Dr. Mark Strom
Program Manager
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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
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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
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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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