WGS-based characterization of the potentially beneficial Enterococcus faecium EFD from a beehive.
Bacteriocins
Enterococcus faecium
Illumina HiSeq
Whole-genome sequencing
Journal
Molecular biology reports
ISSN: 1573-4978
Titre abrégé: Mol Biol Rep
Pays: Netherlands
ID NLM: 0403234
Informations de publication
Date de publication:
Aug 2020
Aug 2020
Historique:
received:
25
03
2020
accepted:
11
07
2020
revised:
07
07
2020
pubmed:
23
7
2020
medline:
27
5
2021
entrez:
23
7
2020
Statut:
ppublish
Résumé
Nowadays, due to their potential application as probiotics for humans or animals, many beneficial lactic acid bacteria have been isolated from different natural environments. These include members of the genus Enterococcus - quite specific due to their ambiguous nature, varying from pathogens to probiotics. In our work we present a whole-genome sequencing (WGS)-based approach for assessing the potential of bacteriocin-producing Enterococcus isolates from beehives to serve as natural preserving agents against bacterial infections associated with honeybees. Potential Enterococcus spp. isolates from pollen granules were tested with the well diffusion assay for bacteriocin activity against Paenibacillus larvae, the causative agent of the American foulbrood disease (AFB). Two of them gave positive results and were determined at species level by 16S rRNA genes sequencing. They were then subjected to WGS using the Illumina HiSeq platform. The resulting raw data reads were processed and further analyzed by using only freely available web-based tools (the Shovill pipeline, QUAST, BAGEL4, ResFinder, VirulenceFinder and PlasmidFinder). The analysis revealed that both of them represent clonally identical isolates of the same strain. This specific strain was named Enterococcus faecium EFD, and was genotyped by the MLST-2.0 Server. Five bacteriocin genes were found in the assembled genome, providing a possible explanation for the antimicrobial properties of the isolate. The protein nature of the inhibitory agent/s was confirmed by treatment with proteinase K. No resistance determinants for clinically important antibiotics and functional virulence factor genes were detected. The bioinformatic analyses of the draft genome sequence suggest that E. faecium EFD is not pathogenic.The observation that E. faecium EFD was present within more than one of the beehives in the apiary proposes the idea that E. faecium EFD is there as a part of the normal beehive microbiota. This finding, in combination with its antibacterial activity against P. larvae, highlights this novel isolate as a potential natural preserving agent against AFB. Furthermore, the WGS-based approach reported here proved to be very cost- and time- efficient, for screening the applicability of new pro- and prebiotic Enterococcus strains as beehive protection agents.
Identifiants
pubmed: 32696346
doi: 10.1007/s11033-020-05663-5
pii: 10.1007/s11033-020-05663-5
doi:
Substances chimiques
Bacteriocins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
6445-6449Subventions
Organisme : Bulgarian National Science Fund
ID : КП-06-Н26/8 from 17.12.2018
Références
Bansal P, Kumar R, Singh J, Dhanda S (2019) Next generation sequencing, biochemical characterization, metabolic pathway analysis of novel probiotic Pediococcusacidilactici NCDC 252 and it’s evolutionary relationship with other lactic acid bacteria. MolBiol Rep 46:5883–5895. https://doi.org/10.1007/s11033-019-05022-z
doi: 10.1007/s11033-019-05022-z
Fisher K, Phillips C (2009) The ecology, epidemiology and virulence of Enterococcus. Microbiology 155:1749–1757. https://doi.org/10.1099/mic.0.026385-0
doi: 10.1099/mic.0.026385-0
pubmed: 19383684
Zommiti M, Ferchichi M, Sebei K, Feuilloley MGJ, Connil N, Boukerb AM (2020) Draft Genome Sequences of Five Potentially Probiotic Enterococcus faecium Strains Isolated from an Artisanal Tunisian Meat (Dried Ossban). Microbiology Resource Announcements 9(3):e01348–e01319. https://doi.org/10.1128/MRA.01348-19
doi: 10.1128/MRA.01348-19
pubmed: 31948960
pmcid: 6965578
Royan M (2019) Mechanisms of Probiotic Action in the Honeybee. Crit Rev Eukaryot Gene Expr 29(2):95–103. https://doi.org/10.1615/critreveukaryotgeneexpr.2019025358
doi: 10.1615/critreveukaryotgeneexpr.2019025358
pubmed: 31679264
Zulkhairi AFA, SabriS, Ismail M, Chan KW, Ismail N, MohdEsaN, Mohd LilaMA, Zawawi N (2020) Probiotic Properties of Bacillus Strains Isolated from Stingless Bee (Heterotrigonaitama) Honey Collected across Malaysia. International Journal of Environmental Research Public Health 17(1):278. https://doi.org/10.3390/ijerph17010278
doi: 10.3390/ijerph17010278
Dimov S, Peykov S, Raykova D, Ivanova P, Kirilov N, Dalgalarrondo M, Chobert J, Haertlé T, Ivanova I (2009) A newly discovered bacteriocin produced by Enterococcus faecalis 3915. BenefMicrob 1:43–51. https://doi.org/10.3920/BM2008.1004
doi: 10.3920/BM2008.1004
Dimov SG (2007) A Novel Bacteriocin-Like Substance Produced by Enterococcus faecium 3587. CurrMicrobiol 55:323–327. https://doi.org/10.1007/s00284-007-0018-0
doi: 10.1007/s00284-007-0018-0
Lane DJ (1991) 16S/23S rRNA sequencing. In: Stackebrandt E, Goodfellow M (eds) Nucleic acid techniques in bacterial systematics. John Wiley and Sons, New York, NY, pp 115–175
Seemann T (2017) Shovill: Faster SPAdes assembly of Illumina reads on https://github.com/tseemann/shovill
Afgan E, Baker D, Batut B, Van Den Beek M, Bouvier D et al (2018) The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2018 update. Nucleic Acids Research 46(W1):W537–W544. https://doi.org/10.1093/nar/gky379
doi: 10.1093/nar/gky379
pubmed: 29790989
pmcid: 6030816
Gurevich A, Saveliev V, Vyahhi N, Tesler G (2013) QUAST: quality assessment tool for genome assemblies. Bioinformatics 29(8):1072–1075. https://doi.org/10.1093/bioinformatics/btt086
doi: 10.1093/bioinformatics/btt086
pubmed: 23422339
pmcid: 3624806
De Jong A, Van Heel AJ, Kok J, Kuipers OP (2010) BAGEL2: mining for bacteriocins in genomic data. Nucleic Acids Res 38(Web Server issue):W647-651. https://doi.org/10.1093/nar/gkq365
doi: 10.1093/nar/gkq365
pubmed: 20462861
pmcid: 2896169
Zankari E, Hasman H, Cosentino S, Vestergaard M, Rasmussen S et al (2012) Identification of acquired antimicrobial resistance genes. J AntimicrobChemother 67(11):2640–2644. https://doi.org/10.1093/jac/dks261
doi: 10.1093/jac/dks261
Joensen KG, Scheutz F, Lund O, Hasman H, Kaas RS et al (2014) Real-time whole-genome sequencing for routine typing, surveillance, and outbreak detection of verotoxigenicEscherichia coli. J Clin Microbiol 52(5):1501–1510. https://doi.org/10.1128/JCM.03617-13
doi: 10.1128/JCM.03617-13
pubmed: 24574290
pmcid: 3993690
Carattoli A, Zankari E, Garcia-Fernandez A, Voldby Larsen M, Lund O et al (2014) In silico detection and typing of plasmids using PlasmidFinder and plasmid multilocus sequence typing. Antimicrob Agents Chemother 58(7):3895–3903. https://doi.org/10.1128/AAC.02412-14
doi: 10.1128/AAC.02412-14
pubmed: 24777092
pmcid: 4068535
Larsen MV, Cosentino S, Rasmussen S, Friis C, Hasman H et al (2012) Multilocus sequence typing of total-genome-sequenced bacteria. J Clin Microbiol 50(4):1355–1361. https://doi.org/10.1128/JCM.06094-11
doi: 10.1128/JCM.06094-11
pubmed: 22238442
pmcid: 3318499
Jaouani I, Abbassi MS, Alessandria V, Bouraoui J, Ben Salem R, Kilani H, Mansouri R, Messadi., Cocolin L (2014) High inhibition of Paenibacillus larvae and Listeria monocytogenes by Enterococcus isolated from different sources in Tunisia and identification of their bacteriocin genes. Lett Appl Microbiol 59:17–25. https://doi.org/10.1111/lam.12239
doi: 10.1111/lam.12239
pubmed: 24698417
Hollenbeck BL, Louis B. Rice LB (2012) Intrinsic and acquired resistance mechanisms in enterococcus. Virulence 3(5):421–433. https://doi.org/10.4161/viru.21282
doi: 10.4161/viru.21282
pubmed: 23076243
pmcid: 3485979