Genomic diversity, antibiotic resistance, and virulence in South African Enterococcus faecalis and Enterococcus lactis isolates.


Journal

World journal of microbiology & biotechnology
ISSN: 1573-0972
Titre abrégé: World J Microbiol Biotechnol
Pays: Germany
ID NLM: 9012472

Informations de publication

Date de publication:
05 Aug 2024
Historique:
received: 27 02 2024
accepted: 27 07 2024
medline: 5 8 2024
pubmed: 5 8 2024
entrez: 5 8 2024
Statut: epublish

Résumé

This study presents the empirical findings of an in-depth genomic analysis of Enterococcus faecalis and Enterococcus lactis isolates from South Africa. It offers valuable insights into their genetic characteristics and their significant implications for public health. The study uncovers nuanced variations in the gene content of these isolates, despite their similar GC contents, providing a comprehensive view of the evolutionary diversity within the species. Genomic islands are identified, particularly in E. faecalis, emphasizing its propensity for horizontal gene transfer and genetic diversity, especially in terms of antibiotic resistance genes. Pangenome analysis reveals the existence of a core genome, accounting for a modest proportion of the total genes, with 2157 core genes, 1164 shell genes, and 4638 cloud genes out of 7959 genes in 52 South African E. faecalis genomes (2 from this study, 49 south Africa genomes downloaded from NCBI, and E. faecalis reference genome). Detecting large-scale genomic rearrangements, including chromosomal inversions, underscores the dynamic nature of bacterial genomes and their role in generating genetic diversity. The study uncovers an array of antibiotic resistance genes, with trimethoprim, tetracycline, glycopeptide, and multidrug resistance genes prevalent, raising concerns about the effectiveness of antibiotic treatment. Virulence gene profiling unveils a diverse repertoire of factors contributing to pathogenicity, encompassing adhesion, biofilm formation, stress resistance, and tissue damage. These empirical findings provide indispensable insights into these bacteria's genomic dynamics, antibiotic resistance mechanisms, and virulence potential, underlining the pressing need to address antibiotic resistance and implement robust control measures.

Identifiants

pubmed: 39102038
doi: 10.1007/s11274-024-04098-5
pii: 10.1007/s11274-024-04098-5
doi:

Substances chimiques

Anti-Bacterial Agents 0
Virulence Factors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

289

Informations de copyright

© 2024. The Author(s).

Références

Al-turfi NAA, Hussein AA (2022) Multidrug Resistance Enterococcus Faecalis isolated from patients with urinary tract infections. Int J Health Sci 6:3473–3483. https://doi.org/10.53730/ijhs.v6ns8.12860
doi: 10.53730/ijhs.v6ns8.12860
Alcock BP, Raphenya AR, Lau TTY, Tsang KK, Bouchard M, Edalatmand A, Huynh W, Nguyen A-LV, Cheng AA, Liu S, Min SY, Miroshnichenko A, Tran H-K, Werfalli RE, Nasir JA, Oloni M, Speicher DJ, Florescu A, Singh B, Faltyn M, Hernandez-Koutoucheva A, Sharma AN, Bordeleau E, Pawlowski AC, Zubyk HL, Dooley D, Griffiths E, Maguire F, Winsor GL, Beiko RG, Brinkman FSL, Hsiao WWL, Domselaar GV, McArthur AG (2019) CARD 2020: antibiotic resistome surveillance with the comprehensive antibiotic resistance database. Nucleic Acids Res 48(D1):D517–D525. https://doi.org/10.1093/nar/gkz935
doi: 10.1093/nar/gkz935 pmcid: 7145624
Ali S, Alemayehu M, Dagnew M, Gebrecherkos T (2018) Vancomycin-Resistant Enterococci and its Associated Risk factors among HIV-Positive and -negative clients attending Dessie Referral Hospital, Northeast Ethiopia. Int J Microbiol 2018:4753460. https://doi.org/10.1155/2018/4753460
doi: 10.1155/2018/4753460 pubmed: 30123274 pmcid: 6079580
Amarasiri M, Sano D, Suzuki S (2020) Understanding human health risks caused by antibiotic resistant bacteria (ARB) and antibiotic resistance genes (ARG) in water environments: current knowledge and questions to be answered. Crit Rev Environ Sci Technol 50(19):2016–2059. https://doi.org/10.1080/10643389.2019.1692611
doi: 10.1080/10643389.2019.1692611
Anderson AC, Jonas D, Huber I, Karygianni L, Wölber J, Hellwig E, Arweiler N, Vach K, Wittmer A, Al-Ahmad A (2016) Enterococcus faecalis from Food, clinical specimens, and oral sites: prevalence of Virulence Factors in Association with Biofilm formation. Front Microbiol 6:1534. https://doi.org/10.3389/fmicb.2015.01534
doi: 10.3389/fmicb.2015.01534 pubmed: 26793174 pmcid: 4707231
Andrews S (2010) FastQC: A Quality Control Tool for High Throughput Sequence Data
Anna Woźniak-Biel GB-P, Burdzy J, Korzekwa K, Ploch S, Wieliczko A (2019) Antimicrobial Resistance and Biofilm formation in Enterococcus spp. Isolated from humans and turkeys in Poland. Microb Drug Resist 25(2):277–286. https://doi.org/10.1089/mdr.2018.0221
doi: 10.1089/mdr.2018.0221 pubmed: 30698495 pmcid: 6441282
Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M (2008) The RAST server: rapid annotations using subsystems technology. BMC Genomics 9(1):1–15
doi: 10.1186/1471-2164-9-75
Bakshi U, Sarkar M, Paul S, Dutta C (2016) Assessment of virulence potential of uncharacterized Enterococcus faecalis strains using pan genomic approach – identification of pathogen–specific and habitat-specific genes. Sci Rep 6(1):38648. https://doi.org/10.1038/srep38648
doi: 10.1038/srep38648 pubmed: 27924951 pmcid: 5141418
Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M, Kulikov AS, Lesin VM, Nikolenko SI, Pham S, Prjibelski AD (2012) SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol 19(5):455–477
doi: 10.1089/cmb.2012.0021 pubmed: 22506599 pmcid: 3342519
Barbosa J, Gibbs PA, Teixeira P (2010) Virulence factors among enterococci isolated from traditional fermented meat products produced in the North of Portugal. Food Control 21(5):651–656. https://doi.org/10.1016/j.foodcont.2009.10.002
doi: 10.1016/j.foodcont.2009.10.002
Bertelli C, Laird MR, Williams KP, Simon Fraser University Research Computing Group, Lau BY, Hoad G, Winsor GL, Brinkman FS (2017) IslandViewer 4: expanded prediction of genomic islands for larger-scale datasets. Nucleic Acids Res 45(W1):W30–W35. https://doi.org/10.1093/nar/gkx343
doi: 10.1093/nar/gkx343 pubmed: 28472413 pmcid: 5570257
Bezuidenhout CC, Molale-Tom LG, Kritzinger RK, Olanrewaju OS (2023) Draft genome sequences of two Bacillus bombysepticus strains from drinking Water. Microbiol Resource Announcements 12(7):e00434–e00423. https://doi.org/10.1128/mra.00434-23
doi: 10.1128/mra.00434-23
Bolger AM, Lohse M, Usadel B (2014) Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 30(15):2114–2120
doi: 10.1093/bioinformatics/btu170 pubmed: 24695404 pmcid: 4103590
Bryan NC, Lebreton F, Gilmore M, Ruvkun G, Zuber MT, Carr CE (2021) Genomic and functional characterization of Enterococcus faecalis isolates recovered from the International Space Station and their potential for pathogenicity. Front Microbiol 11:515319. https://doi.org/10.3389/fmicb.2020.515319
doi: 10.3389/fmicb.2020.515319 pubmed: 33505359 pmcid: 7829349
Camacho C, Coulouris G, Avagyan V, Ma N, Papadopoulos J, Bealer K, Madden TL (2009) BLAST+: architecture and applications. BMC Bioinformatics 10:421. https://doi.org/10.1186/1471-2105-10-421
doi: 10.1186/1471-2105-10-421 pubmed: 20003500 pmcid: 2803857
Choi DG, Baek JH, Han DM, Khan SA, Jeon CO (2024) Comparative pangenome analysis of Enterococcus faecium and Enterococcus lactis provides new insights into the adaptive evolution by horizontal gene acquisitions. BMC Genomics 25(1):28. https://doi.org/10.1186/s12864-023-09945-7
doi: 10.1186/s12864-023-09945-7 pubmed: 38172677 pmcid: 10765913
Dai X, Ma R, Jiang W, Deng Z, Chen L, Liang Y, Shao L, Zhao W (2022) Enterococcus faecalis-Induced Macrophage Necroptosis promotes refractory apical periodontitis. Microbiol Spectr 10(4):e01045–e01022. https://doi.org/10.1128/spectrum.01045-22
doi: 10.1128/spectrum.01045-22 pubmed: 35708336 pmcid: 9431707
Ding Y, Zhao J, He X, Li M, Guan H, Zhang Z, Li P (2016) Antimicrobial resistance and virulence-related genes of Streptococcus obtained from dairy cows with mastitis in Inner Mongolia, China. Pharm Biol 54(1):162–167. https://doi.org/10.3109/13880209.2015.1025290
doi: 10.3109/13880209.2015.1025290 pubmed: 25856704
Duggan JM, Sedgley CM (2007) Biofilm formation of oral and endodontic Enterococcus faecalis. J Endod 33(7):815–818. https://doi.org/10.1016/j.joen.2007.02.016
doi: 10.1016/j.joen.2007.02.016 pubmed: 17804318
Eaton TJ, Gasson MJ (2001) Molecular screening of EnterococcusVirulence determinants and potential for Genetic Exchange between Food and Medical isolates. Appl Environ Microbiol 67(4):1628–1635. https://doi.org/10.1128/AEM.67.4.1628-1635.2001
doi: 10.1128/AEM.67.4.1628-1635.2001 pubmed: 11282615 pmcid: 92779
Eren AM, Esen ÖC, Quince C, Vineis JH, Morrison HG, Sogin ML, Delmont TO (2015) Anvi’o: an advanced analysis and visualization platform for ‘omics data. PeerJ 3:e1319. https://doi.org/10.7717/peerj.1319
doi: 10.7717/peerj.1319 pubmed: 26500826 pmcid: 4614810
Foka FET, Kumar A, Ateba CN (2018) Emergence of vancomycin-resistant Enterococci in South Africa: implications for Public Health. South Afr J Sci 114(9/10):1–7. https://doi.org/10.17159/sajs.2018/4508
doi: 10.17159/sajs.2018/4508
García-Solache M, Rice Louis B (2019) The Enterococcus: a model of adaptability to its environment. Clin Microbiol Rev 32(2). :10.1128/cmr.00058-18 doi:10.1128/cmr.00058-18
Geraldes C, Tavares L, Gil S, Oliveira M (2022) Enterococcus Virulence and Resistant Traits Associated with its permanence in the Hospital Environment Antibiotics. 11:857
Grant JR, Enns E, Marinier E, Mandal A, Herman EK, Chen C-y, Graham M, Van Domselaar G, Stothard P (2023) Proksee: in-depth characterization and visualization of bacterial genomes. Nucleic Acids Res 51(W1):W484–W492. https://doi.org/10.1093/nar/gkad326
doi: 10.1093/nar/gkad326 pubmed: 37140037 pmcid: 10320063
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
Haghi F, Lohrasbi V, Zeighami H (2019) High incidence of virulence determinants, Aminoglycoside and Vancomycin resistance in enterococci isolated from hospitalized patients in Northwest Iran. BMC Infect Dis 19(1):744. https://doi.org/10.1186/s12879-019-4395-3
doi: 10.1186/s12879-019-4395-3 pubmed: 31455296 pmcid: 6712822
Hassoun-Kheir N, Stabholz Y, Kreft J-U, de la Cruz R, Romalde JL, Nesme J, Sørensen SJ, Smets BF, Graham D, Paul M (2020) Comparison of antibiotic-resistant bacteria and antibiotic resistance genes abundance in hospital and community wastewater: a systematic review. Sci Total Environ 743:140804. https://doi.org/10.1016/j.scitotenv.2020.140804
doi: 10.1016/j.scitotenv.2020.140804 pubmed: 32758846
He Q, Hou Q, Wang Y, Li J, Li W, Kwok L-Y, Sun Z, Zhang H, Zhong Z (2018) Comparative genomic analysis of Enterococcus faecalis: insights into their environmental adaptations. BMC Genomics 19(1):527. https://doi.org/10.1186/s12864-018-4887-3
doi: 10.1186/s12864-018-4887-3 pubmed: 29996769 pmcid: 6042284
Hendrickx Antoni PA, van Luit-Asbroek M, Schapendonk Claudia ME, van Wamel Willem JB, Braat Johanna C, Wijnands Lucas M, Bonten Marc JM, Willems Rob JL (2009) SgrA, a nidogen-binding LPXTG surface adhesin implicated in Biofilm formation, and EcbA, a collagen binding MSCRAMM, are two novel adhesins of hospital-acquired Enterococcus faecium. Infect Immun 77(11):5097–5106. https://doi.org/10.1128/iai.00275-09
doi: 10.1128/iai.00275-09 pubmed: 19737906 pmcid: 2772516
Hochstedler-Kramer BR, Ene A, Putonti C, Wolfe AJ (2023) Comparative genomic analysis of clinical Enterococcus faecalis distinguishes strains isolated from the bladder. BMC Genomics 24(1):752. https://doi.org/10.1186/s12864-023-09818-z
doi: 10.1186/s12864-023-09818-z pubmed: 38062354 pmcid: 10701997
Hu Y, Yang X, Qin J, Lu N, Cheng G, Wu N, Pan Y, Li J, Zhu L, Wang X, Meng Z, Zhao F, Liu D, Ma J, Qin N, Xiang C, Xiao Y, Li L, Yang H, Wang J, Yang R, Gao GF, Wang J, Zhu B (2013) Metagenome-wide analysis of antibiotic resistance genes in a large cohort of human gut microbiota. Nat Commun 4(1):2151. https://doi.org/10.1038/ncomms3151
doi: 10.1038/ncomms3151 pubmed: 23877117
Hudson CM, Lau BY, Williams KP (2014) Islander: a database of precisely mapped genomic islands in tRNA and tmRNA genes. Nucleic Acids Res 43(D1):D48–D53. https://doi.org/10.1093/nar/gku1072
doi: 10.1093/nar/gku1072 pubmed: 25378302 pmcid: 4383910
Hui-Ling Ong M, Ho W, Ng W, Chew C (2017) High prevalence of tetM as compared to tetK Amongst Methicillin-Resistant Staphylococcus aureus (MRSA) isolates from hospitals in Perak, Malaysia. Jundishapur J Microbiol 10(6):e13935. https://doi.org/10.5812/jjm.13935
doi: 10.5812/jjm.13935
Joensen KG, Scheutz F, Lund O, Hasman H, Kaas RS, Nielsen EM, Aarestrup FM (2014) Real-time whole-genome sequencing for routine typing, Surveillance, and outbreak detection of Verotoxigenic Escherichia 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
Khalifa L, Shlezinger M, Beyth S, Houri-Haddad Y, Coppenhagen-Glazer S, Beyth N, Hazan R (2016) Phage therapy against Enterococcus faecalis in dental root canals. J Oral Microbiol 8(1):32157. https://doi.org/10.3402/jom.v8.32157
doi: 10.3402/jom.v8.32157 pubmed: 27640530
Kommineni S, Bretl DJ, Lam V, Chakraborty R, Hayward M, Simpson P, Cao Y, Bousounis P, Kristich CJ, Salzman NH (2015) Bacteriocin production augments niche competition by enterococci in the mammalian gastrointestinal tract. Nature 526(7575):719–722. https://doi.org/10.1038/nature15524
doi: 10.1038/nature15524 pubmed: 26479034 pmcid: 4978352
Kreft Ł, Botzki A, Coppens F, Vandepoele K, Van Bel M (2017) PhyD3: a phylogenetic tree viewer with extended phyloXML support for functional genomics data visualization. Bioinformatics 33(18):2946–2947. https://doi.org/10.1093/bioinformatics/btx324
doi: 10.1093/bioinformatics/btx324 pubmed: 28525531
Kritzinger RK, Molale-Tom LG, Olanrewaju OS, Bezuidenhout CC (2023) Draft genome of heterotrophic bacteria Sphingomonas sp. 2R-10 isolated from water treatment plant in South Africa. Microbiol Resource Announcements 0(0):e00437–e00423. https://doi.org/10.1128/MRA.00437-23
doi: 10.1128/MRA.00437-23
Krzywinski MI, Schein JE, Birol I, Connors J, Gascoyne R, Horsman D, Jones SJ, Marra MA (2009) Circos: an information aesthetic for comparative genomics. Genome Res. https://doi.org/10.1101/gr.092759.109
doi: 10.1101/gr.092759.109 pubmed: 19541911 pmcid: 2752132
Kumar S, Devi S, Sood SK, Kapila S, Narayan KS, Shandilya S (2019) Antibiotic resistance and virulence genes in nisin-resistant Enterococcus faecalis isolated from raw buffalo milk modulate the innate functions of rat macrophages. J Appl Microbiol 127(3):897–910. https://doi.org/10.1111/jam.14343
doi: 10.1111/jam.14343 pubmed: 31173435
Lagesen K, Hallin P, Rødland EA, Stærfeldt H-H, Rognes T, Ussery DW (2007) RNAmmer: consistent and rapid annotation of ribosomal RNA genes. Nucleic Acids Res 35(9):3100–3108. https://doi.org/10.1093/nar/gkm160
doi: 10.1093/nar/gkm160 pubmed: 17452365 pmcid: 1888812
Lawrence JG, Ochman H (1998) Molecular archaeology of the < i > Escherichia coli genome. Proceedings of the National Academy of Sciences 95(16):9413–9417 https://doi.org/10.1073/pnas.95.16.9413
Lefort V, Desper R, Gascuel O (2015) FastME 2.0: a Comprehensive, Accurate, and fast Distance-based phylogeny inference program. Mol Biol Evol 32(10):2798–2800. https://doi.org/10.1093/molbev/msv150
doi: 10.1093/molbev/msv150 pubmed: 26130081 pmcid: 4576710
Leonetti CT, Hamada MA, Laurer SJ, Broulidakis MP, Swerdlow KJ, Lee CA, Grossman AD, Berkmen MB (2015) Critical components of the Conjugation Machinery of the integrative and conjugative element ICE Bs1 of Bacillus subtilis. J Bacteriol 197(15):2558–2567. https://doi.org/10.1128/jb.00142-15
doi: 10.1128/jb.00142-15 pubmed: 26013486 pmcid: 4518827
Levin BR, Cornejo OE (2009) The Population and Evolutionary dynamics of homologous gene recombination in Bacteria. PLoS Genet 5(8):e1000601. https://doi.org/10.1371/journal.pgen.1000601
doi: 10.1371/journal.pgen.1000601 pubmed: 19680442 pmcid: 2717328
Lienen T, Schnitt A, Hammerl JA, Maurischat S, Tenhagen B-A (2022) Mammaliicoccus spp. from German dairy farms exhibit a wide range of Antimicrobial Resistance genes and non-wildtype phenotypes to several antibiotic classes. Biology 11(2):152
doi: 10.3390/biology11020152 pubmed: 35205019 pmcid: 8869381
Liu Q, Ponnuraj K, Xu Y, Ganesh VK, Sillanpää J, Murray BE, Narayana SVL, Höök M (2007) The Enterococcus faecalis MSCRAMM ACE binds its ligand by the Collagen hug model. J Biol Chem 282(27):19629–19637. https://doi.org/10.1074/jbc.M611137200
doi: 10.1074/jbc.M611137200 pubmed: 17392280
Lu J, Shen T, Zhang Y, Ma X, Xu S, Awad S, Du M, Zhong Z (2023) Safety assessment of Enterococcus lactis based on comparative genomics and phenotypic analysis. Front Microbiol 14:1196558. https://doi.org/10.3389/fmicb.2023.1196558
doi: 10.3389/fmicb.2023.1196558 pubmed: 37283930 pmcid: 10239811
Mbanga J, Amoako DG, Abia ALK, Allam M, Ismail A, Essack SY (2021) Genomic analysis of Enterococcus spp. Isolated from a Wastewater Treatment Plant and its Associated Waters in Umgungundlovu District, South Africa. Front Microbiol 12:648454. https://doi.org/10.3389/fmicb.2021.648454
doi: 10.3389/fmicb.2021.648454 pubmed: 34194401 pmcid: 8236953
Meier-Kolthoff JP, Göker M (2019) TYGS is an automated high-throughput platform for state-of-the-art genome-based taxonomy. Nat Commun 10(1):1–10
doi: 10.1038/s41467-019-10210-3
Meier-Kolthoff JP, Auch AF, Klenk H-P, Göker M (2013) Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 14(1):60. https://doi.org/10.1186/1471-2105-14-60
doi: 10.1186/1471-2105-14-60 pubmed: 23432962 pmcid: 3665452
Meier-Kolthoff JP, Hahnke RL, Petersen J, Scheuner C, Michael V, Fiebig A, Rohde C, Rohde M, Fartmann B, Goodwin LA, Chertkov O, Reddy TBK, Pati A, Ivanova NN, Markowitz V, Kyrpides NC, Woyke T, Göker M, Klenk H-P (2014) Complete genome sequence of DSM 30083T, the type strain (U5/41T) of Escherichia coli, and a proposal for delineating subspecies in microbial taxonomy. Stand Genomic Sci 9(1):2. https://doi.org/10.1186/1944-3277-9-2
doi: 10.1186/1944-3277-9-2 pubmed: 25780495 pmcid: 4334874
Mogokotleng R, Ismail H, Perovic O, Jallow S (2023) A retrospective analysis of culture-confirmed Enterococci Bloodstream infections in South Africa, 2016–2020: a cross-sectional study. Trop Med Infect Disease 8(1):19. https://doi.org/10.3390/tropicalmed8010019
doi: 10.3390/tropicalmed8010019
Molale-Tom LG, Olanrewaju OS, Kritzinger RK, Fri J, Bezuidenhout CC (2024) Heterotrophic bacteria in drinking water: evaluating antibiotic resistance and the presence of virulence genes. Microbiol Spectr 12(2):e03359–e03323. https://doi.org/10.1128/spectrum.03359-23
doi: 10.1128/spectrum.03359-23 pubmed: 38205959 pmcid: 10845987
Nallapareddy SR, Weinstock GM, Murray BE (2003) Clinical isolates of Enterococcus faecium exhibit strain-specific collagen binding mediated by Acm, a new member of the MSCRAMM family. Mol Microbiol 47(6):1733–1747. https://doi.org/10.1046/j.1365-2958.2003.03417.x
doi: 10.1046/j.1365-2958.2003.03417.x pubmed: 12622825
Nnadozie CF, Odume ON (2019) Freshwater environments as reservoirs of antibiotic resistant bacteria and their role in the dissemination of antibiotic resistance genes. Environ Pollut 254:113067. https://doi.org/10.1016/j.envpol.2019.113067
doi: 10.1016/j.envpol.2019.113067 pubmed: 31465907
Olanrewaju OS, Molale-Tom LG, Kritzinger RK, Bezuidenhout CC (2024) Genome mining of Escherichia coli WG5D from drinking water source: unraveling antibiotic resistance genes, virulence factors, and pathogenicity. BMC Genomics 25(1):263. https://doi.org/10.1186/s12864-024-10110-x
doi: 10.1186/s12864-024-10110-x pubmed: 38459466 pmcid: 10924361
Olawale KO, Fadiora SO, Taiwo SS (2011) Prevalence of Hospital Acquired Enterococci infections in two primary-care hospitals in Osogbo, Southwestern Nigeria. Afr J Infect Dis 5(2):40–46. https://doi.org/10.4314/ajid.v5i2.66513
doi: 10.4314/ajid.v5i2.66513 pubmed: 23878706 pmcid: 3497844
Ondov BD, Treangen TJ, Melsted P, Mallonee AB, Bergman NH, Koren S, Phillippy AM (2016) Mash: fast genome and metagenome distance estimation using MinHash. Genome Biol 17(1):132. https://doi.org/10.1186/s13059-016-0997-x
doi: 10.1186/s13059-016-0997-x pubmed: 27323842 pmcid: 4915045
Page AJ, Cummins CA, Hunt M, Wong VK, Reuter S, Holden MTG, Fookes M, Falush D, Keane JA, Parkhill J (2015) Roary: rapid large-scale prokaryote pan genome analysis. Bioinformatics 31(22):3691–3693. https://doi.org/10.1093/bioinformatics/btv421
doi: 10.1093/bioinformatics/btv421 pubmed: 26198102 pmcid: 4817141
Parker H, Lorenc R, Ruelas Castillo J, Karakousis PC (2020) Mechanisms of antibiotic tolerance in Mycobacterium avium Complex: lessons from related mycobacteria. Front Microbiol 11:573983. https://doi.org/10.3389/fmicb.2020.573983
doi: 10.3389/fmicb.2020.573983 pubmed: 33101247 pmcid: 7554310
Parks DH, Imelfort M, Skennerton CT, Hugenholtz P, Tyson GW (2015) CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res 25(7):1043–1055
doi: 10.1101/gr.186072.114 pubmed: 25977477 pmcid: 4484387
Patiño LA, Courvalin P, Perichon B (2002) vanE Gene Cluster of Vancomycin-resistant Enterococcus faecalis BM4405. J Bacteriol 184(23):6457–6464. https://doi.org/10.1128/jb.184.23.6457-6464.2002
doi: 10.1128/jb.184.23.6457-6464.2002 pmcid: 135418
Paulsen IT, Banerjei L, Myers GSA, Nelson KE, Seshadri R, Read TD, Fouts DE, Eisen JA, Gill SR, Heidelberg JF, Tettelin H, Dodson RJ, Umayam L, Brinkac L, Beanan M, Daugherty S, DeBoy RT, Durkin S, Kolonay J, Madupu R, Nelson W, Vamathevan J, Tran B, Upton J, Hansen T, Shetty J, Khouri H, Utterback T, Radune D, Ketchum KA, Dougherty BA, Fraser CM (2003) Role of mobile DNA in the evolution of vancomycin-resistant Enterococcus faecalis. Science 299(5615):2071–2074. https://doi.org/10.1126/science.1080613
doi: 10.1126/science.1080613 pubmed: 12663927
Pinkston Kenneth L, Gao P, Diaz-Garcia D, Sillanpää J, Nallapareddy Sreedhar R, Murray Barbara E, Harvey Barrett R (2011) The Fsr Quorum-Sensing System of Enterococcus faecalis modulates Surface Display of the collagen-binding MSCRAMM Ace through Regulation of gelE. J Bacteriol 193(17):4317–4325. https://doi.org/10.1128/jb.05026-11
doi: 10.1128/jb.05026-11 pubmed: 21705589 pmcid: 3165527
Pöntinen AK, Top J, Arredondo-Alonso S, Tonkin-Hill G, Freitas AR, Novais C, Gladstone RA, Pesonen M, Meneses R, Pesonen H, Lees JA, Jamrozy D, Bentley SD, Lanza VF, Torres C, Peixe L, Coque TM, Parkhill J, Schürch AC, Willems RJL, Corander J (2021) Apparent nosocomial adaptation of Enterococcus faecalis predates the modern hospital era. Nat Commun 12(1):1523. https://doi.org/10.1038/s41467-021-21749-5
doi: 10.1038/s41467-021-21749-5 pubmed: 33750782 pmcid: 7943827
Power JJ, Pinheiro F, Pompei S, Kovacova V, Yüksel M, Rathmann I, Förster M, Lässig M, Maier B (2021) Adaptive evolution of hybrid bacteria by horizontal gene transfer. Proceedings of the National Academy of Sciences 118(10):e2007873118 https://doi.org/10.1073/pnas.2007873118
Raven KE, Reuter S, Gouliouris T, Reynolds R, Russell JE, Brown NM, Török ME, Parkhill J, Peacock SJ (2016) Genome-based characterization of hospital-adapted Enterococcus faecalis lineages. Nat Microbiol 1(3):15033. https://doi.org/10.1038/nmicrobiol.2015.33
doi: 10.1038/nmicrobiol.2015.33 pubmed: 27572164 pmcid: 4872833
Rich RL, Kreikemeyer B, Owens RT, LaBrenz S, Narayana SVL, Weinstock GM, Murray BE, Höök M (1999) Ace is a collagen-binding MSCRAMM from Enterococcus faecalis. J Biol Chem 274(38):26939–26945. https://doi.org/10.1074/jbc.274.38.26939
doi: 10.1074/jbc.274.38.26939 pubmed: 10480905
Schönknecht G, Chen W-H, Ternes CM, Barbier GG, Shrestha RP, Stanke M, Bräutigam A, Baker BJ, Banfield JF, Garavito RM, Carr K, Wilkerson C, Rensing SA, Gagneul D, Dickenson NE, Oesterhelt C, Lercher MJ, Weber APM (2013) Gene transfer from Bacteria and Archaea facilitated evolution of an Extremophilic Eukaryote. Science 339(6124):1207–1210. https://doi.org/10.1126/science.1231707
doi: 10.1126/science.1231707 pubmed: 23471408
Sillanpää J, Xu Y, Nallapareddy SR, Murray BE, Höök M (2004) A family of putative MSCRAMMs from Enterococcus faecalis. Microbiology 150(7):2069–2078. https://doi.org/10.1099/mic.0.27074-0
doi: 10.1099/mic.0.27074-0 pubmed: 15256550
Sillanpää J, Nallapareddy SR, Houston J, Ganesh VK, Bourgogne A, Singh KV, Murray BE, Höök M (2009) A family of fibrinogen-binding MSCRAMMs from Enterococcus faecalis. Microbiology 155(7):2390–2400. https://doi.org/10.1099/mic.0.027821-0
doi: 10.1099/mic.0.027821-0 pubmed: 19389755 pmcid: 2739004
Sirichoat A, Flórez AB, Vázquez L, Buppasiri P, Panya M, Lulitanond V, Mayo B (2020) Antibiotic resistance-susceptibility profiles of Enterococcus faecalis and Streptococcus spp. From the Human Vagina, and Genome Analysis of the genetic basis of intrinsic and acquired resistances. Front Microbiol 11:1438. https://doi.org/10.3389/fmicb.2020.01438
doi: 10.3389/fmicb.2020.01438 pubmed: 32695087 pmcid: 7333779
Solheim M, Brekke MC, Snipen LG, Willems RJL, Nes IF, Brede DA (2011) Comparative genomic analysis reveals significant enrichment of mobile genetic elements and genes encoding surface structure-proteins in hospital-associated clonal complex 2 Enterococcus faecalis. BMC Microbiol 11(1):3. https://doi.org/10.1186/1471-2180-11-3
doi: 10.1186/1471-2180-11-3 pubmed: 21205308 pmcid: 3022643
Song M, Wu D, Hu Y, Luo H, Li G (2021) Characterization of an Enterococcus faecalis bacteriophage vB_EfaM_LG1 and its synergistic Effect with Antibiotic. Front Cell Infect Microbiol 11:698807. https://doi.org/10.3389/fcimb.2021.698807
doi: 10.3389/fcimb.2021.698807 pubmed: 34336721 pmcid: 8322680
Strateva T, Atanasova D, Savov E, Petrova G, Mitov I (2016) Incidence of virulence determinants in clinical Enterococcus faecalis and Enterococcus faecium isolates collected in Bulgaria. Brazilian J Infect Dis 20(2):127–133. https://doi.org/10.1016/j.bjid.2015.11.011
doi: 10.1016/j.bjid.2015.11.011
Su T, Qiu Y, Hua X, Ye B, Luo H, Liu D, Qu P, Qiu Z (2020) Novel opportunity to reverse antibiotic resistance: to explore traditional Chinese medicine with potential activity against antibiotics-resistance Bacteria. Front Microbiol 11:610070. https://doi.org/10.3389/fmicb.2020.610070
doi: 10.3389/fmicb.2020.610070 pubmed: 33414777 pmcid: 7782309
Suchi SE, Shamsuzzaman S, Uddin BMM, Yusuf MA (2017) Detection of virulence factors and antimicrobial resistance in enterococci isolated from urinary tract infection. Bangladesh J Infect Dis 4(2):30–34. https://doi.org/10.3329/bjid.v4i2.37682
doi: 10.3329/bjid.v4i2.37682
Szadkowska M, Olewniczak M, Kloska A, Jankowska E, Kapusta M, Rybak B, Wyrzykowski D, Zmudzinska W, Gieldon A, Kocot A, Kaczorowska A-K, Nierzwicki L, Makowska J, Kaczorowski T, Plotka M (2022) A Novel cryptic clostridial peptide that kills Bacteria by a cell membrane permeabilization mechanism. Microbiol Spectr 10(5):e01657–e01622. https://doi.org/10.1128/spectrum.01657-22
doi: 10.1128/spectrum.01657-22 pubmed: 36094301 pmcid: 9602519
Szmolka A, Nagy B (2013) Multidrug resistant commensal Escherichia coli in animals and its impact for public health. Front Microbiol 4:00258. https://doi.org/10.3389/fmicb.2013.00258
doi: 10.3389/fmicb.2013.00258
Teng F, Singh Kavindra V, Bourgogne A, Zeng J, Murray Barbara E (2009) Further characterization of the epa gene cluster and Epa polysaccharides of Enterococcus faecalis. Infect Immun 77(9):3759–3767. https://doi.org/10.1128/iai.00149-09
doi: 10.1128/iai.00149-09 pubmed: 19581393 pmcid: 2737988
Touchon M, Moura de Sousa JA, Rocha EPC (2017) Embracing the enemy: the diversification of microbial gene repertoires by phage-mediated horizontal gene transfer. Curr Opin Microbiol 38:66–73. https://doi.org/10.1016/j.mib.2017.04.010
doi: 10.1016/j.mib.2017.04.010 pubmed: 28527384
Virolle C, Goldlust K, Djermoun S, Bigot S, Lesterlin C (2020) Plasmid transfer by conjugation in Gram-negative Bacteria: from the Cellular to the Community Level. Genes 11(11):1239. https://doi.org/10.3390/genes11111239
doi: 10.3390/genes11111239 pubmed: 33105635 pmcid: 7690428
Wei W, Gao F, Du M-Z, Hua H-L, Wang J, Guo F-B (2016) Zisland Explorer: detect genomic islands by combining homogeneity and heterogeneity properties. Brief Bioinform 18(3):357–366. https://doi.org/10.1093/bib/bbw019
doi: 10.1093/bib/bbw019 pmcid: 5429010
Wiedenbeck J, Cohan FM (2011) Origins of bacterial diversity through horizontal genetic transfer and adaptation to new ecological niches. FEMS Microbiol Rev 35(5):957–976. https://doi.org/10.1111/j.1574-6976.2011.00292.x
doi: 10.1111/j.1574-6976.2011.00292.x pubmed: 21711367
Yang F, Zhang S, Shang X, Wang X, Yan Z, Li H, Li J (2019) Short communication: antimicrobial resistance and virulence genes of Enterococcus faecalis isolated from subclinical bovine mastitis cases in China. J Dairy Sci 102(1):140–144. https://doi.org/10.3168/jds.2018-14576
doi: 10.3168/jds.2018-14576 pubmed: 30415850
Yoon S-H, Ha S-M, Kwon S, Lim J, Kim Y, Seo H, Chun J (2017) Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies. Int J Syst Evol MicroBiol 67(5):1613
doi: 10.1099/ijsem.0.001755 pubmed: 28005526 pmcid: 5563544
Yu Y, Xie Z, Yang J, Yang R, Li Y, Zhu Y, Zhao Y, Yang Q, Chen J, Alwathnani HA, Feng R, Rensing C, Herzberg M (2023) Citrobacter portucalensis Sb-2 contains a metalloid resistance determinant transmitted by Citrobacter phage Chris1. J Hazard Mater 443:130184. https://doi.org/10.1016/j.jhazmat.2022.130184
doi: 10.1016/j.jhazmat.2022.130184 pubmed: 36270189
Zhang E, Zong S, Zhou W, Zhou J, Han J, Qu D (2023) Characterization and comparative genomics analysis of RepA_N multi-resistance plasmids carrying optrA from Enterococcus faecalis. Front Microbiol 13:991352. https://doi.org/10.3389/fmicb.2022.991352
doi: 10.3389/fmicb.2022.991352 pubmed: 36777024 pmcid: 9911807
Zhao X, Zhao H, Zhou Z, Miao Y, Li R, Yang B, Cao C, Xiao S, Wang X, Liu H, Wang J, Yang Z (2022) Characterization of extended-spectrum β-Lactamase-producing Escherichia coli isolates that cause Diarrhea in Sheep in Northwest China. Microbiol Spectr 10(4):e01595–e01522. https://doi.org/10.1128/spectrum.01595-22
doi: 10.1128/spectrum.01595-22 pubmed: 35943154 pmcid: 9431196
Zheng J-X, Wu Y, Lin Z-W, Pu Z-Y, Yao W-M, Chen Z, Li D-Y, Deng Q-W, Qu D, Yu Z-J (2017) Characteristics of and Virulence Factors Associated with Biofilm formation in clinical Enterococcus faecalis isolates in China. Front Microbiol 8:2338. https://doi.org/10.3389/fmicb.2017.02338
doi: 10.3389/fmicb.2017.02338 pubmed: 29225595 pmcid: 5705541
Zheng J, Wu Y, Lin Z, Wang G, Jiang S, Sun X, Tu H, Yu Z, Qu D (2020) ClpP participates in stress tolerance, biofilm formation, antimicrobial tolerance, and virulence of Enterococcus faecalis. BMC Microbiol 20(1):30. https://doi.org/10.1186/s12866-020-1719-9
doi: 10.1186/s12866-020-1719-9 pubmed: 32033530 pmcid: 7006429
Zhou Q, Mai K, Yang D, Liu J, Yan Z, Luo C, Tan Y, Cao S, Zhou Q, Chen L, Chen F (2021) Comparative genomic analysis of Mycoplasma anatis strains. Genes Genomics 43(11):1327–1337. https://doi.org/10.1007/s13258-021-01129-5
doi: 10.1007/s13258-021-01129-5 pubmed: 34181213 pmcid: 8237044

Auteurs

Oluwaseyi Samuel Olanrewaju (OS)

Unit for Environmental Sciences and Management, North-West University, Potchefstroom Campus, Private Bag X6001, Potchefstroom, 2520, South Africa. olusam777@gmail.com.

Lesego G Molale-Tom (LG)

Unit for Environmental Sciences and Management, North-West University, Potchefstroom Campus, Private Bag X6001, Potchefstroom, 2520, South Africa. Lesego.molaleTom@nwu.ac.za.

Cornelius C Bezuidenhout (CC)

Unit for Environmental Sciences and Management, North-West University, Potchefstroom Campus, Private Bag X6001, Potchefstroom, 2520, South Africa.

Articles similaires

Genome, Chloroplast Phylogeny Genetic Markers Base Composition High-Throughput Nucleotide Sequencing

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C

Classifications MeSH