References
- Wozniak-Biel A, Bugla-Płoskońska G, Burdzy J, Korzekwa K, Ploch S, Wieliczko A. Antimicrobial resistance and iofilm formation in Enterococcus spp. isolated from humans and turkeys in Poland. Microb Drug Resist. 2019; 25(2):277-86. [DOI:10.1089/mdr.2018.0221] [PMID]
- Khare T, Anand U, Dey A, Assaraf YG, Chen ZS, Liu Z, et al. Exploring phytochemicals for combating antibiotic resistance in microbial pathogens. Front Pharmacol. 2021; 12:720726. [DOI:10.3389/fphar.2021.720726] [PMID]
- Forde BM, Bergh H, Cuddihy T, Hajkowicz K, Hurst T, Playford EG, et al. Clinical implementation of routine whole-genome sequencing for hospital infection control of multi-drug resistant pathogens. Clin Infect Dis. 2023; 76(3):e1277-84. [DOI:10.1093/cid/ciac726] [PMID]
- Marston HD, Dixon DM, Knisely JM, Palmore TN, Fauci AS. Antimicrobial resistance. JAMA. 2016; 316(11):1193-204. [DOI:10.1001/jama.2016.11764] [PMID]
- Lebreton F, Valentino MD, Schaufler K, Earl AM, Cattoir V, Gilmore MS. Transferable vancomycin resistance in clade B commensal-type Enterococcus faecium. J Antimicrob Chemother. 2018; 73(6):1479-86. [DOI:10.1093/jac/dky039] [PMID]
- Elahi Y, Nowroozi J, Fard RMN. Isolation and characterization of bacteriophages from wastewater sources on Enterococcus spp. isolated from clinical samples. Iran J Microbiol. 2021; 13(5):671-7. [DOI:10.18502/ijm.v13i5.7434] [PMID]
- Adeniji OO, Sibanda T, Okoh AI. Recreational water quality status of the Kidd’s Beach as determined by its physicochemical and bacteriological quality parameters. Heliyon. 2019; 5(6):e01893. [DOI:10.1016/j.heliyon.2019.e01893] [PMID]
- Rapid Annotation using Subsystem Technology (RAST). online sequence analysis service [Internet]. 2025 [Updared 25 November 2025]. Available from: [Link]
- DNA Data Bank of Japan. sharing and analysis services for data from life science researches and advances science. Shizuoka: DDBJ Center; 2025. [Link]
- Pulingam T, Parumasivam T, Gazzali AM, Sulaiman AM, Chee JY, Lakshmanan M, et al. Antimicrobial resistance: Prevalence, economic burden, mechanisms of resistance and strategies to overcome. Eur J Pharm Sci. 2022; 170:106103. [DOI:10.1016/j.ejps.2021.106103] [PMID]
- Ayobami O, Willrich N, Reuss A, Eckmanns T, Markwart R. The ongoing challenge of vancomycin-resistant Enterococcus faecium and Enterococcus faecalis in Europe: An epidemiological analysis of bloodstream infections. Emerg Microbes Infect. 2020; 9(1):1180-93. [DOI:10.1080/22221751.2020.1769500] [PMID]
- Gorrie C, Higgs C, Carter G, Stinear TP, Howden B. Genomics of vancomycin-resistant Enterococcus faecium. Microb Genom. 2019; 5(7):e000283. [DOI:10.1099/mgen.0.000283] [PMID]
- Sun L, Xu J, Wang W, He F. Emergence of vanA-type vancomycin-resistant Enterococcus faecium ST 78 strain with a rep2-type plasmid carrying a Tn1546-like element isolated from a urinary tract infection in China. Infect Drug Resist. 2020; 13:949-55. [DOI:10.2147/IDR.S247569]
- Berglund F, Böhm ME, Martinsson A, Ebmeyer S, Österlund T, Johnning A, et al. Comprehensive screening of genomic and metagenomic data reveals a large diversity of tetracycline resistance genes. Microb Genom. 2020; 6(11):mgen000455. [DOI:10.1099/mgen.0.000455] [PMID]
- Tarrah A, Pakroo S, Corich V, Giacomini A. Identification and transferability of tetracycline resistance in Streptococcus thermophilus during milk fermentation, storage, and gastrointestinal transit. Fermentation. 2021; 7(2):65. [DOI:10.3390/fermentation7020065]
- Revtovich AV, Tjahjono E, Singh KV, Hanson BM, Murray BE, Kirienko NV. Development and characterization of high-throughput Caenorhabditis elegans-Enterococcus faecium infection model. Front Cell Infect Microbiol. 2021; 11:667327. [DOI:10.3389/fcimb.2021.667327] [PMID]
- Markwart R, Willrich N, Haller S, Noll I, Koppe U, Werner G, et al. The rise in vancomycin-resistant Enterococcus faecium in Germany: Data from the German Antimicrobial Resistance Surveillance (ARS). Antimicrob Resist Infect Control. 2019; 8:147. [DOI:10.1186/s13756-019-0594-3] [PMID]
- Sanderson H, Ortega-Polo R, Zaheer R, Goji N, Amoako KK, Brown RS, et al. Comparative genomics of multidrug-resistant Enterococcus spp. isolated from wastewater treatment plants. BMC Microbiol. 2020; 20(1):20. [DOI:10.1186/s12866-019-1683-4] [PMID]
- Amachawadi RG, Giok F, Shi X, Soto J, Narayanan SK, Tokach MD, et al. Antimicrobial resistance of Enterococcus faecium strains isolated from commercial probiotic products used in cattle and swine. J Anim Sci. 2018; 96(3):912-20. [DOI:10.1093/jas/sky056] [PMID]
- Bozdogan B, Berrezouga L, Kuo MS, Yurek DA, Farley KA, Stockman BJ, et al. A new resistance gene, linB, conferring resistance to lincosamides by nucleotidylation in Enterococcus faecium HM1025. Antimicrob Agents Chemother. 1999; 43(4):925-9. [DOI:10.1128/AAC.43.4.925] [PMID]
- Edirmanasinghe R, Finley R, Parmley EJ, Avery BP, Carson C, Bekal S, et al. A whole-genome sequencing approach to study cefoxitin-resistant Salmonella enterica serovar Heidelberg isolates from various sources. Antimicrob Agents Chemother. 2017; 61(4):e01919-16. [DOI:10.1128/AAC.01919-16] [PMID]
- Falagas ME, Vouloumanou EK, Samonis G, Vardakas KZ. Fosfomycin. Clin Microbiol Rev. 2016; 29(2):321-47. [DOI:10.1128/CMR.00068-15] [PMID]
- da Silva VL, Caçador NC, da Silva Cdos S, Fontes CO, Garcia GD, Nicoli JR, et al. Occurrence of multidrug-resistant and toxic-metal tolerant enterococci in fresh feces from urban pigeons in Brazil. Microbes Environ. 2012; 27(2):179-85. [DOI:10.1264/jsme2.ME11296] [PMID]
- Amachawadi R, Shelton N, Shi X, Vinasco J, Dritz S, Tokach M, et al. Selection of fecal enterococci exhibiting tcrb-mediated copper resistance in pigs fed diets supplemented with copper. Appl Environ Microbiol. 2011; 77(11). [DOI:10.1128/AEM.00364-11]
- Festa RA, Thiele DJ. Copper at the front line of the host-pathogen battle. PLoS Pathog. 2012; 8(9):e1002887.[DOI:10.1371/journal.ppat.1002887] [PMID]
- Zaidi SE, Zaheer R, Poulin-Laprade D, Scott A, Rehman MA, Diarra M, et al. Comparative genomic analysis of enterococci across sectors of the one health continuum. Microorganisms. 2023; 11(3):727. [DOI:10.3390/microorganisms11030727] [PMID]
- Pal C, Bengtsson-Palme J, Kristiansson E, Larsson DG. Co-occurrence of resistance genes to antibiotics, biocides and metals reveals novel insights into their co-selection potential. BMC Genomics. 2015; 16:964. [DOI:10.1186/s12864-015-2153-5] [PMID]
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