Molecular Analysis of Phylogenetic Diversity of Halophilic Methylotrophic Bacterial Communities
- Авторлар: Shustova M.N.1,2, Kocharovskaya Y.N.1,3, Delegan Y.A.1,3, Kaparullina E.N.1, Doronina N.V.1
-
Мекемелер:
- G.K. Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, Federal Research Center "Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences"
- Pushchino branch of the Federal State Budgetary Educational Institution of Higher Education "Russian Biotechnological University (ROSBIOTECH)"
- Ivanovsky Academy of Biology and Biotechnology, Southern Federal University
- Шығарылым: Том 94, № 6 (2025)
- Беттер: 594–604
- Бөлім: EXPERIMENTAL ARTICLES
- URL: https://journal-vniispk.ru/0026-3656/article/view/358317
- DOI: https://doi.org/10.7868/S3034546425060093
- ID: 358317
Дәйексөз келтіру
Аннотация
Авторлар туралы
M. Shustova
G.K. Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, Federal Research Center "Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences"; Pushchino branch of the Federal State Budgetary Educational Institution of Higher Education "Russian Biotechnological University (ROSBIOTECH)"Pushchino, Moscow oblast, Russia; Pushchino, Moscow oblast, Russia
Yu. Kocharovskaya
G.K. Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, Federal Research Center "Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences"; Ivanovsky Academy of Biology and Biotechnology, Southern Federal UniversityPushchino, Moscow oblast, Russia; Rostov-on-Don, Russia
Ya. Delegan
G.K. Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, Federal Research Center "Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences"; Ivanovsky Academy of Biology and Biotechnology, Southern Federal UniversityPushchino, Moscow oblast, Russia; Rostov-on-Don, Russia
E. Kaparullina
G.K. Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, Federal Research Center "Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences"
Email: lenokap80@gmail.com
Pushchino, Moscow oblast, Russia
N. Doronina
G.K. Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, Federal Research Center "Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences"Pushchino, Moscow oblast, Russia
Әдебиет тізімі
- Доронина Н.В., Торгонская М.Л., Федоров Д.Н., Троценко Ю.А. Аэробные метилобактерии – перспективные объекты современной биотехнологии (обзор) // Прикл. биохимия и микробиология. 2015. Т. 51. С. 111–121.
- Doronina N.V., Torgonskaya M.L., Fedorov D.N., Trotsenko Y.A. Aerobic methylobacteria as promising objects of modern biotechnology (review) // Appl. Biochem. Microbiol. 2015. V. 51. P. 125–134.
- Курочкин В.Ю., Федоров А.А., Хорошавина Е.И., Волкова Н.А. Природные ресурсы озера Медвежье Курганской области, вопросы их формирования, комплексного использования и охраны // Курортная медицина. 2014. № 4. С. 8–13.
- Равин Н.В., Марданов А.В., Скрябин К.Г. Метагеномика как инструмент изучения “некультивируемых” микроорганизмов // Генетика. 2015. T. 51. C. 519–528
- Ravin N.V., Mardanov A.V., Skryabin K.G. Metagenomics as a tool for the investigation of uncultured microorganisms // Russ. J. Gen. 2015. V. 51. P. 431–439.
- Селиванова Е.А., Пошвина Д.В., Хлопко Ю.А., Гоголева Н.Е., Плотников А.О. Разнообразие прокариот в планктонных сообществах соленых Соль-Илецких озер (Оренбургская область) // Микробиология. 2018. Т. 87. С. 432–447.
- Selivanova E.A., Poshvina D.V., Khlopko Y.A., Plotnikov A.O., Gogoleva N.E. Diversity of prokariotes in planktonic communities of saline Sol-Iletsk lakes (Orenburg oblast, Russia) // Microbiology (Moscow). 2018. Т. 87. P. 569–582.
- Шмарева М.Н., Доронина Н.В., Тарлачков С.В., Василенко О.В., Троценко Ю.А. Галоалкалофильный метилотроф выделенный из содового озера Хилганта (Южное Забайкалье, Республика Бурятия) // Микробиология. 2018. Т. 87. С. 23–36.
- Shmareva M.N., Doronina N.V., Tarlachkov S.V., Vasilenko O.V., Trotsenko Y.A. Methylophaga muralis Bur 1, a halophilic methylotroph isolated from the Khilganta soda lake (Southern Transbaikalia, Buryat republic) // Microbiology (Moscow). 2018. V. 87. P. 33–46.
- Ahmad T., Ishaq S.E., Liang L., Xie R., Wang Y., Wang F. A diffusion-based integrative approach for culturing previously uncultured bacteria from marine sediments // Marine Life Sci. Technol. 2024. P. 1–12. https://doi.org/10.1007/s42995-024-00240-2
- Arahal D.R., Ludwig W., Schleifer K.H., Ventosa A. Phylogeny of the family Halomonadaceae based on 23S and 165 rDNA sequence analyses // Int. J. Syst. Evol. Microbiol. 2002. V. 52. P. 241–249.
- Benjamin J.C., Paul J.M., Michael J.R., Andrew W.H., Amy J.A.J., Susan P.H. Dada2: high-resolution sample inference from Illumina amplicon data // Nature Meth. 2016. V. 13. P. 581–583.
- Boden R. Emended description of the genus Methylophaga Janvier et al. 1985 // Int. J. Syst. Evol. Microbiol. 2012. V. 62. P. 1644–1646.
- Bokulich N.A., Kaehler B.D., Rideout J.R., Dillon M., Bolyen E., Knight R., Huttley G.A., Caporaso J.G. Optimizing taxonomic classification of marker-gene amplicon sequences with QIIME 2’s q2-feature-classifier plugin // Microbiome. 2018. V. 6. P. 1–17. https://doi.org/10.1186/s40168-018-0470-z
- Bolyen E., Rideout J.R., Dillon M.R., et al. Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2 // Nat. Biotechnol. 2019. V. 37. P. 852–857.
- Chistoserdova L. Methylotrophy in a lake: from metagenomics to single-organism physiology // Appl. Env. Microbiol. 2011. V. 77. P. 4705‒4711.
- Doronina N.V., Poroshina M.N., Kaparullina E.N., Ezhov V.A., Trotsenko Y.A. Methyloligella halotolerans gen. nov., sp. nov. and Methyloligella solikamskensis sp. nov., two non-pigmented halotolerant obligately methylotrophic bacteria isolated from the Ural saline environments // Syst. Appl. Microbiol. 2013. V. 36. P. 148–154.
- Doronina N.V., Shmareva M.N, Kaparullina E.N., Vasilenko O.V., Tarlachkov S.V., Trotsenko Y.A. Reclassification of Methylarcula marina Doronina et al. 2000 as Paracoccus methylarcula nom. nov. // Microbiology (Moscow). 2020. V. 89. P. 197–204.
- Grice E.A., Kong H.H., Conlan S., Deming C.B., Davis J., Young A.C., NISC Comparative Sequencing Program, Bouffard G.G., Blakesley R.W., [...], Segre J.A. Topographical and temporal diversity of the human skin microbiome // Science. 2009. V. 324. P. 1190–1192.
- Kalyuzhnaya M.G., Lapidus A., Ivanova N., Copeland A.C., McHardy A.C., Szeto E., Salamov A., Grigoriev I.V., Suciu D., Levine S.R., Markowitz V.M., Rigoutsos I., Tringe S.G., Bruce D.C., Richardson P.M., Lidstrom M.E., Chistoserdova L. High-resolution metagenomics targets specific functional types in complex microbial communities // Nat. Biotechnol. 2008. V. 26. P. 1029–1034.
- Kolberg J., Busse H.J., Wilke T., Schubert P., Kämpfer P., Glaeser S.P. Mesonia hippocampi sp. nov., isolated from the brood pouch of a diseased Barbour’s Seahorse (Hippocampus barbouri) // Int. J. Syst. Evol. Microbiol. 2015. V. 65. P. 2241–2247.
- Kumar R., Mishra A., Jha B. Bacterial community structure and functional diversity in subsurface seawater from the western coastal ecosystem of the Arabian Sea, India // Gene. 2019. V. 701. P. 55–64.
- Lahti L., Shetty S. Tools for microbiome analysis in R. Version 2.1. 26 // Bioc Package. 2017.
- Lin K.Y., Sheu S.Y., Chang P.S., Cho J.C., Chen W.M. Oceanicola marinus sp. nov., a marine alphaproteobacterium isolated from seawater collected off Taiwan // Int. J. Syst. Evol. Microbiol. 2007. V. 57. P. 1625–1629.
- Liu J.J., Zhang X.Q., Pan J., Sun C., Zhang Y., Li C.Q., Zhu X.F., Wu M. Aequorivita viscosa sp. nov., isolated from an intertidal zone, and emended descriptions of Aequorivita antarctica and Aequorivita capsosiphonis // Int. J. Syst. Evol. Microbiol. 2013. V. 63. P. 3192–3196.
- Lu J., Salzberg S.L. Ultrafast and accurate 16S rRNA microbial community analysis using Kraken 2 // Microbiome. 2020. V. 8. Art. 124. https://doi.org/10.1186/s40168-020-00900-2
- McMurdie P.J., Holmes S. phyloseq: an R package for reproducible interactive analysis and graphics of microbiome census data // PloS One. 2013. V. 8. Art. e61217. https://doi.org/10.1371/journal.pone.0061217
- Malygina E.V., Imidoeva N.A., Morgunova M.M., Dmitrieva M.E., Belyshenko A.Y., Vlasova A.A., Shelkovnikova V.N., Telnova T.Y., Konovalov A.S., Axenov-Gribanov D.V. First report on truffle-inhabiting fungi and metagenomic communities of Tuber aestivum collected in Russia // J. Exper. Biol. Agricult. Sci. 2024. V. 12. P. 16–35.
- Martin M. Cutadapt removes adapter sequences from high-throughput sequencing reads // EMBnet J. 2011. V. 17. P. 10–12.
- Neufeld J.D., Schäfer H., Cox M.J., Boden R., McDonald I.R., Murrell J.C. Stable-isotope probing implicates Methylophaga spp and novel Gammaproteobacteria in marine methanol and methylamine metabolism // ISME J. 2007. V. 1. P. 480–491.
- Poroshina M.N., Trotsenko Y.A., Doronina N.V. Methylobrevis pamukkalensis gen. nov., sp. nov., a halotolerant restricted facultative methylotroph isolated from saline water // Int. J. Syst. Evol. Microbiol. 2015. V. 65. P. 1321–1327.
- Saitou N., Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees // Mol. Biol. Evol. 1987. V. 4. P. 406–425.
- Schornsteiner E., Mann E., Bereuter O., Wagner M., Schmitz-Esser S. Cultivation-independent analysis of microbial communities on Austrian raw milk hard cheese rinds // Int. J. Food Microbiol. 2014. V. 180. P. 88–97.
- Schäfer H. Isolation of Methylophaga spp. from marine dimethylsulfide-degrading enrichment cultures and identification of polypeptides induced during growth on dimethylsulfide // Appl. Environ. Microbiol. 2007. V. 73. P. 2580–2591.
- Sorokin D.Y., Trotsenko Y.A., Doronina N.V., Tourova T.P., Galinski E.A., Kolganova T.V., Muyzer G. Methylohalomonas lacus gen. nov., sp. nov. and Methylonatrum kenyense gen. nov., sp. nov., methylotrophic gammaproteobacteria from hypersaline lakes // Int. J. Syst. Evol. Microbiol. 2007. V. 57. P. 2762–2769.
- Tamura K., Stecher G., Peterson D., Filipski A., Kumar S. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0 // Mol. Biol. Evol. 2013. V. 30. P. 2725–2729.
- Thompson J.D., Gibson T.J., Plewniak F., Jeanmougin F., Higgins D.G. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools // Nucleic Acids Res. 1997. V. 25. P. 4876–4882.
- Vandecandelaere I., Segaert E., Mollica A., Faimali M., Vandamme P. Leisingera aquimarina sp. nov., isolated from a marine electroactive biofilm and emended description of Leisingera methylohalidovorans Schaefer et al. 2002, Phaeobacter daeponensis Yoon et al. 2007 and Phaeobacter inhibens Martens et al. 2006 // Int. J. Syst. Evol. Microbiol. 2008. V. 58. P. 2788–2793.
- Villeneuve C., Martineau C., Mauffrey F., Villemur R. Methylophaga nitratireducenticrescens sp. nov. and Methylophaga frappieri sp. nov., isolated from the biofilm of the methanol-fed denitrification system treating the seawater at the Montreal Biodome // Int. J. Syst. Evol. Microbiol. 2013. V. 63. P. 2216–2222.
- Quast C., Pruesse E., Yilmaz P., Gerken J., Schweer T., Yarza P., Peplies J., Glöckner F.O. The SILVA ribosomal RNA gene database project: improved data processing and web-based tools // Nucleic Acids Res. 2012. V. 41. D1. P. D590–D596.
- Wei T.T., Zhang R.Y., Quan Z.X. Methylophaga pinxianii sp. nov., isolated from the Mariana Trench // Int. J. Syst. Evol. Microbiol. 2022. V. 72. Art. 005414.
- Wickham H., Averick M., Bryan J., Chang W., McGowan L.D., François R., Grolemund G., Hayes A., Henry L., Hester J., Kuhn M., Pedersen T.L., Miller E., Bache S.M., Müller K., Ooms J., Robinson D., Seidel D.P., Spinu V., Takahashi K., Vaughan D., Wilke C., Woo K., Yutani H. Welcome to the Tidyverse // J. Open Source Software. 2019. V. 4. № 43. Art. 1686. http://dx.doi.org/10.21105/joss.01686
- Wickham H., Sievert C. ggplot2: elegant graphics for data analysis. New York: Springer, 2009. V. 10. P. 978–980.
- Willis A., Bunge J., Whitman T. Improved detection of changes in species richness in high diversity microbial communities // J. Royal Statist. Soc. Ser. C: Applied Statistics. 2017. V. 66. P. 963–977.
- Wood D.E., Salzberg S.L. Kraken: ultrafast metagenomic sequence classification using exact alignments // Genome Biol. 2014. V. 15. Art. R46. https://doi.org/10.1186/gb-2014-15-3-r46
Қосымша файлдар

