Ballast Tank Organisms: Wanted Dead NOT Alive
Transcript of Ballast Tank Organisms: Wanted Dead NOT Alive
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Ballast Tank Organisms:Wanted Dead – NOT Alive
Nick Welschmeyer and Sarah Smith
Moss Landing Marine LaboratoriesMoss Landing CA 95039
California Prevention First, Sept 10th, 2008
Support from:
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•The Problem:Abate Aquatic Invasive Species
•The Solution (partial):Remove or Inactivate Organisms from Ship Ballast Discharge
•The Challenge:Engineer Shipboard Ballast Treatment Systems
•The Situation:Scientists must intelligently and accurately distinguish ‘live’ and
‘dead’ organisms in plankton (including microbes) in order to
evaluate treatment efficacy and to meet regulations
•
Let’s talk about this…
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Table 1. Example regulatory standards for ballast water.
Mesoplankton Nanoplankton Bacteria, Viruses
International Convention
for the Control and
Management of Ships
Ballast Water & Sediments;
IMO 2004
< than 10 viable organisms
per m3 for those organisms
> 50 µm minimum
dimension
< 10 viable organisms per
mL for those organisms >
10 µm but < 50 µm
minimum dimension
< 10 CFU per L of Vibrio
cholorae
< 1000 CFU per L of
intestinal enterococci
< 2500 CFU per L of
Escherichia coli
Ballast Water Management
Act of 2005; US Senate Bill
363, February 10th, 2005
< than 0.1 viable organisms
per m3 for those organisms
> 50 µm minimum
dimension
< 0.1 viable organisms per
mL for those organisms >
10 µm but < 50 µm
minimum dimension
< 10 CFU per L of Vibrio
cholorae
< 330 CFU per L of
intestinal enterococci
< 1260CFU per L of
Escherichia coli
Report and
Recommendation of the
California Advisory Panel
on Ballast Water
Performance Standards
(Staff recommendations,
November 2005)
No detectable viable
organisms > 50 µm
minimum dimension
< 10 viable organisms per L
for those organisms > 10
µm but < 50 µm minimum
dimension
< 10 CFU of bacteria per
mL
< 100 viruses per mL
< 10 CFU per L of Vibrio
cholorae
< 330 CFU per L of
intestinal enterococci
< 1260 CFU per L of
Escherichia coli
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Plankton Size Distribution
(from Veldhuis & Kraay 2000)
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Dead or Alive?Dead Alive Dead Alive
?
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Definition of unicellular viability
• Cells capable of growth (cell division) and metabolism
--Dead
X?Active – non cultivable
-XViable but inactive
Dormant
XXViable
Metabolically activeCapable of growth
To score a cell as truly live or dead, we must measure
growth capacity and metabolic activity
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Colony forming units vs. direct count
www.niwa.cri.nz www.dees.dri.edu(Daley & Hobbie 1975)
• 90 – 99.9% of bacterial cells are…
Dead?
Dormant/Inactive?
Non-cultivable?
0.1-10% of direct count
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The handbook
• All of these stains are designed to be used in human health related research– Mammalian cell lines
– E. coli, other pathogens
• None of these stains is designed for or optimized for environmental studies
• Many not suitable for use with phytoplankton– Autofluorescence interference
– Impaired staining under variable pH, temp, etc.
Chapter 15: Assays
for Cell Viability,
Proliferation and
Function
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Selected Vital StainsStain/Dye Assay target Result
CTC cell respiration Live cells fluoresce red
Calcein AM intracellular esterase activity Live cells fluoresce green
BCECF AM intracellular esterase activity Live cells fluoresce green
FDA intracellular esterase activity Live cells fluoresce green
CFDA-AM intracellular esterase activity Live cells fluoresce green
CDFA intracellular esterase activity Live cells fluoresce green
trypan blue Membrane Integrity Dead cells stain blue
Evan's Blue Membrane Integrity Dead cells stain blue
SYTOX® Green Membrane Integrity DNA of dead cells fluoresce green
7-AAD Membrane integrity DNA of dead cells fluoresce red
EthD-1 Membrane Integrity DNA of dead cells fluoresce red-orange
PI Membrane Integrity DNA of dead cells fluoresce red-orange
DiOC2 mitochondrial membrane potential Mitochondria of live cells fluoresce red
TTC redox potential medium fluoresces red with live cells
XTT redox potential medium turns orange
MTT redox potential medium turns purple
resazurin Unid. intracellular enzymatic/chemical activity medium fluoresces pink in presence of live cells
alamarBlue™ Unid. intracellular enzymatic/chemical activity medium fluoresces pink in presence of live cells
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0
10
20
30
40
50
60
70
80
90
100
1970 1975 1980 1985 1990 1995 2000 2005 2010
Year
Stu
die
s P
ub
lish
ed
(C
um
ula
tive
)
.
total
FDA
SYTOX
Digest
Published phytoplankton viability studies
Selected phytoplankton viability studies published from 1971 to present . Data are cumulative and
represent viability studies from a significant, though not comprehensive, survey of the literature.
(Watt 1971, Crippen & Perrier 1974, Faust & Correll 1977, Paerl 1978, Reynolds et al. 1978, Descolas-Gros 1980, Bentley-Mowat 1982, Gallagher 1984, Berglund & Eversman 1988, Yentsch et al. 1988, Dorsey et al. 1989, Selvin et al. 1989, Gala
& Giesy 1990, Berdalet & Dortch 1991, Gilbert et al. 1992, Arsenault et al. 1993, Minier et al. 1993, Gala & Giesy 1994, Reiriz et al. 1994, Faber et al. 1997, Geary et al. 1997, Lee & Rhee 1997, Murphy & Cowles 1997, Pouneva 1997, Regel 1997,
Berges & Falkowski 1998, Jochem 1999, Lee & Rhee 1999, Okochi et al. 1999, Vardi et al. 1999, Brookes et al. 2000, Onji et al . 2000, Vasconcelos et al. 2000, Brookes et al. 2001, Brussaard et al. 2001, Franklin et al. 2001, Veldhuis et al. 2001,
Agustí & Sanchéz 2002, Regel et al. 2002, Anderson et al. 2003, Segovia et al. 2003, Agustí 2004, Berman-Frank et al. 2004, Franklin & Berges 2004, Franklin et al. 2004, Latour et al. 2004, Regel et al. 2004, Casotti et al. 2005, van de Poll et al.
2005, Agustí et al. 2006, Binet & Stauber 2006, Franklin et al. 2006, Gregg & Hallegraeff 2006, Lawrence et al. 2006, Llabrés & Agustí 2006, Moharikar et al. 2006, van de Poll et al. 2006, Vardi et al. 2006, Garvey et al. 2007, Jansen & Bathmann
2007, Ribalet et al. 2007, Timmermans et al. 2007, Wigglesworth-Cooksey et al. 2007, Hayakawa et al. 2008, Holm et al. 2008, Prince et al. 2008)
33% FDA
22% SYTOX
91 assays
68 publications
7% Digest
Sytox green, introducedProchlorococcusOstreococcus
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SYTOX Green (marks ‘dead’ cells)
Intact Membrane – no stain
LIVEPermeable membrane – stained nucleus
DEAD
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SYTOX® Green Visible Fluorescence
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Fluorescein Diacetate (marks ‘live’
cells)
Enzyme activity – stained
LIVENo enzyme activity – unstained
DEAD
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Fluorescein Diacetate visible Fluorescence
Garvey et al. 2007
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Sample
Hydrodynamic
focusing
Sheath
fluid
laser 2 Scattered
light detectors
3 Fluorescence
detectors
Waste
Anatomy of a Flow Cytometer
Detector Measures
Forward Scatter Size
Side Scatter Shape
Red
Fluorescence
Chlorophyll
autofluorescence
Orange
Fluorescence
Phycobilin
autofluorescence
Green
Fluorescence
Stains
mild autofluorescence
Chlorophyll
Forw
ard
Scatt
er
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Flow Cytometric Analysis of Viability – Sytox Green
Live Phaeodactylum Dead Phaeodactylum (Glutaraldehyde)
Live - Dead
Gre
en
Gre
en
Red
Red
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Unstained
Station 10
Station 5
FDA staining of natural phytoplankton (Elkhorn Slough)
Forward Scatter
Chloro
phyll
Forward Scatter
Green Fluore
scence
Green Fluorescence
Counts
Forward Scatter
Chlorophyll
Forward Scatter
Green Fluore
scence
Green Fluorescence
Counts
Forward Scatter
Chlorophyll
Forward Scatter
Green Fluore
scence
Green Fluorescence
Counts
FDA++
FDA+
FDA-
Cryptophytes
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FDA Staining Results: Continued
Station 10
Station 9
Station 8
Station 7
Station 6
Station 5
Station 2
Station 1
St. 10
St. 9
St. 8
St. 7
St. 6
St. 5
St. 2
St. 1 1600
cells ml-1
155
Station 4
Station 3
St. 4
St. 3
0
10
20
30
40
50
60
70
0 1 2 3 4 5 6 7 8 9 10
Station
Ce
lls m
l-1 .
Cells
per
ml (x
1000)
Station
0%
10%
20%
30%
40%
50%
60%
70%
80%
90%
100%
1 2 3 4 5 6 7 8 9 10
Station
Perc
en
t in
meta
bo
lic c
ate
go
ry .
FDA-
FDA+
FDA++
Pe
rce
nta
ge
in
me
tab
olic
ca
teg
ory
Station
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Viability Summary
0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
0.9
1
0 1 2 3 4 5 6 7 8 9 10 11
Station
Fra
cti
on
FD
A+
+
(no
rmali
zed
to
max v
alu
e w
ith
in c
ruis
e)
Fra
cti
on
FD
A+
+
no
rmali
zed
to
max v
alu
e p
er
cru
ise
Small cryptophytes (~3µm) show an increased fraction of
metabolically active cells in the upper Elkhorn Slough
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Cell-specific viability analysis is not the only show in town…
What about physiological metabolism?
Analysis of viability stains is time-consuming, costly and
impractical at times
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3H-leucine uptake
0.0E+00
2.0E+04
4.0E+04
6.0E+04
Control Treatment
dp
m . m
L-1
5 days after treatment with chlorine dioxide (5 ppm)
M/V Atlantic Compass, February 2007
Smith, Cox and Maranda (unpublished)
Examples of ‘bulk’ metabolic activity in ballast-related experiments
Bacterial
Heterotrophic
Production
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Primary Production
0
5
10
15
20
25
30
Control Treatment
µgC
L-1
d-1
Photosynthesis (14C) Ballast Treatment Expt.
M/V Eversuperb, MARENCO UV/filter treatment
Welschmeyer et al 2007
Examples of ‘bulk’ metabolic activity in ballast-related experiments
Phytoplankton
Photosynthesis
C-14 technique
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Examples of ‘bulk’ metabolic proxies in ballast-related experiments
0
50
100
150
200
250
300
Control Treatment
AT
P (
pm
ol
L-1)
ATP concentration during Ballast Treatment Expt.
M/V Eversuperb, MARENCO UV/filter treatment
Welschmeyer et al 2007
Microbial (<50um)
ATP content
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Rau et al (in prep). CO2 as
a biocide; 7 days after 25%
CO treatment ended.
Day 13 Photosynthesis
0
50
100
150
200
250
300
350
400
450
500
Air CO2 CO2+Light
Treatment
Pri
mary
Pro
du
cti
on
(m
gC
m-3 d
-1)
Day 13 Dark Respiration
0
100
200
300
400
500
600
Air CO2 CO2+Light
Treatment
Resp
irati
on
(m
gO
2 m
-3 d
-1)
mg C
m-3
d-1
mg O
2m
-3d
-1Photosynthetic C-14 uptake
Microbial DarkOxygen Respiration (Winkler)
Examples of ‘bulk’ metabolic activity in ballast-related experiments
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Examples of ‘bulk’ metabolic proxies in ballast-related experiments
-0.3
-0.25
-0.2
-0.15
-0.1
-0.05
0
0.05
1
treatment
mg
O2 / (
L*
h)
live
dead
Zooplankton (>50um)
Zooplankton
Respiration
(oxygen electrode)
1% Sodium Azide
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Examples of ‘bulk’ metabolic proxies in ballast-related experiments
RJP1:(enclosures)
0.0
0.2
0.4
0.6
0.8
0 10 20 30 40 50 60
Time (h)
Ph
oto
ch
em
ical Y
ield
(Fv/F
m)
RJP2: (enclosures)
0.0
0.2
0.4
0.6
0.8
0 50 100 150
Time (h)
Ph
oto
ch
em
ica
l Y
ield
(Fv
/Fm
)
PAM Fluorometry
Phytoplankton
Variable Fluorescence
Control
Control
Treatment (UV)
Treatment (UV)
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So… what do we get when we combine fancy, flow-cytometric
viability analysis with bulk physiological measurements?
Cell specific
Viability
Bulk Physiological
Metabolism?
On one hand…
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Metabolic verification of SYTOX Green™
y = -0.0003x + 0.0003
R2 = 0.9704
0.0E+00
5.0E-05
1.0E-04
1.5E-04
2.0E-04
2.5E-04
3.0E-04
3.5E-04
0 0.2 0.4 0.6 0.8 1
Fraction Dead (SYTOX Green)
Pro
duction R
ate
(pg C
Cell-
1hr-
1)
In laboratory cultures, increased membrane
permeability correlates with a reduction in
photosynthesis
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So… what do we get when we combine fancy, flow-cytometric
viability analysis with bulk physiological measurements?
Cell specific
Viability
Bulk Physiological
Metabolism?
On the other hand…
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Evidence of photosynthetic metabolism in ‘dead’ cells
Primary Production (C-14 uptake) per 'Live' Cell
Surrogate species, Tetraselmis ; NRL January, 2008
0.00
100.00
200.00
300.00
400.00
500.00
600.00
1 2 3 4 5 6
Experiment
Ph
oto
syn
thesis
p
g C
(li
ve c
ell
)-1
Control
UV
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(Becker et al. 2002)
Chlorophyll
Siz
e (
Fo
rwa
rd S
ca
tte
r)
Chlorophyll
Chlorophyll
Ora
ng
e F
luo
resce
nce
Ye
llow
Flu
ore
sce
nce
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Conclusions:
•Determination of live and dead cell concentrations in marine microbes is an
important, but evolving procedure in marine science – it is not yet perfect
•At the moment, the best and most conservative means of establishing
‘ground truth’ in viability studies includes bulk physiological measurements of
metabolism and growth
•The combination of cell-specific viability staining with complementary
physiological measurements will establish confidence in the selection of
methods used to test ballast treatment efficacy
Remember: Ballast tank organisms are ‘Wanted Dead – NOT Alive’