Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Probl Tuberk Bolezn Legk ; (5): 25-31, 2005.
Article in Russian | MEDLINE | ID: mdl-15988974

ABSTRACT

The true prevalence rates of multidrug-resistant tuberculosis (MDRT) are unknown for most regions of Russia. This study was conducted in the Samara Region that differs from other regions in the rapid spread of HIV infection. The purpose of this study was to determine the primary and acquired resistance of Mycobacterium tuberculosis (MBT) to first-line antituberculous drugs in patients from civil and penitentiary sectors and to reveal risk factors of drug resistance of MBT. Six hundred patients (309 civilians and 291 prisoners who had been bacteriologically diagnosed as having tuberculosis. The authors have established the following:--in new cases, primary drug resistance is as follows: to isoniazid [38.9% (95% CI, 31.3-36.9%)], to rifampicin [25.9% (95% CI, 19.4-33.4%)] and to MDRT [23.0% (95% CI, 16.7-30.3%)];--in prisoners, the primary resistance of MBT was statistically more significant than in civilians;--male sex, in adequate prior or current treatment for tuberculosis for more than 4 weeks, the presence of fibrocavernous tuberculosis and previous prison stay are essential risk factors of the development of resistance of MBT to both any first-line drug and MDRT;--HIV infection is unassociated with resistance.


Subject(s)
Antibiotics, Antitubercular/therapeutic use , Mycobacterium tuberculosis/isolation & purification , Prisoners , Tuberculosis, Multidrug-Resistant/microbiology , Adult , Female , Humans , Incidence , Male , Middle Aged , Mycobacterium tuberculosis/drug effects , Risk Assessment/methods , Risk Factors , Russia/epidemiology , Tuberculosis, Multidrug-Resistant/diagnosis , Tuberculosis, Multidrug-Resistant/epidemiology
2.
Mikrobiologiia ; 63(3): 450-6, 1994.
Article in Russian | MEDLINE | ID: mdl-7990733

ABSTRACT

As is shown expression homologous (dihydroxyacetone kinase) and heterologous (HBsAg, beta-galactosidase) genes in methylotrophic yeasts Hansenula polymorpha DL1 negatively affects on the growth parameters of a host strain. The reducing of specific growth rate (mu max) and yield of biomass per the unit of a consumed substrate (Yx/s) were found in all recombinant strains grown on methanol. Overproduction of dihydroxyacetone kinase and beta-galactosidase in recombinant H. polymorpha was accompanied by two-fold increasing of the activity of alcohol oxidase, which is the first enzyme of methanol oxidation. Otherwise, the activity of formaldehyde dehydrogenase two-fold decreased in the recombinant strain overproducing HBsAg compared with the host strain. It is suggested that the over-synthesis of foreign proteins requiring an additional energetic and metabolic expenses might reduce the growth parameters and the activities of some enzymes of methanol metabolism in recombinant methylotrophic yeast H. polymorpha.


Subject(s)
Fungal Proteins/genetics , Genes, Fungal , Methanol/metabolism , Pichia/metabolism , Alcohol Oxidoreductases/genetics , Cloning, Molecular , Escherichia coli , Fungal Proteins/biosynthesis , Hepatitis B Surface Antigens/biosynthesis , Phosphotransferases (Alcohol Group Acceptor)/biosynthesis , Promoter Regions, Genetic , Recombinant Proteins/biosynthesis , beta-Galactosidase/biosynthesis
3.
Mikrobiologiia ; 58(3): 467-70, 1989.
Article in Russian | MEDLINE | ID: mdl-2685517

ABSTRACT

Plasmid pCJ55 with a cloned gene for the large fragment of Escherichia coli DNA polymerase I is stable in the population of a recombinant strain under the conditions of batch and continuous cultivation at different dilution rates in the presence of ampicillin. The level of Klenow fragment expression is determined by at least two factors: the stability of the recombinant strain and its specific growth rate. The maximal activity of the Klenow fragment was found after thermoinduction of the culture growing at a rate of mu = 0.6 h-1 in a synthetic medium with bactopeptone and glucose as a carbon source.


Subject(s)
DNA Polymerase I/genetics , Escherichia coli/genetics , Gene Expression , Plasmids , Cloning, Molecular , DNA Polymerase I/biosynthesis , Escherichia coli/growth & development , Recombination, Genetic
SELECTION OF CITATIONS
SEARCH DETAIL
...