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Microbiology, BKD Vaccines and Chemotherapeutics Research

Microbiology

Dr. Mark Strom
Program Manager

Program Staff Directory



Microbiology Home
 Molecular Pathogenesis
   Aeromonas salmonicida

   Renibacterium salmoninarum

   R. salmoninarum Genome
   Project

   Vibrio vulnificus

 Diagnostics development,
 identification tools

 Applied Studies
   BKD vaccines
   and chemotherapeutics

   Disease Diagnostics
   and Pathology


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Current Research - BKD Vaccines and Chemotherapuetics

Renibacterium salmoninarum is the cause of bacterial kidney disease (BKD), a chronic, debilitating disease with high mortality, that is characterized by granulomatous lesions primarily on the kidney and other organs. The disease occurs worldwide in cultured and wild salmon. BKD affects the health, fitness and survival of salmonids at all life stages during both fresh and saltwater phases. In the Pacific Northwest Columbia River drainage and estuary, it is a serious problem in cultured broodstocks of endangered chinook and sockeye salmon and hatchery raised fish. Currently there are no completely effective vaccines available to prevent R. salmoninarum infections, and antibiotic treatment has also proven less than optimal.

typical BKD lesion on the kidney of a juvenile chinook salmon   Typical BKD lesion on the kidney of a juvenile
  chinook salmon
Measures to control BKD have had limited success and presently there are no satisfactory treatments or an effective vaccine. One of the biggest factors in preventing disease is the fact that R. salmoninarum is passed vertically from the female to her eggs, as well as horizontally from fish to fish. The use of chemotherapeutics including antibiotics has been hampered because of many factors, including the intracellular life cycle of the bacterium in the infected host, and the general problem in delivery of these compounds into the early life stages of salmon when bacterial populations are lowest. The approved antibiotic for treatment of R. salmoninarum infections is erythromycin, a member of the macrolide class. Unfortunately, this antibiotic does not penetrate cells well, bacteria easily develop resistance to it, and continued prophylactic use of it to treat endangered captive broodstock populations can sometimes lead to toxic reactions and lowered reproductive success.

We have approached the problem of treating BKD in endangered captive populations from two points. One is to use the alternative macrolide antibiotic, azithromycin, to treat the infection. Azithromycin has several pharmacological features that may be advantageous in treating BKD, including the ability to cross eukaryotic cell membranes, and a longer active half-life. The second approach is to test various vaccine candidates to assist the fish immune system in preventing or alleviating infections. Both approaches are showing some promise, and it is hoped that applying these strategies to salmon at their earliest life stage may result in populations free of the pathogen.

More Information:

Project lead(s): Rhodes, Harrell, Strom

Publications
Strom, M.S., L.W. Harrell, W.T. Fairgrieve, M.E. Peterson, C.K. Rathbone, and L.D. Rhodes. 2001. Use of antibiotics and new vaccines to reduce mortality from Bacterial Kidney Disease in chinook salmon, pp. 80-85. In B.A. Berejikian and C.E. Nash (ed), Research on captive broodstock programs for Pacific salmon Research, FY2001 Annual Report to Bonneville Power Administration, Contract 00005227.

Strom, M.S., W.T. Fairgrieve, L.W. Harrell, and C.K. Rathbone. 2000. Efficacy and toxicity of treatments for Bacterial Kidney Disease in chinook salmon, pp. 105-110. In B.A. Berejikian (ed), Research on captive broodstock programs for Pacific salmon Research, FY2000 Annual Report to Bonneville Power Administration, Contract 00005227.

Flagg, T. A., B. A. Berejikian, J. E. Colt, W. W. Dickhoff, L. W. Harrell, D. J. Maynard, C. E. Nash, M. S. Strom, R. N. Iwamoto, and C. V. W. Mahnken. 2000. Ecological and behavioral impacts of artificial production strategies on the abundance of wild salmon populations. U. S. Dept. Commerce, NOAA Tech. Memo. NMFS-NWFSC-41, 92 p.

Recent Meeting Presentations:
Rhodes, L. D., L. W. Harrell, C. K. Rathbone, S. C. Corbett, and M. S. Strom. 2001. Studies of major soluble antigen (MSA) in Renibacterium salmoninarum, the causative agent of bacterial kidney disease in salmonid fish. Cold Spring Harbor Laboratory Symposium "Microbial Pathogenesis and Host Defense", Cold Spring Harbor Laboratory, New York, September 12-16, 2001.

Harrell, L. W., C. K. Rathbone, M. E. Peterson, F. T. Poysky, M. J. Crewson and M. S. Strom. 2000. Observations on the Efficacy of Azithromycin for Chemotherapy of Bacterial Kidney Disease. Western Fish Disease Workshop, Gig Harbor, WA, June 28-29, 2000.

Poysky, F. T. , M. E. Peterson, L. D. Rhodes, and M. S. Strom. 2000. Increased growth rate of Renibacterium salmoninarum in modified KDM2 media. Western Fish Disease Workshop, Gig Harbor, WA, June 28-29, 2000

Rathbone, C. K., L. W. Harrell, M. E. Peterson, F. T. Poysky, and M. S. Strom. Preliminary Observations on the Efficacy of Azithromycin for Chemotherapy of Bacterial Kidney Disease. Western Fish Disease Workshop, Fish Health Section/American Fisheries Society Annual Meeting, Twin Falls, Idaho, June 9-11, 1999.


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last modified 12/26/02

              
   
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