Teaching self-destructing Salmonella new tricks to fight cancer Wei Kong and Roy Curtiss III Arizona...
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![Page 1: Teaching self-destructing Salmonella new tricks to fight cancer Wei Kong and Roy Curtiss III Arizona State University, Tempe, Arizona, USA.](https://reader035.fdocuments.us/reader035/viewer/2022062305/5697bf951a28abf838c90d50/html5/thumbnails/1.jpg)
Teaching self-destructing Salmonella new tricks to fight cancer
Teaching self-destructing Salmonella new tricks to fight cancer
Wei Kong and Roy Curtiss IIIArizona State University, Tempe,
Arizona, USA
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Cancer is one of the leading causes of death in the world
An estimated 289,000 Americans are expected to die from lung and other three most common cancers (colon, breast and pancreatic) in 2014
http://www.lung.org
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Tumor hypoxia- a major hazard of cancer therapy
http://www.mc.pref.osaka.jp
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Development of novel therapies targeting hypoxic cancer cells
Bacteria have been investigated as anticancer agents:
•Salmonella •Escherichia •Clostridium•Bifidobacterium•Caulobacter•Listeria•Proteus•Streptococcus, etc.
Bacteria
Live, attenuated or genetically-engineered
Vector
Immunotherapeutic agents
Toxin
Spore
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Motile S. Typhimurium exists as facultative anaerobes, allowing them to survive in both oxygenated and hypoxic conditions.
S. Typhimurium strains have been shown to preferentially accumulate in tumours.
Importantly, S. Typhimurium was shown not only to colonize large established tumors but also exhibit the property to invade and affect metastases.
Salmonella as anti-cancer therapy
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Self-destructing Salmonella - Programmed regulated lysis system
For antigen delivery:
For DNA vaccine delivery:
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Programmed regulated lysis system for antigen delivery
In vitro with arabinose
Plasmid
araC PBADmurA asd P22PR
Ptrc Ag
In vivo without arabinose
Chromosome
araC PBAD murA araC PBADC2 araC PBAD lacI
SCV
nucleus
Host cell
RASV multiplyand antigen synthesis
Endosome escapingRelease Ag by lysis
The
gut e
pith
eliu
m
RASV
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DAP-less and Muramic acid-less Death in Host Strain with Regulated Lysis System Vector
11283
11283(pYA3681)
LB Agar LB Agar + 0.2% Arabinose
+ 50g/ml DAP
LB Agar + 0.2% Arabinose
LB Agar
Recombinant host-vector strain displaying arabinose-dependent growth and regulated cell lysis in the absence of arabinose
The genotype of 11283: asdA::araC PBAD c2 PmurA::araC PBAD murA (wza-wcaM) relA::araC PBAD lacI TTpmiPrfc::TT araC PBAD rfcpagP::Ptrc lpxE
pYA3681 araC PBAD regulated murA+ asdA+
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Self-destructing Salmonella for DNA vaccine delivery- Vector
The synthesis of EGFP from pYA4545 harboring EGFP gene in INT-407 and Vero cell line
5’-ggggactttcc ggggactttcc tccccacgcg ggggactttcc gccacgggc ggggactttcc ggggactttcc
pYA4685 (pYA4545-EGFP)
INT-407
Vero
DTS (II)pYA4272
(pYA3650-EGFP)
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Genotype of the ideal RASV strain: asdA::TT araC PBAD c2 PmurA::TT araC PBAD murArelA (wza-wcaM) pmi pagP::Ptrc lpxE fljBfliCendA sifAPhilA::Ptrc lacO hilAtlpA sseL
Self-destructing Salmonella for DNA vaccine delivery- Strain
Importin family members
RAN
Transcription factors
RASV harboring DNA vaccine vector pYA4545
∆tlpA∆sseL
PhilA :: Ptrc lacOhilA (Hyper-invasive)
Apoptosis/pyroptosis
∆sifA
Salmonella cell lysis
∆asdA∆PmurA
pYA4545
Host Cell
SCV
nucleus
NLS
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Programmed Salmonella regulated lysis system delivering antigens or DNA vaccine induced mucosal and systemic antibody and T-cell
responses protective immunity against various diseases
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Teaching self-destructing Salmonella new tricks to fight cancer
Exhibit diminished toxicity of lipid A to lessen inflammatory responses.
Rapid release of vacuolar Salmonella from the endosome to increase the efficacy of delivery and expression of a DNA vaccine.
Allow in vivo maximized Salmonella localization in tumors.
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11371 (Ptar::Ptrc lacOtar)3761 Chemo attractants: 100 μM Aspartate
3.0 cm 4.3 cm
A. Bacterium swimming test on soft agar plate
113713761
Swim
min
g D
ista
nce
(cm
)
B. Graph of swimming test result
*The data of graph were collected from 4 independent experiments, ρ < 0.05
Modulate Salmonella swimming behavior for enhanced tumor targeting and tumor homing
• ΔPtar::PtrcΔlacO tar• ΔPtsr::Ptrc ΔlacOtsr• Δtrg
Genetically modification of chemoreceptor genes*
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The
ratio
of S
alm
onel
la c
olon
izati
on in
tum
or v
s. s
plee
n
3761
3761+ htrA
3761 + purA
Reduced normal tissue fitness and enhance tumor fitness by genetically modifying RASV strains
Deletion of purA gene:•eliminate the production of adenosine monophosphate (AMP)
Deletion of htrA gene: •Eliminate a bifunctional stress protein HtrA that is required by many bacterial pathogens to successfully cause infection
tumor specific fitness of indicated strains was determined in BALB/c CT-26 subcutaneous tumor bearing mice post IT injection
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Day 0 Day 4 Day 8
BSG
Χ11517(pYA4545)
χ11517(pYA4545 + FasL)
11517
PmurA::TT araC PBAD murA asdA::TT araC PBAD c2 (araC PBAD)::P22 PR araBAD (wza-wcaM)pmi relA::araC PBAD lacI TT pagP::Plpp lpxE endAPhilA::PtrclacOhilA Ptar::Ptrc lacO tar Ptsr::Ptrc lacO tsr trg
Anti-tumor efficacy assay of anti-cancer Salmonella strains by intra-tumoral injection using whole body bioluminescence imaging
breast cancer subcutaneous mouse model
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National Institutes of Health (NIH/NIAID)
U. S. Department of Agriculture (USDA)
Acknowledgements
Project of programmed regulated lysis system:
Dr. Roy Curtiss IIIDr. Shamaila AshrafDr. Keith AmeissDr. Xiangmin ZhangDr. Maria Dolores Juarez-Rodriguez Project of RASV anti-cancer therapeutic vaccine:
Dr. Roy Curtiss IIIMr. Matthew BrovoldMr. Jeffrey TullyMr. Lee BensonMs. Chelsea Warren
National Institutes of Health (NIH/NCI)