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

• Published in: Journal of aquatic animal health Vol. 27; no. 1; pp. 50 - 56
• Main Authors: Nehring, R. Barry, Schisler, George, Chiaramonte, Luciano, Horton, Annie, Poole, Barbara
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 01-03-2015
• Subjects: Animals; fish; hosts; linear models; Myxobolus - physiology; Myxobolus cerebralis; Oligochaeta - parasitology; Oncorhynchus mykiss; regression analysis; sand; Spores, Protozoan; temperature; Tubifex tubifex; viability; whirling disease
• ISSN: 1548-8667; 0899-7659; 1548-8667
• DOI: 10.1080/08997659.2014.976671

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.