<?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">urovest</journal-id><journal-title-group><journal-title xml:lang="ru">Вестник урологии</journal-title><trans-title-group xml:lang="en"><trans-title>Urology Herald</trans-title></trans-title-group></journal-title-group><issn pub-type="epub">2308-6424</issn><publisher><publisher-name>Rostov State Medical University</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21886/2308-6424-2023-11-3-118-130</article-id><article-id custom-type="elpub" pub-id-type="custom">urovest-762</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>ОБЗОРЫ ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS ARTICLE</subject></subj-group></article-categories><title-group><article-title>Микробиота / микробиом кожи полового члена у здоровых мужчин и при некоторых заболеваниях</article-title><trans-title-group xml:lang="en"><trans-title>Penile skin microbiota / microbiome in healthy men and some diseases</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4808-7024</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Набока</surname><given-names>Ю. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Naboka</surname><given-names>Yu. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Юлия Лазаревна Набока — д-р мед. наук, профессор; заведующая кафедрой микробиологии и вирусологии №1</p><p>Ростов-на-Дону</p></bio><bio xml:lang="en"><p>Yulia L. Naboka — M.D., Dr.Sc.(Med), Prof.; Head, Dept. of Microbiology and Virology No.1</p><p>Rostov-on-Don</p></bio><email xlink:type="simple">nagu22@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5595-8799</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Котиева</surname><given-names>Е. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Kotieva</surname><given-names>E. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Елизавета Михайловна Котиева — студентка</p><p>Ростов-на-Дону</p></bio><bio xml:lang="en"><p>Elizaveta M. Kotieva — Student</p><p>Rostov-on-Don</p></bio><email xlink:type="simple">elizaveta.kotieva@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1783-1073</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Котиева</surname><given-names>В. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Kotieva</surname><given-names>V. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Виолетта Михайловна Котиева — студентка</p><p>Ростов-на-Дону</p></bio><bio xml:lang="en"><p>Violetta M. Kotieva — Student</p><p>Rostov-on-Don</p></bio><email xlink:type="simple">kotieva.violetta@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1710-0169</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Коган</surname><given-names>М. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Kogan</surname><given-names>M. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Михаил Иосифович Коган — д-р мед. наук, профессор, заслуженный деятель науки РФ; заведующий кафедрой урологии и репродуктивного здоровья человека (с курсом детской урологии-андрологии)</p><p>Ростов-на-Дону</p></bio><bio xml:lang="en"><p>Mikhail I. Kogan — M.D., Dr.Sc.(Med), Full Prof., Honored Scientist of the Russian Federation; Head, Dept. of Urology, Pediatric Urology &amp; Reproductive Health</p><p>Rostov-on-Don</p></bio><email xlink:type="simple">dept_kogan@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Ростовский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Rostov State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>05</day><month>10</month><year>2023</year></pub-date><volume>11</volume><issue>3</issue><fpage>118</fpage><lpage>130</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Набока Ю.Л., Котиева Е.М., Котиева В.М., Коган М.И., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Набока Ю.Л., Котиева Е.М., Котиева В.М., Коган М.И.</copyright-holder><copyright-holder xml:lang="en">Naboka Y.L., Kotieva E.M., Kotieva V.M., Kogan M.I.</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://www.urovest.ru/jour/article/view/762">https://www.urovest.ru/jour/article/view/762</self-uri><abstract><p>Изучение микробиоты / микробиома кожных покровов мужских половых органов актуально не только для понимания дефиниции «нормы» для данного биотопа, но и для корректной интерпретации результатов, полученных от пациентов с инфекционно-воспалительными заболеваниями или послеоперационными инфекционно-воспалительными осложнениями кожи этой области. Целью исследования является обобщение и критический анализ данных по обсеменённости микроорганизмами различных участков кожи полового члена путём проведения систематического обзора публикаций. Поиск привёл к отбору 8 статей, опубликованных в период с 2011 года по первую половину 2023 года, которые посвящены исследованию особенностей микробиоты / микробиома кожи полового члена в норме и при некоторых заболеваниях. Так, у сексуально активных здоровых мужчин микробиота / микробиом кожи полового члена отчасти отражает вагинальный микробиом половых партнёров. После незащищённого полового контакта в микробиоте полового члена увеличивается частота обнаружения и количество Lactobacillus. В целом на коже полового члена доминируют Corynebacteriaceae, реже регистрируют Prevotellaceae, неклостридиальные (нк) Clostridiales, Porphyromonadaceae, Staphylococcaceae, Bifidobacteriaceae, Lactobacillaceae, Veillonellaceae, Anaerococcus. Существенное влияние на бактериальное разнообразие кожи полового члена оказывает обрезание. Несмотря на скудность данных по микробиоте / микробиому кожи полового члена при различных заболеваниях, были отмечены определённые взаимосвязи. Так, у сексуально активных здоровых мужчин-партнёров женщин с бактериальным вагинозом увеличивается число бактерий, ассоциированных с бактериальным вагинозом, и снижается — Corynebacterium. У ВИЧ-положительных мужчин на коже полового члена преобладают Staphylococcus, Faecalibacterium, Strenotrophominas, Jonquetella, Ruminococcus, Roseburia, Pseudochrobactrum и Lamia. Также отмечено, что обрезание снижает риск развития ВПЧ и ВИЧ-инфекций. Знание не только бактериального, но и грибкового разнообразия микробиоты кожи полового члена имеет важное клиническое значение, ведь условно-патогенные дрожжеподобные грибы при определённых условиях могут вызывать ряд заболеваний. Таким образом, данный обзор представляет собой анализ микробного состава кожи полового члена в норме и при некоторых заболеваниях, выявивший огромный пробел в имеющихся знаниях о сообществах микроорганизмов кожи полового члена. Необходимы исследования, которые помогут детальнее изучить её микробный состав в норме и его влияние на результаты реконструктивно-пластических операций с использованием кожи полового члена.</p></abstract><trans-abstract xml:lang="en"><p>The study of the cutaneous microbiota/microbiome of the male genital is relevant not only to understand "normality" for this biotope but also to correctly interpret the results obtained from patients with infectious-inflammatory diseases or postoperative infectious-inflammatory complications of penile skin. The study aimed to generalize and critically analyze data on microbial contamination of various areas of the penile skin by conducting a systematic review of publications. The search led to the selection of eight articles published in 2011 ­– 2023 that investigated the microbiota / microbiome features of the penile skin in health and some diseases. Thus, in sexually active healthy men, the penile skin microbiota / microbiome partly reflects the vaginal microbiome of sexual partners. After unprotected sexual contact, the frequency of detection and the number of Lactobacillus increase in the penile skin microbiota. In general, Corynebacteriaceae dominate on the penile skin, while Prevotellaceae, nc Clostridiales, Porphyromonadaceae, Staphylococcaceae, Bifidobacteriaceae, Lactobacillaceae, Veillonellaceae, Anaerococcus are less frequently recorded. Circumcision has a significant effect on the bacterial diversity of the penile skin. Although data regarding the penile skin microbiota/microbiome in various diseases are scarce, certain interactions have been noted. Thus, in healthy sexually active male partners of women with bacterial vaginosis, the number of bacteria associated with bacterial vaginosis increases and Corynebacterium decreases. In HIV-positive men, Staphylococcus, Faecalibacterium, Strenotrophominas, Jonquetella, Ruminococcus, Roseburia, Pseudochrobactrum and Lamia predominate on the penis skin. It is also noted that circumcision reduces the risk of HPV and HIV infections. Knowledge of not only the bacterial, but also fungal diversity of the penile skin microbiota is of great clinical importance, because conditionally pathogenic yeast-like fungi under certain conditions can cause a few diseases. Thus, this review analyses the microbial composition of penile skin in normal and some diseases, revealing a great gap in current knowledge of penile skin microbial assemblages. Studies are needed to better understand the microbial composition of normal penile skin and its impact on the results of reconstructive and plastic surgeries using penile skin.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>микробиота и микробиом полового члена</kwd><kwd>здоровые мужчины</kwd><kwd>заболевания кожи полового члена</kwd><kwd>бактериальный вагиноз</kwd><kwd>вирус иммунодефицита человека</kwd><kwd>баланопостит</kwd><kwd>вирус папилломы человека</kwd></kwd-group><kwd-group xml:lang="en"><kwd>microbiota</kwd><kwd>microbiome</kwd><kwd>penis</kwd><kwd>healthy men</kwd><kwd>penile skin diseases</kwd><kwd>bacterial vaginosis</kwd><kwd>balanoposthitis</kwd><kwd>human papillomavirus</kwd><kwd>human immunodeficiency virus</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Byrd AL, Belkaid Y, Segre JA. The human skin microbiome. Nat Rev Microbiol. 2018;16(3):143-155. DOI: 10.1038/nrmicro.2017.157</mixed-citation><mixed-citation xml:lang="en">Byrd AL, Belkaid Y, Segre JA. The human skin microbiome. Nat Rev Microbiol. 2018;16(3):143-155. DOI: 10.1038/nrmicro.2017.157</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Flowers L, Grice EA. The Skin Microbiota: Balancing Risk and Reward. Cell Host Microbe. 2020;28(2):190-200. DOI: 10.1016/j.chom.2020.06.017</mixed-citation><mixed-citation xml:lang="en">Flowers L, Grice EA. The Skin Microbiota: Balancing Risk and Reward. Cell Host Microbe. 2020;28(2):190-200. DOI: 10.1016/j.chom.2020.06.017</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Pistone D, Meroni G, Panelli S, D'Auria E, Acunzo M, Pasala AR, Zuccotti GV, Bandi C, Drago L. A Journey on the Skin Microbiome: Pitfalls and Opportunities. Int J Mol Sci. 2021;22(18):9846. DOI: 10.3390/ijms22189846</mixed-citation><mixed-citation xml:lang="en">Pistone D, Meroni G, Panelli S, D'Auria E, Acunzo M, Pasala AR, Zuccotti GV, Bandi C, Drago L. A Journey on the Skin Microbiome: Pitfalls and Opportunities. Int J Mol Sci. 2021;22(18):9846. DOI: 10.3390/ijms22189846</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Integrative HMP (iHMP) Research Network Consortium. The Integrative Human Microbiome Project. Nature. 2019;569(7758):641-648. DOI: 10.1038/s41586-019-1238-8</mixed-citation><mixed-citation xml:lang="en">Integrative HMP (iHMP) Research Network Consortium. The Integrative Human Microbiome Project. Nature. 2019;569(7758):641-648. DOI: 10.1038/s41586-019-1238-8</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Boxberger M, Cenizo V, Cassir N, La Scola B. Challenges in exploring and manipulating the human skin microbiome. Microbiome. 2021;9(1):125. DOI: 10.1186/s40168-021-01062-5</mixed-citation><mixed-citation xml:lang="en">Boxberger M, Cenizo V, Cassir N, La Scola B. Challenges in exploring and manipulating the human skin microbiome. Microbiome. 2021;9(1):125. DOI: 10.1186/s40168-021-01062-5</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Grice EA, Kong HH, Conlan S, Deming CB, Davis J, Young AC; NISC Comparative Sequencing Program; Bouffard GG, Blakesley RW, Murray PR, Green ED, Turner ML, Segre JA. Topographical and temporal diversity of the human skin microbiome. Science. 2009;324(5931):1190-2. DOI: 10.1126/science.1171700</mixed-citation><mixed-citation xml:lang="en">Grice EA, Kong HH, Conlan S, Deming CB, Davis J, Young AC; NISC Comparative Sequencing Program; Bouffard GG, Blakesley RW, Murray PR, Green ED, Turner ML, Segre JA. Topographical and temporal diversity of the human skin microbiome. Science. 2009;324(5931):1190-2. DOI: 10.1126/science.1171700</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Uberoi A, Bartow-McKenney C, Zheng Q, Flowers L, Campbell A, Knight SAB, Chan N, Wei M, Lovins V, Bugayev J, Horwinski J, Bradley C, Meyer J, Crumrine D, Sutter CH, Elias P, Mauldin E, Sutter TR, Grice EA. Commensal microbiota regulates skin barrier function and repair via signaling through the aryl hydrocarbon receptor. Cell Host Microbe. 2021;29(8):1235-1248.e8. DOI: 10.1016/j.chom.2021.05.011</mixed-citation><mixed-citation xml:lang="en">Uberoi A, Bartow-McKenney C, Zheng Q, Flowers L, Campbell A, Knight SAB, Chan N, Wei M, Lovins V, Bugayev J, Horwinski J, Bradley C, Meyer J, Crumrine D, Sutter CH, Elias P, Mauldin E, Sutter TR, Grice EA. Commensal microbiota regulates skin barrier function and repair via signaling through the aryl hydrocarbon receptor. Cell Host Microbe. 2021;29(8):1235-1248.e8. DOI: 10.1016/j.chom.2021.05.011</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Zheng Y, Hunt RL, Villaruz AE, Fisher EL, Liu R, Liu Q, Cheung GYC, Li M, Otto M. Commensal Staphylococcus epidermidis contributes to skin barrier homeostasis by generating protective ceramides. Cell Host Microbe. 2022;30(3):301-313.e9. DOI: 10.1016/j.chom.2022.01.004</mixed-citation><mixed-citation xml:lang="en">Zheng Y, Hunt RL, Villaruz AE, Fisher EL, Liu R, Liu Q, Cheung GYC, Li M, Otto M. Commensal Staphylococcus epidermidis contributes to skin barrier homeostasis by generating protective ceramides. Cell Host Microbe. 2022;30(3):301-313.e9. DOI: 10.1016/j.chom.2022.01.004</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Nakamura K, O'Neill AM, Williams MR, Cau L, Nakatsuji T, Horswill AR, Gallo RL. Short chain fatty acids produced by Cutibacterium acnes inhibit biofilm formation by Staphylococcus epidermidis. Sci Rep. 2020;10(1):21237. DOI: 10.1038/s41598-020-77790-9</mixed-citation><mixed-citation xml:lang="en">Nakamura K, O'Neill AM, Williams MR, Cau L, Nakatsuji T, Horswill AR, Gallo RL. Short chain fatty acids produced by Cutibacterium acnes inhibit biofilm formation by Staphylococcus epidermidis. Sci Rep. 2020;10(1):21237. DOI: 10.1038/s41598-020-77790-9</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Naik S, Bouladoux N, Wilhelm C, Molloy MJ, Salcedo R, Kastenmuller W, Deming C, Quinones M, Koo L, Conlan S, Spencer S, Hall JA, Dzutsev A, Kong H, Campbell DJ, Trinchieri G, Segre JA, Belkaid Y. Compartmentalized control of skin immunity by resident commensals. Science. 2012;337(6098):1115-9. DOI: 10.1126/science.1225152</mixed-citation><mixed-citation xml:lang="en">Naik S, Bouladoux N, Wilhelm C, Molloy MJ, Salcedo R, Kastenmuller W, Deming C, Quinones M, Koo L, Conlan S, Spencer S, Hall JA, Dzutsev A, Kong H, Campbell DJ, Trinchieri G, Segre JA, Belkaid Y. Compartmentalized control of skin immunity by resident commensals. Science. 2012;337(6098):1115-9. DOI: 10.1126/science.1225152</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Chehoud C, Rafail S, Tyldsley AS, Seykora JT, Lambris JD, Grice EA. Complement modulates the cutaneous microbiome and inflammatory milieu. Proc Natl Acad Sci U S A. 2013;110(37):15061-6. DOI: 10.1073/pnas.1307855110</mixed-citation><mixed-citation xml:lang="en">Chehoud C, Rafail S, Tyldsley AS, Seykora JT, Lambris JD, Grice EA. Complement modulates the cutaneous microbiome and inflammatory milieu. Proc Natl Acad Sci U S A. 2013;110(37):15061-6. DOI: 10.1073/pnas.1307855110</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Braff MH, Zaiou M, Fierer J, Nizet V, Gallo RL. Keratinocyte production of cathelicidin provides direct activity against bacterial skin pathogens. Infect Immun. 2005;73(10):6771-81. DOI: 10.1128/IAI.73.10.6771-6781.2005</mixed-citation><mixed-citation xml:lang="en">Braff MH, Zaiou M, Fierer J, Nizet V, Gallo RL. Keratinocyte production of cathelicidin provides direct activity against bacterial skin pathogens. Infect Immun. 2005;73(10):6771-81. DOI: 10.1128/IAI.73.10.6771-6781.2005</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">De Pessemier B, Grine L, Debaere M, Maes A, Paetzold B, Callewaert C. Gut-Skin Axis: Current Knowledge of the Interrelationship between Microbial Dysbiosis and Skin Conditions. Microorganisms. 2021;9(2):353. DOI: 10.3390/microorganisms9020353</mixed-citation><mixed-citation xml:lang="en">De Pessemier B, Grine L, Debaere M, Maes A, Paetzold B, Callewaert C. Gut-Skin Axis: Current Knowledge of the Interrelationship between Microbial Dysbiosis and Skin Conditions. Microorganisms. 2021;9(2):353. DOI: 10.3390/microorganisms9020353</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Dreno B, Martin R, Moyal D, Henley JB, Khammari A, Seité S. Skin microbiome and acne vulgaris: Staphylococcus, a new actor in acne. Exp Dermatol. 2017;26(9):798-803. DOI: 10.1111/exd.13296</mixed-citation><mixed-citation xml:lang="en">Dreno B, Martin R, Moyal D, Henley JB, Khammari A, Seité S. Skin microbiome and acne vulgaris: Staphylococcus, a new actor in acne. Exp Dermatol. 2017;26(9):798-803. DOI: 10.1111/exd.13296</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Lee SY, Lee E, Park YM, Hong SJ. Microbiome in the Gut-Skin Axis in Atopic Dermatitis. Allergy Asthma Immunol Res. 2018;10(4):354-362. DOI: 10.4168/aair.2018.10.4.354</mixed-citation><mixed-citation xml:lang="en">Lee SY, Lee E, Park YM, Hong SJ. Microbiome in the Gut-Skin Axis in Atopic Dermatitis. Allergy Asthma Immunol Res. 2018;10(4):354-362. DOI: 10.4168/aair.2018.10.4.354</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Paller AS, Kong HH, Seed P, Naik S, Scharschmidt TC, Gallo RL, Luger T, Irvine AD. The microbiome in patients with atopic dermatitis. J Allergy Clin Immunol. 2019;143(1):26-35. Erratum in: J Allergy Clin Immunol. 2019;143(4):1660. DOI: 10.1016/j.jaci.2018.11.015.</mixed-citation><mixed-citation xml:lang="en">Paller AS, Kong HH, Seed P, Naik S, Scharschmidt TC, Gallo RL, Luger T, Irvine AD. The microbiome in patients with atopic dermatitis. J Allergy Clin Immunol. 2019;143(1):26-35. Erratum in: J Allergy Clin Immunol. 2019;143(4):1660. DOI: 10.1016/j.jaci.2018.11.015.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Thomas CL, Fernández-Peñas P. The microbiome and atopic eczema: More than skin deep. Australas J Dermatol. 2017;58(1):18-24. DOI: 10.1111/ajd.12435</mixed-citation><mixed-citation xml:lang="en">Thomas CL, Fernández-Peñas P. The microbiome and atopic eczema: More than skin deep. Australas J Dermatol. 2017;58(1):18-24. DOI: 10.1111/ajd.12435</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Thio HB. The Microbiome in Psoriasis and Psoriatic Arthritis: The Skin Perspective. J Rheumatol Suppl. 2018;94:30-31. DOI: 10.3899/jrheum.180133</mixed-citation><mixed-citation xml:lang="en">Thio HB. The Microbiome in Psoriasis and Psoriatic Arthritis: The Skin Perspective. J Rheumatol Suppl. 2018;94:30-31. DOI: 10.3899/jrheum.180133</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Holmes AD. Potential role of microorganisms in the pathogenesis of rosacea. J Am Acad Dermatol. 2013;69(6):1025-32. DOI: 10.1016/j.jaad.2013.08.006</mixed-citation><mixed-citation xml:lang="en">Holmes AD. Potential role of microorganisms in the pathogenesis of rosacea. J Am Acad Dermatol. 2013;69(6):1025-32. DOI: 10.1016/j.jaad.2013.08.006</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Wang R, Farhat M, Na J, Li R, Wu Y. Bacterial and fungal microbiome characterization in patients with rosacea and healthy controls. Br J Dermatol. 2020;183(6):1112-1114. DOI: 10.1111/bjd.19315</mixed-citation><mixed-citation xml:lang="en">Wang R, Farhat M, Na J, Li R, Wu Y. Bacterial and fungal microbiome characterization in patients with rosacea and healthy controls. Br J Dermatol. 2020;183(6):1112-1114. DOI: 10.1111/bjd.19315</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Воробьева Н.Е., Шипицына Е.В., Савичева А.М. Микробиота кожи женщин репродуктивного возраста в норме и при андрогензависимых дерматозах. Журнал акушерства и женских болезней. 2019;68(2):7-16. DOI: 10.17816/JOWD6827-16</mixed-citation><mixed-citation xml:lang="en">Vorobyova N.E., Shipitsyna E.V., Savicheva A.M. Skin microbiota in women of reproductive age in norm and androgen-dependent dermatoses. Journal of obstetrics and women's diseases. 2019;68(2):7-16. (In Russian). DOI: 10.17816/JOWD6827-16</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Onywera H, Williamson AL, Cozzuto L, Bonnin S, Mbulawa ZZA, Coetzee D, Ponomarenko J, Meiring TL. The penile microbiota of Black South African men: relationship with human papillomavirus and HIV infection. BMC Microbiol. 2020;20(1):78. DOI: 10.1186/s12866-020-01759-x</mixed-citation><mixed-citation xml:lang="en">Onywera H, Williamson AL, Cozzuto L, Bonnin S, Mbulawa ZZA, Coetzee D, Ponomarenko J, Meiring TL. The penile microbiota of Black South African men: relationship with human papillomavirus and HIV infection. BMC Microbiol. 2020;20(1):78. DOI: 10.1186/s12866-020-01759-x</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Liu CM, Hungate BA, Tobian AA, Ravel J, Prodger JL, Serwadda D, Kigozi G, Galiwango RM, Nalugoda F, Keim P, Wawer MJ, Price LB, Gray RH. Penile Microbiota and Female Partner Bacterial Vaginosis in Rakai, Uganda. mBio. 2015;6(3):e00589. DOI: 10.1128/mBio.00589-15</mixed-citation><mixed-citation xml:lang="en">Liu CM, Hungate BA, Tobian AA, Ravel J, Prodger JL, Serwadda D, Kigozi G, Galiwango RM, Nalugoda F, Keim P, Wawer MJ, Price LB, Gray RH. Penile Microbiota and Female Partner Bacterial Vaginosis in Rakai, Uganda. mBio. 2015;6(3):e00589. DOI: 10.1128/mBio.00589-15</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Carda-Diéguez M, Cárdenas N, Aparicio M, Beltrán D, Rodríguez JM, Mira A. Variations in Vaginal, Penile, and Oral Microbiota After Sexual Intercourse: A Case Report. Front Med (Lausanne). 2019;6:178. Erratum in: Front Med (Lausanne). 2020;6:294. DOI: 10.3389/fmed.2019.00178</mixed-citation><mixed-citation xml:lang="en">Carda-Diéguez M, Cárdenas N, Aparicio M, Beltrán D, Rodríguez JM, Mira A. Variations in Vaginal, Penile, and Oral Microbiota After Sexual Intercourse: A Case Report. Front Med (Lausanne). 2019;6:178. Erratum in: Front Med (Lausanne). 2020;6:294. DOI: 10.3389/fmed.2019.00178</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Ravel J, Gajer P, Abdo Z, Schneider GM, Koenig SS, McCulle SL, Karlebach S, Gorle R, Russell J, Tacket CO, Brotman RM, Davis CC, Ault K, Peralta L, Forney LJ. Vaginal microbiome of reproductive-age women. Proc Natl Acad Sci U S A. 2011;108 Suppl 1(Suppl 1):4680-7. DOI: 10.1073/pnas.1002611107</mixed-citation><mixed-citation xml:lang="en">Ravel J, Gajer P, Abdo Z, Schneider GM, Koenig SS, McCulle SL, Karlebach S, Gorle R, Russell J, Tacket CO, Brotman RM, Davis CC, Ault K, Peralta L, Forney LJ. Vaginal microbiome of reproductive-age women. Proc Natl Acad Sci U S A. 2011;108 Suppl 1(Suppl 1):4680-7. DOI: 10.1073/pnas.1002611107</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Mehta SD, Zhao D, Green SJ, Agingu W, Otieno F, Bhaumik R, Bhaumik D, Bailey RC. The Microbiome Composition of a Man's Penis Predicts Incident Bacterial Vaginosis in His Female Sex Partner With High Accuracy. Front Cell Infect Microbiol. 2020;10:433. DOI: 10.3389/fcimb.2020.00433</mixed-citation><mixed-citation xml:lang="en">Mehta SD, Zhao D, Green SJ, Agingu W, Otieno F, Bhaumik R, Bhaumik D, Bailey RC. The Microbiome Composition of a Man's Penis Predicts Incident Bacterial Vaginosis in His Female Sex Partner With High Accuracy. Front Cell Infect Microbiol. 2020;10:433. DOI: 10.3389/fcimb.2020.00433</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Gonçalves MFM, Fernandes ÂR, Rodrigues AG, Lisboa C. Microbiome in Male Genital Mucosa (Prepuce, Glans, and Coronal Sulcus): A Systematic Review. Microorganisms. 2022;10(12):2312. DOI: 10.3390/microorganisms10122312</mixed-citation><mixed-citation xml:lang="en">Gonçalves MFM, Fernandes ÂR, Rodrigues AG, Lisboa C. Microbiome in Male Genital Mucosa (Prepuce, Glans, and Coronal Sulcus): A Systematic Review. Microorganisms. 2022;10(12):2312. DOI: 10.3390/microorganisms10122312</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Nelson DE, Dong Q, Van der Pol B, Toh E, Fan B, Katz BP, Mi D, Rong R, Weinstock GM, Sodergren E, Fortenberry JD. Bacterial communities of the coronal sulcus and distal urethra of adolescent males. PLoS One. 2012;7(5):e36298. DOI: 10.1371/journal.pone.0036298</mixed-citation><mixed-citation xml:lang="en">Nelson DE, Dong Q, Van der Pol B, Toh E, Fan B, Katz BP, Mi D, Rong R, Weinstock GM, Sodergren E, Fortenberry JD. Bacterial communities of the coronal sulcus and distal urethra of adolescent males. PLoS One. 2012;7(5):e36298. DOI: 10.1371/journal.pone.0036298</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Price LB, Liu CM, Johnson KE, Aziz M, Lau MK, Bowers J, Ravel J, Keim PS, Serwadda D, Wawer MJ, Gray RH. The effects of circumcision on the penis microbiome. PLoS One. 2010;5(1):e8422. DOI: 10.1371/journal.pone.0008422</mixed-citation><mixed-citation xml:lang="en">Price LB, Liu CM, Johnson KE, Aziz M, Lau MK, Bowers J, Ravel J, Keim PS, Serwadda D, Wawer MJ, Gray RH. The effects of circumcision on the penis microbiome. PLoS One. 2010;5(1):e8422. DOI: 10.1371/journal.pone.0008422</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Клинические рекомендации – Бактериальный вагиноз – 2022- 2023-2024. Утверждены Минздравом РФ; 2022.</mixed-citation><mixed-citation xml:lang="en">Clinical recommendations – Bacterial vaginosis – 2022- 2023-2024. Approved by the Ministry of Health of the Russian Federation; 2022. (In Russian).</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Vodstrcil LA, Plummer EL, Doyle M, Fairley CK, McGuiness C, Bateson D, Hocking JS, Law MG, Petoumenos K, Donovan B, Chow EPF, Bradshaw CS; StepUp RCT Team. Treating male partners of women with bacterial vaginosis (StepUp): a protocol for a randomised controlled trial to assess the clinical effectiveness of male partner treatment for reducing the risk of BV recurrence. BMC Infect Dis. 2020;20(1):834. DOI: 10.1186/s12879-020-05563-w</mixed-citation><mixed-citation xml:lang="en">Vodstrcil LA, Plummer EL, Doyle M, Fairley CK, McGuiness C, Bateson D, Hocking JS, Law MG, Petoumenos K, Donovan B, Chow EPF, Bradshaw CS; StepUp RCT Team. Treating male partners of women with bacterial vaginosis (StepUp): a protocol for a randomised controlled trial to assess the clinical effectiveness of male partner treatment for reducing the risk of BV recurrence. BMC Infect Dis. 2020;20(1):834. DOI: 10.1186/s12879-020-05563-w</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Zozaya M, Ferris MJ, Siren JD, Lillis R, Myers L, Nsuami MJ, Eren AM, Brown J, Taylor CM, Martin DH. Bacterial communities in penile skin, male urethra, and vaginas of heterosexual couples with and without bacterial vaginosis. Microbiome. 2016;4:16. DOI: 10.1186/s40168-016-0161-6</mixed-citation><mixed-citation xml:lang="en">Zozaya M, Ferris MJ, Siren JD, Lillis R, Myers L, Nsuami MJ, Eren AM, Brown J, Taylor CM, Martin DH. Bacterial communities in penile skin, male urethra, and vaginas of heterosexual couples with and without bacterial vaginosis. Microbiome. 2016;4:16. DOI: 10.1186/s40168-016-0161-6</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Савичева А.М., Шипицына Е.В. Микробиота влагалища при бактериальном вагинозе. Аспекты диагностики и терапии. Медицинский совет. 2014;(9):90-95. eLIBRARY ID: 22411054; EDN: SWKYMD</mixed-citation><mixed-citation xml:lang="en">Savicheva A.M., Shipitsyna E.V. Vaginal microbiota in bacterial vaginosis. Aspects of diagnosis and therapy. Medical council. 2014;(9):90-95. (In Russian). eLIBRARY ID: 22411054; EDN: SWKYMD</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Plummer EL, Vodstrcil LA, Doyle M, Danielewski JA, Murray GL, Fehler G, Fairley CK, Bulach DM, Garland SM, Chow EPF, Hocking JS, Bradshaw CS. A Prospective, Open-Label Pilot Study of Concurrent Male Partner Treatment for Bacterial Vaginosis. mBio. 2021;12(5):e0232321. DOI: 10.1128/mBio.02323-21</mixed-citation><mixed-citation xml:lang="en">Plummer EL, Vodstrcil LA, Doyle M, Danielewski JA, Murray GL, Fehler G, Fairley CK, Bulach DM, Garland SM, Chow EPF, Hocking JS, Bradshaw CS. A Prospective, Open-Label Pilot Study of Concurrent Male Partner Treatment for Bacterial Vaginosis. mBio. 2021;12(5):e0232321. DOI: 10.1128/mBio.02323-21</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Dareng EO, Ma B, Famooto AO, Adebamowo SN, Offiong RA, Olaniyan O, Dakum PS, Wheeler CM, Fadrosh D, Yang H, Gajer P, Brotman RM, Ravel J, Adebamowo CA. Prevalent high-risk HPV infection and vaginal microbiota in Nigerian women. Epidemiol Infect. 2016;144(1):123-37. DOI: 10.1017/S0950268815000965</mixed-citation><mixed-citation xml:lang="en">Dareng EO, Ma B, Famooto AO, Adebamowo SN, Offiong RA, Olaniyan O, Dakum PS, Wheeler CM, Fadrosh D, Yang H, Gajer P, Brotman RM, Ravel J, Adebamowo CA. Prevalent high-risk HPV infection and vaginal microbiota in Nigerian women. Epidemiol Infect. 2016;144(1):123-37. DOI: 10.1017/S0950268815000965</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Lee JE, Lee S, Lee H, Song YM, Lee K, Han MJ, Sung J, Ko G. Association of the vaginal microbiota with human papillomavirus infection in a Korean twin cohort. PLoS One. 2013;8(5):e63514. DOI: 10.1371/journal.pone.0063514</mixed-citation><mixed-citation xml:lang="en">Lee JE, Lee S, Lee H, Song YM, Lee K, Han MJ, Sung J, Ko G. Association of the vaginal microbiota with human papillomavirus infection in a Korean twin cohort. PLoS One. 2013;8(5):e63514. DOI: 10.1371/journal.pone.0063514</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Di Paola M, Sani C, Clemente AM, Iossa A, Perissi E, Castronovo G, Tanturli M, Rivero D, Cozzolino F, Cavalieri D, Carozzi F, De Filippo C, Torcia MG. Characterization of cervico-vaginal microbiota in women developing persistent high-risk Human Papillomavirus infection. Sci Rep. 2017;7(1):10200. DOI: 10.1038/s41598-017-09842-6</mixed-citation><mixed-citation xml:lang="en">Di Paola M, Sani C, Clemente AM, Iossa A, Perissi E, Castronovo G, Tanturli M, Rivero D, Cozzolino F, Cavalieri D, Carozzi F, De Filippo C, Torcia MG. Characterization of cervico-vaginal microbiota in women developing persistent high-risk Human Papillomavirus infection. Sci Rep. 2017;7(1):10200. DOI: 10.1038/s41598-017-09842-6</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Onywera H, Williamson AL, Mbulawa ZZA, Coetzee D, Meiring TL. The cervical microbiota in reproductive-age South African women with and without human papillomavirus infection. Papillomavirus Res. 2019;7:154-163. DOI: 10.1016/j.pvr.2019.04.006</mixed-citation><mixed-citation xml:lang="en">Onywera H, Williamson AL, Mbulawa ZZA, Coetzee D, Meiring TL. The cervical microbiota in reproductive-age South African women with and without human papillomavirus infection. Papillomavirus Res. 2019;7:154-163. DOI: 10.1016/j.pvr.2019.04.006</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Mbulawa ZZ, Coetzee D, Marais DJ, Kamupira M, Zwane E, Allan B, Constant D, Moodley JR, Hoffman M, Williamson AL. Genital human papillomavirus prevalence and human papillomavirus concordance in heterosexual couples are positively associated with human immunodeficiency virus coinfection. J Infect Dis. 2009;199(10):1514-24. DOI: 10.1086/598220</mixed-citation><mixed-citation xml:lang="en">Mbulawa ZZ, Coetzee D, Marais DJ, Kamupira M, Zwane E, Allan B, Constant D, Moodley JR, Hoffman M, Williamson AL. Genital human papillomavirus prevalence and human papillomavirus concordance in heterosexual couples are positively associated with human immunodeficiency virus coinfection. J Infect Dis. 2009;199(10):1514-24. DOI: 10.1086/598220</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Mbulawa ZZ, Marais DJ, Johnson LF, Coetzee D, Williamson AL. Impact of human immunodeficiency virus on the natural history of human papillomavirus genital infection in South African men and women. J Infect Dis. 2012;206(1):15-27. DOI: 10.1093/infdis/jis299</mixed-citation><mixed-citation xml:lang="en">Mbulawa ZZ, Marais DJ, Johnson LF, Coetzee D, Williamson AL. Impact of human immunodeficiency virus on the natural history of human papillomavirus genital infection in South African men and women. J Infect Dis. 2012;206(1):15-27. DOI: 10.1093/infdis/jis299</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Liu CM, Hungate BA, Tobian AA, Serwadda D, Ravel J, Lester R, Kigozi G, Aziz M, Galiwango RM, Nalugoda F, Contente-Cuomo TL, Wawer MJ, Keim P, Gray RH, Price LB. Male circumcision significantly reduces prevalence and load of genital anaerobic bacteria. mBio. 2013;4(2):e00076. DOI: 10.1128/mBio.00076-13</mixed-citation><mixed-citation xml:lang="en">Liu CM, Hungate BA, Tobian AA, Serwadda D, Ravel J, Lester R, Kigozi G, Aziz M, Galiwango RM, Nalugoda F, Contente-Cuomo TL, Wawer MJ, Keim P, Gray RH, Price LB. Male circumcision significantly reduces prevalence and load of genital anaerobic bacteria. mBio. 2013;4(2):e00076. DOI: 10.1128/mBio.00076-13</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Auvert B, Taljaard D, Lagarde E, Sobngwi-Tambekou J, Sitta R, Puren A. Randomized, controlled intervention trial of male circumcision for reduction of HIV infection risk: the ANRS 1265 Trial. PLoS Med. 2005 Nov;2(11):e298. Erratum in: PLoS Med. 2006;3(5):e298. DOI: 10.1371/journal.pmed.0020298</mixed-citation><mixed-citation xml:lang="en">Auvert B, Taljaard D, Lagarde E, Sobngwi-Tambekou J, Sitta R, Puren A. Randomized, controlled intervention trial of male circumcision for reduction of HIV infection risk: the ANRS 1265 Trial. PLoS Med. 2005 Nov;2(11):e298. Erratum in: PLoS Med. 2006;3(5):e298. DOI: 10.1371/journal.pmed.0020298</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Liu CM, Prodger JL, Tobian AAR, Abraham AG, Kigozi G, Hungate BA, Aziz M, Nalugoda F, Sariya S, Serwadda D, Kaul R, Gray RH, Price LB. Penile Anaerobic Dysbiosis as a Risk Factor for HIV Infection. mBio. 2017;8(4):e00996-17. DOI: 10.1128/mBio.00996-17</mixed-citation><mixed-citation xml:lang="en">Liu CM, Prodger JL, Tobian AAR, Abraham AG, Kigozi G, Hungate BA, Aziz M, Nalugoda F, Sariya S, Serwadda D, Kaul R, Gray RH, Price LB. Penile Anaerobic Dysbiosis as a Risk Factor for HIV Infection. mBio. 2017;8(4):e00996-17. DOI: 10.1128/mBio.00996-17</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Anderson D, Politch JA, Pudney J. HIV infection and immune defense of the penis. Am J Reprod Immunol. 2011;65(3):220-9. DOI: 10.1111/j.1600-0897.2010.00941.x</mixed-citation><mixed-citation xml:lang="en">Anderson D, Politch JA, Pudney J. HIV infection and immune defense of the penis. Am J Reprod Immunol. 2011;65(3):220-9. DOI: 10.1111/j.1600-0897.2010.00941.x</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">de Jong MA, Geijtenbeek TB. Human immunodeficiency virus-1 acquisition in genital mucosa: Langerhans cells as key-players. J Intern Med. 2009;265(1):18-28. DOI: 10.1111/j.1365-2796.2008.02046.x</mixed-citation><mixed-citation xml:lang="en">de Jong MA, Geijtenbeek TB. Human immunodeficiency virus-1 acquisition in genital mucosa: Langerhans cells as key-players. J Intern Med. 2009;265(1):18-28. DOI: 10.1111/j.1365-2796.2008.02046.x</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Donoval BA, Landay AL, Moses S, Agot K, Ndinya-Achola JO, Nyagaya EA, MacLean I, Bailey RC. HIV-1 target cells in foreskins of African men with varying histories of sexually transmitted infections. Am J Clin Pathol. 2006;125(3):386-91. PMID: 16613341.</mixed-citation><mixed-citation xml:lang="en">Donoval BA, Landay AL, Moses S, Agot K, Ndinya-Achola JO, Nyagaya EA, MacLean I, Bailey RC. HIV-1 target cells in foreskins of African men with varying histories of sexually transmitted infections. Am J Clin Pathol. 2006;125(3):386-91. PMID: 16613341.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">de Witte L, Nabatov A, Geijtenbeek TB. Distinct roles for DC-SIGN+-dendritic cells and Langerhans cells in HIV-1 transmission. Trends Mol Med. 2008;14(1):12-9. DOI: 10.1016/j.molmed.2007.11.001</mixed-citation><mixed-citation xml:lang="en">de Witte L, Nabatov A, Geijtenbeek TB. Distinct roles for DC-SIGN+-dendritic cells and Langerhans cells in HIV-1 transmission. Trends Mol Med. 2008;14(1):12-9. DOI: 10.1016/j.molmed.2007.11.001</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Gosmann C, Anahtar MN, Handley SA, Farcasanu M, Abu-Ali G, Bowman BA, Padavattan N, Desai C, Droit L, Moodley A, Dong M, Chen Y, Ismail N, Ndung'u T, Ghebremichael MS, Wesemann DR, Mitchell C, Dong KL, Huttenhower C, Walker BD, Virgin HW, Kwon DS. Lactobacillus-Deficient Cervicovaginal Bacterial Communities Are Associated with Increased HIV Acquisition in Young South African Women. Immunity. 2017;46(1):29-37. DOI: 10.1016/j.immuni.2016.12.013</mixed-citation><mixed-citation xml:lang="en">Gosmann C, Anahtar MN, Handley SA, Farcasanu M, Abu-Ali G, Bowman BA, Padavattan N, Desai C, Droit L, Moodley A, Dong M, Chen Y, Ismail N, Ndung'u T, Ghebremichael MS, Wesemann DR, Mitchell C, Dong KL, Huttenhower C, Walker BD, Virgin HW, Kwon DS. Lactobacillus-Deficient Cervicovaginal Bacterial Communities Are Associated with Increased HIV Acquisition in Young South African Women. Immunity. 2017;46(1):29-37. DOI: 10.1016/j.immuni.2016.12.013</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Prodger JL, Abraham AG, Tobian AA, Park DE, Aziz M, Roach K, Gray RH, Buchanan L, Kigozi G, Galiwango RM, Ssekasanvu J, Nnamutete J, Kagaayi J, Kaul R, Liu CM. Penile bacteria associated with HIV seroconversion, inflammation, and immune cells. JCI Insight. 2021;6(8):e147363. DOI: 10.1172/jci.insight.147363</mixed-citation><mixed-citation xml:lang="en">Prodger JL, Abraham AG, Tobian AA, Park DE, Aziz M, Roach K, Gray RH, Buchanan L, Kigozi G, Galiwango RM, Ssekasanvu J, Nnamutete J, Kagaayi J, Kaul R, Liu CM. Penile bacteria associated with HIV seroconversion, inflammation, and immune cells. JCI Insight. 2021;6(8):e147363. DOI: 10.1172/jci.insight.147363</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Bentubo HD, Mantovani A, Yamashita JT, Gambale W, Fischman O. Yeasts of the genital region of patients attending the dermatology service at Hospital São Paulo, Brazil. Rev Iberoam Micol. 2015;32(4):229-34. DOI: 10.1016/j.riam.2014.11.004</mixed-citation><mixed-citation xml:lang="en">Bentubo HD, Mantovani A, Yamashita JT, Gambale W, Fischman O. Yeasts of the genital region of patients attending the dermatology service at Hospital São Paulo, Brazil. Rev Iberoam Micol. 2015;32(4):229-34. DOI: 10.1016/j.riam.2014.11.004</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Li M, Mao JX, Jiang HH, Huang CM, Gao XH, Zhang L. Microbiome Profile in Patients with Adult Balanoposthitis: Relationship with Redundant Prepuce, Genital Mucosa Physical Barrier Status and Inflammation. Acta Derm Venereol. 2021;101(5):adv00466. DOI: 10.2340/00015555-3833</mixed-citation><mixed-citation xml:lang="en">Li M, Mao JX, Jiang HH, Huang CM, Gao XH, Zhang L. Microbiome Profile in Patients with Adult Balanoposthitis: Relationship with Redundant Prepuce, Genital Mucosa Physical Barrier Status and Inflammation. Acta Derm Venereol. 2021;101(5):adv00466. DOI: 10.2340/00015555-3833</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Szczuka E, Krzymińska S, Kaznowski A. Clonality, virulence and the occurrence of genes encoding antibiotic resistance among Staphylococcus warneri isolates from bloodstream infections. J Med Microbiol. 2016;65(8):828-836. DOI: 10.1099/jmm.0.000287</mixed-citation><mixed-citation xml:lang="en">Szczuka E, Krzymińska S, Kaznowski A. Clonality, virulence and the occurrence of genes encoding antibiotic resistance among Staphylococcus warneri isolates from bloodstream infections. J Med Microbiol. 2016;65(8):828-836. DOI: 10.1099/jmm.0.000287</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Doerflinger SY, Throop AL, Herbst-Kralovetz MM. Bacteria in the vaginal microbiome alter the innate immune response and barrier properties of the human vaginal epithelia in a species-specific manner. J Infect Dis. 2014;209(12):1989-99. DOI: 10.1093/infdis/jiu004</mixed-citation><mixed-citation xml:lang="en">Doerflinger SY, Throop AL, Herbst-Kralovetz MM. Bacteria in the vaginal microbiome alter the innate immune response and barrier properties of the human vaginal epithelia in a species-specific manner. J Infect Dis. 2014;209(12):1989-99. DOI: 10.1093/infdis/jiu004</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Happel AU, Kullin B, Gamieldien H, Wentzel N, Zauchenberger CZ, Jaspan HB, Dabee S, Barnabas SL, Jaumdally SZ, Dietrich J, Gray G, Bekker LG, Froissart R, Passmore JS. Exploring potential of vaginal Lactobacillus isolates from South African women for enhancing treatment for bacterial vaginosis. PLoS Pathog. 2020;16(6):e1008559. DOI: 10.1371/journal.ppat.1008559</mixed-citation><mixed-citation xml:lang="en">Happel AU, Kullin B, Gamieldien H, Wentzel N, Zauchenberger CZ, Jaspan HB, Dabee S, Barnabas SL, Jaumdally SZ, Dietrich J, Gray G, Bekker LG, Froissart R, Passmore JS. Exploring potential of vaginal Lactobacillus isolates from South African women for enhancing treatment for bacterial vaginosis. PLoS Pathog. 2020;16(6):e1008559. DOI: 10.1371/journal.ppat.1008559</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Plummer EL, Ratten LK, Vodstrcil LA, Murray GL, Danielewski JA, Fairley CK, Garland SM, Chow EPF, Bradshaw CS. The Urethral Microbiota of Men with and without Idiopathic Urethritis. mBio. 2022;13(5):e0221322. DOI: 10.1128/mbio.02213-22</mixed-citation><mixed-citation xml:lang="en">Plummer EL, Ratten LK, Vodstrcil LA, Murray GL, Danielewski JA, Fairley CK, Garland SM, Chow EPF, Bradshaw CS. The Urethral Microbiota of Men with and without Idiopathic Urethritis. mBio. 2022;13(5):e0221322. DOI: 10.1128/mbio.02213-22</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Olajide AO, Salako AA, Aremu AA, Eziyi AK, Olajide FO, Banjo OO. Complications of transverse distal penile island flap: urethroplasty of complex anterior urethral stricture. Urol J. 2010;7(3):178-82. PMID: 20845294.</mixed-citation><mixed-citation xml:lang="en">Olajide AO, Salako AA, Aremu AA, Eziyi AK, Olajide FO, Banjo OO. Complications of transverse distal penile island flap: urethroplasty of complex anterior urethral stricture. Urol J. 2010;7(3):178-82. PMID: 20845294.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">McAninch JW. Reconstruction of extensive urethral strictures: circular fasciocutaneous penile flap. J Urol. 1993;149(3):488-91. DOI: 10.1016/s0022-5347(17)36125-6</mixed-citation><mixed-citation xml:lang="en">McAninch JW. Reconstruction of extensive urethral strictures: circular fasciocutaneous penile flap. J Urol. 1993;149(3):488-91. DOI: 10.1016/s0022-5347(17)36125-6</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Santucci RA, Mario LA, McAninch JW. Anastomotic urethroplasty for bulbar urethral stricture: analysis of 168 patients. J Urol. 2002;167(4):1715-9. PMID: 11912394.</mixed-citation><mixed-citation xml:lang="en">Santucci RA, Mario LA, McAninch JW. Anastomotic urethroplasty for bulbar urethral stricture: analysis of 168 patients. J Urol. 2002;167(4):1715-9. PMID: 11912394.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Wang CX, Zhang WP, Song HC. Complications of proximal hypospadias repair with transverse preputial island flap urethroplasty: a 15-year experience with long-term follow-up. Asian J Androl. 2019;21(3):300-303. DOI: 10.4103/aja.aja_115_18</mixed-citation><mixed-citation xml:lang="en">Wang CX, Zhang WP, Song HC. Complications of proximal hypospadias repair with transverse preputial island flap urethroplasty: a 15-year experience with long-term follow-up. Asian J Androl. 2019;21(3):300-303. DOI: 10.4103/aja.aja_115_18</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>
