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1.
Appl Environ Microbiol ; 67(10): 4901-7, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11571200

RESUMO

Several natural isolates of Escherichia coli O157:H7 have previously been shown to exhibit stationary-phase-dependent variation in their resistance to inactivation by high hydrostatic pressure. In this report we demonstrate that loss of the stationary-phase-inducible sigma factor RpoS resulted in decreased resistance to pressure in E. coli O157:H7 and in a commensal strain. Furthermore, variation in the RpoS activity of the natural isolates of O157:H7 correlated with the pressure resistance of those strains. Heterogeneity was noted in the rpoS alleles of the natural isolates that may explain the differences in RpoS activity. These results are consistent with a role for rpoS in mediating resistance to high hydrostatic pressure in E. coli O157:H7.


Assuntos
Proteínas de Bactérias/genética , Escherichia coli O157/crescimento & desenvolvimento , Variação Genética , Pressão Hidrostática , Fator sigma/genética , Animais , Proteínas de Bactérias/metabolismo , Sequência de Bases , Bovinos , Clonagem Molecular , Escherichia coli O157/genética , Escherichia coli O157/isolamento & purificação , Humanos , Dados de Sequência Molecular , Análise de Sequência de DNA , Fator sigma/metabolismo
2.
Infect Immun ; 69(7): 4276-86, 2001 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-11401964

RESUMO

In the course of characterizing a locus involved in heme utilization, we identified a Legionella pneumophila gene predicted to encode a protein with homology to the product of the Salmonella enterica serovar Typhimurium pagP gene. In Salmonella, pagP increases resistance to the bactericidal effects of cationic antimicrobial peptides (CAMPs). Mutants with insertions in the L. pneumophila pagP-like gene were generated and showed decreased resistance to different structural classes of CAMPs compared to the wild type; hence, this gene was designated rcp for resistance to cationic antimicrobial peptides. Furthermore, Legionella CAMP resistance was induced by growth in low-magnesium medium. To determine whether rcp had any role in intracellular survival, mutants were tested in the two most relevant host cells for Legionnaires' disease, i.e., amoebae and macrophages. These mutants exhibited a 1,000-fold-decreased recovery during a Hartmannella vermiformis coculture. Complementation of the infectivity defect could be achieved by introduction of a plasmid containing the intact rcp gene. Mutations in rcp consistently reduced both the numbers of bacteria recovered during intracellular infection and their cytopathic capacity for U937 macrophages. The rcp mutant was also more defective for lung colonization of A/J mice. Growth of rcp mutants in buffered yeast extract broth was identical to that of the wild type, indicating that the observed differences in numbers of bacteria recovered from host cells were not due to a generalized growth defect. However, in low-Mg(2+) medium, the rcp mutant was impaired in stationary-phase survival. This is the first demonstration of a pagP-like gene, involved in resistance to CAMPs, being required for intracellular infection and virulence.


Assuntos
Peptídeos Catiônicos Antimicrobianos/farmacologia , Proteínas de Bactérias/fisiologia , DNA Helicases/fisiologia , Proteínas de Ligação a DNA , Genes Bacterianos , Legionella pneumophila/fisiologia , Transativadores/fisiologia , Sequência de Aminoácidos , Animais , Antibacterianos/farmacologia , Proteínas de Bactérias/genética , DNA Helicases/genética , Resistência Microbiana a Medicamentos , Humanos , Líquido Intracelular/microbiologia , Legionella pneumophila/efeitos dos fármacos , Legionella pneumophila/genética , Legionella pneumophila/crescimento & desenvolvimento , Camundongos , Dados de Sequência Molecular , Mutagênese , Peptídeos/farmacologia , Transativadores/genética , Células U937 , Virulência
3.
FEMS Microbiol Lett ; 170(2): 355-61, 1999 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-9933930

RESUMO

We have constructed a DNA library from a virulent Salmonella typhimurium strain, in an avirulent strain. The process of selecting the components of interest from the library involved iterative growth in liquid culture. This resulted, after four cycles, in the culture becoming homogeneous for a single plasmid, which was much smaller than the average size for the library. We have identified the larger precursor of this plasmid which has two regions of sufficient homology to allow recombination resulting in the formation of the small plasmid. S. typhimurium carrying the small plasmid have a smaller genetic burden than other members of the library and survive better in spent culture medium, facilitating selection on repeated subculture. Such rapid adventitious selection has important implications for isolation of clones of interest from genomic libraries.


Assuntos
Cosmídeos/genética , Biblioteca Genômica , Salmonella typhimurium/genética , DNA Bacteriano/análise , Mapeamento por Restrição , Salmonella typhimurium/crescimento & desenvolvimento , Salmonella typhimurium/patogenicidade , Virulência
4.
Invest Ophthalmol Vis Sci ; 33(13): 3481-92, 1992 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-1464493

RESUMO

Rod- and cone-mediated function was studied with psychophysics and electroretinography in members of an X-linked retinitis pigmentosa pedigree with the RP2 genotype. An asymptomatic hemizygote with an early stage of the disease had cone dysfunction in the mid-periphery and an abnormal cone electroretinogram (ERG); rod function was normal. Hemizygotes with more advanced disease had cone and rod dysfunction in the mid-peripheral retina and cone dysfunction in the far periphery; cone and rod ERGs were abnormal. At very advanced stages, there was an absolute mid-peripheral scotoma and marked cone and rod dysfunction in the far peripheral and central retina. Cone and rod ERGs were severely abnormal or not detectable. Heterozygotes showed tapetal-like reflexes, patches of pigmentary retinopathy, and a range of functional findings from no detectable abnormalities to moderate levels of retinal dysfunction. There were regions of normal function adjacent to dysfunctional patches that had greater cone than rod sensitivity losses or comparable cone and rod losses. The results suggest that the phenotype of this RP2 genotype of X-linked retinitis pigmentosa, unlike other forms of retinitis pigmentosa, is first expressed as a cone photoreceptor system dysfunction, and as the disease progresses, both rod and cone systems are involved.


Assuntos
Ligação Genética , Retinose Pigmentar/genética , Cromossomo X , Adulto , Criança , Sensibilidades de Contraste , Adaptação à Escuridão , Eletrorretinografia , Feminino , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Linhagem , Fenótipo , Células Fotorreceptoras/fisiopatologia , Psicofísica , Retinose Pigmentar/fisiopatologia , Testes de Campo Visual , Campos Visuais
5.
Ophthalmology ; 93(5): 552-8, 1986 May.
Artigo em Inglês | MEDLINE | ID: mdl-2425325

RESUMO

We evaluated previously reported and hypothesized risk factors for the development of age-related maculopathy (ARM) in a case-control study. We compared 26 patients with documented disciform scarring or choroidal neovascularization with 23 age- and sex-matched controls. Systolic and diastolic blood pressure, smoking history, glucose, lipoprotein profiles, and serum levels of vitamins A, C, and E did not differ significantly between the two groups. Statistically significant associations (P less than 0.05) identified by univariate analysis include degree of dermal elastotic degeneration in sun-exposed and sun-protected skin, white blood count, increasing age and small posterior lenticular opacities. Using an interactive multivariate model, only extent of elastosis in sun protected dermis, age and white blood count were predictive (Mult R = 0.652, P less than .001). Our data support the concept of a multifactorial etiology of ARM but suggest that generalized increased susceptibility of elastic fibers to photic or other degenerative stimuli is a new and important risk factor for choroidal neovascularization.


Assuntos
Degeneração Macular/complicações , Neovascularização Patológica/etiologia , Fatores Etários , Idoso , Feminino , Humanos , Degeneração Macular/sangue , Degeneração Macular/etiologia , Masculino , Neovascularização Patológica/sangue , Análise de Regressão , Risco
8.
Photochem Photobiol ; 21(5): 363-5, 1975 May.
Artigo em Inglês | MEDLINE | ID: mdl-1208663
18.
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