Discovery of Sea Star Associated Densovirus: Difference between revisions

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The past year has shown a remarkable epidemic among many sea star species largely centered on the Pacific Coast.  This epidemic is notable both because it drastically alters marine ecosystems for which sea stars are keystone predators but also because it is a particularly pervasive and grisly disease – many populations of many species over an impressive geographical distance have been devastated and the disease causes sea stars to eventually just dissolve.  New high-throughput sequencing technologies, most notably metagenomics, have begun to yield answers to the source of this epidemic.  Researchers were surprised to learn that the infectious agent was a densovirus since it had been widely speculated that the disease was bacterial and caused by vibrio bacteria, well-established marine pathogens.  This discovery thus opens up a discussion about newly discovered marine viruses, our expanding ability to detect and characterize them, and their role in marine environments, either natural or used for aquaculture.
Late 2013 and 2014 have shown a remarkable epidemic among many sea star species largely centered on the Pacific Coast.  This epidemic is notable not only because it drastically alters marine ecosystems for which sea stars are keystone predators but also because it is a particularly pervasive and grisly disease – many populations of many species over an impressive geographical distance have been devastated and the disease causes sea stars to eventually just dissolve .  New high-throughput sequencing technologies, most notably [http://en.wikipedia.org/wiki/Metagenomics metagenomics], have begun to yield answers to the source of this epidemic. Sea star wasting disease thus provides a model for the power of new sequencing technologies as a means to identify pathogens extraordinarily rapidly and as a response to a crisis.  Researchers were surprised to discover that the infectious agent was a [http://en.wikipedia.org/wiki/Densovirinae densovirus] since it had been widely speculated that the disease was bacterial and caused by [http://en.wikipedia.org/wiki/Vibrio <i>Vibrio</i>] bacteria, well-established marine pathogens. [http://www.pnas.org/content/111/48/17278 8] This discovery thus opens up a discussion about newly discovered marine viruses, our expanding ability to detect and characterize them, and their role in marine environments, either natural or used for aquaculture.
==SSWD==
==Sea Star Wasting Disease==


[[File:SSWD.jpeg|thumb|300px|right|Progression and Geographic Spread of SSWD from Hewson et. al.Photographs of SSWD-affected stars (A) asymptomatic P. helianthoides, (B) symptomatic P. helianthoides, and (C) symptomatic P. ochraceus. Disease symptoms are consistent with loss of turgor, loss of rays, formation of lesions, and animal decomposition. (D) Map showing occurrence of SSWD based on first reported observation. (E) Transmission electron micrograph of negatively stained (uranyl acetate) viruses extracted from an affected wild E. troschelii from Vancouver . The sample contained 20–25-nm diameter nonenveloped icosohedral viral particles on a background of cellular debris (primarily ribosomal subunits) and degraded viral particles of similar morphology. (Scale bar: 100 nm.) [http://www.pnas.org/content/111/48/17278.abstract Hewson et. al. 2014]]]  
[[File:SSWD.jpeg|thumb|300px|right|Progression and Geographic Spread of SSWD from Hewson et. al. 2014 Figure1: Photographs of SSWD-affected stars (A) asymptomatic P. helianthoides, (B) symptomatic P. helianthoides, and (C) symptomatic P. ochraceus. Disease symptoms are consistent with loss of turgor, loss of rays, formation of lesions, and animal decomposition. (D) Map showing occurrence of SSWD based on first reported observation. (E) Transmission electron micrograph of negatively stained (uranyl acetate) viruses extracted from an affected wild E. troschelii from Vancouver . The sample contained 20–25-nm diameter nonenveloped icosohedral viral particles on a background of cellular debris (primarily ribosomal subunits) and degraded viral particles of similar morphology. (Scale bar: 100 nm.) [http://www.pnas.org/content/111/48/17278.abstract Hewson et. al. 2014]]]  
Sea stars on the California coast are periodically subject to wasting disease epidemics which leave the populations of many sea star species greatly reduced.  Sea stars, particularly serve as keystone predators in their marine ecosystems as they prey on mussels and keep the edges of mussel beds at a remarkably constant location.  This work maintains kelp forests which support many other species and aid in protecting the shore.
Sea stars on the California coast are periodically subject to wasting disease epidemics which leave the populations of many sea star species greatly reduced [http://www.int-res.com/abstracts/dao/v86/n3/p245-251/ 1].  Sea stars serve as [http://en.wikipedia.org/wiki/Keystone_species#Predators keystone predators] in their marine ecosystems as they prey on mussels and keep the edges of mussel beds at a remarkably constant location.  This work maintains kelp forests which support many other species and aid in protecting the shore [http://scholar.google.com/scholar?q=+Sea+star+disease+and+population+declines+at+the+Channel+Islands.+&btnG=&hl=en&as_sdt=0%2C5 5].
<br>Sea star wasting disease (SSWD) is rather grisly disease which causes sea stars to largely disintegrate and which can occur completely in the course of a few days to a few weeks.  The disease begins with a loss of turgor pressure, leading to a deflated appearance, proceeds to the formation of lesions on the sea star, the detachment and “walking away” of individual arms, and, finally, the disintegration and death of the organism.  
<br>Sea star wasting disease (SSWD) is rather grisly disease which causes sea stars to largely disintegrate and which can occur completely in the course of a few days to a few weeks.  The disease begins with a loss of turgor pressure, leading to a deflated appearance, proceeds to the formation of lesions on the sea star, the detachment and “walking away” of individual arms, and, finally, the disintegration and death of the organism. [http://www.eeb.ucsc.edu/pacificrockyintertidal/data-products/sea-star-wasting/ 11]
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<br>As of the summer of 2013, sea stars seem to be undergoing another particularly severe epidemic of this wasting disease.  This epidemic is notable for its remarkable spatial spread – from Alaska to Central America, with some accounts from the east coast – and for the diversity of species affected, up to twelve different species currently identified.  The ravages of this disease are seen even in remarkably protected environments such as the Monterey Bay Aquarium.  The geographic range suggests that there is indeed a pathogenic, instead of environmental, basis to this epidemic.
<br>As of the summer of 2013, sea stars seem to be undergoing another particularly severe epidemic of this wasting disease.  This epidemic is notable for its remarkable spatial spread – from Alaska to Central America, with some accounts from the east coast – and for the diversity of species affected, up to twelve different species currently identified.  The ravages of this disease are seen even in remarkably protected environments such as the Monterey Bay Aquarium.[http://www.eeb.ucsc.edu/pacificrockyintertidal/data-products/sea-star-wasting/ 11] The geographic range suggests that there is indeed a pathogenic, instead of environmental, basis to this epidemic [http://www.pnas.org/content/111/48/17278 8, 11]. 
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<br>In their paper “Sea star disease and population declines at the Channel Islands” Eckert et al outline the extent and background of one such wasting disease epidemic.  In a 1997 wasting disease epidemic, incidence of wasting disease at a site ranged from 0.8% to 59.6%” and, a year later, populations of two sea star species had declined 75% and 56%.  A few other echinoderm species were also affected.  Interestingly, wasting disease epidemics generally seem correlated with marginally warmer water (indeed, affected sea stars removed into cold water recovered in Eckert’s study and the warmer water following El Niño storms seems to have been the ultimate cause, allowing the disease to take its course) which would seem to indicate that this problem may become more frequent and severe as ocean temperatures rise.  However, the current wasting disease epidemic confounds researchers due to the current trend of somewhat cooler ocean temperatures on the West Coast.   
<br>In their paper “Sea star disease and population declines at the Channel Islands” [http://scholar.google.com/scholar?q=+Sea+star+disease+and+population+declines+at+the+Channel+Islands.+&btnG=&hl=en&as_sdt=0%2C5 Eckert et al] outline the extent and background of one such wasting disease epidemic.  In a 1997 wasting disease epidemic, incidence of wasting disease at a site ranged from 0.8% to 59.6%” and, a year later, populations of two sea star species had declined 75% and 56%.  A few other [http://en.wikipedia.org/wiki/Echinoderm echinoderm] species were also affected.  Interestingly, wasting disease epidemics generally seem correlated with marginally warmer water (indeed, affected sea stars removed into cold water recovered in Eckert’s study and the warmer water following El Niño storms seems to have been the ultimate cause, allowing the disease to take its course) which would seem to indicate that this problem may become more frequent and severe as ocean temperatures rise.  However, the current wasting disease epidemic confounds researchers due to the current trend of somewhat cooler ocean temperatures on the West Coast [http://www.eeb.ucsc.edu/pacificrockyintertidal/data-products/sea-star-wasting/ 11].   




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==Metagenomics==
==Metagenomics==
Metagenomics, discussed by Wooley et. al. in his review as the “discipline that enables the genomic study of uncultured microorganisms”, allows researchers to sequence the bulk of bacteria or other microorganisms present in an environmental sample to gain an understanding of what species are present and in what ratios. Considering the impossibility of culturing many microbial species, metagenomics provides a way to gain insight into the diversity of species present.  The review also stresses metagenomics’ ability to shed some light on communities of microorganisms and perhaps their interactions with each other or their host which is said to be more relevant to gaining an accurate picture of what is happening than looking at isolated organisms.  While powerful, metagenomics is a fairly new and extremely noisy technique, as it relies on researcher’s ability to compile many genomes from many different fragments and researchers cannot expect to find full genomes for the species present.  This is made more difficult by the relative newness of whole genome sequencing and the fact that many if not most environmental organisms do not have reference genomes.  Metagenomics relies on gene sequencing, most particularly on newer high-throughput sequencing methods such as Roche or Illumina sequencing.  The particular challenges of the volume and fragmented nature of the data provided by metagenomics has led to significant work in developing computational strategies to organize the data.
Analysis of SSWD is made possible by metagenomics, a relatively new sequencing technology.  Metagenomics, discussed by [http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1000667 Wooley et. al.] in his review as the “discipline that enables the genomic study of uncultured microorganisms”, allows researchers to sequence the bulk of bacteria or other microorganisms present in an environmental sample to gain an understanding of what species are present and in what ratios. Considering the impossibility of culturing many microbial species, metagenomics provides an unprecedented way to gain insight into the diversity of species present and promises to revolutionize both pathogen hunting and characterization of microbial communities: indeed, the review stresses metagenomics’ ability to shed some light on communities of microorganisms and perhaps their interactions with each other or their host which is said to be more relevant to gaining an accurate picture of what is happening than looking at isolated organisms.  At the same time, studies with marine microbes also highlight the challenges associated with metagenomics.  While powerful, metagenomics is a fairly new and extremely noisy technique, as it relies on researcher’s ability to compile many genomes from many different fragments and researchers cannot expect to find full genomes for all or any of the species present.  This is made more difficult by the relative newness of whole genome sequencing and the fact that many if not most environmental organisms, the vast majority of which cannot be cultured, are entirely unknown and, naturally, do not have archived reference genomes.  Metagenomics relies on gene sequencing, most particularly on newer [http://en.wikipedia.org/wiki/DNA_sequencing#Next-generation_methods high-throughput sequencing methods] such as [http://en.wikipedia.org/wiki/DNA_sequencing#Next-generation_methods Roche] or [http://en.wikipedia.org/wiki/DNA_sequencing#Illumina_.28Solexa.29_sequencing Illumina] sequencing.  The particular challenges of the volume and fragmented nature of the data provided by metagenomics has led to significant work in developing computational strategies to organize the data. [http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1000667 10]
[[File:A-Primer-on-Metagenomics-pcbi.1000667.g001.jpg|thumb|256px wide|Metagenomics Schematic: Environmental samples are filtered down to microbes which from which DNA is isolated and sequenced. [http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1000667  Wooley et. al. A Primer on Metagenomics.]]]
[[File:A-Primer-on-Metagenomics-pcbi.1000667.g001.jpg|thumb|256px wide|Metagenomics Schematic: Environmental samples are filtered down to microbes which from which DNA is isolated and sequenced. [http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1000667  Wooley et. al. A Primer on Metagenomics.]]]
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<br>There is ample precedent for using metagenomic analyses to gain insight into marine microbial communities.  Originally, many different environmental samples were analyzed from the Saragasso Sea which yielded insight into many new marine bacteria and established the effectiveness of using metagenomics approaches to understand marine organisms.  Metagenomics has been applied to try to gain insight into a disease, white plague, affecting Mussismilia braziliensis corals.  This study could serve almost as a template for approaches to working with metagenomics and marine organisms, instead of general environmental samples.  The metagenome was sequenced with Roche sequencing which generated 344,000 sequences with and average length of 414 base pairs.  This study saw significant differences in the metagenomes of healthy and sick corals with several different types of bacteria, Bacteroidetes, Cytophaga, Flavobacteria, Rickettsiales, Neisseriales, and Vibrionales, having significantly higher amounts in sick corals and concluded that coral white plague appeared to be a polymicrobial infection.  Unfortunately this study did not validate its findings which would have strengthened their postulate.  However, this study also took into account other types of organisms, eukaryotes and viruses, which were present in the corals, though they did not focus on them as a source of disease, which would be valuable in expanding the search for the pathogen beyond bacteria.  In addition to shedding light on the potential agents behind white plague, this metagenomic analysis provides an initial look into the complexity of the M. braziliensis holobiont through the analysis of levels of known eukaryotic coral symbionts and the relative differences in their amounts between sick and healthy coral.  
<br>There is intriguing precedent for using metagenomic analyses to gain insight into marine microbial communities.  Metagenomics has been applied to try to gain insight into a disease, white plague, affecting [http://www.arkive.org/mussismilia/mussismilia-braziliensis/ <i>Mussismilia braziliensis</i> corals].  This study could serve almost as a template for approaches to working with metagenomics and marine organisms, instead of general environmental samples.  The metagenome was sequenced with Roche sequencing which generated 344,000 sequences with and average length of 414 base pairs.  This study saw significant differences in the metagenomes of healthy and sick corals with several different types of bacteria, <i>[http://en.wikipedia.org/wiki/Bacteroidetes Bacteroidetes], [http://en.wikipedia.org/wiki/Cytophaga Cytophaga], [http://en.wikipedia.org/wiki/Flavobacterium Flavobacteria], [http://en.wikipedia.org/wiki/Rickettsiales Rickettsiales], [http://en.wikipedia.org/wiki/Neisseriaceae Neisseriales]</i>, and <i>[http://en.wikipedia.org/wiki/Vibrionaceae Vibrionales]</i>, having significantly higher amounts in sick corals and concluded that coral white plague appeared to be a polymicrobial infection.  Unfortunately this study did not validate its findings which would have strengthened their postulate.  However, this study also took into account other types of organisms, eukaryotes and viruses, which were present in the corals, though they did not focus on them as a source of disease, which would be valuable in expanding the search for the pathogen beyond bacteria.  In addition to shedding light on the potential agents behind white plague, this metagenomic analysis provides an initial look into the complexity of the <i>M. braziliensis</i> [http://www.thereeftank.com/blog/the-coral-holobiont/ holobiont] through the analysis of levels of known eukaryotic coral symbionts and the relative differences in their amounts between sick and healthy coral. [http://link.springer.com/article/10.1007%2Fs00248-012-0161-4 6]
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<br>Most notably, metagenomics has recently been used to identify a densovirus in sea urchins, the first virus discovered to affect echinoderms.  Researchers chose to focus on sea urchins because these organisms are important both for aquaculture and maintaining a stable ecosystem and because, while the importance of viruses in marine ecosystems is slowly becoming better known, no viruses affecting echinoderms have previously been characterized.  Sea urchin mortality is also known to be affected by other microbial agents and environmental conditions, and a severe epidemic in D. antillarum in the 1980’s followed patterns of a viral outbreak, pointing to the presence of viruses as affecting sea urchin populations.  For the metagenomic analysis, samples from three species’ gonads and digestive tract as well as environmental samples were obtained and filtered to remove cells and organisms larger than virus-sized and the absence of bacterial or eukaryotic DNA was confirmed using PCR to amplify 16S or 18S rRNA.  The remaining viral DNA was amplified and sequenced with Illumina sequencing and the data was analyzed.  Researchers found mainly phages and viruses from the Parvoviridae family and were most interested in the discovery of a densovirus, the form of parvoviridae viruses most likely to infect invertebrates, in sea urchin tissue.  Since the urchins investigated did not seem diseased, this seems to be a non-pathogenic virus though evidence of capsid production seemed to confirm that this virus was not endogenous to the host genome.  This densovirus was familiar to those affecting arthropods, which allowed researchers to develop probes for the virus and look at its presence in environmental samples which showed this densovirus to be present in sediment and the water column. Metagenomics has thus allowed researchers to identify and characterize novel marine viruses in phyla which previously had no known viruses and attest to the important role which these unknown viruses play in marine populations.   
<br>Most notably, metagenomics has recently been used to identify a densovirus in [http://en.wikipedia.org/wiki/Sea_urchin sea urchins], the first virus discovered to affect [http://en.wikipedia.org/wiki/Echinoderm echinoderms].  Researchers chose to focus on sea urchins because these organisms are important both for aquaculture and maintaining a stable ecosystem and because, while the importance of viruses in marine ecosystems is slowly becoming better known, no viruses affecting echinoderms have previously been characterized.  Sea urchin mortality is also known to be affected by other microbial agents and environmental conditions, and a severe epidemic in [http://en.wikipedia.org/wiki/Diadema_antillarum <i>D. antillarum</i>] in the 1980’s followed patterns of a viral outbreak, pointing to the presence of viruses as affecting sea urchin populations.  For the metagenomic analysis, samples from three species’ gonads and digestive tract as well as environmental samples were obtained and filtered to remove cells and organisms larger than virus-sized and the absence of bacterial or eukaryotic DNA was confirmed using [http://en.wikipedia.org/wiki/Polymerase_chain_reaction PCR] to amplify [http://en.wikipedia.org/wiki/16S_ribosomal_RNA 16S] or [http://en.wikipedia.org/wiki/16S_ribosomal_RNA 18S] rRNA.  The remaining viral DNA was amplified and sequenced with Illumina sequencing and the data was analyzed.  Researchers found mainly phages and viruses from the [http://en.wikipedia.org/wiki/Parvoviridae <i>Parvoviridae</i> family] and were most interested in the discovery of a densovirus, the form of <i>Parvoviridae</i> viruses most likely to infect invertebrates, in sea urchin tissue.  Since the urchins investigated did not seem diseased, this seems to be a non-pathogenic virus though evidence of capsid production seemed to confirm that this virus was not endogenous to the host genome.  This densovirus was familiar to those affecting arthropods, which allowed researchers to develop probes for the virus and look at its presence in environmental samples which showed this densovirus to be present in sediment and the water column. [http://vir.sgmjournals.org/content/95/Pt_3/652 7]  Metagenomics has thus allowed researchers to identify and characterize novel marine viruses in phyla which previously had no known viruses and attest to the important role which these unknown viruses play in marine populations.   
   
   
==SSaDV==
==Sea Star Associated Densovirus==
Sea star wasting disease (SSWD) has been recently analyzed by metagenomics by Hewson’s lab, the same group which investigated viruses in sea urchins, and the results point to a densovirus as the responsible pathogen.  Densoviruses belong to the sub-family Densovirinae which, in turn, belongs to the family Parvoviridae.  Densovirinae viruses are distinct in that they generally infect invertebrates either in marine or terrestrial ecosystems.  This family is undergoing continuous redefinition and division into sub-groups as new and diverse viruses which fit its parameters are characterized.  Parvoviridae genomes consist of linear single-stranded DNA and tend to be about 5kb long.  They generally end in short palindromic repeats which create hairpin turns which can serve as almost a sort of primer to permit “rolling hairpin” DNA replication.  Genomes vary, but universally code for a NS1 gene which initiates replication and serves as a helicase, nickase, and ATPase as well as genes for other structural proteins, VP genes, which form the capsid.  
Sea star wasting disease has been recently analyzed with metagenomics by [http://hewsonlab.micro.cornell.edu/home.html Hewson’s lab], the same group which investigated viruses in sea urchins, and the results point to a densovirus as the responsible pathogen [http://www.pnas.org/content/111/48/17278 8].  Densoviruses belong to the sub-family [http://en.wikipedia.org/wiki/Densovirinae <i>Densovirinae</i>] which, in turn, belongs to the family <i>Parvoviridae</i>.  Densovirinae viruses are distinct in that they generally infect invertebrates either in marine or terrestrial ecosystems.  This family is undergoing continuous redefinition and division into sub-groups as new and diverse viruses which fit its parameters are characterized [http://www.ncbi.nlm.nih.gov/pubmed/3980186 9]<i>Parvoviridae</i> genomes consist of linear single-stranded DNA and tend to be about 5kb long.  They generally end in short palindromic repeats which create hairpin turns which can serve as almost a sort of primer to permit [http://viralzone.expasy.org/all_by_species/2656.html “rolling hairpin” DNA replication].  Genomes vary, but universally code for a NS1 gene which initiates replication and serves as a helicase, nickase, and ATPase as well as genes for other structural proteins, VP genes, which form the capsid. These two types of genes are arranged near the 5' ends of both strands in an [http://en.wikipedia.org/wiki/Sense_(molecular_biology)#Ambisense ambisense] genome.  Transcription thus proceeds from both ends of the densovirus genome. [http://www.ncbi.nlm.nih.gov/pubmed/10941568 2],[http://link.springer.com/article/10.1007%2Fs00705-013-1914-1 3]  Densoviruses have an icosahedral structure, as can be seen of SSaDV in the electron micrograph in [http://www.pnas.org/content/111/48/17278 Hewson et. al.]'s figure [http://www.pnas.org/content/111/48/17278/F1.large.jpg 1E].  
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<br>Many researchers expected the pathogen to be a type of vibrio bacteria so these results were surprising.  However, the researcher’s initial analysis did not show signs of bacterial infection and virus-sized particles isolated from affected sea stars were sufficient to cause sea star wasting disease in two rounds of previously unaffected individuals, which established the pathogen as a virusThe fact that the disease had spread to sea stars in aquariums indicates that the virus is water-borne and transmission does not rely on contact between affected and unaffected individuals.
<br> Though metagenomics has been used to identify other marine viruses, the SSWD epidemic and discovery of SSaDV really showcase the increasing power of the method as original signs of SSWD began to be seen in June 2013 [http://www.eeb.ucsc.edu/pacificrockyintertidal/data-products/sea-star-wasting/ 11] and sequencing and analysis technologies have already yielded a completed genome [http://www.pnas.org/content/111/48/17278 8].  This use of metagenomics as a sort of “emergency response” technique seems to be a new development in the use of this technology and opens up intriguing possibilities for metagenomics future useAdditionally, this is first sea star virus which has been discovered and only the second echinoderm virus, setting even more of a metagenomic precedent for identifying novel marine viruses [http://www.pnas.org/content/111/48/17278 8].  
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<br>[[File:SSaDV.jpg|thumb|300px|right|SSaDV Genome. [http://www.pnas.org/content/111/48/17278.abstract Hewson et. al. 2014]]]The virus was analyzed using metagenomics to compare the viral metagenome of both sick and healthy sea stars.  This comparison showed sick sea stars to have a significantly higher level of virus particles from the parvoviridae family.  Further analysis of many samples allowed researchers to compile a nearly complete densovirus genome.  This virus has been named sea star associated densovirus (SSaDV) and is seemingly the only microbe responsible for sea star wasting disease.  This was confirmed by testing multiple species of affected sea stars all of which showed higher levels of SSaDV than any other microbe.  qPCR also confirmed that the amounts of virus present in affected sea stars increased throughout the progression of the disease and, across species, individuals with higher levels of SSaDV were more likely to show disease symptoms.  Indeed, levels of virus present proved to be the greatest indication for SSWD when compared to factors of location, species, and size.  Strikingly, one species, P. ochraceus, showed evidence of the virus both in sick and healthy individuals, indicating a difference in the ways in which different species interact with the virus.  Next, environmental samples were investigated to further examine the manner in which SSaDV spreads among individuals.  SSaDV was found in particulate matter, indicating that it can travel in the water column to infect new populations, and in other apparently unaffected echinoderm species, indicating a potential reservoir of SSaDV in the ecosystem.  Intriguingly, SSaDV has been isolated from diseased sea stars preserved from earlier wasting disease epidemics, which raises questions about why this particular outbreak is so widespread and severe.  Researchers speculate that SSaDV could be exacerbated by unidentified environmental factors, overpopulation, or changes in the virus. The definitive discovery of SSaDV is a triumph for metagenomics and an important step in understand SSWD though many questions remain.   
<br>[[File:ssadv discovery validation.png|thumb|300px|left|Validation of isolated virus as the source of the disease as the isolated virus is able to infect two rounds of previously unaffected individuals [http://www.usgs.gov/envirohealth/images/headline_images/sswd_experiment_figure1_l.png Ben Young Landis/USGS]]]Many researchers expected the pathogen to be a type of <i>Vibrio</i> bacteria so these results were surprising.  However, the researchers' initial analysis did not show signs of bacterial infection and virus-sized particles isolated from affected sea stars were sufficient to cause sea star wasting disease in two rounds of previously unaffected individuals, which established the pathogen as a virus.  The fact that the disease had spread to sea stars in aquariums indicates that the virus is water-borne and transmission does not necessarily rely on contact between affected and unaffected individuals. [http://www.pnas.org/content/111/48/17278 8]
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<br>[[File:SSaDV.jpg|thumb|300px|right|SSaDV Genome. [http://www.pnas.org/content/111/48/17278.abstract Hewson et. al. 2014]]]The virus was analyzed using metagenomics to compare the viral metagenome of both sick and healthy sea stars.  This comparison showed sick sea stars to have a significantly higher level of virus particles from the <i>Parvoviridae</i> family.  Further analysis of many samples allowed researchers to compile a nearly complete densovirus genome.  This virus has been named sea star associated densovirus (SSaDV) and is seemingly the only microbe responsible for sea star wasting disease.  This was confirmed by testing multiple species of affected sea stars all of which showed higher levels of SSaDV than any other microbe.  [http://en.wikipedia.org/wiki/Real-time_polymerase_chain_reaction qPCR] also confirmed that the amounts of virus present in affected sea stars increased throughout the progression of the disease and, across species, individuals with higher levels of SSaDV were more likely to show disease symptoms.  Indeed, levels of virus present proved to be the greatest indication for SSWD when compared to factors of location, species, and size.  Strikingly, one species, [http://en.wikipedia.org/wiki/Pisaster_ochraceus <i>P. ochraceus</i>], showed evidence of the virus both in sick and healthy individuals, indicating a difference in the ways in which different species interact with the virus.  Next, environmental samples were investigated to further examine the manner in which SSaDV spreads among individuals.  SSaDV was found in particulate matter, indicating that it can travel in the water column to infect new populations, and in other apparently unaffected echinoderm species, indicating a potential reservoir of SSaDV in the ecosystem.  Intriguingly, SSaDV has been isolated from diseased sea stars preserved from earlier wasting disease epidemics, which raises questions about why this particular outbreak is so widespread and severe.  Researchers speculate that SSaDV could be exacerbated by unidentified environmental factors, overpopulation, or changes in the virus. [http://www.pnas.org/content/111/48/17278 8] The definitive discovery of SSaDV is a triumph for metagenomics and an important step in understand SSWD though many questions remain to be answered.  
    
==Further Reading==
==Further Reading==
<br> [http://www.eeb.ucsc.edu/pacificrockyintertidal/data-products/sea-star-wasting/ Ecology and Evolutionary Biology]
<br>1.  [http://www.seastarsofthepacificnorthwest.info/index.html Sea Stars of the Pacific Northwest]-This website provides further background on sea star biology.
<br> [http://www.inquisitr.com/1617759/ssadv-world-war-ii-era-virus-is-back-millions-of-dead-sea-animals-alerady/ SSaDV – World War II-Era VIrus Is Back – Millions Of Starfish Dead]
<br>2.  [http://www.annualreviews.org/doi/full/10.1146/annurev-marine-010213-135029 C. Burge et al., Climate change influences on marine infectious diseases: implications for management and society. Annu. Rev. Mar. Sci. 6, (2014).]-Though climate change does not seem to have a direct effect on SSaDV, this is still a factor that can be explored and is relevant to considering the effects of marine pathogens.
<br>3.  [http://www.sciencedirect.com/science/article/pii/S0044848698004396 Roch, P (1999) Defense mechanisms and disease prevention in farmed marine invertebrates. Aquaculture 172, 125–145.]-This paper looks at disease and immunity in aquaculture communities and discusses methods to combat them.  It is interesting to speculate how or if such ideas could be applied to the non-aquaculture populations of sea stars affected by SSaDV. 
<br>4.  [http://www.ncbi.nlm.nih.gov/pubmed/10941569 Afanasiev, B., and Carlson, J. (2000). Densovirinae as gene transfer vehicles. Contrib. Microbiol. 4, 33–58.]-Though the densovirus causing SSaDV is definitively pathogenic, this paper discusses a very different side of densoviruses: their small size makes them effective tools for transfection.


==References==
==References==
[http://www.int-res.com/abstracts/dao/v86/n3/p245-251/ Bates, A., Hilton, B., and Harley, C. (2009). Effects of temperature, season and locality on wasting disease in the keystone predatory sea star Pisaster ochraceus. Dis. Aquat. Organ. 86, 245–251.]
<br> 1.  [http://www.int-res.com/abstracts/dao/v86/n3/p245-251/ Bates, A., Hilton, B., and Harley, C. (2009). Effects of temperature, season and locality on wasting disease in the keystone predatory sea star Pisaster ochraceus. Dis. Aquat. Organ. 86, 245–251.]
<br>[http://link.springer.com/article/10.1007%2Fs00705-013-1914-1 Cotmore, S.F., Agbandje-McKenna, M., Chiorini, J.A., Mukha, D.V., Pintel, D.J., Qiu, J., Soderlund-Venermo, M., Tattersall, P., Tijssen, P., Gatherer, D., et al. (2014). The family Parvoviridae. Arch. Virol. 159, 1239–1247.]
<br> 2.  [http://www.ncbi.nlm.nih.gov/pubmed/10941568 Bergoin, M., and Tijssen, P. (2000). Molecular biology of Densovirinae. Contrib. Microbiol. 4, 12–32.]
<br>[http://cshperspectives.cshlp.org/content/5/2/a012989 Cotmore, S.F., and Tattersall, P. (2013). Parvovirus Diversity and DNA Damage Responses. Cold Spring Harb. Perspect. Biol. 5, a012989–a012989.]
<br> 3.  [http://link.springer.com/article/10.1007%2Fs00705-013-1914-1 Cotmore, S.F., Agbandje-McKenna, M., Chiorini, J.A., Mukha, D.V., Pintel, D.J., Qiu, J., Soderlund-Venermo, M., Tattersall, P., Tijssen, P., Gatherer, D., et al. (2014). The family Parvoviridae. Arch. Virol. 159, 1239–1247.]
<br>[http://link.springer.com/article/10.1007%2Fs00248-012-0161-4 Garcia, G.D., Gregoracci, G.B., de O. Santos, E., Meirelles, P.M., Silva, G.G.Z., Edwards, R., Sawabe, T., Gotoh, K., Nakamura, S., Iida, T., et al. (2013). Metagenomic Analysis of Healthy and White Plague-Affected Mussismilia braziliensis Corals. Microb. Ecol. 65, 1076–1086.]
<br> 4.  [http://cshperspectives.cshlp.org/content/5/2/a012989 Cotmore, S.F., and Tattersall, P. (2013). Parvovirus Diversity and DNA Damage Responses. Cold Spring Harb. Perspect. Biol. 5, a012989–a012989.]
<br>[http://vir.sgmjournals.org/content/95/Pt_3/652 Gudenkauf, B.M., Eaglesham, J.B., Aragundi, W.M., and Hewson, I. (2014). Discovery of urchin-associated densoviruses (family Parvoviridae) in coastal waters of the Big Island, Hawaii. J. Gen. Virol. 95, 652–658.]
<br> 5.  [http://scholar.google.com/scholar?q=+Sea+star+disease+and+population+declines+at+the+Channel+Islands.+&btnG=&hl=en&as_sdt=0%2C5 Eckert, G.L., J.M. Engle and D.J. Kushner. 2000. Sea star disease and population declines at the Channel Islands. Proceedings of the Fifth California Islands Symposium. Minerals Management Service 99-0038: pp. 390-393.]
<br>[http://www.pnas.org/content/111/48/17278 Hewson, I., Button, J.B., Gudenkauf, B.M., Miner, B., Newton, A.L., Gaydos, J.K., Wynne, J., Groves, C.L., Hendler, G., Murray, M., et al. (2014). Densovirus associated with sea-star wasting disease and mass mortality. Proc. Natl. Acad. Sci. 111, 17278–17283.]
<br> 6.  [http://link.springer.com/article/10.1007%2Fs00248-012-0161-4 Garcia, G.D., Gregoracci, G.B., de O. Santos, E., Meirelles, P.M., Silva, G.G.Z., Edwards, R., Sawabe, T., Gotoh, K., Nakamura, S., Iida, T., et al. (2013). Metagenomic Analysis of Healthy and White Plague-Affected Mussismilia braziliensis Corals. Microb. Ecol. 65, 1076–1086.]
<br>[http://www.ncbi.nlm.nih.gov/pubmed/3980186 Siegl, G., Bates, R.C., Berns, K.I., Carter, B.J., Kelly, D.C., Kurstak, E., and Tattersall, P. (1985). Characteristics and taxonomy of Parvoviridae. Intervirology 23, 61–73.]
<br> 7.  [http://vir.sgmjournals.org/content/95/Pt_3/652 Gudenkauf, B.M., Eaglesham, J.B., Aragundi, W.M., and Hewson, I. (2014). Discovery of urchin-associated densoviruses (family Parvoviridae) in coastal waters of the Big Island, Hawaii. J. Gen. Virol. 95, 652–658.]
<br>[http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1000667 Wooley, J.C., Godzik, A., and Friedberg, I. (2010). A Primer on Metagenomics. PLoS Comput. Biol. 6, e1000667.]
<br> 8.  [http://www.pnas.org/content/111/48/17278 Hewson, I., Button, J.B., Gudenkauf, B.M., Miner, B., Newton, A.L., Gaydos, J.K., Wynne, J., Groves, C.L., Hendler, G., Murray, M., et al. (2014). Densovirus associated with sea-star wasting disease and mass mortality. Proc. Natl. Acad. Sci. 111, 17278–17283.]
<br> 9.  [http://www.ncbi.nlm.nih.gov/pubmed/3980186 Siegl, G., Bates, R.C., Berns, K.I., Carter, B.J., Kelly, D.C., Kurstak, E., and Tattersall, P. (1985). Characteristics and taxonomy of Parvoviridae. Intervirology 23, 61–73.]
<br>10.  [http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1000667 Wooley, J.C., Godzik, A., and Friedberg, I. (2010). A Primer on Metagenomics. PLoS Comput. Biol. 6, e1000667.]
<br>11.  [http://www.eeb.ucsc.edu/pacificrockyintertidal/data-products/sea-star-wasting/ Ecology and Evolutionary Biology:Pacific Rocky Intertidal Monitoring]
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Late 2013 and 2014 have shown a remarkable epidemic among many sea star species largely centered on the Pacific Coast. This epidemic is notable not only because it drastically alters marine ecosystems for which sea stars are keystone predators but also because it is a particularly pervasive and grisly disease – many populations of many species over an impressive geographical distance have been devastated and the disease causes sea stars to eventually just dissolve . New high-throughput sequencing technologies, most notably metagenomics, have begun to yield answers to the source of this epidemic. Sea star wasting disease thus provides a model for the power of new sequencing technologies as a means to identify pathogens extraordinarily rapidly and as a response to a crisis. Researchers were surprised to discover that the infectious agent was a densovirus since it had been widely speculated that the disease was bacterial and caused by Vibrio bacteria, well-established marine pathogens. 8 This discovery thus opens up a discussion about newly discovered marine viruses, our expanding ability to detect and characterize them, and their role in marine environments, either natural or used for aquaculture.

Sea Star Wasting Disease

Progression and Geographic Spread of SSWD from Hewson et. al. 2014 Figure1: Photographs of SSWD-affected stars (A) asymptomatic P. helianthoides, (B) symptomatic P. helianthoides, and (C) symptomatic P. ochraceus. Disease symptoms are consistent with loss of turgor, loss of rays, formation of lesions, and animal decomposition. (D) Map showing occurrence of SSWD based on first reported observation. (E) Transmission electron micrograph of negatively stained (uranyl acetate) viruses extracted from an affected wild E. troschelii from Vancouver . The sample contained 20–25-nm diameter nonenveloped icosohedral viral particles on a background of cellular debris (primarily ribosomal subunits) and degraded viral particles of similar morphology. (Scale bar: 100 nm.) Hewson et. al. 2014

Sea stars on the California coast are periodically subject to wasting disease epidemics which leave the populations of many sea star species greatly reduced 1. Sea stars serve as keystone predators in their marine ecosystems as they prey on mussels and keep the edges of mussel beds at a remarkably constant location. This work maintains kelp forests which support many other species and aid in protecting the shore 5.
Sea star wasting disease (SSWD) is rather grisly disease which causes sea stars to largely disintegrate and which can occur completely in the course of a few days to a few weeks. The disease begins with a loss of turgor pressure, leading to a deflated appearance, proceeds to the formation of lesions on the sea star, the detachment and “walking away” of individual arms, and, finally, the disintegration and death of the organism. 11

As of the summer of 2013, sea stars seem to be undergoing another particularly severe epidemic of this wasting disease. This epidemic is notable for its remarkable spatial spread – from Alaska to Central America, with some accounts from the east coast – and for the diversity of species affected, up to twelve different species currently identified. The ravages of this disease are seen even in remarkably protected environments such as the Monterey Bay Aquarium.11 The geographic range suggests that there is indeed a pathogenic, instead of environmental, basis to this epidemic 8, 11.

In their paper “Sea star disease and population declines at the Channel Islands” Eckert et al outline the extent and background of one such wasting disease epidemic. In a 1997 wasting disease epidemic, incidence of wasting disease at a site ranged from 0.8% to 59.6%” and, a year later, populations of two sea star species had declined 75% and 56%. A few other echinoderm species were also affected. Interestingly, wasting disease epidemics generally seem correlated with marginally warmer water (indeed, affected sea stars removed into cold water recovered in Eckert’s study and the warmer water following El Niño storms seems to have been the ultimate cause, allowing the disease to take its course) which would seem to indicate that this problem may become more frequent and severe as ocean temperatures rise. However, the current wasting disease epidemic confounds researchers due to the current trend of somewhat cooler ocean temperatures on the West Coast 11.




Metagenomics

Analysis of SSWD is made possible by metagenomics, a relatively new sequencing technology. Metagenomics, discussed by Wooley et. al. in his review as the “discipline that enables the genomic study of uncultured microorganisms”, allows researchers to sequence the bulk of bacteria or other microorganisms present in an environmental sample to gain an understanding of what species are present and in what ratios. Considering the impossibility of culturing many microbial species, metagenomics provides an unprecedented way to gain insight into the diversity of species present and promises to revolutionize both pathogen hunting and characterization of microbial communities: indeed, the review stresses metagenomics’ ability to shed some light on communities of microorganisms and perhaps their interactions with each other or their host which is said to be more relevant to gaining an accurate picture of what is happening than looking at isolated organisms. At the same time, studies with marine microbes also highlight the challenges associated with metagenomics. While powerful, metagenomics is a fairly new and extremely noisy technique, as it relies on researcher’s ability to compile many genomes from many different fragments and researchers cannot expect to find full genomes for all or any of the species present. This is made more difficult by the relative newness of whole genome sequencing and the fact that many if not most environmental organisms, the vast majority of which cannot be cultured, are entirely unknown and, naturally, do not have archived reference genomes. Metagenomics relies on gene sequencing, most particularly on newer high-throughput sequencing methods such as Roche or Illumina sequencing. The particular challenges of the volume and fragmented nature of the data provided by metagenomics has led to significant work in developing computational strategies to organize the data. 10

Metagenomics Schematic: Environmental samples are filtered down to microbes which from which DNA is isolated and sequenced. Wooley et. al. A Primer on Metagenomics.



There is intriguing precedent for using metagenomic analyses to gain insight into marine microbial communities. Metagenomics has been applied to try to gain insight into a disease, white plague, affecting Mussismilia braziliensis corals. This study could serve almost as a template for approaches to working with metagenomics and marine organisms, instead of general environmental samples. The metagenome was sequenced with Roche sequencing which generated 344,000 sequences with and average length of 414 base pairs. This study saw significant differences in the metagenomes of healthy and sick corals with several different types of bacteria, Bacteroidetes, Cytophaga, Flavobacteria, Rickettsiales, Neisseriales, and Vibrionales, having significantly higher amounts in sick corals and concluded that coral white plague appeared to be a polymicrobial infection. Unfortunately this study did not validate its findings which would have strengthened their postulate. However, this study also took into account other types of organisms, eukaryotes and viruses, which were present in the corals, though they did not focus on them as a source of disease, which would be valuable in expanding the search for the pathogen beyond bacteria. In addition to shedding light on the potential agents behind white plague, this metagenomic analysis provides an initial look into the complexity of the M. braziliensis holobiont through the analysis of levels of known eukaryotic coral symbionts and the relative differences in their amounts between sick and healthy coral. 6

Most notably, metagenomics has recently been used to identify a densovirus in sea urchins, the first virus discovered to affect echinoderms. Researchers chose to focus on sea urchins because these organisms are important both for aquaculture and maintaining a stable ecosystem and because, while the importance of viruses in marine ecosystems is slowly becoming better known, no viruses affecting echinoderms have previously been characterized. Sea urchin mortality is also known to be affected by other microbial agents and environmental conditions, and a severe epidemic in D. antillarum in the 1980’s followed patterns of a viral outbreak, pointing to the presence of viruses as affecting sea urchin populations. For the metagenomic analysis, samples from three species’ gonads and digestive tract as well as environmental samples were obtained and filtered to remove cells and organisms larger than virus-sized and the absence of bacterial or eukaryotic DNA was confirmed using PCR to amplify 16S or 18S rRNA. The remaining viral DNA was amplified and sequenced with Illumina sequencing and the data was analyzed. Researchers found mainly phages and viruses from the Parvoviridae family and were most interested in the discovery of a densovirus, the form of Parvoviridae viruses most likely to infect invertebrates, in sea urchin tissue. Since the urchins investigated did not seem diseased, this seems to be a non-pathogenic virus though evidence of capsid production seemed to confirm that this virus was not endogenous to the host genome. This densovirus was familiar to those affecting arthropods, which allowed researchers to develop probes for the virus and look at its presence in environmental samples which showed this densovirus to be present in sediment and the water column. 7 Metagenomics has thus allowed researchers to identify and characterize novel marine viruses in phyla which previously had no known viruses and attest to the important role which these unknown viruses play in marine populations.

Sea Star Associated Densovirus

Sea star wasting disease has been recently analyzed with metagenomics by Hewson’s lab, the same group which investigated viruses in sea urchins, and the results point to a densovirus as the responsible pathogen 8. Densoviruses belong to the sub-family Densovirinae which, in turn, belongs to the family Parvoviridae. Densovirinae viruses are distinct in that they generally infect invertebrates either in marine or terrestrial ecosystems. This family is undergoing continuous redefinition and division into sub-groups as new and diverse viruses which fit its parameters are characterized 9. Parvoviridae genomes consist of linear single-stranded DNA and tend to be about 5kb long. They generally end in short palindromic repeats which create hairpin turns which can serve as almost a sort of primer to permit “rolling hairpin” DNA replication. Genomes vary, but universally code for a NS1 gene which initiates replication and serves as a helicase, nickase, and ATPase as well as genes for other structural proteins, VP genes, which form the capsid. These two types of genes are arranged near the 5' ends of both strands in an ambisense genome. Transcription thus proceeds from both ends of the densovirus genome. 2,3 Densoviruses have an icosahedral structure, as can be seen of SSaDV in the electron micrograph in Hewson et. al.'s figure 1E.

Though metagenomics has been used to identify other marine viruses, the SSWD epidemic and discovery of SSaDV really showcase the increasing power of the method as original signs of SSWD began to be seen in June 2013 11 and sequencing and analysis technologies have already yielded a completed genome 8. This use of metagenomics as a sort of “emergency response” technique seems to be a new development in the use of this technology and opens up intriguing possibilities for metagenomics future use. Additionally, this is first sea star virus which has been discovered and only the second echinoderm virus, setting even more of a metagenomic precedent for identifying novel marine viruses 8.


Validation of isolated virus as the source of the disease as the isolated virus is able to infect two rounds of previously unaffected individuals Ben Young Landis/USGS

Many researchers expected the pathogen to be a type of Vibrio bacteria so these results were surprising. However, the researchers' initial analysis did not show signs of bacterial infection and virus-sized particles isolated from affected sea stars were sufficient to cause sea star wasting disease in two rounds of previously unaffected individuals, which established the pathogen as a virus. The fact that the disease had spread to sea stars in aquariums indicates that the virus is water-borne and transmission does not necessarily rely on contact between affected and unaffected individuals. 8



SSaDV Genome. Hewson et. al. 2014

The virus was analyzed using metagenomics to compare the viral metagenome of both sick and healthy sea stars. This comparison showed sick sea stars to have a significantly higher level of virus particles from the Parvoviridae family. Further analysis of many samples allowed researchers to compile a nearly complete densovirus genome. This virus has been named sea star associated densovirus (SSaDV) and is seemingly the only microbe responsible for sea star wasting disease. This was confirmed by testing multiple species of affected sea stars all of which showed higher levels of SSaDV than any other microbe. qPCR also confirmed that the amounts of virus present in affected sea stars increased throughout the progression of the disease and, across species, individuals with higher levels of SSaDV were more likely to show disease symptoms. Indeed, levels of virus present proved to be the greatest indication for SSWD when compared to factors of location, species, and size. Strikingly, one species, P. ochraceus, showed evidence of the virus both in sick and healthy individuals, indicating a difference in the ways in which different species interact with the virus. Next, environmental samples were investigated to further examine the manner in which SSaDV spreads among individuals. SSaDV was found in particulate matter, indicating that it can travel in the water column to infect new populations, and in other apparently unaffected echinoderm species, indicating a potential reservoir of SSaDV in the ecosystem. Intriguingly, SSaDV has been isolated from diseased sea stars preserved from earlier wasting disease epidemics, which raises questions about why this particular outbreak is so widespread and severe. Researchers speculate that SSaDV could be exacerbated by unidentified environmental factors, overpopulation, or changes in the virus. 8 The definitive discovery of SSaDV is a triumph for metagenomics and an important step in understand SSWD though many questions remain to be answered.

Further Reading


1. Sea Stars of the Pacific Northwest-This website provides further background on sea star biology.
2. C. Burge et al., Climate change influences on marine infectious diseases: implications for management and society. Annu. Rev. Mar. Sci. 6, (2014).-Though climate change does not seem to have a direct effect on SSaDV, this is still a factor that can be explored and is relevant to considering the effects of marine pathogens.
3. Roch, P (1999) Defense mechanisms and disease prevention in farmed marine invertebrates. Aquaculture 172, 125–145.-This paper looks at disease and immunity in aquaculture communities and discusses methods to combat them. It is interesting to speculate how or if such ideas could be applied to the non-aquaculture populations of sea stars affected by SSaDV.
4. Afanasiev, B., and Carlson, J. (2000). Densovirinae as gene transfer vehicles. Contrib. Microbiol. 4, 33–58.-Though the densovirus causing SSaDV is definitively pathogenic, this paper discusses a very different side of densoviruses: their small size makes them effective tools for transfection.

References


1. Bates, A., Hilton, B., and Harley, C. (2009). Effects of temperature, season and locality on wasting disease in the keystone predatory sea star Pisaster ochraceus. Dis. Aquat. Organ. 86, 245–251.
2. Bergoin, M., and Tijssen, P. (2000). Molecular biology of Densovirinae. Contrib. Microbiol. 4, 12–32.
3. Cotmore, S.F., Agbandje-McKenna, M., Chiorini, J.A., Mukha, D.V., Pintel, D.J., Qiu, J., Soderlund-Venermo, M., Tattersall, P., Tijssen, P., Gatherer, D., et al. (2014). The family Parvoviridae. Arch. Virol. 159, 1239–1247.
4. Cotmore, S.F., and Tattersall, P. (2013). Parvovirus Diversity and DNA Damage Responses. Cold Spring Harb. Perspect. Biol. 5, a012989–a012989.
5. Eckert, G.L., J.M. Engle and D.J. Kushner. 2000. Sea star disease and population declines at the Channel Islands. Proceedings of the Fifth California Islands Symposium. Minerals Management Service 99-0038: pp. 390-393.
6. Garcia, G.D., Gregoracci, G.B., de O. Santos, E., Meirelles, P.M., Silva, G.G.Z., Edwards, R., Sawabe, T., Gotoh, K., Nakamura, S., Iida, T., et al. (2013). Metagenomic Analysis of Healthy and White Plague-Affected Mussismilia braziliensis Corals. Microb. Ecol. 65, 1076–1086.
7. Gudenkauf, B.M., Eaglesham, J.B., Aragundi, W.M., and Hewson, I. (2014). Discovery of urchin-associated densoviruses (family Parvoviridae) in coastal waters of the Big Island, Hawaii. J. Gen. Virol. 95, 652–658.
8. Hewson, I., Button, J.B., Gudenkauf, B.M., Miner, B., Newton, A.L., Gaydos, J.K., Wynne, J., Groves, C.L., Hendler, G., Murray, M., et al. (2014). Densovirus associated with sea-star wasting disease and mass mortality. Proc. Natl. Acad. Sci. 111, 17278–17283.
9. Siegl, G., Bates, R.C., Berns, K.I., Carter, B.J., Kelly, D.C., Kurstak, E., and Tattersall, P. (1985). Characteristics and taxonomy of Parvoviridae. Intervirology 23, 61–73.
10. Wooley, J.C., Godzik, A., and Friedberg, I. (2010). A Primer on Metagenomics. PLoS Comput. Biol. 6, e1000667.
11. Ecology and Evolutionary Biology:Pacific Rocky Intertidal Monitoring

Edited by Kaitlyn Spees, a student of Nora Sullivan in BIOL168L (Microbiology) in The Keck Science Department of the Claremont Colleges Spring 2014.