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Genotyping of Toxoplasma gondii strain directly from human CSF samples of congenital toxoplasmosis clinical case.
New Microbiol. 2017 Apr 03;40(2)
Authors: Pagliuca C, Pastore G, Scaglione E, Migliucci A, Maruotti GM, Cicatiello AG, Salvatore E, Picardi M, Camilla Sammartino J, Consiglio Buonocore M, Martinelli P, Iaccarino E, Colicchio R, Salvatore P
Abstract
This report describes a case of congenital toxoplasmosis in a newborn in Southern Italy. A pregnant mother had been admitted at the 20th week of her pregnancy on account of pharyngodynia and laterocervical lymphadenopathy. Although serological testing of the mother's serum documented a seroconversion with positive IgG and IgM anti-Toxoplasma antibodies during II trimester, the woman refused to perform prenatal diagnosis for congenital toxoplasmosis. Fetal ultrasound scan already showed mild asymmetrical triventricular hydrocephaly and cerebral calcifications. After birth, real-time PCR on cerebrospinal fluid and blood samples of the newborn showed a positive result for 529bp-repeat element DNA of T. gondii, while brain magnetic resonance imaging and computed tomography showed a characteristic diffuse brain tissue loss associated with hydrocephalus. For the first time molecular characterization of T. gondii isolate was performed directly from the newborn's CSF samples by using nested-PCR-RFLP of sag-2 and pk1 genes. The PCR-RLFP analysis revealed that the isolate belongs to the clonal type II, the predominant lineage causing human toxoplasmosis, as confirmed by DNA sequencing.
PMID: 28368078 [PubMed - as supplied by publisher]
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