<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">sibmed</journal-id><journal-title-group><journal-title xml:lang="ru">Сибирский научный медицинский журнал</journal-title><trans-title-group xml:lang="en"><trans-title>Сибирский научный медицинский журнал</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2410-2512</issn><issn pub-type="epub">2410-2520</issn><publisher><publisher-name>ИЦиГ СО РАН</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18699/SSMJ20250209</article-id><article-id custom-type="elpub" pub-id-type="custom">sibmed-2078</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>МЕДИКО-БИОЛОГИЧЕСКИЕ НАУКИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>BIOMEDICINE</subject></subj-group></article-categories><title-group><article-title>Влияние микробиологических особенностей инфекций, вызванных Klebsiella pneumoniae, на антибиотикорезистентность и тяжесть инфекционного процесса</article-title><trans-title-group xml:lang="en"><trans-title>Influence of microbiological characteristics of infections caused by Klebsiella pneumoniae on antibiotic resistance and severity of the infection process</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6753-2074</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Земко</surname><given-names>В. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Zemko</surname><given-names>V. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p> Земко Виктория Юрьевна, к.м.н.</p><p> Республика Беларусь, 210009, г. Витебск, пр. Фрунзе, 27 </p></bio><bio xml:lang="en"><p> Viktoryia Yu. Zemko, candidate of medical sciences </p><p> Republic of Belarus, 210009, Vitebsk, Frunze ave., 27 </p></bio><email xlink:type="simple">viktoryiazia@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8226-6405</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Окулич</surname><given-names>В. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Okulich</surname><given-names>V. K.</given-names></name></name-alternatives><bio xml:lang="ru"><p> Окулич Виталий Константинович, к.м.н. </p><p> Республика Беларусь, 210009, г. Витебск, пр. Фрунзе, 27 </p></bio><bio xml:lang="en"><p> Vitaly K. Okulich, candidate of medical sciences </p><p> Republic of Belarus, 210009, Vitebsk, Frunze ave., 27 </p></bio><email xlink:type="simple">vokul@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Витебский государственный ордена Дружбы народов медицинский университет</institution><country>Беларусь</country></aff><aff xml:lang="en"><institution>Vitebsk State Order of Peoples’ Friendship Medical University</institution><country>Belarus</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>06</day><month>05</month><year>2025</year></pub-date><volume>45</volume><issue>2</issue><fpage>88</fpage><lpage>93</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Земко В.Ю., Окулич В.К., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Земко В.Ю., Окулич В.К.</copyright-holder><copyright-holder xml:lang="en">Zemko V.Y., Okulich V.K.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://sibmed.elpub.ru/jour/article/view/2078">https://sibmed.elpub.ru/jour/article/view/2078</self-uri><abstract><p>Цель исследования ‒ изучить влияние микробиологических особенностей инфекций, вызванных Klebsiella pneumonia, на формирование антибиотикорезистентности и тяжесть инфекционного процесса.Материал и методы. Проведен сравнительный анализ массы биопленки, толщины капсулы K. pneumonia, выделенной у 26 пациентов с сепсисом и у 8 больных хронической обструктивной болезнью легких. Исследовано влияние толщины капсулы на тяжесть инфекционного процесса и антибиотикорезистентность.Результаты и их обсуждение. Масса биопленки K. pneumoniae, выделенной у пациентов с сепсисом, составила 28,2 [16,5; 41,3] мкг/лунку (медиана [нижний квартиль; верхний квартиль]), отличалась устойчивостью к большинству используемых антибактериальных лекарственных средств и была больше массы биопленки, выделенной при хронической обструктивной болезни легких (24,3 [20,0; 28,2] мкг/лунку, p = 0,04), сохранявшей чувствительность к используемым препаратам. Проведена идентификация капсулы бактерий K. pneumoniae как видового признака или свойства патогенности по разработанному методу с использованием альцианового синего. Панрезистентные изоляты K. Pneumoniae имели наиболее толстую капсулу (0,44 [0,32; 0,53] мкм), карбапенемрезистентные изоляты, чувствительные к колистину и тигециклину, – более тонкую капсулу (0,38 [0,35; 0,41] мкм). Толщина капсулы клебсиеллы, сохранившей чувствительность к карбапенемам, была в 4 и 3,5 раза тоньше капсулы панрезистентных (p = 0,031) и карбапенемрезистентных, но чувствительных к колистину и тигециклину изолятов (p = 0,044) соответственно, и составила 0,11 [0,08; 0,16 мкм]. Выявлена положительная корреляция между толщиной бактериальной капсулы, массой микробной биопленки и общей длительностью пребывания в стационаре. Заключение. Патогенность бактерий и тяжесть заболевания объясняется толщиной капсулы K. pneumoniae, которая вносит определенный вклад в формирование антибиотикорезистентности микроорганизмов.</p></abstract><trans-abstract xml:lang="en"><p>The aim of the study was to investigate influence of microbiological characteristics of infections caused by Klebsiella pneumonia on formation of antibiotic resistance and severity of infectious process.Material and methods. A comparative analysis of biofilm mass, thickness of capsule of K. pneumonia isolated from 26 patients with sepsis and from 8 patients with chronic obstructive pulmonary disease was carried out. The influence of capsule thickness on severity of infectious process and antibiotic resistance was studied.Results and discussion. The mass of K. pneumoniae biofilm isolated from patients with sepsis was 28.2 [16.5; 41.3] μg/well (median [lower quartile; upper quartile]), exhibited resistance to most of the antibacterial drugs used, and was greater than the biofilm mass isolated from patients with chronic obstructive pulmonary disease (24.3 [20.0; 28.2] μg/well, p = 0.04), which remained susceptible to the drugs used. K. pneumoniae bacterial capsule was identified as a species characteristic or pathogenicity property using developed method with alcian blue. Panresistant K. pneumoniae isolates had the thickest capsule (0,44 [0,32; 0,53] μm), carbapenem-resistant isolates sensitive to colistin and tigecycline had thinner capsule (0.38; 0.35–0.41 μm). Thickness of capsule of Klebsiella that retained sensitivity to carbapenems was 4 and 3.5 times thinner than thickness of panresistant (p = 0,031) and carbapenem-resistant isolates sensitive to colistin and tigecycline isolates (p = 0,044), respectively and was 0,11 [0,08; 0,16 мкм]. A positive correlation was revealed between thickness of capsule, mass of microbial biofilm and length of hospital stay.Conclusions. The pathogenicity of bacteria and severity of disease are explained by thickness of K. pneumoniae capsule that makes a certain contribution to formation of antibiotic resistance in microorganisms.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>капсула бактерий</kwd><kwd>Klebsiella pneumonia</kwd><kwd>антибиотикорезистентность</kwd></kwd-group><kwd-group xml:lang="en"><kwd>bacteria capsule</kwd><kwd>Klebsiella pneumonia</kwd><kwd>antibiotic resistance</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена в рамках темы НИР «Разработка нового метода диагностики и интенсивной терапии сепсиса» (№ ГР20190090 от 05.02.2019).</funding-statement><funding-statement xml:lang="en">The work was performed as a part of the research topic «Development of a new method for diagnosing and intensive care of sepsis» (state registration No 20190090 from 02.05.2019)</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Voora S., Adey D.B. Management of Kidney transplant recipients by general nephrologists: core curriculum 2019. Am. J. Kidney Dis. 2019;73(6):866–879. doi: 10.1053/j.ajkd.2019.01.031</mixed-citation><mixed-citation xml:lang="en">Voora S., Adey D.B. Management of Kidney transplant recipients by general nephrologists: core curriculum 2019. Am. J. Kidney Dis. 2019;73(6):866–879. doi: 10.1053/j.ajkd.2019.01.031</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Koo H., Allan R.N., Howlin R.P., Stoodley P., Hall-Stoodley L. Targeting microbial biofilms: current and prospective therapeutic strategies. Nat. Rev. Microbiol. 2017;15(12):740–755. doi: 10.1038/nrmicro.2017.99</mixed-citation><mixed-citation xml:lang="en">Koo H., Allan R.N., Howlin R.P., Stoodley P., Hall-Stoodley L. Targeting microbial biofilms: current and prospective therapeutic strategies. Nat. Rev. Microbiol. 2017;15(12):740–755. doi: 10.1038/nrmicro.2017.99</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Pinto R.M., Soares F.A., Reis S., Nunes C., van Dijck P. Innovative strategies toward the disassembly of the EPS matrix in bacterial biofilms. Front. Microbiol. 2020;11:952. doi: 10.3389/fmicb.2020.00952</mixed-citation><mixed-citation xml:lang="en">Pinto R.M., Soares F.A., Reis S., Nunes C., van Dijck P. Innovative strategies toward the disassembly of the EPS matrix in bacterial biofilms. Front. Microbiol. 2020;11:952. doi: 10.3389/fmicb.2020.00952</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Navon-Venezia S., Kondratyeva K., Carattoli A. Klebsiella pneumoniae: a major worldwide source and shuttle for antibiotic resistance. FEMS Microbiol. Rev. 2017;41(3):252–275. doi: 10.1093/femsre/fux013</mixed-citation><mixed-citation xml:lang="en">Navon-Venezia S., Kondratyeva K., Carattoli A. Klebsiella pneumoniae: a major worldwide source and shuttle for antibiotic resistance. FEMS Microbiol. Rev. 2017;41(3):252–275. doi: 10.1093/femsre/fux013</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Verderosa A.D., Totsika M., FairfullSmith K.E. Bacterial biofilm eradication agents: a current review. Front. Chem. 2019;7:824. doi: 10.3389/fchem.2019.00824</mixed-citation><mixed-citation xml:lang="en">Verderosa A.D., Totsika M., FairfullSmith K.E. Bacterial biofilm eradication agents: a current review. Front. Chem. 2019;7:824. doi: 10.3389/fchem.2019.00824</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Khatoon Z., McTiernan C.D., Suuronen E.J., Mah T.F., Alarcon E.I. Bacterial biofilm formation on implantable devices and approaches to its treatment and prevention. Heliyon. 2018;4(12):e01067. doi: 10.1016/j.heliyon.2018.e01067</mixed-citation><mixed-citation xml:lang="en">Khatoon Z., McTiernan C.D., Suuronen E.J., Mah T.F., Alarcon E.I. Bacterial biofilm formation on implantable devices and approaches to its treatment and prevention. Heliyon. 2018;4(12):e01067. doi: 10.1016/j.heliyon.2018.e01067</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Satpathy S., Sen S.K., Pattanaik S., Raut S. Review on bacterial biofilm: an universal cause of contamination. Biocatal. Agric. Biotechnol. 2016;7:56–66. doi: 10.1016/j.bcab.2016.05.002</mixed-citation><mixed-citation xml:lang="en">Satpathy S., Sen S.K., Pattanaik S., Raut S. Review on bacterial biofilm: an universal cause of contamination. Biocatal. Agric. Biotechnol. 2016;7:56–66. doi: 10.1016/j.bcab.2016.05.002</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Lajhar S.A., Brownlie J., Barlow R. Characterization of biofilm-forming capacity and resistance to sanitizers of a range of E. coli O26 pathotypes from clinical cases and cattle in Australia. BMC Microbiol. 2018;18(1):41. doi: 10.1186/s12866-018-1182-z</mixed-citation><mixed-citation xml:lang="en">Lajhar S.A., Brownlie J., Barlow R. Characterization of biofilm-forming capacity and resistance to sanitizers of a range of E. coli O26 pathotypes from clinical cases and cattle in Australia. BMC Microbiol. 2018;18(1):41. doi: 10.1186/s12866-018-1182-z</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Rabin N., Zheng Y., Opoku-Temeng C., Du Y., Bonsu E., Sintim H.O. Biofilm formation mechanisms and targets for developing antibiofilm agents. Future Med. Chem. 2015;7(4):493–512. doi: 10.4155/fmc.15.6</mixed-citation><mixed-citation xml:lang="en">Rabin N., Zheng Y., Opoku-Temeng C., Du Y., Bonsu E., Sintim H.O. Biofilm formation mechanisms and targets for developing antibiofilm agents. Future Med. Chem. 2015;7(4):493–512. doi: 10.4155/fmc.15.6</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Russo T.A., Marr C.M. Hypervirulent Klebsiella pneumoniae. Clin. Microbiol. Rev. 2019;32(3):e00001-19. doi: 10.1128/CMR.00001-19</mixed-citation><mixed-citation xml:lang="en">Russo T.A., Marr C.M. Hypervirulent Klebsiella pneumoniae. Clin. Microbiol. Rev. 2019;32(3):e00001-19. doi: 10.1128/CMR.00001-19</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Gharrah M.M., El-Mahdy A.M., Barwa R.F. Association between virulence factors and extended spectrum beta-lactamase producing Klebsiella pneumoniae compared to nonproducing isolates. Interdiscip. Perspect. Infect. Dis. 2017:2017:7279830. doi: 10.1155/2017/7279830</mixed-citation><mixed-citation xml:lang="en">Gharrah M.M., El-Mahdy A.M., Barwa R.F. Association between virulence factors and extended spectrum beta-lactamase producing Klebsiella pneumoniae compared to nonproducing isolates. Interdiscip. Perspect. Infect. Dis. 2017:2017:7279830. doi: 10.1155/2017/7279830</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Follador R., Heinz E., Wyres K.L., Ellington M.J., Kowarik M., Holt K.E., Thomson N.R. The diversity of Klebsiella pneumoniae surface polysaccharides. Microb. Genom. 2016;2(8):e000073. doi: 10.1099/mgen.0.000073</mixed-citation><mixed-citation xml:lang="en">Follador R., Heinz E., Wyres K.L., Ellington M.J., Kowarik M., Holt K.E., Thomson N.R. The diversity of Klebsiella pneumoniae surface polysaccharides. Microb. Genom. 2016;2(8):e000073. doi: 10.1099/mgen.0.000073</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Paczosa M.K., Mecsas J. Klebsiella pneumoniae: going on the offense with a strong defense. Microbiol. Mol. Biol. Rev. 2016;80(3):629–661. doi: 10.1128/MMBR.00078-15</mixed-citation><mixed-citation xml:lang="en">Paczosa M.K., Mecsas J. Klebsiella pneumoniae: going on the offense with a strong defense. Microbiol. Mol. Biol. Rev. 2016;80(3):629–661. doi: 10.1128/MMBR.00078-15</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Sharma D., Misba L., Khan A.U. Antibiotics versus biofilm: an emerging battleground in microbial communities. Antimicrob. Resist. Infect. Control. 2019;8:76. doi: 10.1186/s13756-019-0533-3</mixed-citation><mixed-citation xml:lang="en">Sharma D., Misba L., Khan A.U. Antibiotics versus biofilm: an emerging battleground in microbial communities. Antimicrob. Resist. Infect. Control. 2019;8:76. doi: 10.1186/s13756-019-0533-3</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Celec P., Vlkova B., Laukova L., Babickova J., Boor P. Cell-free DNA: the role in pathophysiology and as a biomarker in kidney diseases. Expert. Rev. Mol. Med. 2018;20:e1. doi: 10.1017/erm.2017.12</mixed-citation><mixed-citation xml:lang="en">Celec P., Vlkova B., Laukova L., Babickova J., Boor P. Cell-free DNA: the role in pathophysiology and as a biomarker in kidney diseases. Expert. Rev. Mol. Med. 2018;20:e1. doi: 10.1017/erm.2017.12</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Selasi G.N., Nicholas A., Jeon H., Na S.H., Kwon H.I., Kim Y.J., Heo S.T., Oh M.H., Lee J.C. Differences in biofilm mass, expression of biofilm-associated genes, and resistance to desiccation between epidemic and sporadic clones of carbapenem-resistant acinetobacter baumannii sequence type 191. PLoS One. 2016;11(9):e0162576. doi: 10.1371/journal.pone.0162576</mixed-citation><mixed-citation xml:lang="en">Selasi G.N., Nicholas A., Jeon H., Na S.H., Kwon H.I., Kim Y.J., Heo S.T., Oh M.H., Lee J.C. Differences in biofilm mass, expression of biofilm-associated genes, and resistance to desiccation between epidemic and sporadic clones of carbapenem-resistant acinetobacter baumannii sequence type 191. PLoS One. 2016;11(9):e0162576. doi: 10.1371/journal.pone.0162576</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Земко В.Ю., Окулич В.К., Бонцевич С.В. Метод идентификации капсулы микроорганизмов с использованием альцианового синего: рац. предложение № 6 от 10.06.2022, утв. Витебским ГМУ.</mixed-citation><mixed-citation xml:lang="en">Zemko V.Yu., Okulich V.K., Bontsevich S.V. Method for identifying meeting capsules using Alcian blue: rationalization proposal No. 6 dated June 10, 2022, approved by Vitebsk State Medical University. [In Russian].</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">D’Angelo F., Rocha E.P.C., Rendueles O. The capsule increases susceptibility to last-resort polymyxins, but not to other antibiotics, in Klebsiella pneumoniae. Antimicrob. Agents Chemother. 2023;67(4):e00127–23. doi: 10.1128/aac.00127-23</mixed-citation><mixed-citation xml:lang="en">D’Angelo F., Rocha E.P.C., Rendueles O. The capsule increases susceptibility to last-resort polymyxins, but not to other antibiotics, in Klebsiella pneumoniae. Antimicrob. Agents Chemother. 2023;67(4):e00127–23. doi: 10.1128/aac.00127-23</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Ernst C.M., Braxton J.R., Rodriguez-Osorio C.A., Zagieboylo A.P., Li L., Pironti A., Manson A.L., Nair A.V., Benson M., Cummins K. … Hung D.T. Adaptive evolution of virulence and persistence in carbapenem-resistant Klebsiella pneumonia. Nat. Med. 2020;26(5):705–711. doi: 10.1038/s41591-020-0825-4</mixed-citation><mixed-citation xml:lang="en">Ernst C.M., Braxton J.R., Rodriguez-Osorio C.A., Zagieboylo A.P., Li L., Pironti A., Manson A.L., Nair A.V., Benson M., Cummins K. … Hung D.T. Adaptive evolution of virulence and persistence in carbapenem-resistant Klebsiella pneumonia. Nat. Med. 2020;26(5):705–711. doi: 10.1038/s41591-020-0825-4</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Chen T., Ying L., Xiong L., Wang X., Lu P., Wang Y., Shen P., Xiao Y. Understanding carbapenem-resistant hypervirulent Klebsiella pneumoniae: Key virulence factors and evolutionary convergence. hLife. 2024:12(2):611–624. doi: 10.1016/j.hlife.2024.06.005</mixed-citation><mixed-citation xml:lang="en">Chen T., Ying L., Xiong L., Wang X., Lu P., Wang Y., Shen P., Xiao Y. Understanding carbapenem-resistant hypervirulent Klebsiella pneumoniae: Key virulence factors and evolutionary convergence. hLife. 2024:12(2):611–624. doi: 10.1016/j.hlife.2024.06.005</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
