<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Cytokines and inflammation</journal-id><journal-title-group><journal-title xml:lang="en">Cytokines and inflammation</journal-title><trans-title-group xml:lang="ru"><trans-title>Цитокины и воспаление</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1684-7849</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">705434</article-id><article-id pub-id-type="doi">10.17816/CI705434</article-id><article-id pub-id-type="edn">JVBSFU</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Original Study Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Оригинальные исследования</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Lipoxygenases and CFTR inhibitory factors might share the same role in host–microbe interactions</article-title><trans-title-group xml:lang="ru"><trans-title>Липоксигеназы и CFTR-ингибирующие факторы могут играть одинаковую роль во взаимодействии «микроорганизм — хозяин»</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5484-8264</contrib-id><contrib-id contrib-id-type="spin">7543-2903</contrib-id><name-alternatives><name xml:lang="en"><surname>Kurakin</surname><given-names>Georgy F.</given-names></name><name xml:lang="ru"><surname>Куракин</surname><given-names>Георгий Фёдорович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Independent researcher</p></bio><bio xml:lang="ru"><p>Независимый исследователь</p></bio><email>phyzyk@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff id="aff1"><institution></institution></aff><pub-date date-type="preprint" iso-8601-date="2026-07-22" publication-format="electronic"><day>22</day><month>07</month><year>2026</year></pub-date><pub-date date-type="pub" iso-8601-date="2026-08-04" publication-format="electronic"><day>04</day><month>08</month><year>2026</year></pub-date><volume>23</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>43</fpage><lpage>57</lpage><history><date date-type="received" iso-8601-date="2026-04-03"><day>03</day><month>04</month><year>2026</year></date><date date-type="accepted" iso-8601-date="2026-07-08"><day>08</day><month>07</month><year>2026</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2026, Kurakin G.F.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2026, Куракин Г.Ф.</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="en">Kurakin G.F.</copyright-holder><copyright-holder xml:lang="ru">Куракин Г.Ф.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/" start_date="2028-08-04"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by-nc-nd/4.0/</ali:license_ref></license></permissions><self-uri xlink:href="https://cijournal.ru/1684-7849/article/view/705434">https://cijournal.ru/1684-7849/article/view/705434</self-uri><abstract xml:lang="en"><p>Cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel in humans and other vertebrates, whose mutation leads to cystic fibrosis. CFTR inhibitory factor, or Cif, is a recently discovered bacterial epoxide hydrolase that downregulates CFTR protein upon the bacterial infection. However, its cleaving activity has been recently characterized towards fatty acid epoxides—epoxygenase-derived oxylipins. We identified a list of host-associated bacteria with putative Cif proteins, identified their most prevalent ecological functions within a systematic review, and performed similar review for the previously assembled list of host-associated bacteria carrying lipoxygenase (LOX). Both Cif and LOX showed the association with pathogenesis and symbiosis in broad host range, and similar ecological profiles of their carriers suggested that they both might target oxylipin signaling in hosts. We also described the association of Cif with plant hormone biosynthesis and plant growth promotion, which indirectly supports our previous model of bacterial LOX action in plant and vertebrate hosts.</p></abstract><trans-abstract xml:lang="ru"><p>Трансмембранный регулятор проводимости при муковисцидозе (CFTR; от англ. cystic fibrosis transmembrane conductance regulator) — это хлоридный канал человека и других позвоночных, мутация в гене которого приводит к муковисцидозу. CFTR-ингибирующий фактор (Cif) — это недавно открытая бактериальная эпоксидгидролаза, снижающая количество молекул белка CFTR на поверхности клетки при бактериальной инфекции. Однако недавно была также охарактеризована его способность расщеплять эпоксиды жирных кислот — оксилипины, образующиеся по эпоксигеназному пути. Мы идентифицировали бактерии, ассоциированные с каким-либо хозяином и потенциально содержащие Cif, выявили наиболее распространённые экологические функции путём систематического обзора литературы, а также выполнили аналогичный обзор для ранее составленного списка бактерий, связанных с каким-либо хозяином и имеющих липоксигеназу. Как Cif, так и липоксигеназа продемонстрировали ассоциацию с патогенностью и симбиотическим потенциалом в отношении широкого круга хозяев, а сходные экологические профили бактерий-носителей позволили предположить, что оба фермента могут влиять на оксилипиновую сигнализацию хозяев. Мы также описали ассоциацию Cif с биосинтезом фитогормонов и стимуляцией роста растений, что косвенно подтверждает ранее выдвинутую нами гипотезу о механизме действия бактериальных липоксигеназ на растения и позвоночных.</p></trans-abstract><kwd-group xml:lang="en"><kwd>lipoxygenase</kwd><kwd>CFTR inhibitory factor</kwd><kwd>Cif</kwd><kwd>oxylipins</kwd><kwd>host-microbe interactions</kwd><kwd>nosocomial pathogens</kwd><kwd>cystic fibrosis</kwd><kwd>plants</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>липоксигеназа</kwd><kwd>CFTR-ингибирующий фактор</kwd><kwd>Cif</kwd><kwd>оксилипины</kwd><kwd>взаимоотношения «микроорганизм — хозяин»</kwd><kwd>нозокомиальные патогены</kwd><kwd>муковисцидоз</kwd><kwd>растения</kwd></kwd-group><funding-group/></article-meta><fn-group><fn xml:lang="en"><p>This is an original paper which was previously published as a preprint on Preprints.org server under the DOI: <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.20944/preprints202602.1829.v1">https://doi.org/10.20944/preprints202602.1829.v1</ext-link> Depositing papers on the preprint servers is considered a legitimate research practice.</p></fn><fn xml:lang="ru"><p>Это оригинальная статья, которая ранее была опубликована в виде препринта на сервере Preprints.org (DOI: <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.20944/preprints202602.1829.v1">https://doi.org/10.20944/preprints202602.1829.v1</ext-link>). Размещение статей на серверах препринтов считается легитимной исследовательской практикой.</p></fn></fn-group></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Amoah AS, Pestov NB, Korneenko TV, et al. Lipoxygenases at the Intersection of Infection and Carcinogenesis. Int J Mol Sci. 2024;25(7):3961. doi: 10.3390/ijms25073961 EDN: VZPZPZ</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Chrisnasari R, Hennebelle M, Vincken JP, et al. Bacterial lipoxygenases: Biochemical characteristics, molecular structure and potential applications. Biotechnol Adv. 2022;61:108046. doi: 10.1016/j.biotechadv.2022.108046 EDN: LCCXYS</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Kurakin GF, Samoukina AM. Oxylipins: Evolution of Biochemical “Esperanto”. Science First Hand. 2022;60(1):46–63. EDN: ZBLQIZ</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Shao DH, Yao YF, Wang DN. Ferroptosis and iron-based therapies in Pseudomonas aeruginosa infections: From pathogenesis to treatment. Virulence. 2025;16(1):2553787. doi: 10.1080/21505594.2025.2553787 EDN: HDYENP</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Morello E, Pérez-Berezo T, Boisseau C, et al. Pseudomonas aeruginosa Lipoxygenase LoxA Contributes to Lung Infection by Altering the Host Immune Lipid Signaling. Front Microbiol. 2019;10:1826. doi: 10.3389/fmicb.2019.01826 EDN: ERUPAP</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Kurakin GF, Samoukina AM, Potapova NA. Bacterial and Protozoan Lipoxygenases Could be Involved in Cell-to-Cell Signaling and Immune Response Suppression. Biochemistry (Mosc). 2020;85(9):1048–1071. doi: 10.1134/S0006297920090059 EDN: SIAVCK</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Kurakin G. Bacterial lipoxygenases are associated with host-microbe interactions and may provide cross-kingdom host jumps. bioRxiv. 2022. doi: 10.1101/2022.06.21.497025</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Beccaccioli M, Pucci N, Salustri M, et al. Fungal and bacterial oxylipins are signals for intra- and inter-cellular communication within plant disease. Front Plant Sci. 2022;13:823233. doi: 10.3389/fpls.2022.823233 EDN: HZBQLL</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Wang KD, Borrego EJ, Kenerley CM, Kolomiets MV. Oxylipins Other Than Jasmonic Acid Are Xylem-Resident Signals Regulating Systemic Resistance Induced by Trichoderma virens in Maize. Plant Cell. 2020;32(1):166–185. doi: 10.1105/tpc.19.00487</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Yan C, Xie D. Jasmonate in plant defence: sentinel or double agent? Plant Biotechnol J. 2015;13(9):1233–1240. doi: 10.1111/pbi.12417</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Chini A, Cimmino A, Masi M, et al. The fungal phytotoxin lasiojasmonate A activates the plant jasmonic acid pathway. J Exp Bot. 2018;69(12):3095–3102. doi: 10.1093/jxb/ery114</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Kurakin G. May oxylipins make bacteria be out of their tree? A controversial preprint that will not be published. Microbiology, Protocols &amp; Methods, and Cell &amp; Molecular Biology. 2025. Available from: https://communities.springernature.com/posts/may-oxylipins-make-bacteria-be-out-of-their-tree-a-controversial-preprint-that-will-not-be-published</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Hvorecny KL, Bahl CD, Kitamura S, et al. Active-Site Flexibility and Substrate Specificity in a Bacterial Virulence Factor: Crystallographic Snapshots of an Epoxide Hydrolase. Structure. 2017;25(5):697–707.e4. doi: 10.1016/j.str.2017.03.002</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Bahl CD, Madden DR. Pseudomonas aeruginosa Cif defines a distinct class of α/β epoxide hydrolases utilizing a His/Tyr ring-opening pair. Protein Pept Lett. 2012;19(2):186–193. doi: 10.2174/092986612799080392</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Bahl CD, Hvorecny KL, Bridges AA, et al. Signature motifs identify an Acinetobacter Cif virulence factor with epoxide hydrolase activity. J Biol Chem. 2014;289(11):7460–7469. doi: 10.1074/jbc.M113.518092</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Katoh K, Rozewicki J, Yamada KD. MAFFT online service: multiple sequence alignment, interactive sequence choice and visualization. Brief Bioinform. 2019;20(4):1160–1166. doi: 10.1093/bib/bbx108 EDN: TEVOWQ</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Gouveia-Oliveira R, Sackett PW, Pedersen AG. MaxAlign: maximizing usable data in an alignment. BMC Bioinformatics. 2007;8:312. doi: 10.1186/1471-2105-8-312 EDN: FRLLTF</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms. Mol Biol Evol. 2018;35(6):1547–1549. doi: 10.1093/molbev/msy096 EDN: NQRMGQ</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Letunic I, Bork P. Interactive Tree of Life (iTOL) v6: recent updates to the phylogenetic tree display and annotation tool. Nucleic Acids Res. 2024;52(W1):W78–W82. doi: 10.1093/nar/gkae268 EDN: NSXRLC</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Hammer Ø, Harper DA, Ryan PD. PAST: Paleontological statistics software package for education and data analysis. Palaeontologia Electronica. 2001;4(1):1–9.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Ye T, Zhou T, Fan X, et al. Acinetobacter lactucae Strain QL-1, a Novel Quorum Quenching Candidate Against Bacterial Pathogen Xanthomonas campestris pv. campestris. Front Microbiol. 2019;10:2867. doi: 10.3389/fmicb.2019.02867</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Rogel-Hernandez MA, Guerrero G, Rincón-Molina CI, et al. Genome Sequence of Acinetobacter lactucae OTEC-02, Isolated from Hydrocarbon-Contaminated Soil. Genome Announc. 2017;5(21):e00400-17. doi: 10.1128/genomeA.00400-17</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Amar AK, Sawant AR, Manoharan M, et al. Genome sequences of blaNDM-1 producing Acinetobacter lactucae isolated from immunocompromised patients in India. Microbiol Resour Announc. 2023;12(11):e0022023. doi: 10.1128/MRA.00220-23 EDN: PVLRPQ</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Ye T, Zhou T, Xu X, et al. Whole-Genome Sequencing Analysis of Quorum Quenching Bacterial Strain Acinetobacter lactucae QL-1 Identifies the FadY Enzyme for Degradation of the Diffusible Signal Factor. Int J Mol Sci. 2020;21(18):6729. doi: 10.3390/ijms21186729 EDN: IZRWBX</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Ali A, Dindhoria K, Kumar R. Acinetobacter oleivorans IRS14 alleviates cold stress in wheat by regulating physiological and biochemical factors. J Appl Microbiol. 2023;134(8):lxad176. doi: 10.1093/jambio/lxad176 EDN: YMNMRD</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Zhang S, Yang Q, Fu S, et al. Indole decreases the virulence of the bivalve model pathogens Vibrio tasmaniensis LGP32 and Vibrio crassostreae J2-9. Sci Rep. 2022;12(1):5749. doi: 10.1038/s41598-022-09799-1 EDN: FURJWC</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Roager L, Athena-Vasileiadi D, Gram L, Sonnenschein EC. Antagonistic activity of Phaeobacter piscinae against the emerging fish pathogen Vibrio crassostreae in aquaculture feed algae. Appl Environ Microbiol. 2024;90(3):e0143923. doi: 10.1128/aem.01439-23 EDN: BMCOLI</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Yilmaz S, Karataş S, Steinum TM, et al. Isolation, Identification, and Pathogenicity of Vibrio gigantis Retrieved from European Seabass (Dicentrarchus labrax) Farmed in Türkiye. Animals. 2023;13(22):3580. doi: 10.3390/ani13223580 EDN: DVGHMK</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Roux FL, Goubet A, Thompson FL, et al. Vibrio gigantis sp. nov., isolated from the haemolymph of cultured oysters (Crassostrea gigas). Int J Syst Evol Microbiol. 2005;55(Pt 6):2251–2255. doi: 10.1099/ijs.0.63666-0</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Teh LS, Shalom SR, James I, et al. Sodalis praecaptivus subsp. spalangiae subsp. nov., a nascent bacterial endosymbiont isolated from the parasitoid wasp, Spalangia cameroni. Int J Syst Evol Microbiol. 2024;74(10). doi: 10.1099/ijsem.0.006552 EDN: FLZXFE</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Ranson EL, Tsevat RK, von Bredow B, et al. Catheter-Related Bloodstream Infection Caused by Mycolicibacterium iranicum, California, USA. Emerg Infect Dis. 2023;29(1):217–219. doi: 10.3201/eid2901.220851 EDN: FLFKSU</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Xu L, Wu H, Zhou H, et al. Purulent meningitis and secondary epilepsy caused by Mycobacterium iranicum infection: A case report. Int J Infect Dis. 2023;135:5–7. doi: 10.1016/j.ijid.2023.06.002 EDN: SNVQCN</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Chen W, Zhang Y, Mi J. Assessing Antibiotic-Resistant Genes in University Dormitory Washing Machines. Microorganisms. 2024;12(6):1112. doi: 10.3390/microorganisms12061112 EDN: XLNLUH</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Kang Y, Tian L, Gu X, et al. Characterization of the Ocular Surface Microbiome in Keratitis Patients after Repeated Ophthalmic Antibiotic Exposure. Microbiol Spectr. 2022;10(2):e0216221. doi: 10.1128/spectrum.02162-21 EDN: GFFMZG</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Udaondo Z, Ramos JL, Abram K. Unraveling the genomic diversity of the Pseudomonas putida group: exploring taxonomy, core pangenome, and antibiotic resistance mechanisms. FEMS Microbiol Rev. 2024;48(6):fuae025. doi: 10.1093/femsre/fuae025 EDN: LYXGQN</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Gomes NC, Kosheleva IA, Abraham WR, Smalla K. Effects of the inoculant strain Pseudomonas putida KT2442 (pNF142) and of naphthalene contamination on the soil bacterial community. FEMS Microbiol Ecol. 2005;54(1):21–33. doi: 10.1016/j.femsec.2005.02.005 EDN: LJJOXD</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Liu C, Shao Z. Alcanivorax dieselolei sp. nov., a novel alkane-degrading bacterium isolated from sea water and deep-sea sediment. Int J Syst Evol Microbiol. 2005;55(Pt 3):1181–1186. doi: 10.1099/ijs.0.63443-0 EDN: MFGXOT</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Campos FF, Garcia JE, Luna-Finkler CL, et al. Alcanivorax dieselolei, an alkane-degrading bacterium associated with the mucus of the zoanthid Palythoa caribaeorum (Cnidaria, Anthozoa). Braz J Biol. 2015;75(2):431–434. doi: 10.1590/1519-6984.16113</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Bueno-Gonzalez V, Brady C, Denman S, et al. Pseudomonas daroniae sp. nov. and Pseudomonas dryadis sp. nov., isolated from pedunculate oak affected by acute oak decline in the UK. Int J Syst Evol Microbiol. 2019;69(11):3368–3376. doi: 10.1099/ijsem.0.003615 EDN: WWCZKJ</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Skrodenytė-Arbačiauskienė V, Radžiutė S, Stunžėnas V, Būda V. Erwinia typographi sp. nov., isolated from bark beetle (Ips typographus) gut. Int J Syst Evol Microbiol. 2012;62(Pt 4):942–948. doi: 10.1099/ijs.0.030304-0</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Cambronero-Heinrichs JC, Battisti A, Biedermann PHW, et al. Erwiniaceae bacteria play defensive and nutritional roles in two widespread ambrosia beetles. FEMS Microbiol Ecol. 2023;99(12):fiad144. doi: 10.1093/femsec/fiad144 EDN: DADZOV</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Liang LX, Sun QW, Hui N, et al. Phyllobacterium phragmitis sp. nov., an endophytic bacterium isolated from Phragmites australis rhizome in Kumtag Desert. Antonie Van Leeuwenhoek. 2019;112(5):661–668. doi: 10.1007/s10482-018-1195-5 EDN: EJWUPA</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Jeon JS, Carreno-Quintero N, van Eekelen HDLM, et al. Impact of root-associated strains of three Paraburkholderia species on primary and secondary metabolism of Brassica oleracea. Sci Rep. 2021;11(1):2781. doi: 10.1038/s41598-021-82238-9 EDN: VXUKOX</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Qin J, Maixnerová M, Nemec M, et al. Acinetobacter cumulans sp. nov., isolated from hospital sewage and capable of acquisition of multiple antibiotic resistance genes. Syst Appl Microbiol. 2019;42(3):319–325. doi: 10.1016/j.syapm.2019.02.001 EDN: TOSBFQ</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Lin HR, Shu HY, Lin GH. Biological roles of indole-3-acetic acid in Acinetobacter baumannii. Microbiol Res. 2018;216:30–39. doi: 10.1016/j.micres.2018.08.004</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Lee CR, Lee JH, Park M, et al. Biology of Acinetobacter baumannii: Pathogenesis, Antibiotic Resistance Mechanisms, and Prospective Treatment Options. Front Cell Infect Microbiol. 2017;7:55. doi: 10.3389/fcimb.2017.00055 EDN: YGTDBQ</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Harding CM, Hennon SW, Feldman MF. Uncovering the mechanisms of Acinetobacter baumannii virulence. Nat Rev Microbiol. 2018;16(2):91–102. doi: 10.1038/nrmicro.2017.148</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Ibrahim S, Al-Saryi N, Al-Kadmy IMS, Aziz SN. Multidrug-resistant Acinetobacter baumannii as an emerging concern in hospitals. Mol Biol Rep. 2021;48(10):6987–6998. doi: 10.1007/s11033-021-06690-6 EDN: ZYXRQX</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Antunes LC, Visca P, Towner KJ. Acinetobacter baumannii: evolution of a global pathogen. Pathog Dis. 2014;71(3):292–301. doi: 10.1111/2049-632X.12125</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Cerezales M, Xanthopoulou K, Ertel J, et al. Identification of Acinetobacter seifertii isolated from Bolivian hospitals. J Med Microbiol. 2018;67(6):834–837. doi: 10.1099/jmm.0.000751</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Na IY, Seo J, Jin Y, Ko KS. Whole-plasmid analysis of NDM-1-producing Acinetobacter seifertii isolate and its fitness in several Acinetobacter species. J Glob Antimicrob Resist. 2024;38:223–226. doi: 10.1016/j.jgar.2024.05.003 EDN: OZJIGY</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Na IY, Kwon KT, Ko KS. Plasmids Carrying blaVIM-2 in Acinetobacter nosocomialis and A. seifertii Isolates from South Korea. Microb Drug Resist. 2021;27(9):1186–1189. doi: 10.1089/mdr.2020.0442 EDN: IVRXAY</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Kishii K, Kikuchi K, Tomida J, et al. The first cases of human bacteremia caused by Acinetobacter seifertii in Japan. J Infect Chemother. 2016;22(5):342–345. doi: 10.1016/j.jiac.2015.12.002</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Neog N, Phukan U, Puzari M, et al. Klebsiella oxytoca and Emerging Nosocomial Infections. Curr Microbiol. 2021;78(4):1115–1123. doi: 10.1007/s00284-021-02402-2 EDN: VEQWXW</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Liébana-Rodríguez M, Recacha-Villamor E, Díaz-Molina C, et al. Outbreaks by Klebsiella oxytoca in neonatal intensive care units: Analysis of an outbreak in a tertiary hospital and systematic review. Enferm Infecc Microbiol Clin (Engl Ed). 2024;42(6):294-301. doi: 10.1016/j.eimce.2023.04.018 EDN: FMJPUW</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Osbelt L, Wende M, Almási É, et al. Klebsiella oxytoca causes colonization resistance against multidrug-resistant K. pneumoniae in the gut via cooperative carbohydrate competition. Cell Host Microbe. 2021;29(11):1663–1679.e7. doi: 10.1016/j.chom.2021.09.003 EDN: BSEEAA</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Greimel TM, Stampfer L, Leitner E, et al. Toxin-Producing Klebsiella oxytoca in Healthy Infants: Commensal or Pathobiont? J Pediatr Gastroenterol Nutr. 2022;74(1):e1–e7. doi: 10.1097/MPG.0000000000003299 EDN: BLFFXL</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Zhang T, Xu SY, Lin H, et al. Efficient degradation of tylosin by Klebsiella oxytoca TYL-T1. Sci Total Environ. 2022;847:157305. doi: 10.1016/j.scitotenv.2022.157305 EDN: RSPZPS</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Alfaify AM, Mir MA, Alrumman SA. Klebsiella oxytoca: an efficient pyrene-degrading bacterial strain isolated from petroleum-contaminated soil. Arch Microbiol. 2022;204(5):248. doi: 10.1007/s00203-022-02850-9 EDN: LAOYYG</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Lasarte-Monterrubio C, Guijarro-Sánchez P, Bellés A, et al; Spanish National Study Acinetobacter spp. 2020 Group. Carbapenem Resistance in Acinetobacter nosocomialis and Acinetobacter junii Conferred by Acquisition of blaOXA-24/40 and Genetic Characterization of the Transmission Mechanism between Acinetobacter Genomic Species. Microbiol Spectr. 2022;10(1):e0273421. doi: 10.1128/spectrum.02734-21 EDN: HVSGOJ</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Jing L, Xu Z, Zhang Y, et al. Metagenomic Insights into Pathogenic Characterization of ST410 Acinetobacter nosocomialis Prevalent in China. Pathogens. 2022;11(8):838. doi: 10.3390/pathogens11080838 EDN: PBXBRV</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Nho JS, Jun SH, Oh MH, et al. Acinetobacter nosocomialis secretes outer membrane vesicles that induce epithelial cell death and host inflammatory responses. Microb Pathog. 2015;81:39–45. doi: 10.1016/j.micpath.2015.03.012</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Mohd Rani F, Lean SS, A Rahman NI, et al. Comparative genomic analysis of clinical Acinetobacter nosocomialis isolates from Terengganu, Malaysia led to the discovery of a novel tetracycline-resistant plasmid. J Glob Antimicrob Resist. 2022;31:104–109. doi: 10.1016/j.jgar.2022.08.019 EDN: YKNLXQ</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Huang L, Chen TL, Lee YT, et al. Risk factors for imipenem-nonsusceptible Acinetobacter nosocomialis bloodstream infection. J Microbiol Immunol Infect. 2014;47(4):311–317. doi: 10.1016/j.jmii.2013.02.002</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Kim SD, Fuente Lde L, Weller DM, Thomashow LS. Colonizing ability of Pseudomonas fluorescens 2112, among collections of 2,4-diacetylphloroglucinol-producing Pseudomonas fluorescens spp. in pea rhizosphere. J Microbiol Biotechnol. 2012;22(6):763–770. doi: 10.4014/jmb.1112.12039</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Scales BS, Dickson RP, LiPuma JJ, Huffnagle GB. Microbiology, genomics, and clinical significance of the Pseudomonas fluorescens species complex, an unappreciated colonizer of humans. Clin Microbiol Rev. 2014;27(4):927–948. doi: 10.1128/CMR.00044-14</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Durán D, Bernal P, Vazquez-Arias D, et al. Pseudomonas fluorescens F113 type VI secretion systems mediate bacterial killing and adaption to the rhizosphere microbiome. Sci Rep. 2021;11(1):5772. doi: 10.1038/s41598-021-85218-1 EDN: XGAPRH</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Wekesa TB, Onguso JM, Barminga D, Kavesu N. Pseudomonas fluorescens from Lake Bogoria, Kenya: a promising biocontrol agent against Fusarium solani in Phaseolus vulgaris L. Microbiology (Reading). 2025;171(8):001593. doi: 10.1099/mic.0.001593 EDN: KFVCLE</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Zhou JY, Zhao XY, Dai CC. Antagonistic mechanisms of endophytic Pseudomonas fluorescens against Athelia rolfsii. J Appl Microbiol. 2014;117(4):1144–1158. doi: 10.1111/jam.12586 EDN: UONCWD</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Mehar V, Yadav D, Sanghvi J, et al. Pantoea dispersa: an unusual cause of neonatal sepsis. Braz J Infect Dis. 2013;17(6):726–728. doi: 10.1016/j.bjid.2013.05.013</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Hu H, Xu M, Song H, et al. First Report of Pantoea dispersa Causing Brown Blotch Disease in Flammulina filiformis in China. Plant Dis. 2022;106(3):1056. doi: 10.1094/PDIS-06-21-1270-PDN EDN: ZEMKFY</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Tariq M, Hasnain N, Rasul I, et al. Reconnoitering the capabilities of nodule endophytic Pantoea dispersa for improved nodulation and grain yield of chickpea (Cicer arietinum L.). World J Microbiol Biotechnol. 2023;39(3):85. doi: 10.1007/s11274-023-03525-3 EDN: OPCEEI</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Famous ED, Thompson H, Masoud A. Pantoea dispersa Causing Bacteremia and Endocarditis in an Immunocompromised Adult: A Rare Case. Cureus. 2024;16(11):e74433. doi: 10.7759/cureus.74433 EDN: ILLGSS</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Jiang L, Jeong JC, Lee JS, et al. Potential of Pantoea dispersa as an effective biocontrol agent for black rot in sweet potato. Sci Rep. 2019;9(1):16354. doi: 10.1038/s41598-019-52804-3 EDN: FOYLAT</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Ruan XL, Qin X, Li M. Nosocomial bloodstream infection pathogen Pantoea dispersa: a case report and literature review. J Hosp Infect. 2022;127:77–82. doi: 10.1016/j.jhin.2022.06.011 EDN: XUSQGJ</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Su YW, Huang WH, Yeh CF. Pantoea dispersa rhinosinusitis: clinical aspects of a rare sinonasal pathogen. Eur Arch Otorhinolaryngol. 2022;279(9):4389–4395. doi: 10.1007/s00405-022-07266-1 EDN: DGTTRC</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Asai N, Koizumi Y, Yamada A, et al. Pantoea dispersa bacteremia in an immunocompetent patient: a case report and review of the literature. J Med Case Rep. 2019;13(1):33. doi: 10.1186/s13256-019-1969-z EDN: KGKVNK</mixed-citation></ref><ref id="B78"><label>78.</label><mixed-citation>Yang WT, Yi YJ, Xia B. Unveiling the duality of Pantoea dispersa: A mini review. Sci Total Environ. 2023;873:162320. doi: 10.1016/j.scitotenv.2023.162320 EDN: OFNTTV</mixed-citation></ref><ref id="B79"><label>79.</label><mixed-citation>Lai L, Li S, Zhang S, et al. Enhancing Benzo[a]pyrene Degradation by Pantoea dispersa MSC14 through Biostimulation with Sodium Gluconate: Insights into Mechanisms and Molecular Regulation. Microorganisms. 2024;12(3):592. doi: 10.3390/microorganisms12030592 EDN: YMPZLT</mixed-citation></ref><ref id="B80"><label>80.</label><mixed-citation>Singh P, Singh RK, Li HB, et al. Diazotrophic Bacteria Pantoea dispersa and Enterobacter asburiae Promote Sugarcane Growth by Inducing Nitrogen Uptake and Defense-Related Gene Expression. Front Microbiol. 2021;11:600417. doi: 10.3389/fmicb.2020.600417 EDN: PNZKMA</mixed-citation></ref><ref id="B81"><label>81.</label><mixed-citation>Bashizi T, Kim MJ, Lee G, et al. Whole-Genome Sequence of Pseudomonas frederiksbergensis Strain A6, Isolated from the Rhizosphere of Pepper (Capsicum annuum L.). Microbiol Resour Announc. 2023;12(7):e0022923. doi: 10.1128/mra.00229-23 EDN: OASWQW</mixed-citation></ref><ref id="B82"><label>82.</label><mixed-citation>Ruiz ON, Brown LM, Striebich RC, et al. Draft Genome Sequence of Pseudomonas frederiksbergensis SI8, a Psychrotrophic Aromatic-Degrading Bacterium. Genome Announc. 2015;3(4):e00811–e00815. doi: 10.1128/genomeA.00811-15</mixed-citation></ref><ref id="B83"><label>83.</label><mixed-citation>Chatterjee P, Samaddar S, Anandham R, et al. Beneficial Soil Bacterium Pseudomonas frederiksbergensis OS261 Augments Salt Tolerance and Promotes Red Pepper Plant Growth. Front Plant Sci. 2017;8:705. doi: 10.3389/fpls.2017.00705 EDN: YFABSI</mixed-citation></ref><ref id="B84"><label>84.</label><mixed-citation>Ruiz ON, Radwan O, Striebich RC. GC-MS hydrocarbon degradation profile data of Pseudomonas frederiksbergensis SI8, a bacterium capable of degrading aromatics at low temperatures. Data Brief. 2021;35:106864. doi: 10.1016/j.dib.2021.106864 EDN: QUSMLB</mixed-citation></ref><ref id="B85"><label>85.</label><mixed-citation>Andersen SM, Johnsen K, Sørensen J, et al. Pseudomonas frederiksbergensis sp. nov., isolated from soil at a coal gasification site. Int J Syst Evol Microbiol. 2000;50 Pt 6:1957–1964. doi: 10.1099/00207713-50-6-1957</mixed-citation></ref><ref id="B86"><label>86.</label><mixed-citation>González-Tobón J, Diaz A, Helmann TC, et al. Genomic insights into a Pseudomonas amygdali isolate from Hibiscus rosa-sinensis. Genomics. 2023;115(3):110600. doi: 10.1016/j.ygeno.2023.110600 EDN: LKBUNF</mixed-citation></ref><ref id="B87"><label>87.</label><mixed-citation>Nielsen TK, Winther-Have CS, Thomsen IM, et al. Genetic rearrangements in Pseudomonas amygdali pathovar aesculi shape coronatine plasmids. Infect Genet Evol. 2023;113:105486. doi: 10.1016/j.meegid.2023.105486 EDN: NKXQCI</mixed-citation></ref><ref id="B88"><label>88.</label><mixed-citation>Chai A, Yuan L, Li L, et al. Aerosol transmission of Pseudomonas amygdali pv. lachrymans in greenhouses. Sci Total Environ. 2020;748:141433. doi: 10.1016/j.scitotenv.2020.141433 EDN: LUQLWU</mixed-citation></ref><ref id="B89"><label>89.</label><mixed-citation>Zhang S, Wang Y, Hu T, et al. Guttation Fluids Containing Pseudomonas amygdali pv. lachrymans Are a Potential Source of Secondary Infection in Cucumber. Phytopathology. 2021;111(12):2162–2167. doi: 10.1094/PHYTO-02-21-0050-SC EDN: HODFFO</mixed-citation></ref><ref id="B90"><label>90.</label><mixed-citation>Nikolaidis M, Mossialos D, Oliver SG, Amoutzias GD. Comparative Analysis of the Core Proteomes among the Pseudomonas Major Evolutionary Groups Reveals Species-Specific Adaptations for Pseudomonas aeruginosa and Pseudomonas chlororaphis. Diversity. 2020;12(8):289. doi: 10.3390/d12080289 EDN: UZRSSL</mixed-citation></ref><ref id="B91"><label>91.</label><mixed-citation>Xin XF, He SY. Pseudomonas syringae pv. tomato DC3000: a model pathogen for probing disease susceptibility and hormone signaling in plants. Annu Rev Phytopathol. 2013;51:473–498. doi: 10.1146/annurev-phyto-082712-102321</mixed-citation></ref><ref id="B92"><label>92.</label><mixed-citation>Xin XF, Kvitko B, He SY. Pseudomonas syringae: what it takes to be a pathogen. Nat Rev Microbiol. 2018;16(5):316–328. doi: 10.1038/nrmicro.2018.17 EDN: YHFJOX</mixed-citation></ref><ref id="B93"><label>93.</label><mixed-citation>Ibrahim E, Nasser R, Hafeez R, et al. Biocontrol Efficacy of Endophyte Pseudomonas poae to Alleviate Fusarium Seedling Blight by Refining the Morpho-Physiological Attributes of Wheat. Plants. 2023;12(12):2277. doi: 10.3390/plants12122277 EDN: ZPASNR</mixed-citation></ref><ref id="B94"><label>94.</label><mixed-citation>Xia Y, DeBolt S, Ma Q, et al. Improved Draft Genome Sequence of Pseudomonas poae A2-S9, a Strain with Plant Growth-Promoting Activity. Microbiol Resour Announc. 2019;8(15):e00275-19. doi: 10.1128/MRA.00275-19</mixed-citation></ref><ref id="B95"><label>95.</label><mixed-citation>Niem JM, Billones-Baaijens R, Stodart BJ, et al. Biocontrol Potential of an Endophytic Pseudomonas poae Strain against the Grapevine Trunk Disease Pathogen Neofusicoccum luteum and Its Mechanism of Action. Plants. 2023;12(11):2132. doi: 10.3390/plants12112132 EDN: FYUQMV</mixed-citation></ref><ref id="B96"><label>96.</label><mixed-citation>Gogoleva NE, Nikolaichik YA, Ismailov TT, et al. Complete genome sequence of the abscisic acid-utilizing strain Novosphingobium sp. P6W. 3 Biotech. 2019;9(3):94. doi: 10.1007/s13205-019-1625-8 EDN: ZBEZAU</mixed-citation></ref><ref id="B97"><label>97.</label><mixed-citation>Gogoleva NE, Konnova TA, Ismailov TT, et al. Dataset for transcriptome analysis of abscisic acid degrading bacterium Novosphingobium sp. P6W. Data Brief. 2019;28:105001. doi: 10.1016/j.dib.2019.105001 EDN: BBKKIO</mixed-citation></ref><ref id="B98"><label>98.</label><mixed-citation>Belimov AA, Dodd IC, Safronova VI, et al. Abscisic acid metabolizing rhizobacteria decrease ABA concentrations in planta and alter plant growth. Plant Physiol Biochem. 2014;74:84–91. doi: 10.1016/j.plaphy.2013.10.032 EDN: SKKCNL</mixed-citation></ref><ref id="B99"><label>99.</label><mixed-citation>Ghoreshizadeh S, Calvo-Peña C, Ruiz-Muñoz M, et al. Pseudomonas taetrolens ULE-PH5 and Pseudomonas sp. ULE-PH6 Isolated from the Hop Rhizosphere Increase Phosphate Assimilation by the Plant. Plants. 2024;13(3):402. doi: 10.3390/plants13030402 EDN: FFWPQD</mixed-citation></ref><ref id="B100"><label>100.</label><mixed-citation>Gislason AS, de Kievit TR. Friend or foe? Exploring the fine line between Pseudomonas brassicacearum and phytopathogens. J Med Microbiol. 2020;69(3):347-360. doi: 10.1099/jmm.0.001145 EDN: DTRTXE</mixed-citation></ref><ref id="B101"><label>101.</label><mixed-citation>Chen Z, Hu H, Xu P, Tang H. Soil bioremediation by Pseudomonas brassicacearum MPDS and its enzyme involved in degrading PAHs. Sci Total Environ. 2022;813:152522. doi: 10.1016/j.scitotenv.2021.152522 EDN: CRQCUW</mixed-citation></ref><ref id="B102"><label>102.</label><mixed-citation>Nelkner J, Tejerizo GT, Hassa J, et al. Genetic Potential of the Biocontrol Agent Pseudomonas brassicacearum (Formerly P. trivialis) 3Re2-7 Unraveled by Genome Sequencing and Mining, Comparative Genomics and Transcriptomics. Genes. 2019;10(8):601. doi: 10.3390/genes10080601 EDN: BJCEQE</mixed-citation></ref><ref id="B103"><label>103.</label><mixed-citation>Loewen PC, Switala J, Fernando WG, de Kievit T. Genome Sequence of Pseudomonas brassicacearum DF41. Genome Announc. 2014;2(3):e00390-14. doi: 10.1128/genomeA.00390-14</mixed-citation></ref><ref id="B104"><label>104.</label><mixed-citation>Nandi M, Berry C, Brassinga AK, et al. Pseudomonas brassicacearum strain DF41 kills Caenorhabditis elegans through biofilm-dependent and biofilm-independent mechanisms. Appl Environ Microbiol. 2016;82(23):6889–6898. doi: 10.1128/AEM.02199-16</mixed-citation></ref><ref id="B105"><label>105.</label><mixed-citation>Yang M, Mavrodi DV, Mavrodi OV, et al. Exploring the Pathogenicity of Pseudomonas brassicacearum Q8r1-96 and Other Strains of the Pseudomonas fluorescens Complex on Tomato. Plant Dis. 2020;104(4):1026–1031. doi: 10.1094/PDIS-09-19-1989-RE EDN: BWWEBW</mixed-citation></ref><ref id="B106"><label>106.</label><mixed-citation>Achouak W, Sutra L, Heulin T, et al. Pseudomonas brassicacearum sp. nov. and Pseudomonas thivervalensis sp. nov., two root-associated bacteria isolated from Brassica napus and Arabidopsis thaliana. Int J Syst Evol Microbiol. 2000;50 Pt 1:9–18. doi: 10.1099/00207713-50-1-9</mixed-citation></ref><ref id="B107"><label>107.</label><mixed-citation>Poshvina DV, Vasilchenko AV, Vasilchenko AS. Draft Genome Sequence of Pseudomonas brassicacearum Strain UTMN3, a Biological Control Agent from the Rhizosphere of Pisum sativum. Microbiol Resour Announc. 2021;10(45):e0089521. doi: 10.1128/MRA.00895-21 EDN: IPLOXT</mixed-citation></ref><ref id="B108"><label>108.</label><mixed-citation>Ivanova EP, Christen R, Bizet C, et al. Pseudomonas brassicacearum subsp. neoaurantiaca subsp. nov., orange-pigmented bacteria isolated from soil and the rhizosphere of agricultural plants. Int J Syst Evol Microbiol. 2009;59(Pt 10):2476–2481. doi: 10.1099/ijs.0.009654-0 EDN: MWYYVV</mixed-citation></ref><ref id="B109"><label>109.</label><mixed-citation>Jander G, Rahme LG, Ausubel FM. Positive correlation between virulence of Pseudomonas aeruginosa mutants in mice and insects. J Bacteriol. 2000;182(13):3843–3845. doi: 10.1128/jb.182.13.3843-3845.2000</mixed-citation></ref><ref id="B110"><label>110.</label><mixed-citation>Chahtane H, Nogueira Füller T, Allard PM, et al. The plant pathogen Pseudomonas aeruginosa triggers a DELLA-dependent seed germination arrest in Arabidopsis. Elife. 2018;7:e37082. doi: 10.7554/eLife.37082</mixed-citation></ref><ref id="B111"><label>111.</label><mixed-citation>Micek ST, Lloyd AE, Ritchie DJ, et al. Pseudomonas aeruginosa bloodstream infection: importance of appropriate initial antimicrobial treatment. Antimicrob Agents Chemother. 2005;49(4):1306–1311. doi: 10.1128/AAC.49.4.1306-1311.2005</mixed-citation></ref><ref id="B112"><label>112.</label><mixed-citation>Wilson MG, Pandey S. Pseudomonas aeruginosa. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2025.</mixed-citation></ref><ref id="B113"><label>113.</label><mixed-citation>Jurado-Martín I, Sainz-Mejías M, McClean S. Pseudomonas aeruginosa: An Audacious Pathogen with an Adaptable Arsenal of Virulence Factors. Int J Mol Sci. 2021;22(6):3128. doi: 10.3390/ijms22063128 EDN: ASQSAB</mixed-citation></ref><ref id="B114"><label>114.</label><mixed-citation>Jovcic B, Lepsanovic Z, Suljagic V, et al. Emergence of NDM-1 metallo-β-lactamase in Pseudomonas aeruginosa clinical isolates from Serbia. Antimicrob Agents Chemother. 2011;55(8):3929–3931. doi: 10.1128/AAC.00226-11</mixed-citation></ref><ref id="B115"><label>115.</label><mixed-citation>Chari A, Oakeson KF, Enomoto S, et al. Phenotypic characterization of Sodalis praecaptivus sp. nov., a close non-insect-associated member of the Sodalis-allied lineage of insect endosymbionts. Int J Syst Evol Microbiol. 2015;65(Pt 5):1400–1405. doi: 10.1099/ijs.0.000091</mixed-citation></ref><ref id="B116"><label>116.</label><mixed-citation>Enomoto S, Chari A, Clayton AL, Dale C. Quorum Sensing Attenuates Virulence in Sodalis praecaptivus. Cell Host Microbe. 2017;21(5):629–636.e5. doi: 10.1016/j.chom.2017.04.003</mixed-citation></ref><ref id="B117"><label>117.</label><mixed-citation>Flórez LV, Scherlach K, Gaube P, et al. Antibiotic-producing symbionts dynamically transition between plant pathogenicity and insect-defensive mutualism. Nat Commun. 2017;8:15172. doi: 10.1038/ncomms15172</mixed-citation></ref><ref id="B118"><label>118.</label><mixed-citation>Bing XL, Wan YY, Liu HH, et al. Characterization of Pantoea ananatis from rice planthoppers reveals a clade of rice-associated P. ananatis undergoing genome reduction. Microb Genom. 2022;8(12):mgen000907. doi: 10.1099/mgen.0.000907 EDN: CXXAYR</mixed-citation></ref><ref id="B119"><label>119.</label><mixed-citation>De Maayer P, Chan WY, Rubagotti E, et al. Analysis of the Pantoea ananatis pan-genome reveals factors underlying its ability to colonize and interact with plant, insect and vertebrate hosts. BMC Genomics. 2014;15(1):404. doi: 10.1186/1471-2164-15-404 EDN: UPCALL</mixed-citation></ref><ref id="B120"><label>120.</label><mixed-citation>Christiansen L, Pathiraja D, Bech PK, et al. A Multifunctional Polysaccharide Utilization Gene Cluster in Colwellia echini Encodes Enzymes for the Complete Degradation of κ-Carrageenan, ι-Carrageenan, and Hybrid β/κ-Carrageenan. mSphere. 2020;5(1):e00792-19. doi: 10.1128/msphere.00792-19 EDN: TAEJME</mixed-citation></ref><ref id="B121"><label>121.</label><mixed-citation>Wang G, Dang G, Xu S, et al. Aliikangiella coralliicola sp. nov., a bacterium isolated from coral Porites lutea, and proposal of Pleioneaceae fam. nov. to accommodate Pleionea and Aliikangiella. Int J Syst Evol Microbiol. 2020;70(11):5880–5887. doi: 10.1099/ijsem.0.004489 EDN: DFZUPN</mixed-citation></ref><ref id="B122"><label>122.</label><mixed-citation>Meng X, Chang YQ, Wang H, Du ZJ. Algibacillus agarilyticus gen. nov., sp. nov., isolated from the surface of the red algae Gelidium amansii. Int J Syst Evol Microbiol. 2021;71(1). doi: 10.1099/ijsem.0.004558 EDN: ULASMF</mixed-citation></ref><ref id="B123"><label>123.</label><mixed-citation>Ivanova EP, Nedashkovskaya OI, Zhukova NV, et al. Shewanella waksmanii sp. nov., isolated from a sipuncula (Phascolosoma japonicum). Int J Syst Evol Microbiol. 2003;53(Pt 5):1471–1477. doi: 10.1099/ijs.0.02630-0 EDN: LIEQDR</mixed-citation></ref><ref id="B124"><label>124.</label><mixed-citation>Hatanaka T, Shimizu R, Hildebrand D. Expression of a Stokesia laevis epoxygenase gene. Phytochemistry. 2004;65(15):2189–2196. doi: 10.1016/j.phytochem.2004.06.006</mixed-citation></ref><ref id="B125"><label>125.</label><mixed-citation>Pineau E, Sauveplane V, Grienenberger E, et al. CYP77B1 a fatty acid epoxygenase specific to flowering plants. Plant Sci. 2021;307:110905. doi: 10.1016/j.plantsci.2021.110905 EDN: YMDZKX</mixed-citation></ref><ref id="B126"><label>126.</label><mixed-citation>Weimann A, Dinan AM, Ruis C, et al. Evolution and host-specific adaptation of Pseudomonas aeruginosa. Science. 2024;385(6704):eadi0908. doi: 10.1126/science.adi0908 EDN: SETOZF</mixed-citation></ref><ref id="B127"><label>127.</label><mixed-citation>Kulkarni AP. Lipoxygenase—a versatile biocatalyst for biotransformation of endobiotics and xenobiotics. Cell Mol Life Sci. 2001;58(12–13):1805–1825. doi: 10.1007/PL00000820 EDN: ASSOSV</mixed-citation></ref></ref-list></back></article>
