Geology topics

M.L. House

Publications and source records attributed to M.L. House.

3 recordsLinked to original sources

USGS2006

An isolate of Piscirickettsia salmonis from white seabass is fully virulent for coho salmon

The virulence of the WSB-98 isolate of Piscirickettsia salmonis from white seabass Atractoscion nobilis was compared with that of the American Type Culture Collection type strain LF-89, which was originally isolated from coho salmon Oncorhynchus kisutch in Chile. In controlled laboratory challenges of juvenile coho salmon, the isolate from white seabass exhibited virulence that was equal to or greater than that of LF-89. The cumulative percent mortality (CPM) was similar between groups of coho salmon receiving an intraperitoneal injection of WSB-98 at 104.5 tissue culture infectious dose with 50% endpoint (TCID50)/fish (CPM = 98%) or an injection of LF-89 at 104.8 TCID50/fish (CPM = 95%). The mean day to death of 9.3 d for WSB-98 and 18.6 d for LF-89, however, differed significantly (P < 0.0001) between the two isolates. The virulence of an isolate of P. salmonis from white seabass for a salmonid species is consistent with the hypothesis that nonsalmonids can serve as natural marine hosts for the bacterium and potential sources for infection of salmonids. ?? Copyright by the American Fisheries Society 2006.

Journal of Aquatic Animal Health↗

USGS1999

Relative virulence of three isolates of Piscirickettsia salmonis for coho salmon Oncorhynchus kisutch

Piscirickettsia salmonis was first recognized as the cause of mortality among pen-reared coho salmon Oncorhynchus kisutch in Chile. Since the initial isolation of this intracellular Gram-negative bacterium in 1989, similar organisms have been described from several areas of the world, but the associated outbreaks were not reported to be as serious as those that occurred in Chile. To determine if this was due to differences in virulence among isolates of P. salmonis , we conducted an experiment comparing isolates from Chile, British Columbia, Canada, and Norway (LF-89, ATL-4-91 and NOR-92, respectively). For each of the isolates, 3 replicates of 30 coho salmon were injected intraperitoneally with each of 3 concentrations of the bacterium. Negative control fish were injected with MEM-10. Mortalities were collected daily for 41 d post-injection. Piscirickettsiosis was observed in fish injected with each of the 3 isolates, and for each isolate, cumulative mortality was directly related to the concentration of bacterial cells administered. The LF-89 isolate was the most virulent, with losses reaching 97% in the 3 replicates injected with 105.0 TCID50, 91% in the replicates injected with 104.0 TCID50, and 57% in the fish injected with 103.0 TCID50. The ATL-4-91 isolate caused losses of 92% in the 3 replicates injected with 105.0 TCID50, 76% in the fish injected with 104.0 TCID50, and 32% in those injected with 103.0 TCID50. The NOR-92 isolate was the least virulent, causing 41% mortality in the replicates injected with 104.6 TCID50. At 41 d post-injection, 6% of the fish injected with 103.6 TCID50 NOR-92 had died. Mortality was only 2% in the fish injected with 102.6 TCID50 NOR-92, which was the same as the negative control group. Because the group injected with the highest concentration (104.6 TCID50) of NOR-92 was still experiencing mortality at 41 d, it was held for an additional 46 d. At 87 d post-injection, the cumulative mortality in this group had reached 70%. These differences in virulence among the isolates were statistically significant (p < 0.0001), and are important for the management of affected stocks of fish.

Diseases of Aquatic Organisms↗

USGS1998

Soft shell clams Mya arenaria with disseminated neoplasia demonstrate reverse transcriptase activity

Disseminated neoplasia (DN), a proliferative cell disorder of the circulatory system of bivalves, was first reported in oysters in 1969. Since that time, the disease has been determined to be transmissible through water-borne exposure, but the etiological agent has not been unequivocally identified. In order to determine if a viral agent, possibly a retrovirus, could be the causative agent of DN, transmission experiments were performed, using both a cell-free filtrate and a sucrose gradient-purified preparation of a cell-free filtrate of DN positive materials. Additionally, a PCR-enhanced reverse transcriptase assay was used to determine if reverse transcriptase was present in tissues or hemolymph from DN positive soft shell clams Mya arenaria. DN was transmitted to healthy clams by injection with whole DN cells, but not with cell-free flitrates prepared from either tissues from DN positive clams, or DN cells. The cell-free preparations from DN-positive tissues and hemolymph having high levels of DN cells in circulation exhibited positive reactions in the PCR-enhanced reverse transcriptase assay. Cell-free preparations of hemolymph from clams having low levels of DN (<0.1% of cells abnormal), hemocytes from normal soft shell clams, and normal soft shell clam tissues did not produce a positive reaction in the PCR enhanced reverse transcriptase assay.

Diseases of Aquatic Organisms↗