Giant membrane rings/loops in the cytosol of P. falciparum-infected erythrocytes and their relation to the parasite.

Striking morphological transformations characterize the invasion of a red blood cell by the malaria parasite. Shortly after the infection, parasite-induced membranes appear in the cytosol of the affected host erythrocyte. One intensely investigated membrane type, commonly called Maurer's clefts, has a slit-like morphology and can be arranged in the form of extended three-dimensional membrane stacks or networks.

A promising diagnostic tool for toxoplasmic encephalitis: tachyzoite/bradyzoite stage-specific RT-PCR.

Objectives: To determine the diagnostic accuracy, technical benefit, and clinical application of the duplex reverse transcription-PCR (duplex RT-PCR) assay specific to bradyzoite (BAG1) and tachyzoite (SAG1) genes, for diagnosing toxoplasmic encephalitis (TE) in HIV-infected patients, using the US Centers for Disease Control and Prevention (CDC) recommended diagnostic criteria as the reference standard.

Methods: Advanced HIV-infected individuals with central nervous system opportunistic infections were enrolled in a prospective study, performed from July 2007 to January 2009; patients were classified as TE- or non-TE subjects in accordance with the CDC recommended criteria. Blood and cerebrospinal fluid samples were assayed by duplex RT-PCR to detect tachyzoite, bradyzoite, both, or none.

Toxoplasma gondii: Simple duplex RT-PCR assay for detecting SAG1 and BAG1 genes during stage conversion in immunosuppressed mice.

Toxoplasmic encephalitis (TE) is caused by reactivation of dormant bradyzoites into rapidly dividing tachyzoites of the apicomplexan parasite Toxoplasma gondii in immune-compromised hosts. Diagnosis of this life-threatening disease is complicated, since it is difficult to distinguish between these two stages. It is, therefore, mainly based on a test positive for T.

The complex morphology of Maurer's clefts: from discovery to three-dimensional reconstructions.

Over 100 years ago, Georg Maurer wrote one of the finest scientific accounts of what is now known as Maurer's dots, or clefts, describing the intracellular changes in red blood cells infected with Plasmodium falciparum. Maurer's clefts have since attracted much attention, and they form an intriguing aspect of parasite biology that may hold the key to the mechanisms by which the intracellular parasite alters red blood cell properties, leading to host pathogenesis and death. This review will focus on the description of the morphology of these clefts, from the first light-microscopic report up to recent three-dimensional reconstructions.

Growth of benign and malignant schwannoma xenografts in severe combined immunodeficiency mice.

Objectives: Models for the development of new treatment options in vestibular schwannoma (VS) treatment are lacking. The purpose of this study is to establish a quantifiable human VS xenograft model in mice.

Study Design And Methods: Both rat malignant schwannoma cells (KE-F11 and RT4) and human malignant schwannoma (HMS-97) cells were implanted near the sciatic nerve in the thigh of severe combined immunodeficiency (SCID) mice.