126
Views
1
CrossRef citations to date
0
Altmetric
Original Research

Effect of Short-Term Antimicrobial Therapy on the Tolerance and Antibiotic Resistance of Multidrug-Resistant Staphylococcus capitis

, , , , , , & show all
Pages 2017-2026 | Published online: 30 Jun 2020

References

  • Davies J, Davies D. Origins and evolution of antibiotic resistance. Microbiol Mol Biol Rev. 2010;74(3):417–433. doi:10.1128/MMBR.00016-1020805405
  • Harris SR, Clarke IN, Seth-Smith HM, et al. Whole-genome analysis of diverse Chlamydia trachomatis strains identifies phylogenetic relationships masked by current clinical typing. Nat Genet. 2012;44(4):413–419, S411. doi:10.1038/ng.221422406642
  • Choe D, Lee JH, Yoo M, et al. Adaptive laboratory evolution of a genome-reduced Escherichia coli. Nat Commun. 2019;10(1):935. doi:10.1038/s41467-019-08888-630804335
  • Marvig RL, Johansen HK, Molin S, Jelsbak L. Genome analysis of a transmissible lineage of pseudomonas aeruginosa reveals pathoadaptive mutations and distinct evolutionary paths of hypermutators. PLoS Genet. 2013;9(9):e1003741. doi:10.1371/journal.pgen.100374124039595
  • Morelli G, Song Y, Mazzoni CJ, et al. Yersinia pestis genome sequencing identifies patterns of global phylogenetic diversity. Nat Genet. 2010;42(12):1140–1143. doi:10.1038/ng.70521037571
  • Conlan S, Park M, Deming C, et al. Plasmid dynamics in KPC-positive Klebsiella pneumoniae during long-term patient colonization. mBio. 2016;7(3):3. doi:10.1128/mBio.00742-16
  • Lazar V, Pal Singh G, Spohn R, et al. Bacterial evolution of antibiotic hypersensitivity. Mol Syst Biol. 2013;9(1):700. doi:10.1038/msb.2013.5724169403
  • Butin M, Martins-Simoes P, Rasigade JP, Picaud JC, Laurent F. Worldwide endemicity of a multidrug-resistant staphylococcus capitis clone involved in neonatal sepsis. Emerg Infect Dis. 2017;23(3):538–539. doi:10.3201/eid2303.16083328221122
  • Cameron DR, Jiang JH, Hassan KA, et al. Insights on virulence from the complete genome of Staphylococcus capitis. Front Microbiol. 2015;6:980. doi:10.3389/fmicb.2015.0098026441910
  • Institute CaLS. Performance Standards for Antimicrobial Susceptibility Testing. 2018:M100
  • Waterhouse A, Bertoni M, Bienert S, et al. SWISS-MODEL: homology modelling of protein structures and complexes. Nucleic Acids Res. 2018;46(W1):W296–W303. doi:10.1093/nar/gky42729788355
  • Sander P, Springer B, Prammananan T, et al. Fitness cost of chromosomal drug resistance-conferring mutations. Antimicrob Agents Chemother. 2002;46(5):1204–1211. doi:10.1128/AAC.46.5.1204-1211.200211959546
  • Guo B, Abdelraouf K, Ledesma KR, Nikolaou M, Tam VH. Predicting bacterial fitness cost associated with drug resistance. J Antimicrob Chemother. 2012;67(4):928–932. doi:10.1093/jac/dkr56022232512
  • van der Maten E, de Jonge MI, de Groot R, van der Flier M, Langereis JD. A versatile assay to determine bacterial and host factors contributing to opsonophagocytotic killing in hirudin-anticoagulated whole blood. Sci Rep. 2017;7(1):42137. doi:10.1038/srep4213728176849
  • Tsai CJ-Y, Loh JMS, Proft T. Galleria mellonella infection models for the study of bacterial diseases and for antimicrobial drug testing. Virulence. 2016;7(3):214–229. doi:10.1080/21505594.2015.113528926730990
  • Sun F, Li C, Jeong D, Sohn C, He C, Bae T. In the Staphylococcus aureus two-component system sae, the response regulator SaeR binds to a direct repeat sequence and DNA binding requires phosphorylation by the sensor kinase SaeS. J Bacteriol. 2010;192(8):2111–2127. doi:10.1128/JB.01524-0920172998
  • Mehta AP, Hanes JW, Abdelwahed SH, Hilmey DG, Hanzelmann P, Begley TP. Catalysis of a new ribose carbon-insertion reaction by the molybdenum cofactor biosynthetic enzyme MoaA. Biochemistry. 2013;52(7):1134–1136. doi:10.1021/bi301602623286307
  • Yokoyama K, Leimkuhler S. The role of FeS clusters for molybdenum cofactor biosynthesis and molybdoenzymes in bacteria. Biochim Biophys Acta. 2015;1853(6):1335–1349. doi:10.1016/j.bbamcr.2014.09.02125268953
  • Wi YM, Greenwood-Quaintance KE, Brinkman CL, Lee JYH, Howden BP, Patel R. Rifampicin resistance in Staphylococcus epidermidis: molecular characterisation and fitness cost of rpoB mutations. Int J Antimicrob Agents. 2018;51(5):670–677. doi:10.1016/j.ijantimicag.2017.12.01929287710
  • Wichelhaus TA, Schafer V, Brade V, Boddinghaus B. Molecular characterization of rpoB mutations conferring cross-resistance to rifamycins on methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 1999;43(11):2813–2816. doi:10.1128/AAC.43.11.281310543773
  • Bassenden AV, Rodionov D, Shi K, Berghuis AM. Structural analysis of the tobramycin and gentamicin clinical resistome reveals limitations for next-generation aminoglycoside design. ACS Chem Biol. 2016;11(5):1339–1346. doi:10.1021/acschembio.5b0107026900880
  • Becker K, Heilmann C, Peters G. Coagulase-negative staphylococci. Clin Microbiol Rev. 2014;27(4):870–926.25278577
  • Dong Y, Speer CP, Glaser K. Beyond sepsis: staphylococcus epidermidis is an underestimated but significant contributor to neonatal morbidity. Virulence. 2018;9(1):621–633. doi:10.1080/21505594.2017.141911729405832
  • Al Hennawi HET, Mahdi EM, Memish ZA. Native valve Staphylococcus capitis infective endocarditis: a mini review. Infection. 2019.
  • Laurent F, Butin M. Staphylococcus capitis and NRCS-A clone: the story of an unrecognized pathogen in neonatal intensive care units. Clin Microbiol Infect. 2019;25(9):1081–1085. doi:10.1016/j.cmi.2019.03.00930928561
  • Tevell S, Hellmark B, Nilsdotter-Augustinsson A, Soderquist B. Staphylococcus capitis isolated from prosthetic joint infections. Eur J Clin Microbiol Infect Dis. 2017;36(1):115–122. doi:10.1007/s10096-016-2777-727680718
  • Carter GP, Ussher JE, Da Silva AG, et al. Genomic analysis of multiresistant staphylococcus capitis associated with neonatal sepsis. Antimicrob Agents Chemother. 2018;62(11):11. doi:10.1128/AAC.00898-18
  • Butin M, Martins-Simoes P, Pichon B, et al. Emergence and dissemination of a linezolid-resistant Staphylococcus capitis clone in Europe. J Antimicrob Chemother. 2017;72(4):1014–1020. doi:10.1093/jac/dkw51627999045
  • O’Neill AJ, Huovinen T, Fishwick CW, Chopra I. Molecular genetic and structural modeling studies of Staphylococcus aureus RNA polymerase and the fitness of rifampin resistance genotypes in relation to clinical prevalence. Antimicrob Agents Chemother. 2006;50(1):298–309. doi:10.1128/AAC.50.1.298-309.200616377701
  • Munck C, Gumpert HK, Wallin AI, Wang HH, Sommer MO. Prediction of resistance development against drug combinations by collateral responses to component drugs. Sci Transl Med. 2014;6(262):262ra156. doi:10.1126/scitranslmed.3009940
  • Jacoby GA, Blaser MJ, Santanam P, et al. Appearance of amikacin and tobramycin resistance due to 4ʹ-aminoglycoside nucleotidyltransferase [ANT(4ʹ)-II] in gram-negative pathogens. Antimicrob Agents Chemother. 1990;34(12):2381–2386. doi:10.1128/AAC.34.12.23811965106
  • Miller GH, Sabatelli FJ, Hare RS, et al. The most frequent aminoglycoside resistance mechanisms–changes with time and geographic area: a reflection of aminoglycoside usage patterns? Aminoglycoside Resistance Study Groups. Clin Infect Dis. 1997;24(Suppl 1):S46–62. doi:10.1093/clinids/24.Supplement_1.S468994779
  • Nichol D, Rutter J, Bryant C, et al. Antibiotic collateral sensitivity is contingent on the repeatability of evolution. Nat Commun. 2019;10(1):334. doi:10.1038/s41467-018-08098-630659188
  • Imamovic L, Sommer MO. Use of collateral sensitivity networks to design drug cycling protocols that avoid resistance development. Sci Transl Med. 2013;5(204):204ra132. doi:10.1126/scitranslmed.3006609
  • Shapiro RS. mSphere of influence: evolutionary strategies to sensitize drug-resistant pathogens. mSphere. 2019;4:3. doi:10.1128/mSphere.00313-19
  • Kim S, Lieberman TD, Kishony R. Alternating antibiotic treatments constrain evolutionary paths to multidrug resistance. Proc Natl Acad Sci U S A. 2014;111(40):14494–14499. doi:10.1073/pnas.140980011125246554
  • Liu Q, Yeo WS, Bae T. The SaeRS Two-Component System of Staphylococcus aureus. Genes (Basel). 2016;7(10):10. doi:10.3390/genes7100081