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How will a changing climate impact
Vibrio tubiashii growth and pathogenicity
to Pacific oyster larvae?

Elene Dorfmeier, Steven Roberts, Carolyn Friedman
University of Washington | S A F S




PCSGA – NSA Joint Meeting 9-21-11
Aquaculture and Bivalve Larvae
           Regional Problems

     Ü  Limited natural recruitment of
               bivalve species
     Ü Ocean chemistry changes
        Ü Re-emergent disease




                                  Photo: Norbert Dankers
Acidification of Northwest Waters
                           SUMMER 2009:
                    Dabob Bay




                    Totten Inlet




Map: R. Jacobsen       Graphs: Simone Alin et al. NOAA
Environment



Impact of Acidification on C. gigas
  Ü Effects of OA on calcifying marine
    organisms:
         •  Growth and development
         •  Energy allocation
         •  Metabolic depression

  Ü Pathogen – Host interaction?
  Ü Disease susceptibility?
Pathogen



Vibrio tubiashii
Ü  Gram-negative, facultative anaerobe

Ü  Pathogenic to a variety of marine
  invertebrate larvae, including Pacific oyster

Ü  Re-emergent vibriosis in the Northwest




                              Photo: Phetsouvanh et al. 2008
Research Goals

Ü  Investigate how environmental stressors will
  influence Vibrio tubiashii growth


Ü  Determine how elevated pCO2 impacts Pacific
  oyster larval survival and disease susceptibility




                                            Photo: Norbert Dankers
Research Goals

ü  Investigate how environmental stressors will
  influence Vibrio tubiashii growth


Ü  Determine how elevated pCO2 impacts Pacific
  oyster larval survival and disease susceptibility




                                            Photo: Norbert Dankers
Vt growth experimental design

           25°C            25°C

~380                                   750
ppm                                    ppm


           12°C            12°C


                Vt strain RE22
        Inoculation dose: 103 CFU/ml
              3 days of growth
Results: 25°C Vt Growth




     Error Bars = ± 1 SE
Results:
  Vt Growth at elevated pCO2
 Ü  At 25°C, no detectable difference in
     Vt growth at 750 ppm pCO2

 Ü  All stages of growth at 12°C not
     captured within 72 hr experiment




Growth curves fit to Gompertz growth model: y = Ae(-b2*b3)^x
Research Goals
Ü  Investigate how environmental stressors will
  influence Vibrio tubiashii growth


ü  Determine how elevated pCO2 impacts Pacific
  oyster larval survival and disease susceptibility




                                            Photo: Norbert Dankers
Larval Disease Challenge
                        Temperature:
                           16°C


        pCO2:
  ~380 ppm = 8.0 pH                         Disease:
  750 ppm = 7.8 pH                         V. tubiashii
  2000 ppm = 7.4 pH




 Ü  Five Vt doses (102 – 106 CFU/ml), plus sterile control

 Ü  40 larvae per well; 6 replicates per dose of Vt

 Ü  LD50 determination at 24, 48, and 72 hrs

                                           Photo: Ghent University
Overview: Vt Disease Challenge




        Early stage         Late stage
         D-veliger            veliger
        3 days old          10 days old



Photo: FAO
Results: Larval Disease Challenges
         Larval Survival on Day 3



           Early stage              Late Stage




             Error Bars: ± 95% CI
               p-values > 0.05
LD50 Results




LD50 reported in CFU/ml of V. tubiashii
LD50 Results




LD50 reported in CFU/ml of V. tubiashii
LD50 Results




LD50 reported in CFU/ml of V. tubiashii
Larval Disease Challenge: Summary
No detectable difference in Pacific oyster
susceptibility to vibriosis at elevated pCO2.
Considerations:

  Ø  Larval population variation
  Ø  Length of exposure to low pH conditions
  Ø  Carbonate ion availability and saturation
      states during spawning (Gazeau et al. 2011)
  Ø  Vt culture conditions
Conclusions
 Ü  Vt growth at 25°C was not significantly
   different at elevated pCO2
 Ü  12°C Vt growth to be performed again to
   capture full growth curve at 750 ppm
 Ü  No significant differences in susceptibility
   to vibriosis were detected at either larval
   age or pCO2 level in Pacific oysters
     Ø  Important to consider factors that may
        affect host susceptibility that are difficult to
        account for
Next Step: Vt Gene Expression
                         VtpR
               (Hasegawa & Hase 2009)

                        • Metalloprotease
             Toxins       (vtpA)
                        • Hemolysin



                        •  Flagellar
             Motility     expression


                             Photo: NOAA NWFSC
THANK YOU!
Saltonstall-Kennedy Program (NOAA)
UW School of Aquatic & Fishery Sciences
Ed and Vicky Jones - Taylor Shellfish Hatchery
Joth Davis - Taylor Resources
Sam White
Richard Wilson – Bay Center Mariculture
Russell Rogers – WDFW


Generous student support provided by:
Chelsea Farms LLC, Little Skookum Shellfish
Growers, Rock Point Oyster Co., Seattle
Shellfish, and Taylor Shellfish Co.

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Elene Dorfmeier pcsga11

  • 1. How will a changing climate impact Vibrio tubiashii growth and pathogenicity to Pacific oyster larvae? Elene Dorfmeier, Steven Roberts, Carolyn Friedman University of Washington | S A F S PCSGA – NSA Joint Meeting 9-21-11
  • 2. Aquaculture and Bivalve Larvae Regional Problems Ü  Limited natural recruitment of bivalve species Ü Ocean chemistry changes Ü Re-emergent disease Photo: Norbert Dankers
  • 3. Acidification of Northwest Waters SUMMER 2009: Dabob Bay Totten Inlet Map: R. Jacobsen Graphs: Simone Alin et al. NOAA
  • 4. Environment Impact of Acidification on C. gigas Ü Effects of OA on calcifying marine organisms: •  Growth and development •  Energy allocation •  Metabolic depression Ü Pathogen – Host interaction? Ü Disease susceptibility?
  • 5. Pathogen Vibrio tubiashii Ü  Gram-negative, facultative anaerobe Ü  Pathogenic to a variety of marine invertebrate larvae, including Pacific oyster Ü  Re-emergent vibriosis in the Northwest Photo: Phetsouvanh et al. 2008
  • 6. Research Goals Ü  Investigate how environmental stressors will influence Vibrio tubiashii growth Ü  Determine how elevated pCO2 impacts Pacific oyster larval survival and disease susceptibility Photo: Norbert Dankers
  • 7. Research Goals ü  Investigate how environmental stressors will influence Vibrio tubiashii growth Ü  Determine how elevated pCO2 impacts Pacific oyster larval survival and disease susceptibility Photo: Norbert Dankers
  • 8. Vt growth experimental design 25°C 25°C ~380 750 ppm ppm 12°C 12°C Vt strain RE22 Inoculation dose: 103 CFU/ml 3 days of growth
  • 9. Results: 25°C Vt Growth Error Bars = ± 1 SE
  • 10. Results: Vt Growth at elevated pCO2 Ü  At 25°C, no detectable difference in Vt growth at 750 ppm pCO2 Ü  All stages of growth at 12°C not captured within 72 hr experiment Growth curves fit to Gompertz growth model: y = Ae(-b2*b3)^x
  • 11. Research Goals Ü  Investigate how environmental stressors will influence Vibrio tubiashii growth ü  Determine how elevated pCO2 impacts Pacific oyster larval survival and disease susceptibility Photo: Norbert Dankers
  • 12. Larval Disease Challenge Temperature: 16°C pCO2: ~380 ppm = 8.0 pH Disease: 750 ppm = 7.8 pH V. tubiashii 2000 ppm = 7.4 pH Ü  Five Vt doses (102 – 106 CFU/ml), plus sterile control Ü  40 larvae per well; 6 replicates per dose of Vt Ü  LD50 determination at 24, 48, and 72 hrs Photo: Ghent University
  • 13. Overview: Vt Disease Challenge Early stage Late stage D-veliger veliger 3 days old 10 days old Photo: FAO
  • 14. Results: Larval Disease Challenges Larval Survival on Day 3 Early stage Late Stage Error Bars: ± 95% CI p-values > 0.05
  • 15. LD50 Results LD50 reported in CFU/ml of V. tubiashii
  • 16. LD50 Results LD50 reported in CFU/ml of V. tubiashii
  • 17. LD50 Results LD50 reported in CFU/ml of V. tubiashii
  • 18. Larval Disease Challenge: Summary No detectable difference in Pacific oyster susceptibility to vibriosis at elevated pCO2. Considerations: Ø  Larval population variation Ø  Length of exposure to low pH conditions Ø  Carbonate ion availability and saturation states during spawning (Gazeau et al. 2011) Ø  Vt culture conditions
  • 19. Conclusions Ü  Vt growth at 25°C was not significantly different at elevated pCO2 Ü  12°C Vt growth to be performed again to capture full growth curve at 750 ppm Ü  No significant differences in susceptibility to vibriosis were detected at either larval age or pCO2 level in Pacific oysters Ø  Important to consider factors that may affect host susceptibility that are difficult to account for
  • 20. Next Step: Vt Gene Expression VtpR (Hasegawa & Hase 2009) • Metalloprotease Toxins (vtpA) • Hemolysin •  Flagellar Motility expression Photo: NOAA NWFSC
  • 21. THANK YOU! Saltonstall-Kennedy Program (NOAA) UW School of Aquatic & Fishery Sciences Ed and Vicky Jones - Taylor Shellfish Hatchery Joth Davis - Taylor Resources Sam White Richard Wilson – Bay Center Mariculture Russell Rogers – WDFW Generous student support provided by: Chelsea Farms LLC, Little Skookum Shellfish Growers, Rock Point Oyster Co., Seattle Shellfish, and Taylor Shellfish Co.