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Biomedical subjects

S A Bulat

Publications and source records attributed to S A Bulat.

22 records · Page 2Linked to original sources

[Glass slide smears and imprints from infected organs for identification of Leishmania major by polymerase chain reaction methods].

The paper presents data showing that the DNA isolated from the smears and imprints of L. major-infected hamsters is suitable for use in the polymerase chain reaction (PCR) to detect the causative agent of leishmaniasis. The most solid data have been obtained with the smears unexposed to staining and examination by using immersion oil and to benzene treatment. The DNA isolated from these smears infected may preserve for at least 1.5 months in a domestic refrigerator. The immersion oil-treated smears may be also used to identify leishmanias, but DNA should be isolated from the infected specimens of these smears just before PCR. The original primer pair L-unit/L-mail that has shown itself well in the experiments on cultured promastigotes may be, if required, used to differentiate L. major and L. turanica in the infected material collected from infected rodents.

Animals↗

[The identification of marker strains of Leishmania major, L. turanica and L. gerbilli by the polymer chain reaction with a universal primer].

The Leningrad Nuclear Physics Institute, Academy of Science of the USSR, and Martsinovskiĭ Institute of Medical Parasitology and Tropical Medicine, USSR Ministry of Health, developed polymerase chain reaction (PCR) technique with universal primer 3-2 for Leishmania identification. The primers were patented in the USSR (Patent No 4757254, 1989). Reference strains of three Leishmania species were identified: L. major--MRHO/SU/59/Neal P; L. gerbilli--MRHO/CN/60/gerbilli; L. turanica--MRHO/SU/80/Cl 3720 and MRHO/SU/83/KD 051. Each Leishmania species is specific and different in its PCR pattern whereas the two L. turanica strains have identical PCR patterns of the given primer.

Animals↗

[Amplification of DNA for 15-30 minutes in single-use pipette tips].

Amplification of 200-1000-bp DNA fragments was performed in 15-30 min using a rapid thermal cycler based on the commercial instrument TC-1000-1 (IRLEN, St. Petersburg, Russia). Plastic pipette tips were used as thin walled, high surface to volume-ratio tubes, to increase the rate of heating (cooling) of 20 microliters samples, which allowed the time required for DNA amplification to be considerably reduced (5-10 times).

DNA↗

[A polymorphism study of the genomic DNA of trematodes at different phases of development].

Polymorphism of the genome DNA in different development stages of trematodes by means of the polymerase chain reaction (PCR) with universal primers was investigated. Interspecific variation in Trichobilharzia ocellata (cercaria) was shown in samples from the Moscow area and some regions in Byelorussia (Naroch Lake). Population groupments of T. ocellata are correlated with migration routes of subpopulation groupments of city populations of the mallard duck (Anas platyrhynchus). The cercariae of T. ocellata from rather distant geographical isolates (Moscow and Naroch Lake) differ by PCR pattern in greater extent than groupments of cercariae within Moscow. These distant isolates are considered to be members of separate populations. The cercariae of T. ocellata emitted from infected snails belonging to the different species (Lymnaea auricularia, L. ovata, L. pusilla pusilla) and during definite period (6 days with 24 h analysis) do not differ by the PCR patterns. T. ocellata cercariae emitted from L. auricularia in autumn period (from molluscs of the new generation in "new" summer infection) are found to be different significantly from the "spring" cercariae of the same year and the "autumn" ones of the previous year. The study of the experimentally reproduced life cycle of Opisthorchis felineus revealed an essential difference of cercariae genome. DNA from that in other development stages. This indicates, that genetic reorganisation in the genome of products of parthenogenetic development took place in the parthenita stage.

Animals↗