[Sex structure and seed productivity of Mentha canadensis L. from natural flora of primorye of Russia].

The sex structure and seed productivity of Mentha canadensis L. from different climatic regioins of Primorye of Russia was studied. We established that M. canadensis is characterized by a homogeneous population structure due to the formation of vegetative clones. The ratio of female and androgynous individuals was 1:5, and it is possible that this is a species-specific trait. Both sexual forms produced fruits under conditions of isolation from cross-pollination. We discuss the possibility of apomixis and the influence of climatic conditions on seed productivity and morphometric characteristics of plants.

[Phenotypic and phytochemical differences between Mentha arvensis L. and Mentha canadiensis L].

A taxonomic study of anatomical, morphological, and phytochemical characteristics of Mentha arvensis L. and Mentha canadiensis L. using hierarchical cluster analysis has been conducted and the differences between the species studied have been revealed. The ratio between the lengths of the calyx tube and the calyx lobes, the number of secretory glands on the upper and lower surfaces of the leaf, and the composition of the essen- tial oil were shown to be the most appropriate parameters for classification.

[Correlation between the output and composition of essential oil and the level of salicylic acid in mint plants at different ontogenetic stages].

Dynamic changes in the content of acetylsalicylic acid and the output and qualitative composition of essential oil have been studied in mint plants (Mentha spicata L. and cultivar Medichka) during their ontogenesis with allowance for changes in weather conditions. Ontogenetic changes in the level of acetylsalicylic acid in leaf tissues are found to be similar in both cv. Medichka and M. spicata. In the case of cv. Medichka, this change is connected with the dynamics of the production and the qualitative composition of essential oil; in the case of M. spicata, this connection is less expressed. The role of acetylsalicylic acid and essential oil in plant adaptation to the environment is discussed.

[Physiological and biochemical aspects of clary (Salvia sclarea L) overwintering in central Russia].

Changes in the hormonal balance and the contents of carbohydrates, nitrogen, phosphorus, and potassium in overwintering organs of the biennial herb clary (Salvia sclarea L.) have been studied in relation to the adverse influence of environmental factors. Weather-related changes in tissue contents of cytokinins (CTK), abscisic acid (ABA), water-soluble sugars, and mineral nutrients elements have been detected in these organs. Each overwintering organ (rosette leaves, the basal part of the stem with axillary growth buds, and the storage portion of the root) is characterized by specific dynamics of the compounds tested. The role of phytohormones and carbohydrates in realization of plant adaptation potential is discussed.

Generation of monoclonal antibodies of desired specificity using chimeric polyomavirus-derived virus-like particles.

Foreign protein sequences presented on hamster polyomavirus (HaPyV) major capsid protein VP1-derived virus-like particles (VLPs) have been demonstrated to be highly immunogenic. The current study was aimed to evaluate VP1-derived chimeric VLPs as tools for hybridoma technology to generate monoclonal antibodies (mAbs) of desired specificity. Chimeric VLPs containing inserts of different size and origin were used as immunogens. Chimeric VLPs carrying a 9 amino acid (aa)-long cytotoxic T-cell epitope (STAPPVHNV) of human mucin 1 (MUC1) elicited a strong epitope-specific humoral immune response in mice and promoted the production of MUC1-specific mAbs. From a total of seven mAbs of IgG isotype generated against the chimeric VLPs, two mAbs were directed against the MUC1 epitope and five mAbs against the VP1-carrier. Two out of five anti-VP1 mAbs recognized epitopes located at the previously defined insertion site #2 (aa 223/224), which confirms its surface-exposed localization. Chimeric VLPs carrying a 120-aa long sequence of Puumala hantavirus (PUUV) nucleocapsid protein (NP) promoted the generation of five mAbs of IgG isotype specific to PUUV NP. All mAbs recognized the full-length NP of different PUUV strains. In contrast, no VP1-specific mAbs were obtained. The ability of chimeric VLPs to activate antigen-presenting cells was evaluated by studying the uptake of chimeric VLPs by murine spleen cell-derived dendritic cells (DCs). Efficient uptake of VLPs and activation of murine DCs were demonstrated, which may represent the basis of the strong immunogenicity of chimeric VLPs. In conclusion, chimeric VLPs effectively stimulated the production of IgG antibodies specific for foreign epitopes presented at surface-exposed regions. Thus, chimeric HaPyV VP1-derived VLPs represent efficient immunogens for hybridoma technology and provide a promising alternative to chemical coupling of synthetic peptides to carrier proteins.

Polyomavirus infection in hamsters and trichoepitheliomas/cutaneous adnexal tumours.

Multiple skin nodules, with histological features of adnexal tumours consistent with trichoepithelioma, were observed on the head and trunk of Syrian hamsters. Skin biopsies from 20 hamsters from five different colonies were affected, and two of the affected hamsters also had lymphoma. Two owners reported that 16 of 70 hamsters and 50 of 100 hamsters in their colonies had similar skin lesions. These tumours have previously been associated in laboratory colonies with hamster polyomavirus (HaPV) infection. Examination of skin tissues by electron microscopy failed to reveal intranuclear virus particles. Using recombinant major capsid protein VP1 of HaPV, VP1-specific antibodies were detected in sera from 12 of 12 affected hamsters and in four of four unaffected in-contact hamsters, by ELISA. The ELISA data were verified by immunoblot analysis. Eleven of 13 serum samples contained antibodies which reacted with at least one recombinant structural HaPV protein (VP2), including samples from three in-contact unaffected hamsters. Nine of the 11 anti-VP2-positive samples also reacted with recombinant VP3 of HaPV, and six reacted with VP1. Amplification by PCR and sequencing detected VP1 -encoding sequences showing a high degree of homology with HaPV. The findings suggest a possible infection by HaPV or a HaPV-like virus and it is likely that such an infection was enzootic within the affected colonies.

[Phytohormones of rhizomes of the mint of various geographic origin in its annual developmental cycle]. / Fitogormony kornevishch miaty razlichnogo geograficheskogo proiskhozhdeniia v godichnom tsikle ee razvitiia.

We studied the ratio of cytokinins and abscisic acid in the rhizome tissues of two southern introduced forms of mint (GBS 1-94 and GBS 2-94) in the annual cycle of its development under the climatic conditions of the Middle Zone of Russia. The level of cytokinins exceeded that of free abscisic acid during the entire period of rhizome growth and development. Three peaks of an excess--zeatin riboside over abscisic acid were established: (a) during mass flowering, (b) after dying off terrestrial shoots, and (c) before the appearance of shoots of the next year vegetation. These peaks were most distinct in the GBS 2-94 mint. Zeatin riboside was the major identified cytokinin. The role of balance of phytohormones in rhizome tissues upon adaptation of the introduced mint forms to new climatic conditions is discussed.

An immunodominant, cross-reactive B-cell epitope region is located at the C-terminal part of the hamster polyomavirus major capsid protein VP1.

The VP1 represents the major capsid protein of the hamster polyomavirus (HaPV). Here we describe the mapping of epitopes along the VP1 using Escherichia coli-expressed VP1-dihydrofolate reductase (DHFR) fusion proteins and PepScan analysis. By use of DHFR fusion proteins an immunodominant region was localized in the C-terminal part of VP1 between amino acids 320-384. Further epitopes are located in the regions amino acids 1-133 and amino acids 133-320, respectively. There were no obvious differences in the reactivity between sera of tumor-bearing and papilloma-free naturally HaPV-infected hamsters. In contrast, PepScan analysis revealed linear epitopes in the regions amino acids 79-97 and amino acids 353-367 for tumor-bearing animals and amino acids 101-113 and amino acids 165-179 for papilloma-free animals. The region between amino acids 320-384 of HaPV-VP1 was found to be involved in cross-reactivity of VP1 from HaPV and other polyomaviruses. Previously we have demonstrated that heterologous expression of HaPV-VP1 allowed the formation of virus-like particles (VLPs). From epitope mapping data and structural predictions it has been suggested that HaPV-VP1-VLPs may tolerate foreign peptides in the region amino acids 81-88 and the C-terminal part of VP1.

Capsid protein-encoding genes of hamster polyomavirus and properties of the viral capsid.

On the basis of its genome organization the hamster polyomavirus (HaPV) is closely related to the murine polyomavirus Py. But HaPV infection, in contrast to Py infection, gives rise to two different tumor types; depending on the hamster strain used for infection, HaPV induces either epitheliomas or lymphomas. Although the HaPV virions were shown to be similar to those of Py and SV40, more precise information about the structure and protein composition of the HaPV capsid was still missing. Here we describe the primary structure of the capsid protein-encoding HaPV genes and the structure and protein composition of the HaPV capsid. Virions isolated from epitheliomas in HaPV-infected hamsters were shown by electron microscopy to be spherical particles with the typical icosahedral structure of polyomaviruses. However, in contrast to the capsids of SV40 and Py, a T = 7 laevo symmetry of HaPV capsids was observed. Separation of HaPV virions in SDS polyacrylamide gels and Western blotting with VP1-specific antisera identified VP1 as the major capsid protein species corresponding in its molecular weight to the predicted value of 41.8 kDa. Because of the presence of two potential translational initiation sites in the VP1 gene, the N-terminal amino acid sequence of virion VP1 was determined and found to start at the second initiation site. The amino acid homologies of HaPV capsid proteins shared with Py varied between 65.5% (VP1), 45.4% (VP3) and 44.6% (VP2), whereas the homologies to the relevant proteins of other polyomaviruses were found to range between 49.6-57.9% for VP1 and 28.9-41% for VP2/VP3.

[Disorders of interleukin 2 biosynthesis by peripheral blood lymphocytes in patients with schizophrenia]. / Narushenie sinteza interleikina-2 limfotsitami perifericheskoi krovi bo'lnykh shizofreniei.

The aim of this study was to investigate the interleukin-2 (IL-2) production in schizophrenic patients with different forms of disease and controls. 70 schizophrenic patients and 20 healthy subjects were studied. Results obtained have shown that the IL-2 production depend on the forms of disease and different forms of progression. The results showed normal IL-2 production in patients with most forms of progression and decreased IL-2 level in the group with least forms of progression of disease.

[Importance of opiate receptor ligands in regulating lymphocyte proliferative activity]. / Znachenie ligandov opiatnykh retseptorov v reguliatsii proliferativnoi aktivnosti limfotsitov.

Effects of morphine (10(-12)-10(-6) M), metenkephalin (10(-12)-10(-6) M), beta-endorphin (10(-12)-10(-6) M), dalargin--synthetic analogue of leu-enkephalin (10(-12)-10(-7) M) and naloxone (10(-8)-10(-6) M) on lymphocytes of the human peripheral blood stimulated by polyclonal mitogens were studied. It was shown that morphine (10(-8)-10(-6) M) and dalargin (10(-12)-10(-7) M) inhibited the lymphocyte proliferative activity induced by optimal doses of phytohemagglutinin; effects of morphine and dalargin were blocked by naloxone. It was also found that beta-endorphin (10(-11)-10(9) M) inhibited the proliferative activity of lymphocytes stimulated by pokeweed mitogen; naloxone failed to block beta-endorphin effect.

[Effect of beta-endorphin and myelopeptides on the cAMP level and proliferation of lymphocytes in vitro]. / Issledovanie vliianiia beta-éndorfina i mielopeptidov na uroven' tsAMF i proliferatsiiu limfotsitov in vitro.

Beta-endorphin (10(-11)-10(-9) M) has been shown to induce naloxone-independent depression of the proliferative activity of human peripheral lymphocytes (HL), stimulated by pokeweed mitogen without affecting PHA-stimulated HL proliferation. Beta-endorphin (10(-10)-10(-7) M) also caused changes in HL cAMP level, that were blocked by naloxone. Marked individual sensitivity to beta-endorphin effects has been noted. It has been also shown that a bone marrow preparation, stimulating antibody production (myelopeptides), causes naloxone-independent depression in the proliferative activity of HL, stimulated by PHA and pokeweed mitogen, as well as naloxone-blocked decrease in cAMP HL level. It has been concluded that beta-endorphin interacts with several types of opiate lymphocyte receptors and that opioids, contained in myelopeptides, are involved in the realization of myelopeptide effect on lymphocytes.