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ARTICLE

Assessment of the Long-Term Viability of the Myxospores of Myxobolus cerebralis as Determined by Production of the Actinospores by Tubifex tubifex

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Pages 50-56 | Received 14 May 2014, Accepted 27 Sep 2014, Published online: 23 Feb 2015
 

Abstract

While whirling disease was first observed in Rainbow Trout Oncorhynchus mykiss in 1893, the complete life cycle of Myxobolus cerebralis (Mc), the causative agent of the disease, was not understood until 1984, when it was shown to involve two obligate hosts, a salmonid fish and the aquatic oligochaete Tubifex tubifex (Tt). The viability of the triactinomyxon (TAM) actinospores produced by Tt has been well studied, and is known to be temperature dependent and measured in days and weeks. Assertions that Mc myxospores produced by infected fish remain viable for years or even decades were made during the mid-20th century, decades before the Mc life cycle was described. Moreover, the duration of myxospore viability has not been well studied since the life cycle was elucidated. In a series of time-delay treatments, we assessed the long-term viability of Mc myxospores by exposure to Mc-susceptible Tt oligochaetes and quantified TAM production. As the time delay between inoculation and incubation of Mc myxospores in sand and water and exposure to Tt oligochaetes increased, TAM production decreased exponentially. Production among the 15-d time-delay replicates was reduced 74.7% compared with the 0-d treatment. Likewise, total TAM production was reduced 94.5, 99.4, and 99.9%, respectively, in the 90-, 120-, and 180-d time-delay treatments. Linear regression analysis of our data and the absence of TAM production among replicates of Mc myxospores held at 5°C for 365 d prior to exposure to Mc-susceptible Tt oligochaetes indicate that the long-term viability of Mc myxospores is less than 1 year under the conditions of this study.

Received May 14, 2014; accepted September 27, 2014

ACKNOWLEDGMENTS

This study was conducted in 2009–2010 as part of the Whirling Disease Investigations research project F-237R, through the Aquatic Research section of the Wildlife Programs Branch of the Colorado Division of Wildlife. Funding for this study was provided in part by the Federal Aid in Sport Fish Restoration Act. Myxospores of the M. cerebralis parasite were provided by Dolly Baxa and Kavery Mukkatira at the Aquatic Animal Health Research Laboratory at the University of California--Davis. Kurt Fausch and Kevin Rogers provided valuable advice on the design of the study.

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