본문 바로가기
KERD
논문KCI 등재

Optimizing Conditions for the Production of Bacterial Extracellular Vesicles of Vibrio vulnificus and Analysis of the Inner Small RNA Compositions

2

조회

0

다운로드

0

인용

0

참고문헌

키워드

주제분류생물학

초록

Chemical and physical elements affecting the production of bacterial extracellular vesicles (BEVs) of the human pathogen Vibrio vulnificus were quantitatively assessed to optimize the conditions for the BEV production by using the western blot quantification for an outer membrane porin OmpU and by fluorescent dye FM4-64. When cells were cultured at 37o C in an enriched medium (2 × Luria Bertani; 2 × LB) in the presence of EDTA, they produced about 70% more BEVs. BEVs were purified from the cells cultured in the established optimal conditions by the density gradient ultracentrifugation. The dynamic light scattering measurement of the purified BEVs showed that the diameter of them ranged from approximately 25 nm to 161 nm. We hypothesized that there may be some features in nucleotide sequences specific to RNAs packaged in BEVs compared to those in cellular RNA molecules. We compared the nucleotide sequences and abundance of sRNAs between in the cellular fraction and in BEVs through next-generation sequencing (NGS). While no distinct feature was observed in the nucleotide sequences of sRNAs between two groups, the length of sRNA fragments from BEVs were significantly shorter than those in cytoplasm.

Abstract

Chemical and physical elements affecting the production of bacterial extracellular vesicles (BEVs) of the human pathogen Vibrio vulnificus were quantitatively assessed to optimize the conditions for the BEV production by using the western blot quantification for an outer membrane porin OmpU and by fluorescent dye FM4-64. When cells were cultured at 37o C in an enriched medium (2 × Luria Bertani; 2 × LB) in the presence of EDTA, they produced about 70% more BEVs. BEVs were purified from the cells cultured in the established optimal conditions by the density gradient ultracentrifugation. The dynamic light scattering measurement of the purified BEVs showed that the diameter of them ranged from approximately 25 nm to 161 nm. We hypothesized that there may be some features in nucleotide sequences specific to RNAs packaged in BEVs compared to those in cellular RNA molecules. We compared the nucleotide sequences and abundance of sRNAs between in the cellular fraction and in BEVs through next-generation sequencing (NGS). While no distinct feature was observed in the nucleotide sequences of sRNAs between two groups, the length of sRNA fragments from BEVs were significantly shorter than those in cytoplasm.

참고문헌 (54)

  1. Toyofuku M, "Types and origins of bacterial membrane vesicles", Nat. Rev. Microbiol, 17, pp.13~24 (2019)
  2. Juodeikis R, "Outer membrane vesicles : biogenesis, functions, and issues", Microbiol. Mol. Biol. Rev, 86, pp.e00032-00022~ (2022)
  3. Sjöström AE, "Membrane vesicle-mediated release of bacterial RNA", Sci. Rep, 5, pp.15329~ (2015)
  4. Koeppen K, "A Novel mechanism of host-pathogen interaction through sRNA in bacterial outer membrane vesicles", PLoS Pathog, 12, pp.e1005672~ (2016)
  5. Bitto NJ, "Bacterial membrane vesicles transport their DNA cargo into host cells", Sci. Rep, 7, pp.7072~ (2017)
  6. Altindis E, "Proteomic analysis of Vibrio cholerae outer membrane vesicles", Proc. Natl. Acad. Sci. USA, 111, pp.E1548~E1556 (2014)
  7. Orench-Rivera N, "Environmentally controlled bacterial vesicle-mediated export", Cell. Microbiol, 18, pp.1525~1536 (2016)
  8. MacDonald IA, "Stress-induced outer membrane vesicle production by Pseudomonas aeruginosa", J. Bacteriol, 195, pp.2971~2981 (2013)
  9. Manning AJ, "Contribution of bacterial outer membrane vesicles to innate bacterial defense", BMC Microbiol, 11, pp.258~271 (2011)
  10. Kim H-M, "Synthesis of ppGpp impacts type IX secretion and biofilm matrix formation in Porphyromonas gingivalis", NPJ Biofilms Microbiomes, 6, pp.5~ (2020)
  11. Ciofu O, "Chromosomal β-lactamase is packaged into membrane vesicles and secreted from Pseudomonas aeruginosa", J. Antimicrob. Chemother, 45, pp.9~13 (2000)
  12. McMahon KJ, "Biogenesis of outer membrane vesicles in Serratia marcescens is thermoregulated and can be induced by activation of the Rcs phosphorelay system", J. Bacteriol, 194, pp.3241~3249 (2012)
  13. Elhenawy W, "Preferential packing of acidic glycosidases and proteases into bacteroides outer membrane vesicles", mBio, 5, pp.e00909-00914~ (2014)
  14. Kim JH, "Gram-negative and Gram-positive bacterial extracellular vesicles", Semin. Cell. Dev. Biol, 40, pp.97~104 (2015)
  15. Ahmadi Badi S, "Small RNAs in outer membrane vesicles and their function in host-microbe interactions", Front. Microbiol, 11, pp.1209~ (2020)
  16. Reddy GP, "Purification and determination of the structure of capsular polysaccharide of Vibrio vulnificus MO6-24", J. Bacteriol, 174, pp.2620~2630 (1992)
  17. Park D-K, "Cyclo(Phe-Pro)modulates the expression of ompU in Vibrio spp", J. Bacteriol, 188, pp.2214~2221 (2006)
  18. McBroom AJ, "Outer membrane vesicle production by Escherichia coli is independent of membrane instability", J. Bacteriol, 188, pp.5385~5392 (2006)
  19. Yang HC, "Single-step equipment-free extracellular vesicle concentration using super absorbent polymer beads", J. Extracell. Vesicles, 10, pp.e12074~ (2021)
  20. Li K, "Cushioned-density gradient ultracentrifugation(C-DGUC) : A refined and high performance method for the isolation, characterization, and use of exosomes", Methods Mol. Biol, 1740, pp.69~83 (2018)
  21. Ko SH, "High-speed, high-purity separation of gold nanoparticle–DNA origami constructs using centrifugation", Soft Matter, 10, pp.7370~7378 (2014)
  22. Castle JD, "Overview of cell fractionation", Curr. Protoc. Protein Sci. Chapter 4. Unit 4.1, ~ (2001)
  23. Schwechheimer C, "Outer-membrane vesicles from Gram-negative bacteria : biogenesis and functions", Nat. Rev. Microbiol, 13, pp.605~619 (2015)
  24. McBroom AJ, "Release of outer membrane vesicles by Gram-negative bacteria is a novel envelope stress response", Mol. Microbiol, 63, pp.545~558 (2007)
  25. Frias A, "Membrane vesicles : a common feature in the extracellular matter of cold-adapted antarctic bacteria", Microb. Ecol, 59, pp.476~486 (2010)
  26. Florez C, "Membrane distribution of the Pseudomonas quinolone signal modulates outer membrane vesicle production in Pseudomonas aeruginosa", mBio, 8, pp.e01034-17~ (2017)
  27. Reichelt J, "Taxonomy of the marine, luminous bacteria", Arch. Microbiol, 94, pp.283~330 (1973)
  28. Baumgarten T, "Membrane vesicle formation as a multiple-stress response mechanism enhances Pseudomonas putida DOT-T1E cell surface hydrophobicity and biofilm formation", Appl. Environ. Microbiol, 78, pp.6217~6224 (2012)
  29. Prados-Rosales R, "Role for Mycobacterium tuberculosis membrane vesicles in iron acquisition", J. Bacteriol, 196, pp.1250~1256 (2014)
  30. Godlewska R, "Influence of environmental and genetic factors on proteomic profiling of outer membrane vesicles from", Polish J. Microbiol., 68, pp.255~261 (2019)
  31. Gerritzen MJH, "High dissolved oxygen tension triggers outer membrane vesicle formation by Neisseria meningitidis", Microb. Cell Fact, 17, pp.157~166 (2018)
  32. Jan AT, "Outer membrane vesicles(OMVs)of gram-negative bacteria : A perspective update", Front. Microbiol, 8, pp.1053~ (2017)
  33. Van de Waterbeemd B, "Improved production process for native outer membrane vesicle vaccine against Neisseria meningitidis", PLoS One, 8, pp.e65157~ (2013)
  34. Bager RJ, "Outer membrane vesicles reflect environmental cues in Gallibacterium anatis", Vet. Microbiol, 167, pp.565~572 (2013)
  35. Choi CW, "Proteomic characterization of the outer membrane vesicle of Pseudomonas putida KT2440", J. Proteome Res, 13, pp.4298~4309 (2014)
  36. Martin M, "Cutadapt removes adapter sequences from high-throughput sequencing reads", EMBnet J, 17(1), pp.10~12 (2011)
  37. Langmead B, "Fast gapped-read alignment with Bowtie 2", Nat. Methods, 9, pp.357~359 (2012)
  38. Huber M, "Switching fatty acid metabolism by an RNA-controlled feed forward loop", Proc. Natl Acad. Sci. USA, 117, pp.8044~8054 (2020)
  39. Song T, "A new Vibrio cholerae sRNA modulates colonization and affects release of outer membrane vesicles", Mol. Microbiol, 70, pp.100~111 (2008)
  40. Wen Y, "Iron-and quorum-sensing signals converge on small quorum-regulatory RNAs for coordinated regulation of virulence factors in Vibrio vulnificus", J. Biol. Chem, 291, pp.14213~14230 (2016)
  41. Yamamoto S, "Identification of a chitin-induced small RNA that regulates translation of the tfoX gene, encoding a positive regulator of natural competence in Vibrio cholerae", J. Bacteriol, 193, pp.1953~1965 (2011)
  42. Liu B, "GcvB regulon revealed by transcriptomic and proteomic analysis in Vibrio alginolyticus", Int. J. Mol. Sci, 23 (2022)
  43. Moriano-Gutierrez S, "The noncoding small RNA SsrA is released by Vibrio fischeri and modulates critical host responses", PLoS Biol, 18, pp.e3000934~ (2020)
  44. Richard AL, "The Vibrio cholerae virulence regulatory cascade controls glucose uptake through activation of TarA, a small regulatory RNA", Mol. Microbiol, 78, pp.1171~1181 (2010)
  45. Mendez-Contreras SI, "Identifying regulatory targets of the small RNA MtlS in Vibrio cholerae", FASEB J, 32, pp.525~528 (2018)
  46. Plaza N, "Conservation of small regulatory RNAs in Vibrio parahaemolyticus : Possible role of RNA-OUT encoded by the pathogenicity island(VPaI-7)of pandemic strains", Int. J. Mol. Sci, 20, pp.2827~ (2019)
  47. Lenz DH, "CsrA and three redundant small RNAs regulate quorum sensing in Vibrio cholerae", Mol. Microbiol, 58, pp.1186~1202 (2005)
  48. Mandel MJ, "Comparative genomics-based investigation of resequencing targets in Vibrio fischeri : Focus on point miscalls and artefactual expansions", BMC Genomics, 9, pp.138~152 (2008)
  49. Peschek N, "RNA-mediated control of cell shape modulates antibiotic resistance in Vibrio cholerae", Nat. Commun, 11, pp.6067~6077 (2020)
  50. Davis BM, "RNase E-dependent processing stabilizes MicX, a Vibrio cholerae sRNA", Mol. Microbiol, 65, pp.373~385 (2007)
  51. Papenfort K, "Differential RNA-seq of Vibrio cholerae identifies the VqmR small RNA as a regulator of biofilm formation", Proc. Natl. Acad. Sci. USA, 112, pp.E766~E775 (2015)
  52. Altschul SF, "Basic local alignment search tool", J. Mol. Biol, 215, pp.403~410 (1990)
  53. Yoon H, "Bacterial outer membrane viscles as a delivery system for virulence regulation", J. Microbiol. Biotechnol, 26, pp.1343~1347 (2016)
  54. Hampton CM, "The opportunistic pathogen Vibrio vulnificus produces outer membrane vesicles in a spatially distinct manner related to capsular polysaccharide", Front. Microbiol, 8, pp.2177~ (2017)

관련 논문AI추천

이 간행물의 다른 논문 (24건)