pathogenesis of gram positive bacterial infections ... · pathogenesis of gram positive bacterial...
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Turkish Clinical Microbiology and Infectious Diseases Congress (KLIMIK 2019) Gloria Golf Resort Hotel Belek, Antalya
Pathogenesis of Gram positive Bacterial Infections- Optimizing Treatment
Annelies S Zinkernagel
Division of Infectious Diseases & Hospital Epidemiology
University Hospital Zurich
University of Zurich
Switzerland
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6 out of 10 infectious diseases
• Global influenza pandemic
• Antimicrobial resistance
• Ebola and other high-threat pathogens
• Vaccine hesitancy
• Dengue
• HIV
https://www.who.int/news-room/fact-sheets/detail/the-top-10-causes-of-death
in 2019
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Bacteria - Host
Der Spiegel, 21/2007, p. 140
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Commensals can prevent (nasal) colonization of
pathobionts
Silde provided by M. M. RamseyAntagonism
Synergy
Metabolites
or Signals
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Commensal – pathobiont - interactions
direct inhibition
behavior shift
indirect inhibition
Brugger, Bomar, Lemon, PLoSPath, 2016
Zipperer, Nature, 2016, Bomar, mBio, 2016, Ramsey, FrontMicro,2016
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Corynebacterium accolens Releases
Antipneumococcal Free Fatty Acids from Human
Nostril and Skin Surface Triacylglycerols
6
Bomar, Brugger, mBio, 2016
Dolosigranulum spp.
Corynebacterium spp.
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Commensales Misbehaving
Swissnoso Bulletin
Susi, 8yr
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Science 1999;284:1318
Plaque
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Staphylococcus aureus: a commensal
• Gram positive extracellular bacterium
• 30% colonization
(Fowler et al. 2005 JAMA; Cosgrove and Fowler. 2008 CID; Chang et al. 2003 Medicine)
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Staphylococcus aureus: a commensal misbehaving
• Gram positive extracellular bacterium
• 30% colonization
• Increased risk for subsequent infection
– Recurring skin infections – abscesses
– Prosthetic joint infections
– Endocarditis
(Fowler et al. 2005 JAMA; Cosgrove and Fowler. 2008 CID; Chang et al. 2003 Medicine)
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Chronic –recurring infections - Biofilm-related infections
David Lebeaux et al. Microbiol. Mol. Biol. Rev. 2014;78:510-543
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How do bacteria withstand antibiotics?
Resistance - MRSA
Susceptible
• 1. ‘Location’:
– in ‘privileged’ sites such as abscess,
intracellular, biofilm
– > AB do not reach bacteria, milieux
• 2. ‘Growth’
– Stationary bacteria
– Persisters = metabolically inactiveLancet
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Rate of bacterial killing by beta-lactams is proportional to the
bacterial growth rate
Generation time
Tuomanen et al, J Gen Microbiology, 1986
High inoculum – stationary
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Rate of bacterial killing by beta-lactams is proportional to the
bacterial growth rate
Generation time
Tuomanen et al, J Gen Microbiology, 1986J Ex Med 1956
High inoculum – stationary
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1947
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J Ex Med 1949
Curative dose of penicillin increases
with the size of the inoculum, and
increases also with the age of the
infection (paradoxical more-drug-
kills-less Eagle effect)
UBI PUS IBI EVACUA
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Chronic –recurring infections
Surgery: Scars- morbidity -mortality
• Removal of infected tissue -foreign body» Therapy of Staphylococcus aureus Bacteremia Associated with a Removable Focus of
Infection, PAUL B. IANNINI, M.D.; KENT CROSSLEY, M.D. 1976
Antibiotics: Long treatment duration, i.v.
– Endocarditis: >4 weeks
•1943: Mortality 100% -now with antibiotic therapy 30%
– Osteomyelitis/ Orthopedic implant associated
infections: 6-12 weeks
? How long is long enough? What is most effective?
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Biphasic killing kinetics of bactericidal antibiotic treatment.
Alexander Harms et al. Science 2016;354:aaf4268
Persisters = metabolically inactive bacteria
Conlon et al., 2013
Growing Dormant
E.coli, Tbc, S.aureus, Salmonella ssp.Stressors: reactive oxygen species (ROS), lack in nutrients,
low pH, antibiotics
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Persisters
Conlon et al., 2013
Growing Dormant
Phenotypic Resistance
Persistenz, Toleranz
Natural Resistanceouter Membrane Gram-
Genetic Resistance
Mutations
Effluxpumps upregulated
Modified enzymes
Growth – No Growth
Genetic Resistant
timesusceptible
Lo
g C
FU
ml-
1
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• Challenging detection – reduced growth
• Phenotype switching, revert to normal colony phenotyp
• Indispensable feature for recurrent infections
• In contrast to stable SCV - genetically determined– Electron transport-defective SCVs, auxotroph for hemin, menadione, thymidine (hemB, menD,
thyD)
Small Colony Variants (SCV) in clinical isolates:
ko
wt
von Eiff, 2006
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Long tailed size distribution
Heterogenous colony size
• semi-automated colony growth analysis• analyzing time lapse movies with MATLAB for growth rate and lag-time
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Heterogeneity?
1. Difference in growth rate? Do they grow slower?
2. Difference in growth start? Do they start later?
3. Difference in growth end? Do they stop growing?
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Nonstable SCVs are bacteria withlong lag
SCV formation is a consequence of a late emergence of colonies
Nature Communications 2018
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Phenotype switching, revert to normal colony phenotyp
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SCV formation is a consequence of a late emergence of colonies
Stable SCVs are bacteriawhichgrow slower
auxotroph for hemin
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S. aureus recovered from human and murine abscesses
Microscopic timelapse
Heterogeneous and lag
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heterogeneous colony size - delay in the first division at the level of single cells
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Non dividing bacteria withstand antibiotics
Tolerance by growthNature Communications 2018
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lag time of individual bacterial cells
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The proportion of bacteria in lag phase correlates
with the proportion of bacteria surviving antibiotics
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How do S.aureus withstand antibiotics?
Resistance - MRSA
Susceptible
• 1. ‘Location’:
– in ‘privileged’ sites such as abscess,
intracellular, biofilm
– > AB do not reach bacteria, milieux
• 2. ‘Growth’
– Stationary bacteria
– Persisters = metabolically inactiveLancet
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Recurrence: Weeks - years after apparent cure
Fowler VG Jr et al. 2006;355:653-665
Daptomycin versus Standard Therapy for Bacteremia and Endocarditis Caused
by Staphylococcus aureus -open-label, randomized trial
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Staphylococcus epidermidis
Medical implant (pacemaker surface)
• Gram-positive coagulase-negative staphylococcus
• Commensal: skin and mucosa
• Less virulent than S. aureus (less toxins and aggressive exoenzymes)
• Opportunistic pathogen:
– Nosocomial bacteraemia
– Biofilm associated infections
• Major cause of medical device associated infections– Prosthetic valve infections
– Pacemaker associated infections
Endocarditis
bloodstream
Adapted from Paharik and Horswill Microbiol Spectr. 4(2) 2016
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A
pacemaker pocket infection
Pacemaker pocket infection in 40 year old
male, debridement of the pacemaker pocket,
vacuum assisted closure therapy (VAC), antibiotics
Staphylococcus epidermidis
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A
pacemaker pocket infection
Pacemaker pocket infection in 40 year old
male, debridement of the pacemaker pocket,
vacuum assisted closure therapy (VAC), antibiotics
Staphylococcus epidermidis
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A
pacemaker associated endocarditis
Explantation of pacemakerBacteremia,
vegetation in
echocardiography
Pacemaker pocket infection in 40 year old
male, debridement of the pacemaker pocket,
vacuum assisted closure therapy (VAC), antibiotics
Staphylococcus epidermidis
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Rifampicin resistent
clinical isolates
Phylogenetic tree of the clinical S. epidermidis isolates
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Biofilm
Scanning Electron Microscopy
Nature communications 2019
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Biofilm
Lag phase
Ciprofloxacin MIC 40 x
time kill curves
Scanning Electron Microscopy
Nature communications 2019
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How do S.epidermidis withstand antibiotics?
Resistance - rifampicin
Susceptible
• 1. ‘Location’:
– in ‘privileged’ sites such as abscess,
intracellular, biofilm
– > AB do not reach bacteria, milieux
• 2. ‘Growth’
– Stationary bacteria
– Persisters = metabolically inactive
– in host evolutionLancet
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Invasive Group A Streptococcal Disease
Global burden of disease / year:
663,000 invasive infections
- 163,000 deaths
- streptococal toxic shock syndrome
- necrotizing fasciitis
Rapidly-progressive, destructive
infection of the soft tissues.
Requires extensive surgical
debridement, intravenous
antibiotics, and ICU care.
High lethality (~35%)
Necrotizing fasciitis
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Why does treatment fail?
Rapidely progressive disease
Doc:
• quick diagnosis, surgery + ‘wright’ antimicrobials
Patient:
• Delay in presentation, necrotic tissue
Bug:
• Extracellular bacterium, 100% peni susceptible
• Many bacteria
• Virulence factors
• Biofilms
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Necrotizing fasciitis - 2 days ceftriaxone
bacterial count
bacte
ria/m
l
day 0 day 21100 0
1100 2
1100 4
1100 6
1100 8
necrotic tissue
healthy tissue
2 4Ceftriaxone
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Group A Streptococcus - Streptococcus pyogenes
bacterial count
bacte
ria/m
l
day 0 day 21100 0
1100 2
1100 4
1100 6
1100 8
necrotic tissue
healthy tissue
2 4Ceftriaxone
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J Ex Med 1949
Curative dose of penicillin increases
with the size of the inoculum, and
increases also with the age of the
infection (paradoxical more-drug-
kills-less Eagle effect)
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High inoculum – stationary
J Ex Med 1956
Once there is a high inoculum of
Strep and it reaches the stationary
phase of growth, Strep does not
express penicillin-binding proteins
and thus is less susceptible to beta-
lactams.
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Antibiotics: Eliminate + Disarm
• Cell wall active antibiotic:
– Penicillin: 100% susceptibility
– Penicillin should be given as quickly as possible
• Protein synthesis inhibitor:
– Clindamycin
• clindamycin is not affected by the inoculum size or
stage of bacterial growth
• suppressor of bacterial toxin synthesis• Sriskandan et al., J Antimicrob Chemother. 1997
• Mascini et al., Int J Antimicrib Agents 2001
• Goscinski G et al., Scand J Infect Dis 2006
IDSA Guidelines, CID 2005
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RealityObservational prospective surveillance of iGAS in Victoria, Australia (4.9mio), 3/2002-8/2004.
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Reduced virulence … in vivo
+ -DNase1Control Clindamycin
CI529
cfu
/g t
issu
e
control CLI
1.0100
1.0102
1.0104
1.0106
1.0108
Andreoni F. et al., J Infect Dis. 2016
GAS CI416
dilution factor
SL
O h
em
oly
tic a
cti
vit
y
[OD
541n
m]
12481632641280.00
0.05
0.10
0.15
0.20
0.25
0.30
0.35control
CLI
Lesion size
0 1 2 30
5
10
15
20control
CLI
day
les
ion
siz
e
[mm
2]
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RealityObservational prospective surveillance of iGAS in Victoria, Australia (4.9mio), 3/2002-8/2004.
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bacterial count
cfu
/g t
issu
e
skin spleen1100 0
1100 2
1100 4
1100 6
1100 8
1101 0
control s.c.
IVIG s.c.
ns ns
ns
SLO activity
% o
f sam
ple
s w
ith
acti
vit
y
control IVIG0
20
40
60
80
100
*
lesion size
day
lesio
n s
ize [
mm
2]
0 1 2 30
5
10
15
20ctrl s.c.
IVIG s.c.
**
***
IVIG inhibit VF activity + reduce lesion size
Tarnutzer A, et al, CMI 2018
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• Virus
• Lytic
• Resistances - Cocktails
• FDA approved for treatment of
Listeria monocytogenes
contamination in food industry
(poultry & cattle)
• Aquaculture & sewage treatment
Fischetti et al, 2006, Matsuda e al 2005, Huff et al 2003, Coates et al 2007, Doyle et al 2006
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AMR CONTROL
2015
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• Phages used to transport and target antibiotics into
bacteria» Yacoby et al, 2006, AAC Targeting Antibacterial Agents by Using Drug-Carrying
Filamentous Bacteriophages
• Rapid resistance development
• Phage lysins = cell wall hydrolases, bind to peptidoglycans
-> disrupt cell walls of Gram pos bacteria
AMR CONTROL
2015
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Endolysins
• Bacteriophage endolysins (=peptidoglycan hydrolase
enzymes) are enzymes which cleave essential bonds
in the peptidoglycans of bacterial cell wall for phage
progeny release
• can cause ‘‘lysis from without.’’
• Endolysins can act synergistically with antibiotics by
resensitizing bacteria to non-susceptible antibiotics
• No strains resistant to phage endolysin
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SpyCEP reduces biofilmB
iofi
lm
Andreoni et al. 2014
JCI Insight. 2016
Jul 7; 1(10): e87882.
GAS make biofilm
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Antibiotic activity against planktonic and
biofilm-embedded Streptococcus pyogenes
J Antimicrob Chemother 2017; 72: 3085–3092
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Fresh Garlic Extract Enhances the
Antimicrobial Activities
Ajoene, a sulfur-rich molecule from garlic
- prevents bacteria from secreting the toxin
rhamnolipid which destroys neutrophils
- inhibits genes controlled by quorum
sensing
- promotes rapid clearing of pulmonary
Pseudomonas aeruginosa infections.
- renders P. aeruginosa sensitive to
tobramycin, respiratory burst and
phagocytosis by PMNs
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Fresh Garlic Extract Enhances the
Antimicrobial Activities
Ajoene, a sulfur-rich molecule from garlic
- prevents bacteria from secreting the toxin
rhamnolipid which destroys neutrophils
- inhibits genes controlled by quorum
sensing
- promotes rapid clearing of pulmonary
Pseudomonas aeruginosa infections.
- renders P. aeruginosa sensitive to
tobramycin, respiratory burst and
phagocytosis by PMNs
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pathogen directed therapy
Adapted from
Nadia Keller
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host directed therapypathogen directed therapy
Adapted from
Nadia Keller
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host directed therapy
• Activation/boosting of eukaryotic effector mechanisms
– increase neutrophil numbers
– antimicrobial peptides,
– nitric oxide,
– reactive oxygen species
• Vitamin D, HIF-1α inducers, IL-4, Interferon α
kill the bacteria
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Vitamin D
• potent inducer of antimicrobial peptides
• link between vitamin D deficiency and the recurrence of GAS
tonsillopharyngitis.
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Atopic Dermatitis
• Allergic ‘type-2’ inflammation (IL4)-> hampers neutrophil
expansion and migration
• Why are atopic individuals more prone to infections
with Gram positive bacteria?
Ref: Adachi et al., JDS 1998;
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IL4-complex = fewer neutrophils, anti-IL4 = more neutrophils
Atopic Dermatitis
J. Woytschak et al., Immunity 2016
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Exogenous IFN-α boots GAS killing
Uchiyama, Keller et al., JID 2016
GAS survival in patient
whole bloodNeutrophil counts
over time of therapyGAS survival in IFN-α
stimulated neutrophils
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Infected with
GAS WT
enriched
pDCs
WT
condition
Infected with
GAS WT
enriched
pDCsWT
condition
* **
*
Infected with
GAS WT
enriched
pDCs
WT
condition
Endogenous IFN-α improves outcome
Type I interferon levels Bacterial load Lesion sizes
Keller N et al, Journal Inv. Dermatology 2018
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Antibiotics and beyond for treating invasive GAS infections
• Pathogen directed therapy
– Killing
• beta lactams, phages, endolysine
– Anti- toxine strategies
• Protein synthesis inhibitors
• IVIG
– Anti- biofilm strategies
• Host directed therapy
– Vitamin D, HIF-1α inducers, IL-4,
Interferon α
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Pathogenesis of Gram positive Bacterial Infections
• Commensals Misbehaving• Susceptible Staphylococci spp.
1. ‘Location’: abscess, intracellular, biofilm
2. ‘Growth’: stationary bacteria, persisters
-> Removal of infectious source crucial
-> Antibiotics: The proportion of bacteria in lag
phase correlates with the proportion of bacteria
survivng antibiotics
• Group A Streptococci: high inocculum, many
virulence factors – combination therapy penicillin,
clinda plus IVIG
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Many thanks
Klinik für Infektionskrankheiten &
Spitalhygiene
EawagProf. M. Ackermann and C. Vulin, PhD
Federica Andreoni
Andrea Tarnutzer
Markus Huemner
Nicola Häffner
Vanina Hauenreiter Dengler
Yvonne Achermann
Mathilde Boumasmoud
Srikanth MairpadyShambat
Alejandro Gomez Mejia
Tizian Schweizer
Carmen Menzi
Dennis Wipfli
Kati Seidl
Nadia Keller
Sandra Götschi
Nadja Leimer
Carol Rachmühl
Miguel Palheiros Marques
Sandro Pereira
Milton Meerwein
Michèle Leemann
Satoshi Uchiyama
Claudia Zürcher
Katrin Schilcher
Rey Gaffner
Kardiologie und Herzchirurgie USZ