Laboratory of Veterinary and Medical Protistology

Mission

The focus is to determine the zoonotic sources of emerging parasitic diseases, especially the opportunistic nature of the occurrence of cryptosporidia, microsporidia and giardia in wild and domestic animals and in immunodeficient (e.g. AIDS) and immunocompetent patients.

Head: Martin Kváč

Selected publications

International collaboration

Graduated students

Current research projects

Immune response in gastric mucosa during Cryptosporidium muris infection

Although scarcely any T-cells are presented in gastric mucosa of healthy rodent hosts, significantly elevated migration of T-lymphocytes (more than 10,000 fold), especially CD8+ T-lymphocytes, to the stomach mucosa occurred during primary infection and persisted for more than two months after its resolution. Most immunocompetent hosts self-cured during 35 days post infection (DPI). The ex vivo cultures of splenocytes revealed very low levels of IFN-? production during the course of the primary infection. These infected animals acquire a protective immunity against re-infection with same or another gastric Cryptosporidium. No cross immunity between gastric Cryptosporidium species of mammals and C. parvumhas been detected. The hosts with CD8+ or CD4+ T-cells deficiency suffered from chronic cryptosporidiosis; nevertheless, they were able to self-cure during 100 or 150 DPI, respectively.

Molecular epidemiology of cryptosporidiosis

Cryptosporidium andersoni and C. muris are two known species of gastric cryptosporidia recorded from mammals. The infectivity and pathogenity of C. andersoni in neonatal calves and both gastric Cryptosporidium species in Mongolian gerbils (Meriones unguiculatus) were molecularly and histologically characterized. Mastomys coucha was described as a new host susceptible to C. andersoni. Neonatal animals were more susceptible to infection with gastric cryptosporidia. The changes of viability and infectivity of gastric and intestinal cryptosporidia are studied in long-term experiments.

Pig cryptosporidiosis has been described in all age categories. Cryptosporidium suis and Cryptosporidium pig genotype II were dominant species in pigs. Very low occurrence of C. parvum in pigs has been recorded but C. parvum and C. andersoni were dominant species infecting cattle younger than two months of age and adult animals, respectively. Cryptosporidium bovis was found with very low prevalence and C. ryanae was not detected. All C. parvum isolates belonged to subtype family IIa. The susceptibility of adult rodents to C. parvum and sheep to C. muris has been proved experimentally. The first report of human infection with
Cryptosporidium pig genotype II was reported. While the occurrence of cryptosporidiosis in pig is breeding hygiene-dependent, in cattle it is breeding type-dependent.

Morphological variability of C. suis oocysts, studied using digital image analysis, revealed that the strains of C. suis oocysts in naturally infected pigs from farms in the Czech Republic were morphologically different from those originally described as C. suis.

Epidemiology and immunology of microsporidiosis

Electron micrograph of Trachipleistophora extenrec. Late meronts with several nu

The immune response mechanisms against the microsporidian Encephalitozoon cuniculi were studied. The role of specific anti-microsporidia antibodies in protection of infected mice was described based on results of experimental infections of immunocompetent mice compared with those of immunodeficient mice. Mice with disrupted IFN-? or IL-12 genes, and those with severe combined immunodeficiency, served as models of immunodeficient hosts. Adoptive transfer experiments of CD4+ and CD8+ T lymphocytes, in combination with antibodies applied in vivo, were used to examine the contribution of antibodies to protective immunity against microsporidians.

Free-living and captured mammals and birds are examined for microsporidia spores. New species of the genus Trachipleistophora has been described from muscles of Tenrec ecaudatus

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Sections > Organismal and Evolutionary Parasitology > Laboratory of Veterinary and Medical Protistology