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  1. 1
    Academic Journal

    Source: IX Всероссийская Пущинская конференция «Биохимия, физиология и биосферная роль микроорганизмов».

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    Academic Journal

    Source: VII Пущинская конференция «Биохимия, физиология и биосферная роль микроорганизмов», шко- ла-конференция для молодых ученых, аспирантов и студентов «Генетические технологии в микробио- логии и микробное разнообразие».

  3. 3
    Academic Journal

    Source: VII Пущинская конференция «Биохимия, физиология и биосферная роль микроорганизмов», шко- ла-конференция для молодых ученых, аспирантов и студентов «Генетические технологии в микробио- логии и микробное разнообразие».

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    Academic Journal

    Contributors: The research was carried out partly within the state assignment of Ministry of Science and Higher Education of the Russian Federation (theme №1023031500033-11.6.7, 1.6.4, 1.6.8) and was partially funded by the Ministry of Science and Higher Education of the Russian Federation (Ural Federal University Program of Development within the Priority-2030 Program), Работа выполнена частично в рамках государственного задания Министерства науки и высшего образования Российской Федерации (тема №1023031500033-1-1.6.7, 1.6.8 «Функциональная и структурная организация сложных, мультикомпонентных биологических систем и их динамика») и частично при финансовой поддержке Министерства науки и высшего образования Российской Федерации в рамках Программы развития Уральского федерального университета имени первого Президента России Б.Н. Ельцина в соответствии с программой стратегического академического лидерства «Приоритет-2030»

    Source: Arctic and Antarctic Research; Том 70, № 4 (2024): Специальный выпуск Исследования подледникового озера Восток; 554-564 ; Проблемы Арктики и Антарктики; Том 70, № 4 (2024): Специальный выпуск Исследования подледникового озера Восток; 554-564 ; 2618-6713 ; 0555-2648

    File Description: application/pdf

    Relation: https://www.aaresearch.science/jour/article/view/671/310; Bulat S., Petit J.R. Vostok, Subglacial Lake. In: Gargaud M. (ed.) Encyclopedia of Astrobiology. Berlin, Heidelberg: Springer; 2023. P. 3206–3212. https://doi.org/10.1007/978-3-662-65093-6_1765; Siegert M.J. Lakes beneath the ice sheet: the occurrence, analysis, and future exploration of Lake Vostok and other Antarctic Subglacial Lakes. Annual Review of Earth and Planetary Sciences. 2005;33:215–245. https://doi.org/10.1146/annurev.earth.33.092203.122725; Kotlyakov V.M., Krenev V.A. Who discovered the Lake Vostok? Led i Sneg = Ice and Snow. 2016;56(3):427–432. (In Russ). https://doi.org/10.15356/2076-6734-2016-3-427-432; Kapitsa A.P., Ridley J.K., Robin G. de Q., Siegert M.J., Zotikov I.A. A large deep freshwater lake beneath the ice of central East Antarctica. Nature. 1996;381:684–686. https://doi.org/10.1038/381684a0; Priscu J.C., Adams E.E., Lyons W.B., Voytek M.A., Mogk D.W., Brown R.L., McKay C.P., Takacs C.D., Welch K.A., Wolf C.F., Kirshtein J.D., Avci R. Geomicrobiology of subglacial ice above Lake Vostok, Antarctica. Science. 1999;286:2141–2144. https://doi.org/10.1126/science.286.5447.2141; Karl D.M., Bird D.F., Bjorkman K., Houlihan T., Shakelford R., Tupas L. Microorganisms in the accreted ice of Lake Vostok. Science. 1999;286:2144–2147. https://doi.org/10.1126/science.286.5447.2144; D’Elia T., Veerapaneni R., Rogers S.O. Isolation of microbes from Lake Vostok accretion ice. Applied Environmental Microbiology. 2008;74:4962–4965. https://doi.org/10.1128/AEM.02501-07; Shtarkman Y.M., Koçer Z.A., Edgar R., Veerapaneni R.S., Morris P.F., Rogers S.O. Subglacial Lake Vostok (Antarctica) accretion ice contains a diverse set of sequences from aquatic, marine and sediment-inhabiting bacteria and eukarya. PLOS ONE. 2013;8(7):e67221. https://doi.org/10.1371/journal.pone.0067221; Rogers S.O., Shtarkman Yu.M., Koçer Z.A., Edgar R., Veerapaneni R., D’Elia T. Ecology of subglacial Lake Vostok (Antarctica), based on metagenomic/metatranscriptomic analyses of accretion ice. Biology. 2013;2:629–650. https://doi.org/10.3390/biology2020629; Epova E.Y., Shevelev A.B., Akbayev R.M., Biryukova Y.K., Zylkova M.V., Bogdanova E.S., Guseva M.A., Tynio Y.Y., Egorov V.V. Heterotrophic microbiota from the oligotrophic waters of Lake Vostok, Antarctica. International Journal of Environmental Research and Public Health. 2022;19:4025. https://doi.org/10.3390/ijerph19074025; Bulat S.A. Microbiology of the subglacial Lake Vostok: first results of borehole-frozen lake water analysis and prospects for searching lake inhabitants. Philosophical Transactions of the Royal Society A . 2016;374:20140292. https://doi.org/10.1098/rsta.2014.0292; Bulat S. SubglacialAntarctic Lake Vostok vs. subglacial South Pole Martian Lake and hypersaline Canadian Arctic Lakes — prospects for life. In: Proceeding of the JpGU Meeting 2019, Makuhari Messe, Chiba, Japan. 2019;PPS04-12. https://confit.atlas.jp/guide/event-img/jpgu2019/PPS04-12/public/pdf?type=in; Lukin V.V., Vasiliev N.I. Technological aspects of the final phase of drilling borehole 5G and unsealing Vostok subglacial lake, East Antarctica. Annals of Glaciology. 2014;55(65):83–89. https://doi.org/10.3189/2014AoG65A002; Ciuffreda L., Rodríguez-Pérez H., Flores C. Nanopore sequencing and its application to the study of microbial communities. Computational Structural Biotech Journal. 2021;19:1497–1511. https://doi.org/10.1016/j.csbj.2021.02.020; National Academies of Sciences, Engineering, and Medicine. Technology developments to advance Antarctic research: Proceedings of a workshop. Washington, DC: The National Academies Press; 2022. https://doi.org/10.17226/26699; Bulat S.A., Alekhina I.A., Blot M., Petit J.-R., de Angelis M., Wagenbach D., Lipenkov V.Ya., Vasilyeva L.P., Wloch D.M., Raynaud D., Lukin V.V. DNA signature of thermophilic bacteria from the aged accretion ice of Lake Vostok, Antarctica: implications for searching for life in extreme icy environments. International Journal of Astrobiology. 2004;3(1):1–12. https://doi.org/10.1017/S1473550404001879; Merkel A.Y., Pimenov N.V., Rusanov I.I., Slobodkin A.I., Slobodkina G.B., Tarnovetckii I.Yu., Frolov E.N., Dubin A.V., Perevalova A.A., Bonch-Osmolovskaya E.A. Microbial diversity and autotrophic activity in Kamchatka hot springs. Extremophiles. 2017;21:307–317. https://doi.org/10.1007/s00792-016-0903-1; Sriaroon P., Elizalde A., Perez E.E., Leiding J.W., Aldrovandi G.M., Sleasman J.W. Psychrobacter immobilis septicemia in a boy with X-linked chronic granulomatous disease and fulminant hepatic failure. J. Clin. Immunol. 2014;34(1):39–41. https://doi.org/10.1007/s10875-013-9961-7; Gomes da Rocha I.M., Torrinhas R., Fonseca D., de Oliveira Lyra C., de Sousa J.L., Neri A., Balmant B.D., Callado L., Charlton K., Queiroz N., Waitzberg D.L. Pro-inflammatory diet Is correlated with high Veillonella rogosae, gut inflammation and clinical relapse of inflammatory bowel disease. Nutrients. 2023;15(19):4148. https://doi.org/10.3390/nu15194148; Bulat S., Doronin M., Sumbatyan D. The uppermost water horizon of the subglacial Antarctic Lake Vostok is microbial DNA-free as proven by Oxford Nanopore sequencing technology. In: Full Abstract Book. Antarctica in a changing World. SCAR Open Science Conference 2022, 1–10 August, 2022; Hyderabad, India. 2022; P. 612.; Lipenkov V.Y., Ekaykin A.A., Polyakova E.V., Raynaud D. Characterization of subglacial Lake Vostok as seen from physical and isotope properties of accreted ice. Philosophical Transactions of the Royal Society A 2016;374:20140303. https://doi.org/10.1098/rsta.2014.0303; Chopra A., Lineweaver C.H. The case for a Gaian Bottleneck: The biology of habitability. Astrobiology. 2016;16:7–22. https://doi.org/10.1089/ast.2015.1387; https://www.aaresearch.science/jour/article/view/671

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    Conference

    Relation: Экология и безопасность в техносфере: современные проблемы и пути решения : сборник трудов Всероссийской научно-практической конференции молодых ученых, аспирантов и студентов, г. Юрга, 23-25 ноября 2017 г. — Томск, 2017.; http://earchive.tpu.ru/handle/11683/46649

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    Academic Journal

    Source: Agricultural Science Euro-North-East; № 3 (2018); 13-21 ; Аграрная наука Евро-Северо-Востока; № 3 (2018); 13-21 ; 2500-1396 ; 2072-9081

    File Description: application/pdf

    Relation: https://www.agronauka-sv.ru/jour/article/view/215/215; Kong К-F., Schneper L., Mathee K. Beta-lactam Antibiotics: From Antibiosis to Resistance and Bacteriology // APMIS: actapathologica, microbiologica, etimmunologica Scandinavica. 2010. 118 V. 1. R 1-36. DOI:10.1111/j. 1600-0463.2009.02563.x.; King D.T., Sobhanifar S., Strynadka N.C.J. One ring to rule them all: Current trends in combating bacterial resistance to the beta-lactams // Protein Science. 2016. V. 25, № 4. P. 787-803. DOI:10.1002/pro.2889.; Roca I., Akova M., Baquero F., et al. The global threat of antimicrobial resistance: science for intervention // New Microbes and New Infections. 2015. №. 6. P. 22-29. DOI:10.1016/j.nmni.2015.02.007.; Nikaido H. Multidrug Resistance in Bacteria // Annual review of biochemistry. 2009. № 78. P 119-146. DOI: 10 1146/annnrevbiochem 78.082907.145923; Dyar O.J., Huttner B., Schouten J., Pulcini C. Antimicrobi EESG: What is antimicrobial stewardship? // Clinical Microbiology and Infection. 2017. V. 23(11). P. 793-798. DOI:10.1016/j.cmi.2017.08.026.; Karam G.,Chastre J.,Wilcox M.H., Vincent J.L. Antibiotic strategies in the era of multidrug resistance // Critical Care. 2016. № 20. 9 p. DOI:10.1186/s13054-016-1320-7).; Панин A.H., Комаров A.A., Куликовский A.B., Макаров Д.А. Проблема резистентности к антибиотикам возбудителей болезней, общих для человека и животных // Ветеринария, зоотехния и биотехнология. 2017. № 5. С. 18-24.; Leisner J.J., Jorgensen N.O.G., Middelboe М. Predation and selection for antibiotic resistance in natural environments. // Evolutionary Applications. 2016. V. 9. № 3. P. 427-434. DOI:10.1111/eva.l2353.; Nikolaidis I., Favini-Stabile S., Dessen A. Resistance to antibiotics targeted to the bacterial cell wall. // Protein Science: A Publication of the Protein Society. 2014. V. 23. № 3. P. 243-259. DOI:10.1002/pro.2414.; Nikaido H., Pages J-M. Broad Specificity Efflux pumps and Their Role in Multidrug Resistance of Gram Negative Bacteria // FEMS microbiology reviews. 2012. V. 36. № 2. P. 340-363. DOI:10.1111/j.l574-6976.2011.00290.x.; Hollenbeck B.L., Rice L.B. Intrinsic and acquired resistance mechanisms in enterococcus // Virulence. 2012. V. 3. № 5. P. 421-569. DOI: 10.416l/viru.21282).; Hughes D., Andersson D.I. Environmental and genetic modulation of the phenotypic expression of antibiotic resistance // FEMS Microbiology Reviews. 2017. V. 41. № 3. P. 374-391. DOI:10.1093/femsre/fux004).; Munita J.M., Arias C.A. Mechanisms of Antibiotic Resistance // Microbiology Spectrum. 2016. V. 4. № 2. 24 p. DOI:10.1128/microbiolspec.VMBF-0016-2015).; Culyba M. J., Mo C.Y., Kohli R.M. Targets for Combating the Evolution of Acquired Antibiotic Resistance // Biochemistry. 2015. V. 54. № 23. P. 3573-3582 DOI:10.1021/acs.biochem.5b00109).; Cooper R.M., Tsimring L., Hasty J. Inter-species population dynamics enhance microbial horizontal gene transfer and spread of antibiotic resistance // Elife. 2017. № 6. DOI:10.7554/eLife.25950.; Van Hoek A., Mevius D., Guerra В., Mullany P, Roberts A.P., Aarts H.J.M. Acquired antibiotic resistance genes: an overview // Frontiers in Microbiology. 2011. № 2. 27 p. DOI:10.3389/fmicb.2011.00203.; Beceiro A., Tomas M., Bou G. Antimicrobial Resistance and Virulence: a Successful or Deleterious Association in the Bacterial World? // Clinical Microbiology Reviews. 2013. V. 26. № 2. P 185-230. DOI:10.1128/cmr.00059-12.; Miller W.R., Munita J.M., Arias C.A. Mechanisms of antibiotic resistance in enterococci // Expert review of anti-infective therapy. 2014. V. 12. № 10. P. 1221-1236. DOI:10.1586/14787210.2014.956092.; Ghai I., Ghai S. Exploring bacterial outer membrane barrier to combat bad bugs // Infection and Drug Resistance. 2017. № 10. R 261-273. DOI:10.2147/idr.sl44299.; Hawkey PM. The origins and molecular basis of antibiotic resistance // British Medical Journal. 1998. V. 317(7159). P. 657-660. DOI:10.1136/bmj.317.7159.657.; Шкурат M.A., Покудина И.О., Баталов Д.В. Резистентность микроорганизмов к атимикробным препаратам // Живые и биокосные системы: электронный журнал. 2014. № 10. URL: http://jbks.ru/archive/issue-10/article-10. (Дата обращения: 26.04.2018).; Schroeder M., Brooks B.D., Brooks A.E. The Complex Relationship between Virulence and Antibiotic Resistance // Genes. 2017. V. 8.№ 1. 23 p. DOI:10.3390/genes8010039.; Tran T.T., Munita J.M., Arias C.A. Mechanisms of Drug Resistance: Daptomycin Resistance // Annals of the New York Academy of Sciences. 2015. V. 1354. P. 32-53. DOI:10.1111/nyas.12948.; Tran T.T., Miller W.R., Shamoo Y., Arias C.A. Targeting cell membrane adaptation as a novel antimicrobial strategy // Current Opinion in Microbiology. 2016. № 33. P. 91-96. DOI:10.1016/j.mib.2016.07.002.; Bush K., Jacoby G.A. Updated Functional Classification of beta-Lactamases // Antimicrobial Agents and Chemotherapy. 2010. V. 54. № 3. P 969-976. DOI:10.1128/aac.01009-09.; Bush K., Jacoby G. A., Medeiros A.A. A functional classification scheme for beta-lactamases and for its correlation with molecular-structure // Antimicrobial Agents and Chemotherapy. 1995. V. 39. № 6. P 12111233. DOI:10.1128/AAC.39.6.1211.; Verraes C., Van Boxstael S., Van Meervenne E., et al. Antimicrobial Resistance in the Food Chain: A Review // International Journal of Environmental Research and Public Health. 2013. V. 10. № 7. P. 2643-2669. DOI:10.3390/ijerphl0072643.; Soto S.M. Role of efflux pumps in the antibiotic resistance of bacteria embedded in a biofilm // Virulence. 2013. V. 4. № 3. P. 223-229. DOI:10.4161/viru.23724.; Лазовская А.Л. Воробьёва З.Г., Слинина K.H., Биология микобактерий птичьего вида. Нижний Новгород, 2011. 47 с.; Vega N.M., Gore J. Collective antibiotic resistance: mechanisms and implications // Current Opinion in Microbiology. 2014. №. 21. P. 28-34. DOI:10.1016/j.mib.2014.09.003.; Маянский A.M. Патогенетическая микробиология: руководство. Нижний Новгород: Изд-во НижГМА, 2006. 520 с.; Титов Л.П., Вотяков В.И., Кожемякин А.К., Мосина Л.И. Эволюция микробов и её медицинское значение // Здравоохранение. 2002. №. 8. С. 30-35.; Kalia V.C., Wood Т.К., Kumar P. Evolution of resistance to quorum sensing inhibitors // Microbial ecology. 2014. V. 68. № 1. P. 13-23. DOI:10.1007/s00248-013-0316-y.; Baquero F., Lanza V.F., Canton R., Coque T.M. Public health evolutionary biology of antimicrobial resistance: priorities for intervention // Evolutionary Applications. 2015. V. 8. № 3. P. 223-239. DOI:10.1111/eva.12235.; Wang J., Ma Z-В., Zeng Z-L., Yang X-W., Huang Y., Liu J-H. The role of wildlife (wild birds) in the global transmission of antimicrobial resistance genes // Zoological Research. 2017. V. 38. № 2. P. 55-80. DOI:10.24272/j.issn.2095-8137.2017.003.; Potter R.F., D’Souza A.W., Dantas G. The rapid spread of carbapenem-resistant Enterobacteriaceae // Drug resistance updates: reviews and commentaries in antimicrobial and anticancer chemotherapy. 2016. № 29. P. 30-46. DOI:10.1016/j.drup.2016.09.002.; Pagano M., Martins A.F., Barth A.L. Mobile genetic elements related to carbapenem resistance in Acinetobacter baumannii // Brazilian Journal of Microbiology. 2016. № 47(4). P. 785-792. DOI:10.1016/j.bjm.2016.06.005).; Li H., Liu F., Zhang Y., et al. Evolution of Carbapenem-Resistant Acinetobacter baumannii Revealed through Whole-Genome Sequencing and Comparative Genomic Analysis // Antimicrobial Agents and Chemotherapy. 2015. V. 59. № 2. P. 1168-1176. DOI:10.1128/AAC.04609-14).; Cabot G., Zamorano L., Moyà В., et al. Evolution of Pseudomonas aeruginosa Antimicrobial Resistance and Fitness under Low and High Mutation Rates // Antimicrobial Agents and Chemotherapy. 2016. V. 60. № 3. P. 1767-1778. DOI:10.1128/AAC.02676-15).; Costa S.S., Viveiros M., Rosato A.E., Melo-Cristino J., Couto I. Impact of efflux in the development of multidmg resistance phenotypes in Staphylococcus aureus II BMC Microbiology. 2015. № 15. 232 p. DOI:10.1186/sl2866-015-0572-8.; Zaidi M.B., Estrada-Garcia T. Shigella: A Highly Virulent and Elusive Pathogen // Current tropical medicine reports. 2014. V. 1. № 2. P. 1-87. DOI:10.1007/S40475-014-0019-6.; Chang H-H., Cohen T., Grad Y.H., Han-age W.P., O’Brien T.F., Lipsitch M. Origin and Proliferation of Multiple-Drug Resistance in Bacterial Pathogens // Microbiology and Molecular Biology Reviews: MMBR. 2015. V. 79. № 1. P. 101-116. DOI:10.1128/MMBR.00039-14.; Nguyen L. Antibiotic resistance mechanisms in M. tuberculosis', an update // Archives of toxicology. 2016. V. 90. № 7. P. 1585-1604. DOI:10.1007/s00204-016-1727-6.; Al-Saeedi M., Al-Hajoj S. Diversity and evolution of drug resistance mechanisms in Mycobacterium tuberculosis II Infection and Drug Resistance. 2017. № 10. P. 333-342. DOI:10.2147/IDR.S144446.; Huyen M.N.T., Cobelens F.G.J., Buu T.N., Lan N.T.N., Dung N.H., Kremer K., Tiemersma E.W., van Soolingen D. Epidemiology of Isoniazid Resistance Mutations and Their Effect on Tuberculosis Treatment Outcomes // Antimicrobial Agents and Chemotherapy. 2013. V. 57. № 8. P. 3620-3627. DOI:10.1128/AAC.00077-13.; Васильева E.А., Анохина И.В., Далии M.B., Кравцов Э.Г., Васильев A.C., Яшина H.В., Слинина К.Н., Лискова Е.А. Значение спорового пробиотика Балис для комбинированной терапии туберкулёза с широкой лекарственной устойчивостью // Естественные и гуманитарные науки - устойчивому развитию общества: Межд. сб. науч трудов, посвящённый году Германии в России. М., 2013. С. 35-41.; Dheda K., Gumbo T., Gandhi N.R., Murray M., Theron G., Udwadia Z., Migliori G. B. Warren R. Global control of tuberculosis: from extensively drug-resistant to untreatable tuberculosis // The Lancet Respiratory medicine. 2014. № 2(4). P. 321-338. DOI:10.1016/S2213-2600(14)70031-1.

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    Conference

    Contributors: Рихванов, Леонид Петрович

    Relation: Творчество юных - шаг в успешное будущее : материалы VIII Всероссийской научной студенческой конференции с элементами научной школы имени профессора М.К. Коровина, г. Томск, 23-27 ноября 2015 г. — Томск, 2015.; http://earchive.tpu.ru/handle/11683/15821