Center of Pediatric Infectious Diseases, Institute of Immunology and Infectious Diseases, Iran University of Medical Sciences, Tehran, Iran

2. Eye Research Center, the five Senses Institute, Iran University of Medical Sciences, Tehran, Iran

3. Noor Ophthalmology Research Center, Noor Eye Hospital, Tehran, Iran

4. Antimicrobial Resistance Research Center, Institute of Immunology and Infectious Diseases, Iran University of Medical Sciences, Tehran, Iran

5. Department of Virology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran

6. Vice Chancellor for Healthcare, Iran University of Medical Sciences, Tehran, Iran

7. Student Research Committee, School of Medicine, Iran University of Medical Sciences, Tehran, Iran

Abstract

Abstract Background Toxoplasmic chorioretinitis may occur as a result of acquired toxoplasmosis or reactivated congenital toxoplasmosis. In this study, Toxoplasma gondii bradyzoite genes along with the B1 gene were evaluated to detect T. gondii DNA in serum and peripheral blood mononuclear cells (PBMCs) of patients with toxoplasmic chorioretinitis. Methods Blood samples were collected from 10 patients (7 cases of active chorioretinal lesions and 3 cases of old chorioretinal scars). The genomic DNA was extracted from the patients’ serum and PBMCs and a polymerase chain reaction (PCR) assay was performed using bradyzoite genes along with B1. The subjects were also evaluated in terms of the T. gondii antibodies. Results The PCR results were positive in four of seven patients (57.1%) with active ocular toxoplasmosis lesions. In three patients (42.8%), the PCR results were positive for MAG-1 and SAG-4 and in one patient (14.3%) the PCR results were only positive for the B1 gene. The PCR results were positive only in the PBMCs, whereas they were negative in the serum samples. Two patients with positive PCR results showed high Toxoplasma immunoglobulin G (IgG) antibody titres. However, none of the patients showed positive Toxoplasma IgM antibodies. Conclusions The PBMCs are suitable for evaluating toxoplasmic chorioretinitis. The present results showed that PCR with bradyzoite genes is useful in the diagnosis of toxoplasmic chorioretinitis in PBMCs.

Funder

Research Center of Pediatric Infectious Diseases

Iran University of Medical Sciences

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Public Health, Environmental and Occupational Health,General Medicine,Parasitology

Reference25 articles.

1. Toxoplasmic chorioretinitis in the setting of acute acquired toxoplasmosis;Montoya;Clin Infect Dis,1996

2. Eye manifestations of congenital toxoplasmosis;Mets;Am J Ophthalmol,1997

3. Toxoplasmosis, an overview with emphasis on ocular involvement;Klaren;Ocul Immunol Inflamm,2002

4. Analysis of aqueous humor in ocular toxoplasmosis;Brézin;N Engl J Med,1991

5. Ocular toxoplasmosis: value of immunoblotting for the determination of an intra-ocular synthesis of antibodies;Riss;Pathol Biol (Paris),1995

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