Education
Ph.D.,
Molecular
Microbiology,
May 1998
University of
Nebraska-Lincoln
Bio:
Dr. Wen
received his
PhD in
Molecular
Microbiology
from the
University of
Nebraska-Lincoln,
NE in May
1998. He
worked as a
Postdoctoral
Fellow at the
University of
Rochester
Center for
Oral Biology,
Rochester, New
York from 1998
to 2001 and as
a Research
Assistant
Professor in
the Department
of Oral
Biology at the
University of
Florida,
Gainesville,
Florida from
2001 to 2008.
Dr. Wen joined
the faculty at
LSU Health
Sciences
Center in May
26, 2008 as an
Assistant
Professor with
a primary
appointment in
the Department
of Oral and
Craniofacial
Biology.
Research
Interests:
The primary
interest of
Dr. Wen's
research is on
the ecology of
oral biofilms
with a focus
on molecular
regulation of
Streptococcus
mutans biofilm
formation and
a long-term
goal in
identification
of novel
strategies
against
cariogenic
biofilms and
human dental
caries. It is
being carried
out using a
combination of
modern
microbiological,
molecular and
computational
techniques and
various in
vitro and in
vivo models.
Sponsored
by NIH/NIDCR,
one of Dr.
Wen’s major
projects is on
"BrpA in
virulence
modulation of
Streptococcus
mutans".
As a major
etiological
agent of human
dental caries,
S. mutans
lives
primarily on
the tooth
surface in
tenacious
biofilms. The
abilities to
colonize and
to persist on
the tooth
surface are
essential for
the bacterium
to cause
disease.
Identified
using
functional
genomics
approach,
BrpA, for biofilm
regulatory
protein
A, is
shown to play
a major role
in regulation
of acid- and
oxidative
stress
tolerance
response and
biofilm
formation,
traits
critical to
pathogenicity
of S.
mutans.
Predicted as a
surface-associated
protein, BrpA
also possesses
compositional
and structural
features that
appear to be
unique to S.
mutans in
the oral
flora. This
study is
designed to
explore the
structure-function
relationships
of BrpA and
the potential
of BrpA in
strategy
against S.
mutans.
Another
major aspect
of Dr. Wen's
research
focuses on
intra- and
inter-species
communication
and its impact
on the
development
and
ultimately,
the
pathogenicity
of the plaque
biofilms.
Dental plaque
is a highly
complex,
dynamic
microbial
community
consisting of
more than 700
hundred
different
species. This
study uses
multiple-species
consortium and
systems
biology
approach to
investigate
the
interactions
between S.
mutans and
other major
species in the
supragingival
plaque,
including
Lactobacillus
spp., and
their effects
on S. mutans’
colonization,
persistence
and
competitiveness,
the community
composition
and stability,
and
ultimately,
its
pathogenicity.
In this highly
collaborative
effort, Dr.
Wen works
closely with a
multi-disciplinary
team of
experts in
transcriptomics,
metabolomics,
computational
biology, and
animal
modeling from
several
different
institutions.
Dr. Wen is
also working
together with
the Xu group
in
Biomaterials
Sciences to
develop novel
antibacterial
dental
materials and
materials for
oral and
facial tissues
repair.
Currently, he
is serving as
a
co-investigator
on Dr. Xu's
R01 grant
"High
Performance
Antimicrobial
Fluoride
Releasing
Dental
Materials"
sponsored by
NIH/NIDCR.
Research
Interest--Keywords: Streptococcus mutans,
Lactobacillus
spp., eDNA,
biofilms,
ecology of
oral biofilms,
bacterial
cell-cell
communication,
bacterial
genetics,
virulence
regulation,
and human
dental caries.
Teaching
Activities:
Advanced
Bacteriology,
Oral
Microbiology
and
Immunology, DH
Oral
Microbiology,
Research
Methods, and
Dental Grant
Rounds. In
addition, Dr.
Wen's
laboratories
offer a
variety of
training
opportunities
for LSUHSC
undergraduate
and graduate
students, DDS
residents, and
MD/PhD
postdoctoral
fellows.
Selected
Publications:
Katherine
Rainey,
Suzanne
Michalek, Z.
T. Wen*,
and Hui Wu.
2019.
Glycosyltransferase
mediated
biofilm matrix
dynamics and
virulence of
Streptococcus
mutans". Appl
Environ
Microbiol.
2019 Feb
20;85(5).
pii:
e02247-18.
doi:
10.1128/AEM.02247-18.
Print 2019 Mar
1.
PMID:30578260;
Abranches J.,
L. Zeng, J. K.
Kajfasz, S. R.
Palmer, B.
Chakraborty,
Z. T. Wen, V.
P. Richards,
L. J. Brady,
J. A. Lemos.
2018. Biology
of Oral
Streptococci.
Microbiol
Spectr. 2018
Oct;6(5).
doi:
10.1128/microbiolspec.GPP3-0042-2018.
PMID:3033875;
Lemos JA,
Palmer SR,
Zeng L, Wen
ZT, Kajfasz
JK, Freires
IA, Abranches
J, Brady LJ.
Wen,
Z. T.*,
K. Scott-Anne,
S. Liao, A.
De, M. Luo, C.
Kovacs, B. S.
Narvaez, R.
Faustoferri,
Q. Yu, C. M.
Taylor, R. G.
Quivey. 2018.
Deficiency of
BrpA in
Streptococcus
mutans Reduces
Virulence in
Rat Caries
Model. Mol.
Oral
Microbiol.
2018 Jun 11.
doi:
10.1111/omi.12230.
[Epub ahead of
print]
PMID:
29888871.
Lee, J., J.
A. Townsend*,
T. Thompson,
A. De, T.
Garitty, Q.
Yu, B. Peters,
and Z.
T. Wen*.
2017. Analysis
of the
Cariogenic
Potential of
Various Almond
Milk Beverages
Using
Streptococcus
mutans Biofilm
Model In
Vitro. Caries
Research
2018;52(1-2):51-57.
doi:
10.1159/000479936.
Epub 2017 Dec
15.
PMID:29241218.
Wen,
Z. T.,
S. Liao, J. P.
Bitoun, A. De,
A. N.
Jorgensen, S.
Feng, X. Xu,
P. S. G Chain,
P. W.
Caufield, H.
Koo, Y. Li.
2017.
Streptococcus
mutans
displays
altered stress
responses
while
enhancing
biofilm
formation by
Lactobacillus
casei in
mixed-species
consortium.
Front Cell
Infect
Microbiol.
2017 Dec
20;7:524.
doi:
10.3389/fcimb.2017.00524.
eCollection
2017. (PMID:
29326887).
De, A., S.
Liao, J. P.
Bitoun, R.
Roth, W. L.
Beatty, H. Wu,
and Z.
T. Wen*.
2017.
Deficiency of
RgpG causes
major defects
in cell
division and
biofilm
formation, and
deficiency of
LCP proteins
leads to
accumulation
of cell wall
antigens in
culture medium
by
Streptococcus
mutans. Appl.
Environ.
Microbiol.
2017 Jul 7.
pii:
AEM.00928-17.
doi:
10.1128/AEM.00928-17.
(PMID:
28687645).
Besingi, R.
N., I. B.
Wenderska, D.
B.
Senadheeram,
D. G.
Cvitkovitch,
J. R. Long, Z.
T. Wen,
L. J. Brady.
2017.
Functional
Amyloids in
Streptococcus
mutans, their
use as Targets
of Biofilm
Inhibition and
Initial
Characterization
of SMU_63c.
Microbiology.
2017
Apr;163(4):488-501.
(PMID:28141493).
Additional
Info:
Publication at
Pubmed (https://www.ncbi.nlm.nih.gov/pubmed/?term=wen+zt)