Pfiesteria: Review of the Science and Identification of Research Gaps. Report for the National Center for Environmental Health, Centers for Disease Control and Prevention
Abstract:The Pfiesteria organism was first identified and named in the early 1990s and its ability to kill fish was documented at the time. Research on the effects of exposure to its toxin on humans is more recent, sparked largely by widely publicized fish kills in the late 1990s and reports of adversely affected persons present at the scenes of the kills. Consequently, the peer-reviewed literature is still limited and substantial research is in progress at institutions in the Atlantic coast states of Maryland, North C… Show more
“…Burkholder et al, 1999;Magnien, 2001;Samet et al, 2001;Glibert et al, 2001, although many of these links have emphasized the potentially high P demands of these cells, rather the N demands. Toxic Pfiesteria outbreaks generally occur in waters that are shallow, poorly flushed, and enriched with nutrients.…”
Section: Eutrophication and Pfiesteria Sppmentioning
“…Burkholder et al, 1999;Magnien, 2001;Samet et al, 2001;Glibert et al, 2001, although many of these links have emphasized the potentially high P demands of these cells, rather the N demands. Toxic Pfiesteria outbreaks generally occur in waters that are shallow, poorly flushed, and enriched with nutrients.…”
Section: Eutrophication and Pfiesteria Sppmentioning
“…Like many other toxic algal species (see review in Burkholder et al 2001a), toxic Pfiesteria species have naturally occurring toxic strains, as well as apparently benign strains with respect to toxicity (Burkholder et al 1999, 2001a,b,c, Marshall et al 2000, Stoecker et al 2002, Springer et al 2002). In Pfiesteria , the latter strains have been designated as non‐inducible, operationally defined as strains that are unable to kill fish with toxin in appropriately conducted fish bioassays (Turgeon et al 2001, Samet et al 2001). Non‐inducible strains have not shown fish‐killing activity with toxin in these bioassays, and rarely have produced amoeboid stages (Marshall et al 2000, Burkholder et al 2001a,b).…”
Section: Use Of Non‐inducible Strainsmentioning
confidence: 99%
“…Actively toxic strains are capable of causing fish death rapidly (minutes to <6 h on average; Burkholder et al 2001a, Glasgow et al 2001a. Thus far the longest a toxic Pfiesteria strain has maintained toxicity has been 4 years (Burkholder et al 2001a); like other toxic algae, many toxic Pfiesteria strains have lost toxic activity over time in culture (Burkholder et al 2001a,c; Samet et al 2001). Non‐inducible strains have been shown to be capable of causing death of young fish slowly (>24 h) by physical attack (Burkholder et al 2001a).…”
Despite use of excellent molecular techniques, Litaker et al. (2002) cannot provide insights about the life history of toxic Pfiesteria piscicida because they showed no data in support of having used toxic strains; rather they presented evidence that they used non‐inducible strains. Litaker et al. did not find amoeboid stages or a chrysophyte‐like cyst stage in several cultures and unequivocally concluded that the stages do not exist in all P. piscicida strains. Thus, they did not consider the tenet that absence of evidence does not constitute proof of absence. Apparent discrepancies between the research by Litaker et al. and previous research on Pfiesteria can be resolved as follows: First, Litaker et al. did not use toxic strains. We have reported findings (similar to Litaker et al.) showing few amoeboid transformations in non‐inducible strains, which manifest some but not all of the forms that have been documented in some toxic strains. We, and others, have documented active toxicity to fish, transformations to amoebae, and chrysophyte‐like cysts in some clonal toxic strains. Second, the data from several recent publications, which were available but not mentioned by Litaker et al. or by Coats (2002) in accompanying commentary, have verified P. piscicida amoebae, chrysophyte‐like cysts, and other stages in some toxic strains through a combination of approaches including PCR data from clonal cultures.
“…The heterotrophic/mixotrophic dinoflagellate, P. piscicida has several reported nutritional modes, including photoautotrophy via kleptoplastidy, osmotrophic use of organic substrates, and phagotrophic uptake of a range of microalgae, bacteria, microzooplankton, mesozooplankton, and fish tissue and cellular contents (Burkholder and Glasgow, 1997;Glasgow et al, 1998;Lewitus et al, 1999a,b;Samet et al, 2001;Springer et al, 2002). Burkholder et al (2001a) obtained evidence of a relatively greater capability to grow herbivorously and to take up inorganic nutrients in TOX-B and NON-IND than in TOX-A P. piscicida.…”
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