17 research outputs found
Study of the UV Irradiation and Nalidicsic Acid Effect on the RecA-protein Induction in <i>Francisella tularensis</i> 15/10 Cells
Studied is the UV irradiation and nalidicsic acid effect on the RecA-protein synthesis in Francisella tularensis 15/10 cells. Obtained is the specific murine serum to the recombinant RecA-protein. The results of immunoblotting with this specific serum demonstrate that the amount of RecA-protein in Francisella tularensis 15/10 cells is not increased after the exposure to these damaging factors
Immunobiological Properties of <i>Francisella tularensis</i> 15/10 Strain with Deleted recA Gene
Deletion of recA gene in Francisella tularensis 15/10 genome leads to the increase in its sensitivity to ultraviolet irradiation, reduction of the homologous recombination capacity, and a slight decline of virulence for mice. Efficacy of Francisella tularensis 15/10ΞrecA reproduction within microphage-like cells, its resistance to normal rabbit serum, and protective properties on the mouse model of tularemia are the same as in original Francisella tularensis 15/10
Construction and Investigation of the Vaccine Strain Francisella tularensis without iglC genes. Communication 1
Using site-specific mutagenesis constructed were the variants of the vaccine strain F. tularensis subsp. holarctica 15 with the deleted iglC genes. Identified was the fact that genome of the strain 15 contained two copies of iglC gene. Deletion of one of them as well as both had little effect on the cultural-morphological and growth properties of the microbe. At the same time F. tularensis 15 lacking one copy of the iglC gene propagated in mice macrophages several times slower, than the original strain. Inactivation of both of the copies in the chromosome leaded to the emergence of a variant incapable of intracellular reproduction. This capacity in F. tularensis 15/23-2 with two inactivated iglC gene copies was partially recovered after integration of a complementing plasmid. Therewith the data mentioned above testifies to the significance of iglC gene for the process of reproduction in macrophages
Construction and Investigation of the Variants of the Vaccine Strain <I>Francisella tularensis</I> Lacking <I>iglC </I>Genes. Communication 2
for BALB/c mice by an order while retaining protective properties. Strain Francisella tularensis 15 lacking two copies of the iglC gene cannot replicate in mice organism, induces weak humoral response, is fully avirulent, and has decreased protective activity. Treatment of mice with sera obtained from the animals immunized on day 49 post immunization both with the stock F. tularensis 15 strain and its variants with one or two inactivated iglC genes has provided for 100 % protection from challenge with 200 DCL of F. tularensis 15 strain. However in case of BALB/c mice exposure to virulent F. tularensis 503 and F. tularensis Schu strains (50 DCL and 25 DSL, respectively), treated with immune sera 24 hours before, registered has been only mean lifetime increase
Isolation of Central Asian Subspecies of Tularemia Agent in the Altai Territory
Within the frames of activities attributed to the Reference Center for tularemia monitoring at SRC AMB, genetically identified are 4 isolates of Francisella tularensis , isolated in 2011 in the Altai Territory. These bacteria prove to be virulent for BALB/c mice, DCL being lower than 10 CFU. Using single-primer PCR-typing and MLVA assay distinguished have been the subspecies of the isolates. Three of them refer to the Central Asian subspecies, one β to the Holarctic, the former being isolated in the territory of the Russian Federation for the first time ever
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ΠΡΡ ΠΈΠ΄Π½ΡΠ΅ Π ΠΎΡΡΠΈΠΈ : (Π±ΠΈΠΎΠ»ΠΎΠ³ΠΈΡ, ΡΠΊΠΎΠ»ΠΎΠ³ΠΈΡ ΠΈ ΠΎΡ ΡΠ°Π½Π°) [Orchids of Russia : (biology, ecology and protection)]
Π ΠΊΠ½ΠΈΠ³Π΅ ΠΈΠ·Π»ΠΎΠΆΠ΅Π½Ρ ΡΠ΅Π·ΡΠ»ΡΡΠ°ΡΡ Π±ΠΎΠ»Π΅Π΅ ΡΠ΅ΠΌ ΡΡΠΈΠ΄ΡΠ°ΡΠΈΠ»Π΅ΡΠ½Π΅Π³ΠΎ ΠΈΠ·ΡΡΠ΅Π½ΠΈΡ Π΄ΠΈΠΊΠΎΡΠ°ΡΡΡΡΠΈΡ
ΠΎΡΡ
ΠΈΠ΄Π½ΡΡ
(Orchidaceae) Π² ΡΠ°Π·Π»ΠΈΡΠ½ΡΡ
ΡΠ΅Π³ΠΈΠΎΠ½Π°Ρ
Π ΠΎΡΡΠΈΠΈ (ΠΎΡ ΠΠ°Π»ΠΈΠ½ΠΈΠ½Π³ΡΠ°Π΄ΡΠΊΠΎΠΉ ΠΎΠ±Π»Π°ΡΡΠΈ Π΄ΠΎ ΠΠ°Π»ΡΠ½Π΅Π³ΠΎ ΠΠΎΡΡΠΎΠΊΠ°, ΠΎΡ ΠΠΎΠ»ΡΡΠΊΠΎΠ³ΠΎ ΠΏ-ΠΎΠ²Π° Π΄ΠΎ ΠΠ°Π²ΠΊΠ°Π·Π°) ΠΈ Π·Π° Π΅Ρ ΠΏΡΠ΅Π΄Π΅Π»Π°ΠΌΠΈ. ΠΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½Ρ ΡΠ°Π·Π»ΠΈΡΠ½ΡΠ΅ Π°ΡΠΏΠ΅ΠΊΡΡ ΠΆΠΈΠ·Π½ΠΈ ΠΎΡΡ
ΠΈΠ΄Π½ΡΡ
β ΠΌΠΎΡΡΠΎΠ»ΠΎΠ³ΠΈΡ ΠΈ ΠΎΠ½ΡΠΎΠ³Π΅Π½Π΅Π·, ΡΠΊΠΎΠ»ΠΎΠ³ΠΈΡ ΠΈ ΡΠΈΡΠΎΡΠ΅Π½ΠΎΠ»ΠΎΠ³ΠΈΡ, ΠΌΠΈΠΊΠΎΡΠΈΠ·ΠΎΠΎΠ±ΡΠ°Π·ΠΎΠ²Π°Π½ΠΈΠ΅, ΡΠ΅Π·ΠΎΠ½Π½ΡΠΉ ΡΠΈΡΠΌ, ΡΠΏΠΎΡΠΎΠ±Ρ ΠΈ ΠΈΠ½ΡΠ΅Π½ΡΠΈΠ²Π½ΠΎΡΡΡ ΡΠ°Π·ΠΌΠ½ΠΎΠΆΠ΅Π½ΠΈΡ, Π²ΠΎΠ·ΡΠ°ΡΡΠ½Π°Ρ ΡΡΡΡΠΊΡΡΡΠ°, ΡΡΡΠΎΠΉΡΠΈΠ²ΠΎΡΡΡ ΠΈ Π΄ΠΈΠ½Π°ΠΌΠΈΠΊΠ° ΠΏΠΎΠΏΡΠ»ΡΡΠΈΠΉ, ΡΠ΅Π°ΠΊΡΠΈΡ Π½Π° ΡΠ°Π·Π»ΠΈΡΠ½ΡΠ΅ ΡΠΎΡΠΌΡ Π°Π½ΡΡΠΎΠΏΠΎΠ³Π΅Π½Π½ΠΎΠ³ΠΎ Π²ΠΎΠ·Π΄Π΅ΠΉΡΡΠ²ΠΈΡ, ΡΠΎΡΡΠΎΡΠ½ΠΈΠ΅ ΠΈΡ
ΠΎΡ
ΡΠ°Π½Ρ. ΠΠ±ΠΎΠ±ΡΡΠ½ Π±ΠΎΠ»ΡΡΠΎΠΉ ΠΎΠ±ΡΡΠΌ ΠΎΡΠ΅ΡΠ΅ΡΡΠ²Π΅Π½Π½ΠΎΠΉ ΠΈ ΠΈΠ½ΠΎΡΡΡΠ°Π½Π½ΠΎΠΉ Π»ΠΈΡΠ΅ΡΠ°ΡΡΡΡ. ΠΠΎΠ»ΡΡΠ΅Π½Π½ΡΠ΅ ΡΠ΅Π·ΡΠ»ΡΡΠ°ΡΡ Π»Π΅Π³Π»ΠΈ Π² ΠΎΡΠ½ΠΎΠ²Ρ Ρ
Π°ΡΠ°ΠΊΡΠ΅ΡΠΈΡΡΠΈΠΊ ΡΠ²ΡΡΠ΅ 125 Π²ΠΈΠ΄ΠΎΠ² ΡΠ΅ΠΌΠ΅ΠΉΡΡΠ²Π° Orchidaceae, ΠΎΡΠΌΠ΅ΡΠ΅Π½Π½ΡΡ
Π½Π° ΡΠ΅ΡΡΠΈΡΠΎΡΠΈΠΈ Π ΠΎΡΡΠΈΠΈ. ΠΡΠΈΠ²Π΅Π΄Π΅Π½Ρ ΠΊΠ°ΡΡΡ Π°ΡΠ΅Π°Π»ΠΎΠ² ΠΈ ΡΠ²Π΅ΡΠ½ΡΠ΅ ΠΈΠ·ΠΎΠ±ΡΠ°ΠΆΠ΅Π½ΠΈΡ ΠΊΠ°ΠΆΠ΄ΠΎΠ³ΠΎ Π²ΠΈΠ΄Π°. - ΠΠ½ΠΈΠ³Π° ΠΌΠΎΠΆΠ΅Ρ Π±ΡΡΡ ΠΏΠΎΠ»Π΅Π·Π½Π° ΡΡΠ΅Π½ΡΠΌ-Π±ΠΎΡΠ°Π½ΠΈΠΊΠ°ΠΌ, ΠΏΡΠ΅ΠΏΠΎΠ΄Π°Π²Π°ΡΠ΅Π»ΡΠΌ Π²ΡΡΡΠΈΡ
ΡΡΠ΅Π±Π½ΡΡ
Π·Π°Π²Π΅Π΄Π΅Π½ΠΈΠΉ ΠΈ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½Π° ΠΏΡΠΈ ΡΠ°Π·ΡΠ°Π±ΠΎΡΠΊΠ΅ ΠΏΡΠ°ΠΊΡΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΌΠ΅Ρ ΠΏΠΎ ΡΠΎΡ
ΡΠ°Π½Π΅Π½ΠΈΡ Π²ΠΈΠ΄ΠΎΠ² ΡΡΠΎΠ³ΠΎ ΡΠ΅ΠΌΠ΅ΠΉΡΡΠ²Π°.
The book presents the results of a long-term (over 30 years) study of the family Orchidaceae across Russia: from Kaliningrad Province to the Far East and from the Cola Peninsula to the Caucasus, as well as in surrounding countries. Along with an insight into a history of orchid research in Russia, the book provides a review of modern knowledge in orchid morphology, habitats and seasonal development, and reproductive strategies, mycorrhiza, pollination and species geographic range and conservation status in Russia. The book includes descriptions of more than 125 orchid species illustrated with colour images and maps
PCR Differentiation of <i>Francisella tularensis</i> Subspecies Using One Primer
Presented are experimental data of size distribution of amplicons obtained with the help of the primer consisting of Escherichia coli chi-sequence and DNA from different subspecies of Francisella tularensis strains. Analysis of this distribution permitted to determine five informative regions on the electrophoregrams (in the regions of 190, 280, 500-570, 830 and 950 b.p.), that made it possible to perform subspecies differentiation of tularemia microbe strains. Thus, the subspecies of F. tularensis clinical isolates can be identified by safe, fast and convenient method - the PCR analysis using only one primer Chi 1f despite the slight genetic heterogeneity of tularemia agent strains