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1.
Mol Ecol ; 12(12): 3383-401, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14629354

ABSTRACT

Until recently, Histoplasma capsulatum was believed to harbour three varieties, var. capsulatum (chiefly a New World human pathogen), var. duboisii (an African human pathogen) and var. farciminosum (an Old World horse pathogen), which varied in clinical manifestations and geographical distribution. We analysed the phylogenetic relationships of 137 individuals representing the three varieties from six continents using DNA sequence variation in four independent protein-coding genes. At least eight clades were idengified: (i) North American class 1 clade; (ii) North American class 2 clade; (iii) Latin American group A clade; (iv) Latin American group B clade; (v) Australian clade; (vi) Netherlands (Indonesian?) clade; (vii) Eurasian clade and (viii) African clade. Seven of eight clades represented genetically isolated groups that may be recognized as phylogenetic species. The sole exception was the Eurasian clade which originated from within the Latin American group A clade. The phylogenetic relationships among the clades made a star phylogeny. Histoplasma capsulatum var. capsulatum individuals were found in all eight clades. The African clade included all of the H. capsulatum var. duboisii individuals as well as individuals of the other two varieties. The 13 individuals of var. farciminosum were distributed among three phylogenetic species. These findings suggest that the three varieties of Histoplasma are phylogenetically meaningless. Instead we have to recognize the existence of genetically distinct geographical populations or phylogenetic species. Combining DNA substitution rates of protein-coding genes with the phylogeny suggests that the radiation of Histoplasma started between 3 and 13 million years ago in Latin America.


Subject(s)
Evolution, Molecular , Geography , Histoplasma/classification , Histoplasma/genetics , Models, Genetic , Phylogeny , Cluster Analysis , Sequence Analysis, DNA , Species Specificity
2.
Rev. Inst. Med. Trop. Säo Paulo ; 44(6): 299-302, Nov.-Dec. 2002. tab
Article in English | LILACS | ID: lil-326346

ABSTRACT

Serotype, mating type and ploidy of 84 strains of Cryptococcus neoformans isolated from 61 AIDS and 23 non-AIDS patients admitted in a tertiary teaching hospital in Sõo Paulo, Brazil were examined. Among 61 strains isolated from AIDS patients, 60 strains were var. grubii (serotype A). Only one strain was var. gattii (serotype B). No var. neoformans (serotype D) was found. Among 23 strains isolated from non-AIDS patients, 15 were var. grubii (serotype A) and the remaining 8 were var. gattii, all of which were serotype B. Seventy-three of the 75 serotype A strains were the heterothallic alpha type (MATalpha) and the remaining 2 were untypable (asexual). Most of the MATalpha strains (69/73) were haploid and the remaining 4 strains were diploid. Similarly, both of the 2 asexual strains among the 75 serotype A strains were haploid. There were no alpha-mating type (MATalpha) strains among the 84 isolates. All of the 8 var. gattii strains were serotype B and haploid. Among a total of 84 strains tested, neither serotype AD nor serotype D were found. Neither triploid nor tetraploid were found. These results suggest that the serological, sexual and ploidy characteristics in C. neoformans strains isolated from AIDS patients in Sõo Paulo were rather simple, whereas strains isolated from non-AIDS patients presented serotype A and B with predominance of serotype A


Subject(s)
Humans , AIDS-Related Opportunistic Infections , Cryptococcosis , Cryptococcus neoformans , Genes, Fungal , Ploidies , Brazil , Cryptococcus neoformans , Genetic Variation , Serotyping
3.
Rev Inst Med Trop Sao Paulo ; 44(6): 299-302, 2002.
Article in English | MEDLINE | ID: mdl-12532211

ABSTRACT

Serotype, mating type and ploidy of 84 strains of Cryptococcus neoformans isolated from 61 AIDS and 23 non-AIDS patients admitted in a tertiary teaching hospital in São Paulo, Brazil were examined. Among 61 strains isolated from AIDS patients, 60 strains were var. grubii (serotype A). Only one strain was var. gattii (serotype B). No var. neoformans (serotype D) was found. Among 23 strains isolated from non-AIDS patients, 15 were var. grubii (serotype A) and the remaining 8 were var. gattii, all of which were serotype B. Seventy-three of the 75 serotype A strains were the heterothallic alpha type (MATalpha) and the remaining 2 were untypable (asexual). Most of the MATalpha strains (69/73) were haploid and the remaining 4 strains were diploid. Similarly, both of the 2 asexual strains among the 75 serotype A strains were haploid. There were no alpha-mating type (MATalpha) strains among the 84 isolates. All of the 8 var. gattii strains were serotype B and haploid. Among a total of 84 strains tested, neither serotype AD nor serotype D were found. Neither triploid nor tetraploid were found. These results suggest that the serological, sexual and ploidy characteristics in C. neoformans strains isolated from AIDS patients in São Paulo were rather simple, whereas strains isolated from non-AIDS patients presented serotype A and B with predominance of serotype A.


Subject(s)
AIDS-Related Opportunistic Infections/microbiology , Cryptococcosis/microbiology , Cryptococcus neoformans/genetics , Ploidies , Brazil , Cryptococcus neoformans/classification , Cryptococcus neoformans/pathogenicity , Genetic Variation , Humans , Serotyping
4.
Arq. neuropsiquiatr ; 51(3): 395-8, set.-nov. 1993. ilus
Article in Portuguese | LILACS | ID: lil-127741

ABSTRACT

Os autores registram um caso de neurocriptococose em paciente HIV-positivo, por Cryptococcus neofarmans acapsulado ou deficiente em cápsula. O quadro neurológico era de meningoencefalite subaguda, compatível ao diagnóstico de neurotuberculose, pelo exame do líquido cefalorraqueano (LCR). Estruturas leveduriformes foram encontradas no interior de macrófagos, ao exame citomorfológico do LCR. Cultivo do sedimento do LCR revelou a presença de Cryptococcus neoformans näo capsulado (identificaçäo bioquímica). A inoculaçäo da amostra em camundongo, por via intraperitoneal, permitiu a produçäo de cápsula que desaparecia em cultivos. Foi estudada a micromorfologia do fungo à microscopia eletrônica de varredura. A evoluçäo foi favorável com o emprego da anfotericina B associada a 5-fluoreocitosina. Näo foi caracterizada a variedade de Criptococcus neoformans agente do processo


Subject(s)
Humans , Male , Aged , Cryptococcosis/diagnosis , Cryptococcosis/cerebrospinal fluid , Cryptococcus neoformans/ultrastructure
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