about omics group - d2cax41o7ahm5l.cloudfront.net€¦ · 2.00e+10 2.50e+10 3.00e+10 0 20 40 60 80...
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![Page 1: About OMICS Group - d2cax41o7ahm5l.cloudfront.net€¦ · 2.00E+10 2.50E+10 3.00E+10 0 20 40 60 80 100 Time (h) CFU) CFU) 5.00E+06 1.05E+08 2.05E+08 3.05E+08 4.05E+08 5.05E+08 0 20](https://reader034.vdocument.in/reader034/viewer/2022042317/5f06cc397e708231d419c913/html5/thumbnails/1.jpg)
About OMICS Group OMICS Group is an amalgamation of Open Access publications and worldwide
international science conferences and events. Established in the year 2007 with the sole aim of making the information on Sciences and technology ‘Open Access’, OMICS Group publishes 500 online open access scholarly journals in all aspects of Science, Engineering, Management and Technology journals. OMICS Group has been instrumental in taking the knowledge on Science & technology to the doorsteps of ordinary men and women. Research Scholars, Students, Libraries, Educational Institutions, Research centers and the industry are main stakeholders that benefitted greatly from this knowledge dissemination. OMICS Group also organizes 500 International conferences annually across the globe, where knowledge transfer takes place through debates, round table discussions, poster presentations, workshops, symposia and exhibitions.
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About OMICS International Conferences
OMICS International is a pioneer and leading science event organizer, which publishes around 500 open access journals and conducts over 500 Medical, Clinical, Engineering, Life Sciences, Pharma scientific conferences all over the globe annually with the support of more than 1000 scientific associations and 30,000 editorial board members and 3.5 million followers to its credit.
OMICS Group has organized 500 conferences, workshops and national symposiums across the major cities including San Francisco, Las Vegas, San Antonio, Omaha, Orlando, Raleigh, Santa Clara, Chicago, Philadelphia, Baltimore, United Kingdom, Valencia, Dubai, Beijing, Hyderabad, Bengaluru and Mumbai.
.
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Novel forces shaping Beneficial
Bacterial Biofilms
Dept. of Mol. Genetics Weizmann institute of Science
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Dietrich et al., 2013 Sriramulu et al., 2005
Pseudomonas aeruginosa
Bacillus subtilis
Biofilms are multicellular communities of bacteria
Bacteria in the biofilm state:
- Adhere stronger to the host
- Are more resistant to:
antibiotics, sterilizing
agents, and the immune
system
-Biofilm formation Plays an
important role in promoting
beneficial interactions, and
in pathogenicity
2µm
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Bacillus subtilis is a Gram-positive beneficial bacterium forms biofilms in soils and on plant roots
Biofilm formation in the lab
Yaara Oppenheimer-Shaanan
Biofilm formation on the root
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So far, biofilm morphology was considered a direct output of organic matter
secretion, a protein and carbohydrate-rich polymeric extracellular matrix (ECM)
Wild Type tasA eps ywqC-F
tasA; amyloid-like fibers
epsA-O; exopolysaccharides
ywqC-F; acidic exopolysaccharides
What genetic and biochemical factors are essential for biofilm formation?
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• No similarity in ECM genes and in extracellular matrix components.
• In many cases organic ECM is highly produced but biofilm architecture is defective.
• Oxygen depravation triggers morphogenesis (Kolodkin-Gal et al., Gene Dev 2013, Mcloon and Kolodkin-Gal et al., JBact, 2012).
Pseudomonas
chlororaphis
Salmonella
enterica
Gram-Negative Gram-Positive
Bacillus
subtilis
Mycobacterium
smegmatis
What genetic and biochemical factors are essential
for biofilm formation?
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Biofilm formation is dependent on calcium
Day7
- Ca2+ +Ca2+
Day3
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Calcium carbonate is a mineral produced in access of calcium and carbon dioxide,
and participates in shaping multicellular organisms.
Biofilm formation is dependent on carbon dioxide
- Ca2+ +Ca2+ +Ca2+
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Calcium carbonate minerals are used to build shells and skeletons of
higher organism
Corals (argonite) Starfish (calcite)
Biomineralization; The process through which organisms are involved in mineral
formation
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Do bacterial colonies form minerals similar to skeleton formation?
Aragonite Calcite Vaterite
Calcite fingerprint FTIR
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1 2 10
Applied with Ca2+
21
Are mineral scaffolds involved in morphogenesis of bacterial biofilms?
Phase
X-Ray
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Minerals provide mechanical support throughout the wrinkles
Wild type
Mineral thickness
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3
4
Urease
Urea
Ammonia
1
2
Spontaneous
Do mutants defective in biomineralization have a
developmental defect?
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Wild type
ΔureA-C
pH 5.5 pH 7.0
OD
[6
00
nm
]
0
0.2
0.4
0.6
0.8
1
1.2
1.4
0 2.5 5 7.5 10 12.5 15
wild type
ΔureaseABC
Do mutants defective in biomineralization have a
developmental defect?
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lcfA serves to compartmentalize the
membrane
Wild type ΔlcfA
H+
Ca2+
H+
pH
Ca2+
Bacterial cell
Carbonate precipitation Ca2+ + HCO3
- CaCO3 + H+
X-Ray
Mutants defective in MVPs synthesis have a biomineralization
and a morphology defect
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Calcite morphology is determined via interaction with charges EPS
Wild-Type ΔywqC-F
ywqC-F is a novel operon responsible for producing negatively charged
exopolysaccharides that have a significant influence on the calcite morphology
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Calcite morphology is
determined via
interaction with charges
EPS
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Bacteria
Calcite crystals provide phenotypic Antibiotic resistance?
Bacteria
Water Diffusion coefficient: Polysaccharides film (cellulose)- 4-14 X10-8 cm2/sec Calcium carbonate- 20 X10-6 cm2/sec (May-Crespo et al., 2010) Calcite crystal- up to 5 X10-2 cm2/sec (Alkattan et al., 1998)
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Mineral accumulation provides phenotypic resistance to 70% Ethanol
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Living bacteria reside within mineral scaffolds
40 % viable
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Phylogenetic tree
Kinsella R J et al. PNAS 2003
Can mineral precipitation promote morphogenesis in other bacterial
species?
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- Ca2+ Day 5 Day 20
Applied with Ca2+
Day3
Calcite scaffolds promote morphogenesis in Mycobacterium
smegmatis
X-RAY
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• Rigidity and structuring of bacterial biofilms requires
biologically controlled biomineralization
• ECM is essential, but Calcite scaffolds are also essential for bacterial development.
• The organic and non-organic scaffolds strongly shape each other
• How are bacteria survive within minerals?
• Bacterial “Osteoblasts”?
Summary
Oppenheimer-Shaanan & Sibony-Nevo et al, Under review
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Yeda-Sela Center for Basic Research
ISF-icore
Yad Hanadiv
A research grant from Ayala Benjamin-Mashat
Kamin program for R & D
Angel-Fiavovich fund for ecological research
Thanks
Current Lab members
Dr. Yaara Oppenheimer-Shaanan
Gili Rozenberg
Nitai Steinberg
Tabitha Bucher
Dr. Hadas Ganin
Natalia Kampfer
Dan Pollack
Ronit Suissa
Dr. Iris Krukner
Former Lab members
Dr. Zohar Bloom-Ackermann
Odelia Sibony-Nevo
Collaborators:
Prof. Stephen Weiner, Prof. Lia Addadi, Prof. Michael Meijler, Prof. Rotem Sorek,
Prof. Avraham Shenzer, Prof. Ian Baltimore (Max Plank), Dr. Shmuel Rubinstein
(Harvard)
Funding:
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How is flexibility achieved?
B. subtilis B. simplex
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What happens when two complex biofilms meet?
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Contact Engulfment Covering Prior to contact
24h 48h 72h 96h
The interaction between B. subtilis and B. simplex occurs in coordinated stages
2mm
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Prior to contact Post contact
B. simplex B. simplex + B. subtilis
membrane staining DNA staining B. subtilis (GFP)
5µm
Stage 1: Contact between the two biofilms leads to the invasion of B. subtilis into B. simplex colony
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Stage 2: B. subtilis engulfs the biofilm of B. simplex by recruiting flagellated motility
2mm
WT
∆hag
Phag amyE locus
Phag-gfp
0.00E+00
3.00E+07
6.00E+07
WT Δ hag
0
3x107
6x107
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Stage 3: B. simplex population is eradicated by secretion of small diffusible molecules by B. subtilis
0.00E+00
5.00E+09
1.00E+10
1.50E+10
2.00E+10
2.50E+10
3.00E+10
0 20 40 60 80 100
Time (h)
B. S
imp
lex
(CFU
) B
. Su
bti
lis (
CFU
)
5.00E+06
1.05E+08
2.05E+08
3.05E+08
4.05E+08
5.05E+08
0 20 40 60 80 1000.01x108
1.01x108
2.01x108
3.01x108
4.01x108
5.01x108
5.0x109
1.0x1010
1.5x1010
2.0x1010
2.5x1010
3.0x1010 supernatant
Hydrophobic Interaction
Chromatography
Size exclusion
Cannibalism toxins
surfactin
Contact Engulfment Cover
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a b
c f
j k
WT Δ Sdp Δ skf Δ srfAA
0%
20%
40%
60%
80%
100%
B. subtilis
B. simplex
% C
FU
Δ srfAA Δ sdpC Δ skfA
B. sim
B. sim
B. su
b
Interactio
n
B. sim
B. su
b
Interactio
n
Stage 3: B. simplex population is eradicated by secretion of Surfactin and “cannibalism” toxins by B. subtilis
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Novel roles for molecules previously considered solely as biofilm regulators
sdp
skf
surfactin
Channels forming by surfactants
Biofilm matrix
SdpC & SkfA Cannibalism
toxins
surfactin
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Stage 4: B. subtilis population changes genetically in the course of the interspecies interaction
Interaction “mutants”
WT
Whole genome sequencing of the strains derived from the interspecies interaction had no chromosomal mutations
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Interaction derived strain
Rap-P
Spo0A P
ComA
P
Surfactant Cannibalism toxins
Loss of B. subtilis natural plasmid leads to the hyperrugose biofilm phenotype reminiscent of interaction-derived strains
Neiditch MB et al., 2013 Plasmid cured
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0
0.1
0.2
0.3
0.4
0.5
0.6
6 8 10 12 14 16
Time (h)
OD
60
0 o
f B
. sim
ple
x cu
ltu
re
+ WT sup. + Plasmid cured sup. + Interaction mutants sup.
Applied with Sup.
supernatant
Plasmid cured
Interaction mutant
WT
Stage 5: The loss of B. subtilis natural plasmid increases the virulence factors that allow the elimination of B. simplex biofilms
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The loss of B. subtilis natural plasmid may be common among root-
associated B. subtilis
Chen et al., 2011
We Suspect plasmid loss occurs for Isolates with Enhanced biocontrol
properties
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B. simplex population changes genetically in the course of the interspecies interaction
B. simplex - mutation analysis
Mutant Protein Affect Change Mut 1 Spo0A Nonsynonymous G643A Mut 2 Spo0A Frameshift deletion 534_535del Mut 3 Spo0A Nonsynonymous T193G Mut 4 Tyrosine - protein kinase EpsD Frameshift deletion 556_559del Mut 5 UDP - glucose dehydrogenase Frameshift deletion 918delA
B
WT Interaction driven
Biofilm driven Biofilm driven
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• Reservoir of motile cells is actively maintained to enable spreading to new niches from the rigid structures
• Bet-hedging strategy of plasmid loss enables rising of violent isolates during interspecies interactions
• The changes in the single cell morphology and in the toxin secretion are reversible
Strategies to enable flexibility of Bacillus subtilis biofilms to improve competition
during interspecies interactions
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Yeda-Sela Center for Basic Research
ISF-icore
Yad Hanadiv
A research grant from Ayala Benjamin-Mashat
Kamin program for R & D
Angel-Fiavovich fund for ecological research
Thanks
Current Lab members
Dr. Yaara Oppenheimer-Shaanan
Gili Rozenberg
Nitai Steinberg
Tabitha Bucher
Dr. Hadas Ganin
Natalia Kampfer
Dan Pollack
Ronit Suissa
Dr. Iris Krukner
Former Lab members
Dr. Zohar Bloom-Ackermann
Odelia Sibony-Nevo
Collaborators:
Prof. Stephen Weiner, Prof. Lia Addadi, Prof. Michael Meijler, Prof. Rotem Sorek,
Prof. Avraham Shenzer, Prof. Ian Baltimore (Max Plank), Dr. Shmuel Rubinstein
(Harvard)
Funding:
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