Florida in a tank - the role of experiments in ecosystem restoration
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Bane Schill
Publications and source records attributed to Bane Schill.
Non-lethal sampling for the detection of Myxobolus cerebralis in asymptomatic rainbow trout
We have described in previous reports (Schill et al., 1998) the development of a polymerase chain reaction (PCR) amplification of 18S ribosomal RNA for the detection of Myxozoan parasites. Oligonucleotide primers were developed by multiple alignment of Myxozoan sequence information and analysis by a custom-written computer program (PRIM). Candidate pairs of primer sequences were then analyzed for specificity by BLAST (Basic Local Alignment Search Tool). From these, a set of promising primers (MYXFWD and MYXREV) was chosen for further testing. These were chosen because they should direct detection of a number of Myxozoan species (Table 1). PCR using MXYFWD and MYXREV proved to be robust and relatively free of artifact products. Further, we were able to routinely detect Myxobolus cerebralis in fish tissues (Figure 1).
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Preliminary effects of water hardness on triactinomyxon production and development from eastern tubifex worms infected with Myxobolus cerebralis
Whirling disease is caused by Myxobolus cerebralis and requires an intermediate oligochaete host identified as Tubifex tubifex (Wolf, Markiw, and Hiltunen, 1986). M. cerebralis spores ingested by the tubifex worms develop into triactinomyxons (tams) that are eventually released into the water column to infect salmonid fish. There may be many environmental parameters, biotic or abiotic, that may affect the development of waterborne tams in eastern tubifex worms. This study will focus on one of those environmental parameters, total water hardness. Total water hardness is defined as the concentration of calcium and magnesium in a water sample expressed in milligrams per liter of equivalent CACO 3 (Boyd, 1990). This study will address whether different levels of water hardness affect the development and production of tams released by infected tubifex worms.
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Influence of temperature and substrate on infection rate, triactinomyxon production, and release duration from eastern tubifex worms infected with Myxobolus cerebralis
Salmonid whirling disease is caused by Myxobolus cerebralis , a metazoan parasite with a two host life cycle involving salmonid fish a an aquatic oligochaete, Tubifex tubifex (Wolf, Markiw and Hiltunen, 1986). Whirling disease has been reported in 22 U.S. states with the greatest losses occurring in the salmonid fisheries of western and Midwestern states. Although whirling disease is endemic in the eastern United States, serious documented losses to wild populations have not been reported. Two high priority research needs identified in 1996 were a better understanding of how worm and parasite populations might differ from different geographic areas and how environmental factors affect the various stages of whirling disease. To begin to address these research needs we established "eastern" populations of worms, parasite and fish hosts. This abstract will present data on the effects of temperature and substrate upon eastern T. tubifex worms infected with an eastern isolate of M. cerebralis . The influences of these abiotic factors upon the ability to infect the worms and subsequently their ability to produce waterborne triactinomyxons.
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