Antibiotic Resistance a Mechanistic verview BSc PhD FRCPath Consultant Clinical Scientist 1 Polymyxin Colistin Daptomycin Mechanisms of antibiotic action Quinolones Mupirocin Nitrofurans Nitroimidazoles Wall synthesis β-lactams Bacitracin Cycloserine Fosfomycin Glycopeptides Ramoplanin Cytoplasmic membrane Topoisomerase DNA Polypeptide Folic acid synthesis Ribosome RNA Polymerase mrna Sulphonamides Trimethoprim Aminoglycosides Chloramphenicol Fusidic Acid Rifamycins Ketolides Lincosamides Macrolides xazolidinones Courtesy of Ian Chopra Streptogramins 2 Tetracyclines + tigecycline Resistance is as old as antibiotics (not just human use of them) Penicillin isolated in 1928 Resistant E. coli discovered in 1940 but antibiotics and bacteria have co-existed for millions of years Fleming 3 1
Antibiotic resistance mechanisms antibiotics antibiotics reduced uptake antibiotics www.scq.ubc.ca 4 Types of resistance Intrinsic (or inherent) resistance Resistance to an agent is normal for a genus, species or bacterial group (lack the target, or drug can t get to target) Glycopeptide resistance in Gram-negatives Aztreonam resistance in Gram-positives Acquired resistance Most isolates of a genus, species or bacterial group are susceptible, but resistance may arise via: Mutation (usually of a chromosomal gene) e.g., Rif R ; FQ R Acquisition of new DNA conferring resistance (horizontal spread) 5 Defining resistance Courtesy: biomerieux Biological - the inhibition zone is smaller (or MIC is higher) than normal for the species, so it s resistant Pharmacological - the MIC is 32 mg/l, but the drug has a serum peak of 150 mg/l, so it s sensitive Clinical - I know that strains like this don t respond in the patient 6 2
Susceptibility / resistance of every bacterial isolate reflects interplay of multiple factors External [drug] Efflux Pump Non- Specific Porin Specific Pore (D2) V Entry + V Efflux Periplasmic [drug] V Hydrolysis V Binding 7 Antibiotics select resistant bacteria: mutational resistance A mutant emerges randomly Sensitive bacteria killed by antibiotic Mutant s progeny survive and grow I have called this principle, by which each slight variation, if useful, is preserved, Natural Selection 8 Bacteria carry resistance in their DNA Mutations in chromosomal DNA can cause resistance Many bacteria have extra DNA in small rings, known as plasmids plasmids can also carry resistance 9 3
and they don t keep resistance to themselves Antibiotic resistance 10 Three routes that bacteria use to transfer resistance Most efficient between closely related bacteria, but unrelated bacteria often exchange DNA too http://bioinfo.bact.wisc.edu/themicrobialworld/homepage 11 The Red Queen Principle Evolution is often an arms race Antibiotic development vs. antibiotic resistance Bacteria evolve in real-time Now, here, you see, it takes all the running you can do, to keep in the same place" Van Valen L. A New Evolutionary Law. Evolutionary Theory 1973;1:1-30 12 4
Resistance is inevitable even to new antibiotics Antibiotic resistance Considered by all companies developing new agents Search for cross-resistance Assess activity vs. clinical strains resistant to other agents? resistance reservoir if product is natural (or semi-synthetic) In-vitro development of resistance by mutation Not reliable predictors; Ideal scenarios: Penicillin vs. Strep. pyogenes: no resistance Vancomycin: resistance emerged after c. 30 years use Will resistance to compound X emerge: Quickly, in target species, and will it be transferable? 13 How quickly does resistance emerge? Linezolid: a synthetic drug Bacteria have never seen anything like it Excellent activity against almost all Gram-positive species Clinical use sets them a new challenge N N NH F H 3 C 14 xazolidinone timeline Class discovered Influenced by many factors, including: Use of agent (how much, by whom?) Cross-resistance to other antibiotics Type of resistance UK licensing of linezolid Investigation restarted 1 st LRE in UK Will we have a major resistance problem? 1985 1990 2000 2001 2002 2015 15 5
Mechanism 1: alteration of the target Linezolid resistance and 23S rrna Antibiotic resistance nly G2576U in clinical isolates (MICs, 8-128 mg/l) Prystowsky et al., AAC 2001;45:2145-56 16 The forensics of antibiotic resistance Resistance involves Emergence of mutations Spread of resistance genes (plasmids, transposons, integrons) Spread of resistant strains and clones of bacteria Tracking and characterizing The resistant strains: in hospitals and in the community Their resistance genes Surveillance and good microbiology 17 Epidemiological investigation can be applied to every level Genes Gene carriers IS, In, Tn, plasmids Host species Strains, clones, phylogenetic groups, virulence traits, co-resistance Patients Hospital / community setting; risk factors Courtesy of Rafael Canton 18 6
Surveillance of resistance Antibiotic resistance Informs on prevalence and changes in antibiotic resistance Guides empirical prescribing & control strategies Assess if control is working Surveillance shortfalls Lack of clinical denominators Need more community based surveillance Need to link antibiotic consumption to resistance Must be supported by good microbiology (not just number crunching) 19 Similar trend, but is there a causal association? % MRSA bacteraemias Rise of clones 50 45 40 35 30 25 20 15 10 5 0 91 '92 '93 '94 '95 '96 '97 '98 '99 '00 '01 '02 '03 '04 Year A % MRSA pitals Number of Hosp 150 125 100 75 50 25 0 E-15 (ST22) E-16 (ST36) E-3 (ST05) 93 94 95 96 97 Year Data: HPA 20 Mechanism 2: metabolic by-pass β-lactam resistance in MRSA New peptidoglycan Methicillin inhibits PBPs 1,2,3 Cross-linked wall MRSA produce PBP2, decreased binding, clinical resistance to most available β-lactams Ceftobiprole 21 7
Cephalosporin-resistant E. coli from bacteraemias An explosive increase recorded since start of 21 st century In the UK, c. 20,000 cases E. coli bacteraemia p.a. (voluntary) c. 12% CTX and/or CAZ resistance = c. 2400 cases p.a. Antibiotic resistance 2001 http://www.earss.nivm.nl 2008 22, but hang on a minute; Why might resistance rates rise? Technical (artefacts) Change in surveillance methods (e.g., mandatory vs. voluntary) Lowering of breakpoints (isolates previously S, now R) Education / awareness (more people look, and so find) Better screening methods Biological (real) Expansion of resistant clones / strains Emergence of resistance in new clones / strains De novo emergence (mutation) Horizontal spread of plasmids between strains 23 Understanding rising prevalence: SE England, 2004 600 500 CTX-M ther ESBL AmpC ther 400 300 200 100 0 E. coli K. pneumoniae Enterobacter spp. 24 8
H 2 N S Mechanism 3: drug destruction β-lactamases: xyimino-aminothiazolyl or methoxy groups: R N N NH CH 3 S Evade classical penicillinases Hinders access to active site No hydrolysis N H R ESBLs are able to hydrolyse β-lactam bond Allow hydrolysis Confer resistance 25 Global explosion of CTX-M ESBLs in Enterobacteriaceae 2001-2002 Endemic Spordic reports Courtesy of Rafael Canton 2007 2005 26 Multi-resistance plasmids: how bad is bad? Antibiotic classes Genes Mechanism Aminoglycosides aac6 -Ib-cr aada5 Modify drug β-lactams bla CTX-M-15 bla XA-1 Destroy drug bla TEM-1 Chloramphenicol catb4 Modify drug Macrolides mph(a) Efflux Fluoroquinolones aac6 -Ib-cr Modify drug Sulfonamides suli By-pass Trimethoprim dhfr XVII By-pass Tetracycline tet(a) Efflux pek499 (118 kb) encodes CTX-M-15 ESBL in a prevalent UK strain of E. coli Woodford, Carattoli et al., AAC 27 9
E. coli & Klebsiella with ESBLs or AmpC: can it get worse? Carbapenems Standard i.v. therapy for ESBL / AmpC producers 600 500 400 300 200 100 0 <=0.12 0.25 0.5 Ertapenem Imipenem Meropenem which leads to an all-too-familiar situation use = selective pressure = resistant isolates 1 2 4 8 >=16 28 Mechanism 4: reduced uptake porin-mediated carbapenem resistance E. coli strain A usually encodes 3 β-lactamases: A 1 A 2 B C D E CTX-M-15; XA-1; TEM-1 In 1 centre it has acquired an additional AmpC β-lactamase: CMY-23 and carbapenem resistance isolate A 2 : ETP, 4 mg/l, IPM / MEM, 0.5-1 mg/l mpc loss 29 Restore porins and reverse carbapenem resistance MIC (mg/l) Strain Plasmid ETP IPM MEM - 16 0.5 2 Klebsiella ptr 16 0.5 2 ptrompk36 0.5 0.25 0.125 Doumith et al., JAC 2009; 63: 659-67 30 10
Carbapenemase-mediated resistance in the UK Carbapenemase producers: ARMRL referrals 60 50 40 30 20 10 0 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 HPA ARMRL, Unpublished data Enterobacteriaceae Non-Fermenter 31 Another multi-resistant epidemic bacterial clone: A. baumannii, XA-23 clone 1 Prevalent UK strain First appeared in 2002 >50 UK centres affected Multi-resistant lineage Typically susceptible only to CL and TIG XA-23 clone 1 in UK (and Ireland) 32 Mechanism 5: up-regulated efflux Tigecycline resistance in A. baumannii: adeb expression ssion Relative expres 1 0.9 0.8 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0 0.946 Adapted, Lomovskyaya et al., 2007 0.131 0.003 Pre Rx Post Rx Lab mutant TIG MIC: 0.5 16 64 33 11
Recap: mechanisms of resistance Antibiotic resistance Target site modification / protection (mutation or enzymic) e.g., changes in a PBP, the ribosome, DNA gyrase By-pass (acquired target unaffected by antibiotic) e.g., PBP2 ; mupirocin HL resistance; trimethoprim resistance Enzymic inactivation / modification of antibiotic e.g., β-lactamases, aminoglycoside-modifying enzymes Impermeability (porin loss) e.g., ETP R Enterobacteriaceae; prd (D2) in Ps. aeruginosa Active efflux e.g., tigecycline resistance in A. baumannii; non-specific (affects multiple drug classes); diverse pump types 34 Undefined mechanism of action (daptomycin) 35 = undefined resistance mechanisms Sabol et al., Antmicrob Agents Chemother 2005;49:1664-5 36 12
Summary Resistance is complex Not a new phenomenon; discovered by us in last 70 years New drug = new selective pressure = bacterial response; mechanisms are diverse ESBLs (CTX-M types) in E. coli are a major new resistance problem for the 21 st century Resistance associated with plasmids encoding multi-resistance Potential to develop further resistance; mutation and other plasmids Surveillance & microbiology to understand dominant & emerging resistances Rational antibiotic usage needed to limit increasing resistance 37 Acknowledgements Colleagues at the Health Protection Agency Students and collaborators, 1988-2009 Thank you for listening 38 39 13