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1.
J Infect Dis ; 183(2): 269-276, 2001 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-11120932

RESUMO

Chlamydia trachomatis and Neisseria gonorrhoeae are universally acknowledged as urethral pathogens, yet the etiology in the majority of cases of urethritis is unclear. Our case-control study assessed the association of Mycoplasma genitalium, Ureaplasma urealyticum, and other potential pathogens with acute nongonococcal urethritis (NGU) in heterosexual men presenting to an urban sexually transmitted diseases clinic. M. genitalium was detected in 27 (22%) of 121 NGU case patients and in 5 (4%) of 117 control subjects (P<.01). Although C. trachomatis was detected in 36 (30%) of 121 NGU case patients and in 4 (3%) of 117 control subjects (P<.01), only 3 men with NGU were infected with both C. trachomatis and M. genitalium. U. urealyticum was not associated with NGU. By multivariate analyses, controlling for age, race, history of prior urethritis, and chlamydial infection, M. genitalium was associated with a 6.5-fold increased risk of urethritis (95% confidence interval, 2.1-19.5), which supports a role of this organism in the etiology of NGU.


Assuntos
Doenças dos Genitais Masculinos/microbiologia , Heterossexualidade , Infecções por Mycoplasma/microbiologia , Mycoplasma/isolamento & purificação , Uretrite/microbiologia , Adolescente , Adulto , Estudos de Casos e Controles , Chlamydia trachomatis/isolamento & purificação , Humanos , Masculino , Pessoa de Meia-Idade , Mycoplasma/genética , Reação em Cadeia da Polimerase/métodos , Comportamento Sexual , Doenças Bacterianas Sexualmente Transmissíveis/microbiologia , Ureaplasma urealyticum/isolamento & purificação , Urina/microbiologia
2.
Antimicrob Agents Chemother ; 43(10): 2493-6, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10508030

RESUMO

The role of mutations in the genes for GyrA and ParC in quinolone resistance in Mycoplasma hominis was studied. Selection with sparfloxacin gave mutations at GyrA83 (Ser-->Leu; Escherichia coli numbering) or GyrA87 (Glu-->Lys), and mutants had increased levels of resistance to sparfloxacin (8- to 16-fold) but not to ofloxacin. Selection with ofloxacin gave changes at ParC80 (Ser-->Ile) or ParC84 (Glu-->Lys), and mutants were four- to eightfold more resistant to ofloxacin but not to sparfloxacin. Selection of second-step mutants from strains with ParC mutations with either quinolone yielded double mutants with additional mutations at GyrA83 (Ser-->Trp or Ser-->Leu) or GyrA87 (Glu-->Lys). Second-step selection of GyrA mutants gave additional mutations at ParC80 (Ser-->Ile) or ParC84 (Glu-->Lys). Two-step mutants showed high levels of resistance to ofloxacin (MICs, 64 to 128 microg/ml) and moderate levels of resistance to sparfloxacin (MICs, 2 to 8 microg/ml). The primary target of ofloxacin in first-step mutants of Mycoplasma hominis was ParC, whereas that for sparfloxacin was GyrA.


Assuntos
Anti-Infecciosos/farmacologia , DNA Topoisomerases Tipo II/genética , Fluoroquinolonas , Mycoplasma hominis/efeitos dos fármacos , Ofloxacino/farmacologia , DNA Topoisomerase IV , Resistência Microbiana a Medicamentos/genética , Mycoplasma hominis/enzimologia , Mycoplasma hominis/genética , Mutação Puntual
3.
J Intellect Disabil Res ; 42 ( Pt 3): 246-53, 1998 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-9678409

RESUMO

Predictions derived from North American formulations of normalization suggest that contemporary care policies for people with intellectual disabilities will have a positive impact on societal perceptions of this group. To test this, adolescents' attitudes towards the community presence of people with disabilities in a normalization-advanced country (Sweden) and a relatively less normalization-advanced country (England) were compared. It was expected that Swedish and English participants would hold equally positive views of people with a non-intellectual disability, whereas English participants would hold less positive views than Swedish participants of people with an intellectual disability. The results gave limited support to this expectation when dimensions of participants' attitudes derived from a factor analysis were analysed. These results are discussed with reference to other factors that may influence attitudes in the two countries. In addition, implications for future research and practice are outlined.


Assuntos
Comportamento do Adolescente/psicologia , Atitude , Desinstitucionalização , Deficiência Intelectual , Adolescente , Feminino , Humanos , Inclusão Escolar , Masculino , Suécia , Reino Unido
4.
Int J Syst Bacteriol ; 40(4): 456-61, 1990 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-2275861

RESUMO

Four species in the order Mycoplasmatales, Mycoplasma capricolum, Mycoplasma hominis, Mycoplasma arginini, and Acholeplasma laidlawii, were compared for their ability to accumulate radiolabeled amino acids and polyamines. The use of a novel high-molecular-weight (HMW) medium, from which molecules of less than 12,000 molecular weight had been removed by extensive dialysis, allowed us to discern significant differences among the species in their relative accumulations of [3H]methionine and [3H]leucine and of [3H]spermidine and [3H]putrescine. Accumulation of radiolabeled amino acids in control low-molecular-weight (LMW) medium was small (0.2 to 2% of the label), and the species did not differ in their proportional accumulations of methionine and leucine. Accumulation of methionine was significantly enhanced (5- to 12-fold) in all species in HMW medium. In contrast, leucine accumulation was enhanced sevenfold for A. laidlawii but only twofold for M. hominis and M. capricolum in HMW medium. The nonglycolytic species, M. hominis and M. arginini, accumulated radiolabeled putrescine and spermidine in both media, whereas the glycolytic species, M. capricolum and A. laidlawii, accumulated only radiolabeled spermidine. The ability to accumulate putrescine appeared to be a differential characteristic for nonfermentative, arginine-utilizing mycoplasmas. HMW medium was much more effective than LMW medium for use in radiolabeling M. capricolum proteins with [35S]methionine.


Assuntos
Acholeplasma/metabolismo , Aminoácidos/metabolismo , Mycoplasma/metabolismo , Poliaminas/metabolismo , Acholeplasma/crescimento & desenvolvimento , Leucina/metabolismo , Metionina/metabolismo , Peso Molecular , Mycoplasma/crescimento & desenvolvimento , Putrescina/metabolismo , Espermidina/metabolismo , Isótopos de Enxofre
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