Abstract:Blue crab diseases, parasites, and commensals are not well studied in the Gulf of Mexico, and their prevalence rates have only been sporadically determined. Commercial soft shell shedding facilities in Louisiana experience high mortality rates of pre-molt crabs, and some of these deaths may be attributable to diseases or parasites. During the active shedding season in 2013, we determined the prevalence of shell disease, Vibrio spp., Lagenophrys callinectes, and Hematodinium perezi at 4 commercial shedding faci… Show more
“…It is likely that CsRV1 is ubiquitous in blue crabs throughout their range. This is supported by the discovery of CsRV1 in Brazilian blue crabs, together with previously published reports that CsRV1 is present in all the North American populations sampled ( Bowers et al, 2010 ; Rogers et al, 2014 ; Flowers et al, 2015 ). The genetic divergence of the RdRP sequence of CsRV1 from Brazil, relative to North American strains, suggests that the virus has been a part of the blue crab ecology for a long time, and that the virus genome may be a useful marker to understand blue crab population connectivity over large spatial and temporal scales.…”
Section: Discussionsupporting
confidence: 77%
“…Blue crab populations are themselves subject to control by numerous factors, including predation and disease ( Johnson, 1977 ; Hines, 2007 ; Shields and Overstreet, 2007 ; Schott and Messick, 2010 ; van Montfrans et al, 2010 ). Blue crabs are infected by a pathogenic virus, C. sapidus reovirus 1 (CsRV1, also called RLV for reo-like virus), throughout the studied US range from Louisiana to Massachusetts ( Johnson, 1977 ; Bowers et al, 2010 ; Rogers et al, 2014 ; Flowers et al, 2015 ). Originally described in captive crabs, CsRV1 has been reported at an average prevalence of 20% in wild populations, with peak prevalence often exceeding 50% ( Johnson and Bodammer, 1975 ; Flowers et al, 2015 ).…”
The blue crab, Callinectes sapidus Rathbun, 1896, which is a commercially important trophic link in coastal ecosystems of the western Atlantic, is infected in both North and South America by C. sapidus Reovirus 1 (CsRV1), a double stranded RNA virus. The 12 genome segments of a North American strain of CsRV1 were sequenced using Ion Torrent technology. Putative functions could be assigned for 3 of the 13 proteins encoded in the genome, based on their similarity to proteins encoded in other reovirus genomes. Comparison of the CsRV1 RNA-dependent RNA polymerase (RdRP) sequence to genomes of other crab-infecting reoviruses shows that it is similar to the mud crab reovirus found in Scylla serrata and WX-2012 in Eriocheir sinensis, Chinese mitten crab, and supports the idea that there is a distinct “Crabreo” genus, different from Seadornavirus and Cardoreovirus, the two closest genera in the Reoviridae. A region of 98% nucleotide sequence identity between CsRV1 and the only available sequence of the P virus of Macropipus depurator suggests that these two viruses may be closely related. An 860 nucleotide region of the CsRV1 RdRP gene was amplified and sequenced from 15 infected crabs collected from across the geographic range of C. sapidus. Pairwise analysis of predicted protein sequences shows that CsRV1 strains in Brazil can be distinguished from those in North America based on conserved residues in this gene. The sequencing, annotation, and preliminary population metrics of the genome of CsRV1 should facilitate additional studies in diverse disciplines, including structure-function relationships of reovirus proteins, investigations into the evolution of the Reoviridae, and biogeographic research on the connectivity of C. sapidus populations across the Northern and Southern hemispheres.
“…It is likely that CsRV1 is ubiquitous in blue crabs throughout their range. This is supported by the discovery of CsRV1 in Brazilian blue crabs, together with previously published reports that CsRV1 is present in all the North American populations sampled ( Bowers et al, 2010 ; Rogers et al, 2014 ; Flowers et al, 2015 ). The genetic divergence of the RdRP sequence of CsRV1 from Brazil, relative to North American strains, suggests that the virus has been a part of the blue crab ecology for a long time, and that the virus genome may be a useful marker to understand blue crab population connectivity over large spatial and temporal scales.…”
Section: Discussionsupporting
confidence: 77%
“…Blue crab populations are themselves subject to control by numerous factors, including predation and disease ( Johnson, 1977 ; Hines, 2007 ; Shields and Overstreet, 2007 ; Schott and Messick, 2010 ; van Montfrans et al, 2010 ). Blue crabs are infected by a pathogenic virus, C. sapidus reovirus 1 (CsRV1, also called RLV for reo-like virus), throughout the studied US range from Louisiana to Massachusetts ( Johnson, 1977 ; Bowers et al, 2010 ; Rogers et al, 2014 ; Flowers et al, 2015 ). Originally described in captive crabs, CsRV1 has been reported at an average prevalence of 20% in wild populations, with peak prevalence often exceeding 50% ( Johnson and Bodammer, 1975 ; Flowers et al, 2015 ).…”
The blue crab, Callinectes sapidus Rathbun, 1896, which is a commercially important trophic link in coastal ecosystems of the western Atlantic, is infected in both North and South America by C. sapidus Reovirus 1 (CsRV1), a double stranded RNA virus. The 12 genome segments of a North American strain of CsRV1 were sequenced using Ion Torrent technology. Putative functions could be assigned for 3 of the 13 proteins encoded in the genome, based on their similarity to proteins encoded in other reovirus genomes. Comparison of the CsRV1 RNA-dependent RNA polymerase (RdRP) sequence to genomes of other crab-infecting reoviruses shows that it is similar to the mud crab reovirus found in Scylla serrata and WX-2012 in Eriocheir sinensis, Chinese mitten crab, and supports the idea that there is a distinct “Crabreo” genus, different from Seadornavirus and Cardoreovirus, the two closest genera in the Reoviridae. A region of 98% nucleotide sequence identity between CsRV1 and the only available sequence of the P virus of Macropipus depurator suggests that these two viruses may be closely related. An 860 nucleotide region of the CsRV1 RdRP gene was amplified and sequenced from 15 infected crabs collected from across the geographic range of C. sapidus. Pairwise analysis of predicted protein sequences shows that CsRV1 strains in Brazil can be distinguished from those in North America based on conserved residues in this gene. The sequencing, annotation, and preliminary population metrics of the genome of CsRV1 should facilitate additional studies in diverse disciplines, including structure-function relationships of reovirus proteins, investigations into the evolution of the Reoviridae, and biogeographic research on the connectivity of C. sapidus populations across the Northern and Southern hemispheres.
“…Reaction mixtures and thermocycling conditions described previously were modified slightly (Rogers et al 2015). Briefly, reactions (10 µl) included a negative (no template) control and a positive control of DNA extracted from ethanol-preserved hemolymph of a known infected crab provided kindly by Dr. Jeffrey Shields, Virginia Institute of Marine Science.…”
Section: Detection Of Hematodinium Perezimentioning
Louisiana has one of the largest blue crab (Callinectes sapidus) fisheries in the USA, but little is known about blue crab diseases, parasites, and symbionts in this area. In 2013-2014, large juvenile and adult blue crabs were collected at 4 diverse sites to determine the prevalence of the protozoan symbionts associated with black gill disease (Lagenophrys callinectes), buckshot crabs (Urosporidium crescens), and bitter crab disease (Hematodinium perezi). A high aggregate prevalence of L. callinectes (93.2%) was identified across all seasons at all 4 collection sites regardless of salinity. A moderately low aggregate prevalence of U. crescens (22.4%) was identified across all seasons and sites. Prevalence of U. crescens depended on site salinity, with only 10% of infections detected at sites with <6.3 ppt salinity, and no infections detected at the low salinity site. While L. callinectes and U. crescens are commensal parasites of blue crabs, infections can result in unmarketable and unappealing meat. In the Louisiana fishery, H. perezi has been blamed circumstantially for adult mortalities in the low salinity nearshore fishing grounds. Despite this, H. perezi was not detected in any of the large crabs sampled, even from the low salinity sites. The prevalence data reported here for these 3 protozoans are the first to include blue crabs sampled seasonally at multiple locations along the Louisiana coast over the period of a year.
“…Unlike shrimp species, mud crab is usually free from disease and slower growth issues (Ahmed et al, 2013;Rogers, Taylor, Hawke, Schott, & Lively, 2015). Moreover, mud crab can be cultured with relatively low-cost feed compared with either shrimp or prawn (Cui et al, 2015;Wang et al, 2019;Wang, 2011).…”
Change in environmental salinity level is a major limiting factor for the aquaculture productivity because it imposes severe stress on organisms that in turn retards growth. The orange mud crab (Scylla olivacea) is an important coastal aquaculture species (farming is practised in 10‰–20‰ salinity levels) in Bangladesh. The present study was conducted to investigate the changes in growth, O2 consumption and mRNA expression levels of five selected genes in the orange mud crab (S. olivacea) exposed to three different experimental salinity levels (0‰, 10‰ and 20‰) for three months. Crabs reared at 10‰ and 20‰, showed significantly higher (p < .05) growth performance and expression of growth regulatory genes (Actin and α‐amylase). The highest levels (p < .05) of O2 consumption and expression of ion regulatory genes (Na+‐K+‐ATPase, V‐type H+‐ATPase and Diuretic Hormone) were obtained at 0‰. Moderate levels of growth and expression of selected candidate genes were observed at 10‰ treatment while the highest levels of growth and gene expression were obtained at 20‰ (control salinity). Strong interactions were observed between growth performance and expression of growth genes (R2 = 0.81–0.91), and rate of O2 consumption and expression of ion regulatory genes (R2 = 0.83–0.93), implying that the selected genes are important candidates for growth and ionic balance in S. olivacea. Growth performance was found to be very low at 0‰ initially, after 30 days crabs showed better growth performance at this salinity level. It is thus inferred that orange mud crab individuals might require 3–5 days for acclimation to salinity stress but it can take at least 30 days for acclimation to regular growth. Results indicate that with proper acclimation, the orange mud crab (Scylla olivacea) can be farmed at low salinity conditions and possibly in freshwater condition.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.