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Applied and Environmental Microbiology, July 2004, p. 4144-4150, Vol. 70, No. 7
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.7.4144-4150.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Respiration Strategies Utilized by the Gill Endosymbiont from the Host Lucinid Codakia orbicularis (Bivalvia: Lucinidae)

Melinda R. Duplessis,1* Wiebke Ziebis,2 Olivier Gros,3 Audrey Caro,3 Julie Robidart,1 and Horst Felbeck1

Marine Biology Research Division, Scripps Institution of Oceanography, La Jolla, California 92093-0202,1 Department of Biological Sciences, University of Southern California, Los Angeles, California 92089,2 Laboratoire de Biologie Marine, Département de Biologie, Université des Antilles et de la Guyane, 97159 Pointe-à-Pitre Cedex, Guadeloupe3

Received 27 August 2003/ Accepted 9 April 2004

The large tropical lucinid clam Codakia orbicularis has a symbiotic relationship with intracellular, sulfide-oxidizing chemoautotrophic bacteria. The respiration strategies utilized by the symbiont were explored using integrative techniques on mechanically purified symbionts and intact clam-symbiont associations along with habitat analysis. Previous work on a related symbiont species found in the host lucinid Lucinoma aequizonata showed that the symbionts obligately used nitrate as an electron acceptor, even under oxygenated conditions. In contrast, the symbionts of C. orbicularis use oxygen as the primary electron acceptor while evidence for nitrate respiration was lacking. Direct measurements obtained by using microelectrodes in purified symbiont suspensions showed that the symbionts consumed oxygen; this intracellular respiration was confirmed by using the redox dye CTC (5-cyano-2,3-ditolyl tetrazolium chloride). In the few intact chemosymbioses tested in previous studies, hydrogen sulfide production was shown to occur when the animal-symbiont association was exposed to anoxia and elemental sulfur stored in the thioautotrophic symbionts was proposed to serve as an electron sink in the absence of oxygen and nitrate. However, this is the first study to show by direct measurements using sulfide microelectrodes in enriched symbiont suspensions that the symbionts are the actual source of sulfide under anoxic conditions.


* Corresponding author. Present address: Department of Biology, University of Washington, UW Box 355325, Seattle, WA 98195. Phone: (206) 632-1188. Fax: (206) 685-1728. E-mail: mdupless{at}u.washington.edu.


Applied and Environmental Microbiology, July 2004, p. 4144-4150, Vol. 70, No. 7
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.7.4144-4150.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Caro, A., Got, P., Bouvy, M., Troussellier, M., Gros, O. (2009). Effects of Long-Term Starvation on a Host Bivalve (Codakia orbicularis, Lucinidae) and Its Symbiont Population. Appl. Environ. Microbiol. 75: 3304-3313 [Abstract] [Full Text]  
  • Caro, A., Gros, O., Got, P., De Wit, R., Troussellier, M. (2007). Characterization of the Population of the Sulfur-Oxidizing Symbiont of Codakia orbicularis (Bivalvia, Lucinidae) by Single-Cell Analyses. Appl. Environ. Microbiol. 73: 2101-2109 [Abstract] [Full Text]