Vol 8, No 2 (2018)
- Year: 2018
- Published: 10.09.2018
- Articles: 17
- URL: https://iimmun.ru/iimm/issue/view/33
- DOI: https://doi.org/10.15789/2220-7619-2018-2
Full Issue
REVIEWS
GENOMOSYSTEMATICS OF RICKETTSIAE
Abstract
The definition of the term genome was given by the German botanist G. Winkler almost one hundred years ago in 1920. A genome definition for bacterial (rickettsia) with a single chromosome was recently presented from the perspective of information theory, biology and bioinformatics as the information chain of nucleotides. The systematics of rickettsiae (obligate intracellular microorganisms) is based on a limited number of phenotypic characters. Classifications built on the analysis of genes, fragments of genomes and their concatenations cause discussion. Application of the Formal Order Analysis (FOA, http://foarlab.org) in the study of complete genomes allowed to submit the systematics of representatives of the family Rickettsiaceae. This approach confirmed the existence of typhus group (TG), spotted fever group (SFG), and an «ancestral» group within the genus Rickettsia, and allowed the isolation of the Rickettsia felis group within this genus, located between the «ancestral» group and the SFG and the R. akari group on the border between the SFG group and the genus Orientia. The development of the tools of FOA — «Map of Genes» and «Matrix of Similarity» — helped to conduct an in-depth study of the complete genomes of rickettsia, taking into account the characteristics of their genes and noncoding sequences. Application of these instruments, with the help of the obtained classification, confirmed the notion of ecological features of rickettsia, the structure of nosological forms and the epidemiological patterns of rickettsiosis, and made it possible to assess the virulence of the strains of the two most pathogenic species of rickettsia, R. prowazekii and R. rickettsia. In this work, for the first time, a holistic, consistent and multidimensional observation of a set of closely related bacteria (a family of bacteria) and the manifestations associated with them was carried out. The basis of the developed and herein described systematic approach to the study of bacteria is a new mathematical model — the arrangement of nucleotides in a complete genome and its sensitive unambiguous numerical characteristics. A new methodological approach named genomosystematics and based on mathematical modeling of complete genomes of rickettsiae (bacteria) using FOA. Classification of rickettsiae and rickettsioses obtained with the help of this approach corresponds to ecological, epidemiological and etiological principles. Application of the genomosystematics can serve the goals and objectives of preventive medicine. The publication completes a series of scientific works presenting the methodology of an integrated approach based on the application of mathematical analysis tools in the study of objects and laws of natural science disciplines of biological and medical profile.
DISTURBANCE OF AN APOPTOSIS OF NEUTROPHILS AT A SEPSIS
Abstract
The sepsis represents life-endangering disturbances of functions of the internals caused by a dizregulyation of a macroorganism to the infectious agent and is difficult interaction of pro-inflammatory and antiinflammatory processes that not seldom defines the fate of patients. The predetermining factor of a sepsis is the originator. The immunosupression caused by the originator promotes generalization of an infection, and the intensive bacteriemia caused by generalization leads to the accruing endotoxinemia that aggravates immunosupression even more and leads finally to systemic inflammatory reaction — the main and most dangerous implication of a sepsis. The syndrome of systemic inflammation with uncontrollable emission of cytokines is the cornerstone of a sepsis. The pathophysiology of a sepsis begins with impassioned inflammatory reaction which can last several days, and then passes into more lingering immunosupressivny period where the outcome depends on the immune system of the patient. Cellular apoptosis is one of leaders in sepsis immunosupression development. In article mechanisms of disturbance of an apoptosis of neutrophils are described that, undoubtedly, affects weighting of a current of a sepsis and as a result, a failure. Migration of neutrophils under natural conditions includes four various phases which during a sepsis are broken. The mechanisms worsening migration of neutrophils, contributing to the development of a sepsis were investigated in numerous scientific works. Authors of Peking University offered schemes of a way of disturbance of an apoptosis of neutrophils and migration of neutrophils at a sepsis. Despite the extensive accumulated experience on studying of a pathogenesis of septic states, there are no effective and specific remedies of fight from a sepsis now. Perhaps, by prevention of disturbance of the programmed death of a cell the cytokines developed anti-apoptotic, caspase inhibitors will be.
THE PREVALENCE OF HIV RECOMBINANT FORMS IN RUSSIA AND COUNTRIES OF THE CIS: SYSTEMATIC REVIEW AND METAANALYSIS
Abstract
This review was to aimed to access the prevalence of HIV recombinant forms in Russia and countries of the CIS, which have close social and economic ties. We conducted a search in Russian Science Citation Index and PubMed for a depth of 8 years. We included 22 articles, which contained the results of 35 independent cross-sectional studies, in our review. Meta-analysis of HIV recombinant forms prevalence was conducted in Open Meta-analyst with the use of Der Simonian & Laird method, arcsin transformation and correction factor for zero values. Subgroup analysis was used along with meta-regression (by date of collection). Pooled prevalence of HIV recombinant forms was 21.3% (95% CI 16.2–26.5) and was highly heterogeneous. Blood samples from 3,494 HIV patients living in various regions of the Russian Federation and CIS countries — Belarus, Kazakhstan, Kyrgyzstan, Uzbekistan, Tajikistan, Armenia, Georgia — were examined. Among subtypes of HIV-1, the main share was occupied by subtype A — 75.6% (n = 2643), subtype B — 5.5% (n = 193), C — 0.8% (n = 31), G — 0.2% (n = 7), F — 0.14% (n = 5). Among the recombinant forms (n = 616), the fraction of CRF02_ AG was 39.6% (n = 244), CRF02_AG/A was 32.9% (n = 203), CRF63_02A1 was 15.9% (n = 98), CRF03_AB — 5.2% (n = 32), CRF06_cpx — 2.1% (n = 13). Unique recombinant forms were 2.7% (n = 17), including URF63_A1 (2.5%). In Russia, the highest prevalence of recombinant forms of HIV-1 was registered in the Siberian Federal District (33.2% (95% CI 12.2– 54.1), the lowest in the Northwest Federal District — 1.6% (95% CI 0.9–2.3). In the CIS countries, the highest prevalence of recombinant forms of HIV-1 is found in a subgroup of the Central Asian republics — Uzbekistan, Tajikistan, Kyrgyzstan, Kazakhstan — 51.7% (95% CI 38.5–64.9). The significant upward trend was shown with a meta-regression. Our review is the first such research in Russia and thus is of significant interest, but the result should be applied with caution due to high risk of publication bias as well as significant heterogeneity of our results.
IMMUNE RECONSTITUTION INFLAMMATORY SYNDROME IN HIV INFECTION
Abstract
Antiretroviral therapy (ART) leads to suppression of HIV replication, contributes to increase in the number of CD4-lymphocytes count and partial restoration or activation of the immune system. The consequence is a reduction of incidence of opportunistic diseases, increase in the duration and quality of life of people living with HIV (PLHIV). However, in some patients with severe immunosuppression, this may be accompanied by a worsening of the condition and risks of formation of the immune reconstitution inflammatory syndrome (IRIS), which manifests itself in the development of new or previously treated opportunistic, secondary and exacerbating non- infectious diseases against a virologically effective ART. The frequency of the development of IRIS varies widely, in cases of tuberculosis-associated manifestation it can reach 50%. Risk factors for the development of IRIS are low initial CD4-lymphocyte count and a high load of HIV RNA in the blood, the presence of opportunistic infections during the initiation of ART. Discussed terminology issues, other possible risk factors for the development of the syndrome, regularities of the pathological process are considered. Epidemiological statistics of IRIS, pathogenetic bases, variants of clinical and laboratory manifestations of complications are given. The criteria for diagnosis of the syndrome, as well as the necessary conditions for its occurrence, are considered. Particular attention is paid to the most common opportunistic infections that cause the manifestation of IRIS, the peculiarities and polymorphism of clinical manifestations and the prevention of their occurrence. Currently, there is an increasing incidence of HIV infection in the late stages. Laboratory and clinical differences in the manifestations of acquired immunodeficiency syndrome (AIDS) and IRIS have been sanctified. In view of the blurring of the diagnostic criteria, in the Russian Federation specialists rarely expose IRIS to clinical or pathological diagnoses, therefore it is rather difficult to trace the frequency of occurrence of this condition. Clinical and laboratory manifestations are systematized, which allows to formulate this diagnosis on the basis of their totality. Prevention of IRIS is the prudent prescription of antiretroviral drugs. It is neces sary to conduct a qualitative and timely diagnosis of concomitant diseases of infectious and non-infectious nature before the initiation of ART and during treatment, the appointment of effective etiotropic therapy for opportunistic and secon dary infections. In order to improve the prognosis of HIV infection, preferably early onset of ART with stable CD4-lym phocyte counts and low HIV RNA levels in the blood.
ORIGINAL ARTICLES
CHANGES MONOCYTE CHEMOATTRACTANTS PROTEIN-1 IN HELICOBACTER PYLORIASSOCIATED GASTRODUODENAL DISEASES
Abstract
Chemoattractants monocyte protein-1 (MCP-1) is a low molecular weight cytokine, secreted by many cells of the body. The synthesis of MCP-1 can induce the lipopolysaccharides of bacteria, a range of cytokines. It is believed that MCP-1 regulates the migration and infiltration of tissue by monocytes, T-lymphocytes memory, natural killer cells, is involved in differentiation of naive T-helper cells. There is evidence oncogenic and antitumor activity of MCP-1 at different stages of tumor progression. The aim of this work was the determination and comparison of serum level of MCP-1 by infection with Helicobacter (H.) pylori in precancerous conditions and gastric cancer.
Material and methods. Surveyed with the informed consent 204 patients with precancerous diseases of the stomach, 40 patients with gastric cancer and 40 healthy volunteers. Patients at esophagogastroduodenoscopy conducted the fence of material for target biopsy for histological and microbiological studies. Blood on the immunoassay climbed in the morning on an empty stomach from the cubital vein in a volume of 5 ml in a vial without preserving agent, the serum was separated by centrifugation for 10 minutes. By ELISA in the serum of patients determined the level of MCP-1, titer of total antibodies to the cytotoxin-associated protein of H. pylori. The obtained data statistically processed.
Results. The amount of MCP-1 in serum of the patients significantly exceeded the data of healthy individuals in all groups of comparison. Values of MCP-1 during exacerbation of gastric ulcer was higher than patients with exacerbation of chronic not atrophic and focal atrophic gastritis. The concentration of MCP-1 > 280 pg/ml was detected in 17.6% of patients with pre-cancerous conditions of the stomach. When ulceration process there was a strong direct correlation of the severity of its course and the number of MCP-1 in serum. Serum level of MCP-1 in 5.0% of patients with gastric cancer was at the upper limit of normal values, and 77.5% of patients exceeded it. Indicator in gastric cancer significantly prevailed over the values in precancerous conditions, was correlated with the tumor stage. The level of MCP-1 in serum of the examined healthy volunteers, patients with exacerbation of chronic gastritis, gastric ulcer disease, polyposis, gastric cancer was correlated with the titers of total antibodies to the cytotoxin-associated protein of H. pylori.
Conclusion. Determination of serum level of MCP-1 in precancerous conditions and gastric cancer is diagnostically valuable. Comparison of indicator values with the titers of total antibodies to the cytotoxin- associated protein of H. pylori prognostically significant, as it allows to assess the intensity of the induction signal to production of a cytokine.
OXYGEN-DEPENDENT PHAGOCYTOSIS OF BLOOD MONOCYTES IN CHILDREN WITH HELICOBACTER PYLORI-ASSOCIATED GASTRIC AND DUODENAL EROSIONS AND ULCER
Abstract
The aim of the research is to study oxygen-dependent phagocytosis of blood monocytes in children with gastric and duodenal erosions and ulcers by chemiluminescence analysis. The subjects of the research were blood monocytes, extracted from blood in 44 children with gastric and duodenal erosions and ulcers in the ages from 11 to 18 years. Microscopic tests for the bioptats of gastric mucosa of both standard regions and edges of ulcer defects had resulted in the determination of 2 groups of the patients with gastric and duodenal erosions and ulcers. The 1st group was represented by Helicobacter pylori high dissemination. As for the 2nd group, the patients showed low bacterization. The tests for luminol-dependent hemiluminescence of blood monocytes in patients with H. pylorihigh dissemination of gastric and duodenal mucosa demonstrated the significant increase of the intensity and the growth of areas both under the curve of spontaneous response and under the curve in the zimozan-induced process as compared to the monocyte activity in the group with low dissemination. Following the lucigenin- dependent chemiluminescence reactions in the group with H. pylori high dissemination we had found significant increase of the time of approaching the peak in both spontaneous response and zimozan- induced processes while the activation index was higher in comparison with phagocyte activities of monocytes in the group with low dissemination. Further stage of the research was to identify CagA-positive strains of H. pylori in the children with gastric and duodenal erosions and ulcers. Studying chemiluminescence activity of blood lymphocytes in the patients with anti-CagA antibodies we found the true increase of the time of reaching the peak, the intensity and the area under the curve in spontaneous process in luminol-dependent response and the time of reaching intensity peak and the intensity of spontaneous chemiluminescence reaction, lucigenin being an activator. So we marked the increase of the activity of oxygen-dependent phagocytosis of blood monocytes in children with H. pylori associated with gastric and duodenal erosions and ulcers related to H. pylori increased bacterization. The growth of H. pylori dissemination results in the higher stage of stomach mucosa inflammation. Therefore active phagocytes generate more intensively the formation of active forms of oxygen, free radicals and the products of peroxide oxidation. CagA-positive strains of H. pylori, as a rule, are associated with the higher level of inflammatory activity than CagA-negative ones. As a result of such influence the functional activity of monocytes increases, because they are «professional » phagocytes. The ability to perform phagocytosis is better expressed in them as compared to other leukocytes.
DIFFICULTIES IN IDENTIFICATION OF СOMAMONAS KERSTERSII STRAINS ISOLATED FROM INTESTINAL MICROBIOTA OF RESIDENTS OF REPUBLIC OF GUINEA AND RUSSIAN FEDERATION
Abstract
The Сomamonas genus, described in 1985, included one species — Сomamonas terrigena. At present, the Сomamonas genus includes 21 species. The ability of Comamonas to survive in environmental objects (samples of water, soil and plants), including hospital environment and medical equipment, allows them to be considered as opportunistic microorganisms. The purpose of the research was to study the biological properties and antimicrobial susceptibility of Сomamonas kerstersii strains isolated from fecal samples of healthy people living in Saint Petersburg (Russian Federation) and the Republic of Guinea. The study was carried out in the laboratory of enteric infections of the St. Petersburg Pasteur Institute. 1532 fecal samples were obtained from residents of St. Petersburg and 46 samples from residents of the Republic of Guinea. The generic and species identification of the isolated microorganisms was carried out using routine biochemical tests, the NEFERM test24 commercial test system (MIKROLATEST, Erba Rus, Russia) and Vitek 2 Compact (BioMerieux). The difficult for identification microorganisms were studied by MALDI-TOF mass spectrometry, on a “Microflex LRF” mass-spectrometer. Antimicrobial susceptibility was determined by the gradient method with MICEvaluator™ (OXOID, UK) on Müller– Hinton agar (Russia). In the intestine microbiota of 1532 St. Petersburg residents among the opportunistic microorganisms two strains of С. kerstersii were isolated (0.13%). In a survey of 46 residents of the Republic of Guinea in 8 cases (17.4%) С. kerstersii were isolated. The identification of C. kerstersii strains using various methods and biochemical tests has shown different results: routine biochemical tests allowed the strains to be assigned to the group of non-fermenting gram-negative bacteria; NEFERM test24 kit identified all strains as С. testosteroni; VITEC 2 referred all strains to С. testosteroni; using mass spectrometry with a coincidence ratio of 2.19–2.33, all strains were identified as С. kerstersii. It should be taken into account that the С. kerstersii bacteria cannot be identified by the tests of NEFERM test24 kit and the GN VITEC 2 card, since only the С. testosteroni is represented in the databases of both methods. The taxonomic base of mass spectrometry includes reference spectra of five species of Сomamonas from 21 known ones, including С. kerstersii. Strains isolated from the inhabitants of the Republic of Guinea were unsusceptible to at least one tested antibiotic: ciprofloxacin (4 strains), tetracycline (5 strains) and trimethoprim/sulfamethoxazole (5 strains), almost all strains being simultaneously unsusceptible to several antibio tics: ciprofloxacin and trimethoprim/sulfamethoxazole (2 strains), tetracycline and trimethoprim/sulfamethoxazole (2 strains), ciprofloxacin and tetracycline (1 strain). One strain was unsusceptible to ciprofloxacin, tetracycline, and trimethoprim/sulfamethoxazole.
REGULATION OF IMMUNE RESPONSE AGAINST MYCOBACTERIUM TUBERCULOSIS BY THE POPULATION OF REGULATORY DENDRITIC CELLS
Abstract
On the background of a high level of genetic susceptibility to tuberculosis infection (TB), granulomatous reactions in the lung tissue fail to effectively isolate infection foci and rather result in diffuse pathology, confluence of granulomata and formation of necrotic zones. Uncontrolled inflammation severely affect breathing function of the lung. Thus, effective disease control requires a good balance between protective and pathogenic immune responses. Immature regulatory dendritic cells (DCreg) and regulatory T lymphocytes (Treg) represent a pool of important cellular regulators of inflammation. Earlier we have demonstrated that stromal lung cells support development of CD11b+CD11clowCD103– DCreg from their bone marrowderived precursors in in vitro cultures. In addition, significantly larger population size and more rapid development of the lung CD4+Foxp3+ Treg cells characterize TB- resistant B6 mice compare to their TB-susceptible I/St counterparts. Here, we report that adoptive transfer of DCreg cells into TB-infected I/St mice is capable to enlarge the population of Treg cells in the lungs. This, in turn, attenuates lung pathology, decreases mycobacterial multiplication and diminishes lung infiltration with neutrophils, i.e., selectively restricts the population of cell largely responsible for TB pathogenesis. The key difference in lung pathology between DCreg recipients and control animals was the lack of tissue-destructive foci and necrotic zones in the former group. Meanwhile, the groups of mice did not differ in production of regulatory (IL-10 and TGF-β) and key inflammatory (IFNγ and IL-6) cytokines by lung cells. The latter result suggests that contact rather than secretory mechanisms underlie moderate attenuation of the TB process in the lungs of mice with an elevated lung Treg level, given that plethora of such mechanisms were described for Treg functioning. Although therapeutic effects were relatively weak, our results indicate that cell therapy approaches are applicable to regulation of lung tissue inflammation during TB course.
THE GROWTH RATE PHENOTYPIC PROPERTY OF MYCOBACTERIUM TUBERCULOSIS CLINICAL STRAINS: DEPENDENCE ON TUBERCULOSIS LOCALIZATION, TREATMENT, DRUG SUSCEPTIBILITY
Abstract
The phenotypic properties of the M. tuberculosis strains obtained from patients with pulmonary or extra-pulmonary tuberculosis are determined by a complex set of factors: the genetic characteristics of the pathogen, its ability to adapt in vivo and in vitro, the influence of the host’s immune system and chemotherapy. The growth rate as the phenotypic property is the most accessible for the study of the host-pathogen relationships at the level of host/strain population interactions. The aim of the study is to assess in vitro of the growth rate of M. tuberculosis strains isolated from patients with pulmonary and extra-pulmonary tuberculosis: untreated and treated (with surgical and non-surgical treatment) and also sensitive and resistant isolates in comparison with the reference strain H37Rv. To estimate the growth rate of 116 clinical isolates we have used the modified method originally developed by von Groll and co-authors: to get the bacteria growth curve the fluorescence intensity of growing strains (with indicator resazurin) has been measured daily for 8 days in 96- well plate. The growth rate is determined as the slope of the growth curve. The mean values of the growth rate have been calculated in the following groups of patients: 1 — untreated patients with pulmonary tuberculosis (PT), respiratory material; 2 — non-surgical treated PT patients, respiratory material; 3 — surgical treated PT patients (mainly with chronic and hyperchronic process), respiratory material; 4 — patients like in 3rd group, surgical material; 5 — bone and joint tuberculosis (BJT), surgical material. In addition, groups of sensitive and resistant strains have been examined, but there are no significant differences in growth rates. It has been obtained that the growth rate of strains isolated from the PT patients is higher than in BJT patients: it can be explained less favorable conditions for the pathogen vegetation in the BJT. In the case of a closed tuberculous lesion where the pathogen transmission to another host is impossible, then the selection of strains with the property to survive in the tissues of the osteoarticular system is impossible too, therefor it should be observed only an adaptation of the pathogen strain population to the individual host. The growth rate of isolates from untreated PT patients is higher than that of the treated ones. Comparison of the growth parameters of only MDR strains 1–5 groups to eliminate the influence of the sensitivity/resistance has resulted in the same conclusions. We suggest that the decrease in the growth rate of strains from the treated PT patients is in not only result of the treatment, but also is conditioned by adaptation of the pathogen to its external environment, which is the internal environment of the macroorganism. To confirm this assumption, the bacterial load of 1,083 diagnostic specimens grouped in a similar manner has been estimated, taking into account only MDR/XDR strains. In the group of treated patients the frequency of high bacterial load (CFU ≥ 100) reached 52.5–63.8% that shows the conserved fitness of bacteria in such patients. The mean values of the growth rate of the strain H37Rv non-adapted to the macroorganism (due to numerous passages on artificial media) are higher than in all groups of clinical strains. Thus, heterogeneity of phenotypic properties of M. tuberculosis clinical strains on the basis of growth rate has been obtained. The growth rate of M. tuberculosis clinical strains is depended on the tuberculosis localization (PT, BJT) and on the joint effect of patient treatment and pathogen adaptation to the host.
DYNAMICS OF IL-2 PLASMA LEVELS IN HIV PATIENTS WITH CONSIDERING DRUGS RESISTANCE
Abstract
Interleukin-2 (IL-2) is one of the most important cytokines involved in the regulation of innate and adaptive immunity. Its main immunological function is to regulate a specific (antigen-dependent) immune response by stimulating proliferation and differentiation of immune cells involved in its realization, including Т-lymphocytes. Dysfunction of cellular immunity is the main pathogenetic mechanism for the development of HIV infection.
Objective: to identify patterns of IL-2 levels change in HIV-infected patients on the background of drug resistance at the later stages of infection. The study included 83 patients with HIV infection receiving highly active antiretroviral therapy; the control group consisted of 20 healthy blood donors. All patients underwent a study of the effectiveness of antiretroviral therapy, including an assessment of HIV viral load and CD4+ Т lymphocyte levels. In patients with ineffective antiretroviral therapy, a study of drug resistance to HIV by Senger sequencing was additionally conducted. According to the results of genome sequencing, HIV-infected patients with ineffective antiretroviral therapy were divided into two subgroups — with revealed drug resistance (58.5%) and absence of detectable resistance mutations in the genome (41.5%). Levels of IL-2 were measured in all persons included in the study by the method of enzyme immunoassay. When comparing the levels of IL-2 between groups of patients with continuing viral load on the background of antiretroviral therapy (viral load is detected) with drug resistance and without it, significant differences were obtained (1.75±0.26 pg/ml versus 1.95±0.29 pg/ml, p ≤ 0.05, U-criterion, respectively). The content of IL-2 is statistically significantly lower in the group of patients who did not succeed with antiretroviral therapy than in the group of patients with treatment efficacy (1.83±0.29 pg/ml versus 4.89±0.55 pg/ml, respectively, p < 0.001, U-criterion). Thus, it is shown that in patients with revealed drug resistance against the background of progression of HIV infection there is a decrease in levels of IL-2. The increase in its levels in patients with HIV infection who have reached virological and immunological success of therapy is due to the reduction in the number of the cytokine-producing immune cells (T-lymphocytes). We assume that a significant decrease in the levels of IL-2 makes an additional contribution to the disruption of the processes of proliferation and differentiation of immunocompetent cells in HIV infection, which is of great importance in the formation of drug resistance of HIV in conditions of constant viral replication.
PROTECTIVE ACTIVITY OF NOVEL BENZIMIDAZOLE DERIVATIVES AT EXPERIMENTAL INFLUENZA INFECTION
Abstract
Influenza is an acute respiratory viral infection, which represents an important health problem. Every year, influenza causes epidemics and pandemics, leading to increase in morbidity and mortality in all regions of the globe. Due to the segmental organization of the genome and low accuracy of its replication, the influenza virus is capable of escaping the host’s immune response (antigenic drift), as well as the selection of drug-resistant variants. This calls for constant monitoring of the sensitivity of viral isolates to antiviral drugs and the development of new etiotropic antiviral agents that have alternative targets and mechanisms of activity. The purpose of this study was to characterize the new aminobenzimidazole derivatives as protective agents in lethal influenza infection in white mice. The efficacy of the compounds was assessed by their ability to reduce specific mortality of animals in the course of lethal influenza pneumonia caused by the influenza A/Puerto Rico/8/34 (H1N1) irus, increase the life duration of animals, and normalize the morphological structure of lung tissue comparing to the placebo group. For all the compounds studied, a decrease in the specific mortality of animals (from 20 to 60%) has been shown. The reference drug (oseltamivir phosphate) reduced the mortality of mice by 80%. The benzimidazole derivative 2519 demonstrated the highest indices of protective activity, its use reduced the mortality of animals by 60% and increased their mean day of death by 1.6 days in comparison with the control group. Morphological analysis showed that the activity of derivative 2519 was manifested in the normalization of the morphological structure of lung tissue in the course of influenza pneumonia. On day 5 after infection, the cells of the bronchial epithelium looked intact, in contrast to destroyed cells with numerous viral inclusions in control animals. The foci of inflammation themselves occupied a smaller area compared to the control. At the same time, there was no correlation between the previously obtained data on the virus-inhibiting effect of these compounds in vitro and the data obtained in animals. This suggests that despite the presence of direct antiviral activity detected previously in in vitro experiments, the protective properties of the studied aminobenzimidazoles on animals are caused, in addition to the etiotropic effect, by other pathogenetic factors. In conclusion, amino derivatives of benzimidazole should be considered as compounds that are promising for further development and introduction as an anti-influenza agents.
REGULATORY INFLUENCE OF BLOOD MONOCYTES ON THE POPULATION COMPOSITION OF GRANULOCYTES AND THE STATE OF THEIR RESPIRATORY BURST IN THE WIDESPREAD PURULENT PERITONITIS
Abstract
The aim of the study was to investigate the regulatory effect of monocytes and their subpopulations on the population composition of granulocyte leukocytes and the state of their respiratory burst in widespread purulent peritonitis (WPP). The study involved 24 patients aged 30-65 with acute surgical diseases and injuries of abdominal organs complicated by WPP. As a control 25 relatively healthy people of the same age range were examined. A study of the population composition of monocytes and granulocyte leukocytes in blood was performed using a two-platform technology on the hematological analyzer Sysmex XE-5000 (Sysmex Inc., USA) and FC-500 flow cytometer (Beckman Coulter, USA) using the Cytodiff antibody kit (Beckman Coulter, USA). A study of the monocytes number expressing HLA-DR- and CD64-receptor was performed by flow cytometry using direct immunofluorescence of whole peripheral blood. The respiratory burst state of neutrophilic granulocytes was studied by chemiluminescence analysis on a 36-channel chemiluminescence analyzer BLM-3607 (MedBioTech, Russia). As indicators of chemiluminescence were used luminol and lucigenin. The enhancement of chemiluminescence induced by zymosan was evaluated by the ratio of the area of the induced chemiluminescence to the spontaneous area and was defined as the activation index. It has been established that the immune-inflammatory process in WPP is characterized by a decrease in the number of classical monocytes in the peripheral blood and an increase in the content of non-classical monocytes. In WPP in peripheral blood the level of monocytes expressing HLA-DR receptors decreases. The change in the ratio of monocytes subpopulations characterizes the increase in the role of the proinflammatory fraction in the WPP pathogenesis. Changes in the population composition of granulocytes in the blood in patients with WPP also characterize the development of an acute inflammatory process. In this case, there is a decrease in the number of basophils in the peripheral blood, which, apparently, is determined by the presence of an allergic component in WPP and, accordingly, their migration to the inflammation area. In patients with WPP activation of a respiratory burst of granulocytes of blood was detected, the intensity of which is determined by the synthesis of primary and secondary active oxygen species. The results of the correlation analysis made it possible to establish that in WPP the regulatory role of non-classical monocytes increases aimed at stimulating the inflammatory processes (an increase in the number of mature and immature forms of neutrophils and stimulation of the activity of a respiratory explosion of granulocytes). The revealed features of the regulatory effect of monocytes on the population composition and the intensity of the respiratory burst of granulocytes can be used in the development of immunotherapeutic methods aimed at reducing the activity of the inflammatory process in WPP.
THE ROLE OF ARGININE DEIMINASE FROM STREPTOCOCCUS PYOGENES IN INHIBITION MACROPHAGES NITROGEN MONOXIDE (NO) SYNTHESIS
Abstract
The protective role of macrophages closely related to the production of bactericidal molecules, in which nitrogen monoxide (NO) play an important role. Arginine serves as a substrate for inducible NO synthase (iNOS) in course of NO production. Expression and activity of iNOS are regulated by the availability of the substrate (arginine) in the intercellular space. The bacterial enzyme arginine deiminase also uses arginine as a substrate, causing its deficiency for host cells. The aim of this study was to confirm the possible role of arginine deiminase from S. pyogenes in inhibiting NO synthesis by macrophages. For this purpose, a comparative study was made of the effect on the synthesis of NO by macrophages of the products of destruction of two strains: the initial S. pyogenes M49-16 and the isogenic mutant S. pyogenes M49-16 delArcA with the inactivated arginine deiminase gene (arcA). It has been shown that the ability of S. pyogenes M49-16 to inhibit production of NO by macrophages depends on its arginine deiminase activity because the isogenous mutant of S. pyogenes M49-16 delArcA with the inactivated gene arcA has lost its ability to inhibit NO synthesis. This allows us to consider the effects of S. pyogenes M49-16 as effects of arginine deiminase. An analysis of the inhibitory mechanisms of the enzyme showed that suppression of NO synthesis was not associated with the effect of destruction products of S. pyogenes M49-16 on the viability of macrophages. According to data of flow cytometry, incubation of cells in the presence of S. pyogenes destruction products of the original and mutant strains did not affect the level of iNOS expression, i.e. did not alter synthesis or stability of this enzyme. At the same time, the decrease in NO production under the influence of the original S. pyogenes strain M49-16 correlated with a decrease in the content of arginine in the culture medium. When exogenous arginine to the culture medium was added, the effect of the original strain of the suppression of NO production was declined. This confirms that the depletion of arginine is the main mechanism of the inhibitory effect of arginine deiminase on the production of NO by macrophages. The deficiency of NO production in the course of streptococcal infection can lead to a weakening of bactericidal activity of macrophages and to a decrease in the effectiveness of antimicrobial protection.
SHORT COMMUNICATIONS
BACTERIAL AND VIRAL PATHOGENS IN IXODES SP. TICKS IN ST. PETERSBURG AND LENINGRAD DISTRICT
Abstract
Tick-borne infections are the most common group of zooanthroponotic diseases in the Northern Hemisphere. For the Baltic Sea region and Fennoscandia, the dominant infectious pathologies transmitted by ticks are tick-borne borreliosis and tick- borne encephalitis. The presence of vast forested areas, actively visited by people in St. Petersburg and the Leningrad region, contributes to a rather high level of encroachment on the flares and intelligence of the borreliosis and tick-borne encephalitis among the population of these regions. The relatively dangerous pathogens that can be transmitted with the tick bite are also of particular danger: Anaplasma sp., Ehrlichia sp., Coxiella burnetii, Rickettsia sp. In this work, detection was performed using molecular genetic methods of TBE virus, B. burgdorferi sensu lato and Rickettsia sp. in engorged ticksple, as well as questing ticks collected from vegetation. The established levels of infection of TBE on infected ticks, levels of infection by pathogenic Borrelia of questing and engorgeded ticks were approximately equal. Rickettsia was not found in the ticks. The conducted analysis of the pathogens prevalence in comparison with the data of russian and foreign authors. Monitoring the prevalence of tick-borne pathogens is an important issue in the prevention of tick- borne infections in the North-Western Russia.
DETERMINATION OF SOME IMMUNOLOGICAL FEATURES OF HHV-6-MEDIATED INFECTIOUS MONONUCLEOSIS IN CHILDREN BY THE METHOD OF DISCRIMINATORY ANALYSIS
Abstract
Human herpesvirus type 6 (HHV-6) is a lymphotropic virus that is an etiological agent of infectious mononucleosis (IM) in children. HHV-6- mediated infectious mononucleosis (HHV-6M) does not have clearly defined clinical features. Nowadays immunopathogenetic aspects of this disease have not been fully understood. The purpose of this work was to study the characteristics of the quantitative composition of populations of immunocompetent cells of peripheral blood in children with HHV-6M. The material for the study was samples of peripheral blood from children with “infectious mononucleosis” diagnosis and from virtually healthy children. Depending on the etiologic cause of the disease, children with IM were divided into three groups: HHV-6M, IM of other etiology and mixed infection (combination of HHV-6 and Epstein–Barr virus and/or Cytomegalovirus). Virtually healthy children formed the fourth group. In blood samples, the absolute content of the following populations of immunocompetent cells was determined by the method of flow cytometry: the total population of T-lymphocytes, T- helpers, cytotoxic T-lymphocytes, double positive T-lymphocytes (CD4+CD8+), NK cells and B-lymphocytes. Discriminant analysis was carried out: based on the obtained data on the population composition of blood cells we constructed a model of a child’s attribution to one of the four groups analyzed in pairs. We used the method of machine learning — the algorithm of gradient boosting over decision trees. It was determined whether it is possible to classify patients on the basis of the studied indicators and which combination of indicators is optimal for classification. As a result of the study it was possible to classify the following pairs of groups: healthy children — children with HHV- 6M, healthy children — children with IM of other etiology, children with HHV-6M — children with IM of other etiology. When solving the problem of classifying children from group with mixed infection and from any other group, it was not possible to find a model of satisfactory quality. In comparison with virtually healthy children, children with HHV-6M were characterized by an increased content of the total population of T-lymphocytes and cytotoxic T-cells, as well as by a reduced content of doub le-positive T-lymphocytes. Compared with children with IM of other etiology, children with HHV-6M were characterized by an increased content of cytotoxic T-lymphocytes, T- helpers, B-lymphocytes and a reduced number of double-positive T cells. Our results indicate that HHV-6-mediated infectious mononucleosis causes changes in the quantitative composition of certain populations of immunocompetent cells of peripheral blood, different from those of other etiology, in children.
STUDY OF ELISA TEST-SYSTEMS OF DIFFERENT FORMATS FOR DETECTION OF MEASLES VIRUS SPECIFIC IgM IN DIFFERENT GEOGRAPHIC ZONES
Abstract
Detection of the measles virus (MV) specific IgM antibodies in blood serum of patients is considered to be the main standard for the laboratory confirmation of measles diagnosis, the test being acknowledged by WHO. As it was demonstrated earlier the specific IgM antibodies as the marker of the acute MV infection were detected in 97.2–100% of blood serum samples from patients using the ELISA test-systems of the “capture” format (Microimmun Ltd. and Vector Best). In case when the ELISA test-system of the “indirect” format (Siemens, Germany) was used only 63.9% of these sera turned to be IgM positive. And on the contrary using the “indirect” format ELISA test-system Euroimmun, Germany, for detection of the MV specific IgM the false positive results were obtained.
The aim of the study was the comparative evaluation of the different format ELISA test-systems used for the detection of the MV specific IgM antibodies in blood sera of patients and healthy adults collected in different geographic zones.
Materials and methods. In total 108 serum specimens collected in 2015–2017 were studied: from healthy adult Guineans, residents of the Republic of Guinea (RG); patients aged 1–70 with the initial “infectious mononucleosis”, “infectious cytomegalovirus” and “rubella” diagnosis and taken from the bank of sera in the Subnational Measles/Rubella laboratory, StP Measles/Rubella RC in NWFR. The MV specific IgM antibodies were detected using the commercial ELISA test-systems “VectoMeasles-IgM” (Vector-Best, Russia) (“capture” format) and “Anti-Measles Virus ELISA IgM (NP)” (Euroimmun Medizinische Labordiagnostik AG, Germany) («indirect» format). The specific Epshtein-Barr Virus (EBV) IgM and IgG antibodies were detected with the commercial ELISA test-systems «DS-ELISA-anti-EBV-VCA-M», «DS-ELISA-anti-EBV-EA-G» and «DS-ELISA-anti-EBV-NA-G» (“Diagnostic Systems”, Russia).
Results and discussion. The MV specific IgM antibodies were not revealed in the total of 108 blood serum samples from the healthy adults and patients, residents of the Russia and of the RG, with the “capture” format “VectoMeasles-IgM” ELISA test-system. The absence of the acute MV infection was also confirmed by the high measles immunity level (i.e. IgG MV antibodies titers) as well as by detection of the IgG antibodies of high avidity. At the same time in 6 of 108 total sera (5.5%) IgM MV antibodies were detected with the «indirect» format ELISA test system Euroimmun, Germany. In these 6 sera the EBV specific antibodies were also evidenced. The results obtained demonstrate the nonspecific reaction due to the possible reactivity with anti-EBV antibodies. Besides this the different percentage of the false positive reactions in sera from healthy adults, residents of the RG and residents of Russia was determined — 8.5±4.0% and 3.2±2.2% correspondently. Thus the preliminary results, and to get the final results for general conclusions increase of the total amount of the clinical specimens under studying is of extremely importance.
GENETIC AND INFECTIOUS MARKERS OF INFERTILITY
Abstract
The report presents the results of own research of the most important factors in the genesis of various forms of sterility. A married couples (n = 50) was examined with regard to possible etiological structure of these forms of pathology — infections of the family herpes (Herpes simplex types 1, 2, Cytomegalovirus hominis (CMV), Epstein–Barr virus (EBV) and genetic distribution for the second class of histocompatibilit (HLA II class): HLA-DRB1, HLA- DQA1 и HLA-DQB1. The authors present own data on genetic typing of the couples for the second class of histocompatibility, which allow to correlate these data with clinical and laboratory associations with infectious agents (infections of the herpes family). The genetic characteristics that determine the reproductive ability of the couple are associated with susceptibility to certain infectious markers. It is shown that the dominant majority of couples determined the HLA- DRB1 gene, which is more frequently associated with infections of the herpes family. Despite the fact that the level of positive PCR results in the group of couples with primary infertility was higher than in couples with secondary sterility (100 and 92%, respectively), maximum titers of specific antibodies to infections of the herpes family, including the frequency of markers of exacerbation, definition of IgM was higher than in the group of couples with primary infertility, and significantly higher than in couples with normal fertility. So, this antigen histocompatibility (HLA-DRB1) is associated with significant frequency of sterility, especially the secondary one, and infectious contamination infections of the family of herpes — HSV 1, 2 types, CMV, EBV in the study group — couples with secondary infertility. Marker HLA-DRB1, the most frequent in coup les with infertility, including idiopathic, associated in this group not only with significant contamination of infectious of the herpes family, but the presence of a chronic infectious process at the stage of reactivation. Conducted clinical and immunological studies clearly demonstrate the need for a comprehensive survey of women with disabilities in the system of immunogenesis with the mandatory assessment of the level of infectious (viral) contamination. Analysis of the results of their clinical and immunological studies allows us to propose an algorithm of complex examination in functional disorders in the system of immunogenesis, including the study of viral load as a necessary component.