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ПНЕВМОВИРУСЫ В ИНФЕКЦИОННОЙ ПАТОЛОГИИ ЧЕЛОВЕКА 人类传染病中的肺炎病毒
Q3 Medicine Pub Date : 2017-12-28 DOI: 10.36233/0372-9311-2017-6-95-105
S. B. Yatsyshina
This review presents the actual data about structure, genetic diversity and pathogenicity factors of human respiratory syncytial virus (hRSv) and human metapneumovirus - which are the members of new Pneumoviridae family, according to updated taxonomy accepted by the International Committee on Taxonomy of Viruses (ICTV) in 2016. The results of own epidemiological and clinical studies are presented in comparison with literature data. Cyclic recurrence of hRSv circulation was revealed. The clinical and epidemiological characteristics of hRSv and hMpv infections were compared. The leading role of the hRSv in ARVI in children and the importance of hMpv as an etiological agent of respiratory infection in adults are shown. Significance of both viruses as the agents of the lower respiratory tract infections is emphasized. The factors contributing to the prevalence of the hRSv in children with ARI are analyzed. Prevention measures for these infections are considered.
本文综述了国际病毒分类委员会(ICTV) 2016年更新的新肺炎病毒科成员——人呼吸道合胞病毒(hRSv)和人嗜肺病毒的结构、遗传多样性和致病性等方面的实际资料。本文将流行病学和临床研究结果与文献资料进行比较。发现hRSv循环复发。比较hRSv和hMpv感染的临床和流行病学特征。hRSv在儿童ARVI中的主要作用以及hMpv作为成人呼吸道感染的病原的重要性。强调了这两种病毒作为下呼吸道感染病原体的意义。分析了导致急性呼吸道感染儿童中hRSv流行的因素。考虑了这些感染的预防措施。
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引用次数: 0
MODERN EPIDEMIOLOGICAL CHARACTERISTICS OF NOROVIRUS INFECTION IN MOSCOW 莫斯科诺如病毒感染的现代流行病学特征
Q3 Medicine Pub Date : 2017-12-28 DOI: 10.36233/0372-9311-2017-6-32-37
V. Kovalev, N. Filatov, M. Loktionova, T. G. Frolovskaya, A. Linok, G. A. Zhukova, A. A. Goliusov
Aim. Norovirus infection (NVI) epidemiological characteristics evaluation in Moscow at municipal and district levels. Materials and methods. A retrospective analysis of NVI incidence rate was conducted according to the 2009 - 2016 state statistical reporting forms data. Results. In 2009 - 2016 NVI incidence rate has a trend to increase in Moscow, either at municipal and district levels. NVI cases were registered among children mostly (78% in the SEAD of Moscow, 80% in Moscow and 81% in Russia), at the same time adults proportion of NVI incidence rate increased significantly (up to 42,7% in Moscow and 13,9% in the Russian Federation) by 2016. The morbidity dynamics in different child population age groups was effected by the outbreaks cases. Totally in 2011 - 2016 33 outbreaks were registered in Moscow (24,3% from all acute diarrheal infection outbreaks in Moscow for the same period), where 64,3% with nonpercutaneous channel of infection and 35,7% alimentary. Outbreaks were more often recorded in children’s organized collectivity (69,7%). Conclusion. Nowadays in Moscow there is an NVI incidence increase trend is evidenced, with an increase of the adult population proportion in morbidity structure. At this stage, main contribution to group morbidity was made by children 7 - 14 and 15 - 17 years old. One of the reasons for the NVI incidence rate growth in Moscow (2016) could possibly be the lack of effective prevention measures. Actually, specific NVI diagnostics provided only in outbreaks, due to the lack of routine diagnostic tools. The main reason for the NVI group morbidity effective disease area formation is still sanitary and anti-epidemic regime violation at sites and facilities.
的目标。莫斯科市、区两级诺如病毒感染流行病学特征评价材料和方法。根据2009 - 2016年国家统计报告表数据对NVI发病率进行回顾性分析。结果。在2009年至2016年期间,莫斯科的非传染性疾病发病率有上升趋势,无论是在市还是区级。NVI病例以儿童为主(莫斯科SEAD为78%,莫斯科为80%,俄罗斯为81%),同时到2016年,成人NVI发病率比例显著增加(莫斯科为42.7%,俄罗斯联邦为13.9%)。不同年龄组儿童发病动态受疫情影响。2011年至2016年期间,莫斯科共发生了33起暴发(24.3%来自莫斯科同期所有急性腹泻感染暴发),其中64.3%为非经皮感染渠道,35.7%为消化道感染。疫情更常发生在有组织的儿童集体中(69.7%)。结论。目前,莫斯科的NVI发病率呈上升趋势,发病率结构中成年人口的比例有所增加。在这个阶段,群体发病率的主要贡献是7 - 14岁和15 - 17岁的儿童。莫斯科(2016年)NVI发病率增长的原因之一可能是缺乏有效的预防措施。实际上,由于缺乏常规诊断工具,仅在爆发时提供特定的NVI诊断。NVI群体发病有效病区形成的主要原因仍然是现场和设施违反卫生防疫制度。
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引用次数: 0
ПОЛУЧЕНИЕ РЕКОМБИНАНТНОГО АНАЛОГА КАПСИДНОГО БЕЛКА ВИРУСА ГЕПАТИТА Е 1 ГЕНОТИПА: КЛОНИРОВАНИЕ, ЭКСПРЕССИЯ, ОЧИСТКА, ОЦЕНКА АНТИГЕННЫХ СВОЙСТВ 复制型肝炎病毒e - 1型基因组蛋白:克隆、表达、精炼、抗原评估
Q3 Medicine Pub Date : 2017-12-28 DOI: 10.36233/0372-9311-2017-6-72-80
G. I. Alatortseva, Sidorov Av, L. Nesterenko, L. N. Luhverchik, V. Dotsenko, I. I. Amiantova, V. Y. Kabargina, A. V. Milovanova, D. S. Vorobev, Yu. I. Ammur, V. M. Blinov, A. Z. Nurmatov, Z. S. Nurmatov, D. A. Baiyzbekova, O. T. Kasymov, K. K. Kyuregyan, M. I. Mikhailov, S. V. Zhavoronok, Zverev Vv
Aim. The development of the hepatitis E virus (HEV) genotype 1 recombinant capsid protein. Materials and methods. Escherichia coli strains, plasmid vectors, serological and clinical samples, ELISA reagent kits, molecular biological, bioinformatic, biotechnological, biochemical and serological methods. Results. Using HEV genotype 1 DNA copy of subgenomic virus RNA we made E.coli strains producing recombinabt capsid protein, containing C-terminal fragment of ORF2 protein fused to E.coli beta-galactosidase. Recombinant protein ORF2 had been isolated from the inclusion bodies of the E.coli biomass and purified by size exclusion chromatography. By Western blotting it had been shown specific interaction of the recombinant polypeptide with anti-HEV IgG from pool of positive sera. Antigenic specificity of the recombinant polypeptide had been confirmed by enzyme-linked immunosorbent assay with sera of hepatitis E patients and reference groups: healthy donors, patients with hepatitis А, В, C, infectious mononucleosis and cytomegalovirus infection, HIV-infected patients. Conclusion. HEV genotype 1 ORF2 recombinant antigen had been developed, and its possible use in diagnostic tests had been experimentally shown.
的目标。戊型肝炎病毒(HEV)基因1型重组衣壳蛋白的研制。材料和方法。大肠杆菌菌株,质粒载体,血清学和临床样品,ELISA试剂盒,分子生物学,生物信息学,生物技术,生化和血清学方法。结果。利用亚基因组病毒RNA的HEV基因型1 DNA拷贝,我们制备了产生重组衣壳蛋白的大肠杆菌菌株,该蛋白含有ORF2蛋白的c端片段,与大肠杆菌β -半乳糖苷酶融合。从大肠杆菌生物量包涵体中分离得到重组蛋白ORF2,并采用大小排斥层析法纯化。Western blotting显示重组多肽与阳性血清抗hev IgG有特异性相互作用。重组多肽的抗原特异性已通过酶联免疫吸附试验在戊型肝炎患者和对照组血清中得到证实:健康献血者、А、В、丙型肝炎患者、传染性单核细胞增多症和巨细胞病毒感染患者、hiv感染者。结论。已经开发出HEV基因1型ORF2重组抗原,并通过实验证明其可能用于诊断试验。
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引用次数: 4
EPSTEIN - BARR VIRAL INFECTION: MODERN SITUATION AND CLINICAL-EPIDEMIOLOGICAL FEATURES AMONG FERTILE WOMEN AND NEWBORNS 爱泼斯坦-巴尔病毒感染:育龄妇女和新生儿的现代状况和临床流行病学特征
Q3 Medicine Pub Date : 2017-12-28 DOI: 10.36233/0372-9311-2017-6-25-31
A. A. Asratyan, E. G. Simonova, S. Kazaryan, O. A. Orlova, K. V. Ilenkina, S. R. Raichich, N. B. Sipacheva, N. Karazhas
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引用次数: 3
MANIFESTATIONS OF EPIDEMIC PROCESS OF ROTAVIRUS INFECTION IN NIZHNY NOVGOROD IN PRE-VACCINATION PERIOD 下诺夫哥罗德市轮状病毒感染接种前流行过程的表现
Q3 Medicine Pub Date : 2017-10-28 DOI: 10.36233/0372-9311-2017-5-46-52
N. Novikova, T. A. Sashina, L. Solntsev, Epifanova Nv, A. Y. Kashnikov, L. V. Pogodina, I. Okun, O. N. Knyagina
Aim. Study the manifestations of epidemic process of rotavirus infection in Nizhny Novgorod in pre-vaccination period to evaluate the possible effect on morbidity for the rotavirus vaccine application introduction. Materials and methods. Rotavirus morbidity data were analyzed for the 12-year period (2005 - 2016), as well as its age and season distribution. Rotavirus genotyping was carried out using multiplex PCR and partial sequencing of VP4 and VP7 genes. Results. RVI morbidity in Nizhny Novgorod was shown to be at a moderate level when specific prophylaxis was not applied, multi-year dynamics for morbidity reflects the all-Russian state. 2015 - 2016 were characterized by intensification of the epidemic process in age groups of organized children (3 - 6 and 7 - 14) and adults. Season increase included December-May. seasonal morbidity maximums in different age groups took place during different months. Genetic structure of Nizhny Novgorod population PV-A during this time was presented by 10 types with G9P[8] (44,4%) dominating. Conclusion. Growth of RVI morbidity in Nizhny Novgorod in 2015 - 2016 and changes in age and season manifestations of the infection took place under the condition of change of the dominating genotype PV-A (G4P[8] to G9P[8]).
的目标。研究下诺夫哥罗德市轮状病毒感染在疫苗接种前的流行过程表现,评价轮状病毒疫苗的应用对发病率的影响。材料和方法。分析了2005 - 2016年12年期间轮状病毒发病率数据及其年龄和季节分布。采用多重PCR和VP4、VP7基因部分测序进行轮状病毒分型。结果。下诺夫哥罗德的RVI发病率在不采用特定预防措施的情况下处于中等水平,发病率的多年动态反映了全俄罗斯的状况。2015 - 2016年的特点是有组织儿童(3 - 6岁和7 - 14岁)和成人年龄组的流行过程加剧。季节增长包括12月至5月。不同年龄组的季节性发病率高峰出现在不同的月份。下诺夫哥罗德群体PV-A在这一时期的遗传结构呈现为10个型,G9P[8](44.4%)占主导地位。结论。2015 - 2016年下诺夫哥罗德地区RVI发病率的增长以及感染年龄和季节表现的变化是在主导基因型PV-A (G4P[8]到G9P[8])发生变化的情况下发生的。
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引用次数: 3
OBTAINING FUSED RECOMBINANT PROTEINS OprF-ΔOprI, ΔOprF-ΔOprI AND OprF-aTox-ΔOprl OF PSEUDOMONAS AERUGINOSA
Q3 Medicine Pub Date : 2017-10-28 DOI: 10.36233/0372-9311-2017-5-32-38
A. Kaloshin, A. Soldatenkova, E. M. Zimina, N. Mikhailova
Aim. Obtaining fused recombinant proteins of Pseudomonas aeruginosa that have protective properties against experimental pseudomonas infection. Materials and methods. Fused sequences of P. aeruginosa genes oprF, oprl and deleted form of toxA were cloned in plasmids for the expression in Escherichia coli. The synthesized recombinant proteins were purified in Ni-sepharose columns. Recombinant proteins were administered to mice intraperitonealiy twice with a 2 week interval to evaluate protective properties. Virulent culture of P. aeruginosa strain PA103 was injected into the animals intraperitonealiy 2 weeks after the immunization course as experimental challenge. Results. 3 fused recombinant proteins were produced: 1. OprF-ΔOprl included full sequence of OprF protein and deletion variant of OprI (lacking first 20 amino acids); 2. AOprF-AOprl consisted of C-terminal region (192 - 342 amino acids) OprF and deletion variant of Oprl protein; 3. OprF-aTox-ΔOprI included full sequence of OprF protein, sequence of nontoxic variant of exotoxin A (without 106 C-terminal amino acids) and deletion variant of Oprl protein. Fused recombinant proteins OprF-AOprl and OprF-aTox-ΔOprI at immunization doses of 25 and 50 pg for the first and second protein, respectively, were shown to have the best protective properties. Conclusion. The results obtained open perspectives for further studies to create specific immune biological preparations based on fused recombinant proteins of P. aeruginosa.
的目标。获得铜绿假单胞菌对实验性假单胞菌感染具有保护作用的融合重组蛋白。材料和方法。将铜绿假单胞菌基因oprF、oprl和弓形虫缺失型的融合序列克隆到质粒中,在大肠杆菌中表达。合成的重组蛋白在Ni-sepharose柱中纯化。小鼠腹腔注射重组蛋白两次,每隔2周评估其保护作用。免疫2周后腹腔注射铜绿假单胞菌PA103毒力培养物作为实验攻毒。结果:获得了3个融合重组蛋白;OprF-ΔOprl包含OprF蛋白全序列和OprI缺失变体(缺失前20个氨基酸);2. AOprF-AOprl由c端区(192 ~ 342个氨基酸)OprF和Oprl蛋白的缺失变体组成;3.。OprF- atox -ΔOprI包括OprF蛋白全序列、外毒素A无毒变异序列(不含106个c端氨基酸)和Oprl蛋白缺失变异序列。融合重组蛋白OprF-AOprl和OprF-aTox-ΔOprI分别在免疫剂量为25和50 pg时显示出最好的保护性能。结论。该结果为进一步研究以铜绿假单胞菌融合重组蛋白为基础制备特异性免疫生物制剂开辟了前景。
{"title":"OBTAINING FUSED RECOMBINANT PROTEINS OprF-ΔOprI, ΔOprF-ΔOprI AND OprF-aTox-ΔOprl OF PSEUDOMONAS AERUGINOSA","authors":"A. Kaloshin, A. Soldatenkova, E. M. Zimina, N. Mikhailova","doi":"10.36233/0372-9311-2017-5-32-38","DOIUrl":"https://doi.org/10.36233/0372-9311-2017-5-32-38","url":null,"abstract":"Aim. Obtaining fused recombinant proteins of Pseudomonas aeruginosa that have protective properties against experimental pseudomonas infection. Materials and methods. Fused sequences of P. aeruginosa genes oprF, oprl and deleted form of toxA were cloned in plasmids for the expression in Escherichia coli. The synthesized recombinant proteins were purified in Ni-sepharose columns. Recombinant proteins were administered to mice intraperitonealiy twice with a 2 week interval to evaluate protective properties. Virulent culture of P. aeruginosa strain PA103 was injected into the animals intraperitonealiy 2 weeks after the immunization course as experimental challenge. Results. 3 fused recombinant proteins were produced: 1. OprF-ΔOprl included full sequence of OprF protein and deletion variant of OprI (lacking first 20 amino acids); 2. AOprF-AOprl consisted of C-terminal region (192 - 342 amino acids) OprF and deletion variant of Oprl protein; 3. OprF-aTox-ΔOprI included full sequence of OprF protein, sequence of nontoxic variant of exotoxin A (without 106 C-terminal amino acids) and deletion variant of Oprl protein. Fused recombinant proteins OprF-AOprl and OprF-aTox-ΔOprI at immunization doses of 25 and 50 pg for the first and second protein, respectively, were shown to have the best protective properties. Conclusion. The results obtained open perspectives for further studies to create specific immune biological preparations based on fused recombinant proteins of P. aeruginosa.","PeriodicalId":24020,"journal":{"name":"Zhurnal mikrobiologii, epidemiologii, i immunobiologii","volume":"43 1","pages":"32-38"},"PeriodicalIF":0.0,"publicationDate":"2017-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73796924","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
КОГНИТИВНАЯ ОСЬ СТАРОСТИ: ВОСПАЛЕНИЕ - МИКРОБИОТА ТОНКОГО КИШЕЧНИКА 老年认知轴:炎症是小肠的微生物。
Q3 Medicine Pub Date : 2017-10-28 DOI: 10.36233/0372-9311-2017-5-3-9
Ю. Ю. Филиппова, Александра Леонидовна Бурмистрова
Aim. Detect connection between cognitive dysfunction in senior people with systemic infection profile and small intestine microbiota structure. Materials and methods. 42 senior individuals were included into the study All the examined have been divided into 2 groups based on the results of psychic status: 20 individuals with moderate cognitive disorders - «active longevity» group and 22 individuals with pronounced cognitive deficiency - «mercy» group. Systemic inflammation status and structure and quantitative composition of microbiota of small intestine was determined in all the senior individuals using gas chromatography mass-spectrometry of microbial markers. Results. Interconnection between systemic level of cytokines and microbiota structure of small intestine in senior people with various cognitive status was determined. Significant correlations between levels of pro-inflammatory cytokine IL-6 in blood plasma and quantity of Propionibacterium jensenii, Moraxella spp., Bacillus cereus and Fusobacterium spp. in small intestine and the degree of cognitive failure were detected for the first time. Conclusion. The parameters obtained could be used as predictive biomarkers of cognitive dysfunction in senior people.
的目标。检测全身性感染老年人认知功能障碍与小肠微生物群结构之间的联系。材料和方法。42名老年人被纳入研究,所有被调查者根据心理状态的结果被分为两组:20名中度认知障碍的人-“积极长寿”组和22名明显认知缺陷的人-“慈悲”组。采用气相色谱-质谱法测定所有老年人的全身炎症状态和小肠微生物群的结构和定量组成。结果。研究了不同认知状态老年人小肠系统细胞因子水平与肠道菌群结构的相互关系。首次检测到血浆促炎细胞因子IL-6水平与小肠延senpropionibacterium、Moraxella、cereus、Fusobacterium的数量与认知功能障碍程度有显著相关性。结论。所获得的参数可作为预测老年人认知功能障碍的生物标志物。
{"title":"КОГНИТИВНАЯ ОСЬ СТАРОСТИ: ВОСПАЛЕНИЕ - МИКРОБИОТА ТОНКОГО КИШЕЧНИКА","authors":"Ю. Ю. Филиппова, Александра Леонидовна Бурмистрова","doi":"10.36233/0372-9311-2017-5-3-9","DOIUrl":"https://doi.org/10.36233/0372-9311-2017-5-3-9","url":null,"abstract":"Aim. Detect connection between cognitive dysfunction in senior people with systemic infection profile and small intestine microbiota structure. Materials and methods. 42 senior individuals were included into the study All the examined have been divided into 2 groups based on the results of psychic status: 20 individuals with moderate cognitive disorders - «active longevity» group and 22 individuals with pronounced cognitive deficiency - «mercy» group. Systemic inflammation status and structure and quantitative composition of microbiota of small intestine was determined in all the senior individuals using gas chromatography mass-spectrometry of microbial markers. Results. Interconnection between systemic level of cytokines and microbiota structure of small intestine in senior people with various cognitive status was determined. Significant correlations between levels of pro-inflammatory cytokine IL-6 in blood plasma and quantity of Propionibacterium jensenii, Moraxella spp., Bacillus cereus and Fusobacterium spp. in small intestine and the degree of cognitive failure were detected for the first time. Conclusion. The parameters obtained could be used as predictive biomarkers of cognitive dysfunction in senior people.","PeriodicalId":24020,"journal":{"name":"Zhurnal mikrobiologii, epidemiologii, i immunobiologii","volume":"34 1","pages":"3-9"},"PeriodicalIF":0.0,"publicationDate":"2017-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75620891","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
MICROBIOCENOSIS OF SKIN IN BROMHIDROSIS PATIENTS 腋臭患者皮肤微生物病
Q3 Medicine Pub Date : 2017-10-28 DOI: 10.36233/0372-9311-2017-5-53-58
Aleshkin Av, O. Borisova, Gadua Nt, S. Bochkareva, V. A. Chernova, Trebunskikh Ip, B. A. Efimov, L. Kafarskaya, S. Afanasiev, Aleshkin Va, M. Afanasiev, A. Borisova, A. Karaulov
Aim. Evaluate the composition of microorganisms of skin microbiocenosis of axilla in brom-hidrosis patients. Materials and methods. 23 patients were examined (11 - 17 years) under the observation at Pirogov CCDC of the National Medical-Surgery Centre. Identification was carried out using biochemical test-systems BioMerieux VITEK MS MALDI-TOF («bioMerieux», France) and 16SrRNA genesequencing with consequent juxtaposition with EMBL/NCBI. Medium and high degree of skin seeding with microbiota was present in most of the patients with bromhidrosis (52.2 and 43.5%). 137 strains belonging to 5 genera of microorganisms were identified - Corynebacterium, Staphylococcus, Moraxella, Micrococcus, Candida and Bacillus spp. Coiynehacte-rium genus strains (8 species) and Staphylococcus genus (5 species) prevailed in microbiocenosis (89.1%). C. tuberculostearicum strains dominated among Corynebacterium, and S. hominis - Staphylococcus. Conclusion. In most of the cases (82.6%) in patients microbiocenosis of skin of axilla was presented by consortiums of microorganisms with prevalence of Corynebacterium and Staphylococcus microorganisms.
的目标。评价溴化氢患者腋窝皮肤微生物病的微生物组成。材料和方法。23名患者(11 - 17岁)在国家外科医疗中心皮罗戈夫中心接受了检查。使用生化检测系统BioMerieux VITEK MS MALDI-TOF(«BioMerieux»,法国)进行鉴定,并对16SrRNA基因进行测序,随后与EMBL/NCBI并并。腋臭患者皮肤中、高度微生物群播种率分别为52.2%和43.5%。共检出杆状杆菌、葡萄球菌、莫拉菌、微球菌、念珠菌和芽孢杆菌5属137株,其中以coiynehacium属(8种)和葡萄球菌属(5种)为主(89.1%)。硬脂结核杆菌在棒状杆菌和人型葡萄球菌中占主导地位。结论。腋窝皮肤微生物性病变以棒状杆菌和葡萄球菌为主的微生物群为主,占82.6%。
{"title":"MICROBIOCENOSIS OF SKIN IN BROMHIDROSIS PATIENTS","authors":"Aleshkin Av, O. Borisova, Gadua Nt, S. Bochkareva, V. A. Chernova, Trebunskikh Ip, B. A. Efimov, L. Kafarskaya, S. Afanasiev, Aleshkin Va, M. Afanasiev, A. Borisova, A. Karaulov","doi":"10.36233/0372-9311-2017-5-53-58","DOIUrl":"https://doi.org/10.36233/0372-9311-2017-5-53-58","url":null,"abstract":"Aim. Evaluate the composition of microorganisms of skin microbiocenosis of axilla in brom-hidrosis patients. Materials and methods. 23 patients were examined (11 - 17 years) under the observation at Pirogov CCDC of the National Medical-Surgery Centre. Identification was carried out using biochemical test-systems BioMerieux VITEK MS MALDI-TOF («bioMerieux», France) and 16SrRNA genesequencing with consequent juxtaposition with EMBL/NCBI. Medium and high degree of skin seeding with microbiota was present in most of the patients with bromhidrosis (52.2 and 43.5%). 137 strains belonging to 5 genera of microorganisms were identified - Corynebacterium, Staphylococcus, Moraxella, Micrococcus, Candida and Bacillus spp. Coiynehacte-rium genus strains (8 species) and Staphylococcus genus (5 species) prevailed in microbiocenosis (89.1%). C. tuberculostearicum strains dominated among Corynebacterium, and S. hominis - Staphylococcus. Conclusion. In most of the cases (82.6%) in patients microbiocenosis of skin of axilla was presented by consortiums of microorganisms with prevalence of Corynebacterium and Staphylococcus microorganisms.","PeriodicalId":24020,"journal":{"name":"Zhurnal mikrobiologii, epidemiologii, i immunobiologii","volume":"63 1","pages":"53-58"},"PeriodicalIF":0.0,"publicationDate":"2017-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88049264","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
BIOLOGICAL SAFETY OF MASS ACTIONS: TOPICAL ISSUES AND PRINCIPLES 大规模行动的生物安全:专题问题和原则
Q3 Medicine Pub Date : 2017-10-28 DOI: 10.36233/0372-9311-2017-5-10-17
D. V. Efremenko, O. Maletskaya, V. Orobey, V. Efremenko
Topical issues of ensuring biological safety of mass actions are considered in the article. According to the purpose and content are allocated two interdependent and supplementing each other within the system of supervision and monitoring of biological safety — the measures for prophylaxis of emergency situations and the measures for ensuring readiness for emergency situ­ ations. Actions of separate functional elements of system of rather accompanying epidemiological risks focused on their decrease and monitoring are analyzed. The attributive base is developed for the principles of ensuring biological safety (rationality, competence, efficiency, flexibility, control­ lability, preventiveness, coherence) which are considered as determinants of solvable tasks during the periods of preparation and holding mass actions.
文章考虑了确保大规模行动的生物安全的专题问题。根据目的和内容,在生物安全监督和监测系统内分配了两项相互依存和相辅相成的措施,即预防紧急情况的措施和确保对紧急情况做好准备的措施。分析了非伴生流行病学风险系统各功能要素在降低和监测流行病学风险方面的作用。属性基础是为确保生物安全的原则(合理性,能力,效率,灵活性,控制-不稳定性,预防性,一致性)而开发的,这些原则被认为是准备和举行大规模行动期间可解决任务的决定因素。
{"title":"BIOLOGICAL SAFETY OF MASS ACTIONS: TOPICAL ISSUES AND PRINCIPLES","authors":"D. V. Efremenko, O. Maletskaya, V. Orobey, V. Efremenko","doi":"10.36233/0372-9311-2017-5-10-17","DOIUrl":"https://doi.org/10.36233/0372-9311-2017-5-10-17","url":null,"abstract":"Topical issues of ensuring biological safety of mass actions are considered in the article. According to the purpose and content are allocated two interdependent and supplementing each other within the system of supervision and monitoring of biological safety — the measures for prophylaxis of emergency situations and the measures for ensuring readiness for emergency situ­ ations. Actions of separate functional elements of system of rather accompanying epidemiological risks focused on their decrease and monitoring are analyzed. The attributive base is developed for the principles of ensuring biological safety (rationality, competence, efficiency, flexibility, control­ lability, preventiveness, coherence) which are considered as determinants of solvable tasks during the periods of preparation and holding mass actions.","PeriodicalId":24020,"journal":{"name":"Zhurnal mikrobiologii, epidemiologii, i immunobiologii","volume":"194 1","pages":"10-17"},"PeriodicalIF":0.0,"publicationDate":"2017-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73278463","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
AN ACCELERATED METHOD OF DIPHTHERIA GENE DIAGNOSTICS BASED ON ISOTHERMAL AMPLIFICATION TO DETECT DNA OF THE CAUSATIVE AGENT 基于等温扩增检测白喉病原体DNA的白喉基因快速诊断方法
Q3 Medicine Pub Date : 2017-10-28 DOI: 10.36233/0372-9311-2017-5-24-32
O. Borisova, A. S. Pimenova, A. V. Chaplin, L. Kafarskaya, S. Afanasiev, Aleshkin Va, Aleshkin Av, M. Afanasiev, A. Karaulov
of C. from bacteriological the and sent to the of Epidemiology and Microbiology. Strain isolation was carried out in accordance with MI 4.2.698-98 and 4.2.3065-13. Chromosomal DNA was isolated by standard heating method, as well as using 3 commercial kits. Detection of the amplification results was carried out in horizontal electrophoresis in 1.5% agarose gel. Results. The developed method of gene diagnostics was established to allow detection of DNA of toxi­ genic C. diphtheriae strains of 2 biovars, as well as DNA of non-toxigenic tox-gene bearing strains (NTTB) of C. diphtheriae mitis biovar with mechanisms of lack of expression of diphtheria toxin gene due to the presence of deletion or mobile genetic IS element in the tox gene. Non-toxigenic tox-gene bearing C. diphtheriae strain with the mechanism of lack of diphtheria toxin gene expres­ sion due to the presence oftransposon in the tox gene are identified as non-toxigenic. Evaluation of the analytical sensitivity in comparative studies using 3 commercial kits for FNA isolation has shown that sensitivity reached 4.5x10' GE/ml using Ribo-prep kit. High specificity of the developed method is shown, it was evaluated in 18 strains of 16 other members of the Corynebacterium genus and 20 typical strains of microorganisms isolated from oropharynx or causing infections of the respiratory tract. Approbation of the developed method was carried out in model experiments in imitators of clinical samples by infection of single-use sterile dry tampons by consecutive dilutions of the bacterial cultures (with parallel seeding into dense nutrient media) and was 103 GE/ml. Conclusion. The developed method of accelerated gene diagnostics of the diphtheria infection has a high diagnostic effectiveness, specificity and sensitivity, allows to detect 103 — 4.5x10 GE/ml C. diphtheriae in clinical material with simultaneous verification of toxigenic and non-toxigenic strains. fused recombinant proteins of Pseudomonas that infection. P.
C.从细菌学的,并送到流行病学和微生物学。菌株分离按照MI 4.2.698-98和4.2.3065-13进行。染色体DNA采用标准加热法分离,并使用3个商用试剂盒分离。用1.5%琼脂糖凝胶水平电泳检测扩增结果。结果。本研究建立了一种基因诊断方法,用于检测2种生物变种白喉原毒菌株的DNA,以及由于毒素基因中存在缺失或移动的遗传IS元件而导致白喉原毒基因表达缺失的白喉原毒基因携带菌株(NTTB)的DNA。非产毒的含毒基因白喉支原菌被鉴定为非产毒菌株,其机制是由于毒素基因中存在转座子而导致白喉毒素基因缺乏表达。使用3种商用试剂盒对FNA分离的分析灵敏度进行比较研究,结果表明,使用Ribo-prep试剂盒的灵敏度达到4.5x10’GE/ml。结果表明,该方法具有很高的特异性,并对其他16种棒状杆菌属的18株菌株和20株从口咽分离或引起呼吸道感染的典型微生物进行了评估。通过连续稀释细菌培养物(平行播种到密集的营养培养基中)感染一次性无菌干卫生棉条,在临床样品仿制品的模型实验中对所开发的方法进行了验证,其浓度为103 GE/ml。结论。所建立的白喉感染加速基因诊断方法具有较高的诊断有效性、特异性和敏感性,可在临床材料中检测出103 ~ 4.5 × 10 GE/ml的白喉链球菌,同时对产毒株和非产毒株进行验证。感染假单胞菌的融合重组蛋白。P。
{"title":"AN ACCELERATED METHOD OF DIPHTHERIA GENE DIAGNOSTICS BASED ON ISOTHERMAL AMPLIFICATION TO DETECT DNA OF THE CAUSATIVE AGENT","authors":"O. Borisova, A. S. Pimenova, A. V. Chaplin, L. Kafarskaya, S. Afanasiev, Aleshkin Va, Aleshkin Av, M. Afanasiev, A. Karaulov","doi":"10.36233/0372-9311-2017-5-24-32","DOIUrl":"https://doi.org/10.36233/0372-9311-2017-5-24-32","url":null,"abstract":"of C. from bacteriological the and sent to the of Epidemiology and Microbiology. Strain isolation was carried out in accordance with MI 4.2.698-98 and 4.2.3065-13. Chromosomal DNA was isolated by standard heating method, as well as using 3 commercial kits. Detection of the amplification results was carried out in horizontal electrophoresis in 1.5% agarose gel. Results. The developed method of gene diagnostics was established to allow detection of DNA of toxi­ genic C. diphtheriae strains of 2 biovars, as well as DNA of non-toxigenic tox-gene bearing strains (NTTB) of C. diphtheriae mitis biovar with mechanisms of lack of expression of diphtheria toxin gene due to the presence of deletion or mobile genetic IS element in the tox gene. Non-toxigenic tox-gene bearing C. diphtheriae strain with the mechanism of lack of diphtheria toxin gene expres­ sion due to the presence oftransposon in the tox gene are identified as non-toxigenic. Evaluation of the analytical sensitivity in comparative studies using 3 commercial kits for FNA isolation has shown that sensitivity reached 4.5x10' GE/ml using Ribo-prep kit. High specificity of the developed method is shown, it was evaluated in 18 strains of 16 other members of the Corynebacterium genus and 20 typical strains of microorganisms isolated from oropharynx or causing infections of the respiratory tract. Approbation of the developed method was carried out in model experiments in imitators of clinical samples by infection of single-use sterile dry tampons by consecutive dilutions of the bacterial cultures (with parallel seeding into dense nutrient media) and was 103 GE/ml. Conclusion. The developed method of accelerated gene diagnostics of the diphtheria infection has a high diagnostic effectiveness, specificity and sensitivity, allows to detect 103 — 4.5x10 GE/ml C. diphtheriae in clinical material with simultaneous verification of toxigenic and non-toxigenic strains. fused recombinant proteins of Pseudomonas that infection. P.","PeriodicalId":24020,"journal":{"name":"Zhurnal mikrobiologii, epidemiologii, i immunobiologii","volume":"98 1","pages":"24-32"},"PeriodicalIF":0.0,"publicationDate":"2017-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82665891","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
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