Lindsay DS, Dubey JP, Blagburn BL, 1997. Biology of Isospora spp. from humans, nonhuman primates, and domestic animals. Clin Microbiol Rev 10 :19–34.
Zaman V, 1968. Observations on human Isospora. Trans R Soc Trop Med Hyg 62 :556–557.
Morakote N, Muangyimpong Y, Somboon P, Khamboonruang C, 1987. Acute human isosporiasis in Thailand: a case report. Southeast Asian J Trop Med Public Health 18 :107–111.
DeHovitz JA, Pape JW, Boncy M, Johnson WD, 1986. Clinical manifestations and therapy of Isospora belli infection in patients with the acquired immunodeficiency syndrome. N Engl J Med 315 :87–90.
Pape JW, Verdier RI, Johnson WD Jr, 1989. Treatment and prophylaxis of Isospora belli infection in patients with the acquired immunodeficiency syndrome. N Engl J Med 320 :1044–1047.
Certad G, Arenas-Pinto A, Pocaterra L, Ferrara G, Castro J, Bello A, Nunez L, 2003. Isosporiasis in Venezuelan adults infected with human immunodeficiency virus: clinical characterization. Am J Trop Med Hyg 69 :217–222.
Brandborg LL, Goldberg SB, Breidenbach WC, 1970. Human coccidiosis: a possible cause of malabsorption. N Engl J Med 283 :1306–1313.
Jongwutiwes S, Sampatanukul P, Putaporntip C, 2002. Recurrent isosporiasis over a decade in an immunocompetent host successfully treated with pyrimethamine. Scand J Infect Dis 34 :859–862.
Tiangtip R, Jongwutiwes S, 2002. Molecular analysis of Cryptosporidium species isolated from HIV-infected patients in Thailand. Trop Med Int Health 7 :357–364.
Morgan U, Weber R, Xiao L, Sulaiman I, Thompson RC, Ndiritu W, Lal A, Moore A, Deplazes P, 2000. Molecular characterization of Cryptosporidium isolates obtained from human immunodeficiency virus-infected individuals living in Switzerland, Kenya, and the United States. J Clin Microbiol 38 :1180–1183.
Xiao L, Ryan UM, 2004. Cryptosporidiosis: an update in molecular epidemiology. Curr Opin Infect Dis 17 :483–490.
Jongwutiwes S, Tiangtip R, Yentakarm S, Chantachum N, 2002. Simple method for long-term copropreservation of Cryptosporidium oocysts for morphometric and molecular analysis. Trop Med Int Health 7 :257–264.
Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG, 1997. The Clustal X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 25 :4876–4882.
Siebert S, Backofen R, 2005. MARNA: multiple alignment and consensus structure prediction of RNAs based on sequence structure comparisons. Bioinformatics 21 :3352–3359.
Kumar S, Tamura K, Nei M, 2004. MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment. Brief Bioinform 5 :150–163.
Franzen C, Muller A, Bialek R, Diehl V, Salzberger B, Fatkenheuer G, 2000. Taxonomic position of the intestinal protozoan parasite Isospora belli as based on ribosomal RNA sequences. Parasitol Res 86 :669–676.
Bialek R, Binder N, Dietz K, Knobloch J, Zelck UE, 2002. Comparison of autofluorescence and iodine staining for detection of Isospora belli in feces. Am J Trop Med Hyg 67 :304–305.
Mahrt JL, 1968. Sporogony of Isospora rivolta oocysts from the dog. J Protozool 15 :308–312.
Lepp D, Todd KS, 1976. Sporogony of the oocysts of Isospora canis. Trans Am Microsc Soc 95 :89–103.
Linsay DS, Current WL, Ernst JV, 1982. Sporogony of Isospora suis Biester, 1934 of swine. J Parasitol 68 :861–865.
Matsui T, Ito S, Fujino T, Morii T, 1993. Infectivity and sporogony of Caryospora-type oocyst of Isospora rivolta obtained by heating. Parasitol Res 79 :599–602.
Ferrer C, Colom F, Frasés S, Mulet E, Abad JL, Alió JL, 2001. Detection and identification of fungal pathogens by PCR and by ITS2 and 5.8S ribosomal DNA typing in ocular infections. J Clin Microbiol 39 :2873–2879.
Young I, Coleman AW, 2004. The advantages of the ITS2 region of the nuclear rDNA cistron for analysis of phylogenetic relationships of insects: a Drosophila example. Mol Phylogenet Evol 30 :236–242.
Prakash A, Walton C, Bhattacharyya DR, Loughlin SO, Mohapatra PK, Mahanta J, 2006. Molecular characterization and species identification of the Anopheles dirus and An. minimus complexes in north-east India using r-DNA ITS-2. Acta Trop 100 :156–161.
Past two years | Past Year | Past 30 Days | |
---|---|---|---|
Abstract Views | 13 | 13 | 13 |
Full Text Views | 732 | 476 | 38 |
PDF Downloads | 547 | 383 | 29 |
To investigate the extent of genetic heterogeneity in the genus Isospora infecting patients in Thailand, a total of 38 fecal samples containing Isospora oocysts from human immunodeficiency virus/acquired immunodeficiency syndrome patients (n = 30), corticosteroid-treated patients (n = 3) and immunocompetent individuals (n = 5) were recruited for analysis. Remarkable variation in the maximum width and length of oocysts both within and between isolates was observed. However, the average length-width ratio of oocysts was within the range for I. belli (> 1.2). Ex vivo sporogonic development of freshly passed oocysts in feces from three of these isolates was observed longitudinally, showing that 27% of these oocysts underwent complete sporulation. Interestingly, 95% of sporulated oocysts contained two sporocysts in an oocyst with four sporozoites in each sporocyst, and Caryospora-like oocysts, characterized by eight sporozoites enclosed by a single sporocyst, were also detected (5%). The small subunit ribosomal RNA (rRNA), 5.8S rRNA, internal transcribed spacer 1 (ITS-1), and ITS-2 were highly conserved, indicating that there were no cryptic species or extensive strain variation.