<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>shrimp aquaculture &#8211; Science</title>
	<atom:link href="https://scienmag.com/tag/shrimp-aquaculture/feed/" rel="self" type="application/rss+xml" />
	<link>https://scienmag.com</link>
	<description></description>
	<lastBuildDate>Thu, 24 Sep 2026 21:03:28 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=7.1.2</generator>

<image>
	<url>https://scienmag.com/wp-content/uploads/2024/07/cropped-scienmag_ico-32x32.jpg</url>
	<title>shrimp aquaculture &#8211; Science</title>
	<link>https://scienmag.com</link>
	<width>32</width>
	<height>32</height>
</image> 
<site xmlns="com-wordpress:feed-additions:1">73899611</site>	<item>
		<title>Red Seaweeds Turn Shrimp Farm Waste Into Clean Water in Just Days</title>
		<link>https://scienmag.com/red-seaweeds-turn-shrimp-farm-waste-into-clean-water-in-just-days/</link>
		
		<dc:creator><![CDATA[Alan Morgan]]></dc:creator>
		<pubDate>Thu, 24 Sep 2026 21:03:28 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[algal remediation of shrimp farm waste]]></category>
		<category><![CDATA[bioremediation]]></category>
		<category><![CDATA[blue biotechnology wastewater treatment]]></category>
		<category><![CDATA[coastal pollution]]></category>
		<category><![CDATA[environmental impact of shrimp farming]]></category>
		<category><![CDATA[eutrophication]]></category>
		<category><![CDATA[Gracilaria corticata]]></category>
		<category><![CDATA[IMTA]]></category>
		<category><![CDATA[intertidal seaweed pollution mitigation]]></category>
		<category><![CDATA[marine algae bioremediation]]></category>
		<category><![CDATA[nutrient pollution in coastal ecosystems]]></category>
		<category><![CDATA[nutrient removal from aquaculture wastewater]]></category>
		<category><![CDATA[nutrient uptake]]></category>
		<category><![CDATA[red algae]]></category>
		<category><![CDATA[red seaweed biofiltration]]></category>
		<category><![CDATA[red seaweed species for wastewater purification]]></category>
		<category><![CDATA[Sarconema filiforme]]></category>
		<category><![CDATA[seaweed]]></category>
		<category><![CDATA[Seaweed-based wastewater treatment]]></category>
		<category><![CDATA[shrimp aquaculture]]></category>
		<category><![CDATA[shrimp farm effluent pollution]]></category>
		<category><![CDATA[sustainable aquaculture]]></category>
		<category><![CDATA[sustainable aquaculture practices]]></category>
		<category><![CDATA[wastewater treatment]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=212483</guid>

					<description><![CDATA[Five native Indian red seaweed species removed up to 100 percent of nitrate and most phosphate and ammonium from shrimp farm effluent within 96 hours, though only the hardy Gracilaria corticata survived prolonged exposure, pointing to a sequential bioremediation strategy for sustainable aquaculture.]]></description>
										<content:encoded><![CDATA[<p>Shrimp farming has become one of the world&#8217;s fastest-growing food industries, and India now ranks as the second-largest shrimp farming nation on the planet. But behind every plate of farmed shrimp lies a hidden cost: effluent water loaded with ammonium, nitrate, and phosphate that flows into coastal ecosystems, triggering algal blooms, oxygen depletion, and mass die-offs of marine life. Now, a team of researchers at CSIR-Central Salt and Marine Chemicals Research Institute in Bhavnagar, India, has shown that humble intertidal red seaweeds could be the answer, scrubbing these pollutants out of shrimp farm wastewater with remarkable efficiency, sometimes in a matter of hours.</p>
<p>The new study, published in the journal Blue Biotechnology, put five native red seaweed species to the test: Sarconema filiforme, Gracilaria corticata, Scinaia carnosa, Gracilaria dura, and Acanthophora sp. All were collected from the intertidal rocky shore at Veraval on Gujarat&#8217;s coast, while the effluent came from a shrimp farm at Mithi Virdi in Bhavnagar. The researchers cultivated the seaweeds in controlled laboratory tanks at 24 degrees Celsius with a 12:12 light-dark cycle and constant aeration, then transferred precisely weighed two-gram samples into flasks containing 400 milliliters of effluent water. Over the following days, they sampled the water at intervals ranging from fifteen minutes to 96 hours, measuring how quickly each species stripped nutrients from the polluted medium.</p>
<p>The analytical approach was rigorous. Phosphate concentrations were determined using the ascorbic acid method, with the resulting blue complex measured at 880 nanometers on a UV-Vis spectrophotometer. Nitrate was quantified through the vanadium chloride method, detected as a pink complex at 543 nanometers, while ammonium was estimated via the phenate method, which produces indophenol blue measured at 640 nanometers. Calibration curves with R-squared values above 0.99 were required for valid quantification, and all analyses were run in duplicate alongside blanks and standards to guard against contamination and instrument drift. This colorimetric toolkit allowed the team to track the disappearance of each nutrient with high precision across the entire time course.</p>
<p>The results were striking. Sarconema filiforme emerged as the overall champion, achieving the highest removal efficiencies across the board: roughly 85.77 percent of phosphate, 100 percent of nitrate, and 73.80 percent of ammonium within the experimental window. When uptake was normalized to biomass, S. filiforme again led the pack, absorbing nitrate at 1.18 micromoles per gram of wet weight per hour and ammonium at 2.16 micromoles per gram of wet weight per hour. Phosphate removal was also strong across all species, with Scinaia carnosa, Gracilaria corticata, and Gracilaria dura each removing more than 81 percent, while Acanthophora sp. trailed at about 63 percent but with high variability.</p>
<p>Nitrate proved to be the nutrient the seaweeds craved most. All five species achieved near-complete nitrate removal, and Acanthophora sp. accomplished something remarkable: complete nitrate uptake in just 48 hours, the fastest assimilation pattern recorded in the study. The overall preference followed a clear sequence of nitrate greater than phosphate greater than ammonium, a pattern the researchers attribute to red algae&#8217;s protein-rich pigments and high nitrogen quotas, which make them especially effective at assimilating nitrogen compounds. Ammonium, by contrast, was taken up more slowly, likely because high concentrations are toxic and most seaweeds preferentially use nitrate as their nitrogen source when both are available.</p>
<p>The physiological mechanisms behind this cleanup are well understood. Seaweeds absorb dissolved inorganic nutrients through a combination of passive diffusion, facilitated diffusion, and active transport via carrier proteins embedded in their cell membranes. Ammonium is the energetically cheapest nitrogen source, requiring no chemical reduction before incorporation into amino acids, while nitrate must be converted to nitrite and then ammonium inside the cell before it can be used to build proteins. Phosphate enters through dedicated transporters and fuels energy transfer via ATP, nucleic acid synthesis, and membrane formation. This dual passive-and-active uptake machinery allows seaweeds to keep functioning even when ambient nutrient concentrations are low, and to surge when nutrients are abundant, exactly the conditions found in aquaculture effluent.</p>
<p>But the study also delivered a sobering caveat: the best removers are not necessarily the best survivors. Despite its stellar uptake numbers, Sarconema filiforme showed signs of physiological stress under prolonged exposure and eventually died in the high-ammonium effluent. Acanthophora sp., the nitrate sprinter, likewise suffered high mortality after its rapid initial performance. High ammonium is known to suppress the light-saturated photosynthetic electron transport rate and maximum quantum yield in other seaweed species, inhibiting photosynthesis to the point of death, and the researchers believe a similar mechanism may have doomed their top performer. Only Gracilaria corticata remained viable after extended exposure, staying healthy even after 20 days in effluent water, by which point the water&#8217;s color had visibly faded, a sign that the seaweed had absorbed most of the dissolved nutrients.</p>
<p>This survival difference carries a crucial lesson for designing real-world treatment systems: nutrient removal efficiency alone is not enough. Longevity and tolerance under high nutrient loads matter just as much. The effluent itself was punishingly concentrated, containing 14.56 milligrams per liter of phosphate, 18.34 milligrams per liter of nitrate, 57.38 milligrams per liter of ammonium, and a salinity of 18.56 grams per liter. The authors therefore propose a sequential bioremediation strategy that deploys multiple species in stages, matching each seaweed&#8217;s uptake profile and environmental tolerance to the conditions it will face. Fast but fragile species like Acanthophora sp. could handle the initial nitrate pulse, while hardy generalists like Gracilaria corticata provide sustained, long-term polishing.</p>
<p>The broader context makes this work especially timely. The concept of Integrated Multi-Trophic Aquaculture, or IMTA, pairs fed species like shrimp with extractive species like seaweeds and filter-feeding invertebrates, so that the waste of one becomes the resource of another. Seaweeds in such systems do more than clean the water; they also yield valuable biomass that can be harvested for food, agar and carrageenan production, fertilizers, medicines, and biofuels, turning a pollution problem into a secondary crop. Gujarat&#8217;s coastline alone hosts around 285 seaweed species, and the researchers emphasize that using indigenous, locally adapted species avoids the ecological risks of introducing invasive aliens while ensuring compatibility with local temperature and salinity regimes.</p>
<p>For a coastal industry that generates both export income and employment across India, the prospect of a low-cost, nature-based solution to effluent pollution is compelling. The study demonstrates that five common intertidal red seaweeds can strip the three principal eutrophying nutrients from shrimp farm wastewater within 96 hours, with one species achieving complete nitrate removal in half that time. The challenge now is scaling from laboratory flasks to farm-scale treatment channels, where light, temperature, and nutrient loads fluctuate far more than they did under controlled conditions. If the sequential approach holds up in the field, shrimp farms of the future may grow their own cleanup crews, harvesting both protein and clean water from the same system.</p>
<p><strong>Subject of Research:</strong> Nutrient uptake efficiency of intertidal red seaweeds for bioremediation of shrimp farm effluent</p>
<p><strong>Article Title:</strong> Time-course nutrient uptake efficiency of intertidal red seaweeds in shrimp farm effluent: a sustainable bioremediation approach</p>
<p><strong>Article References:</strong> Jaiswar, S., Raval, D., Patel, P., &amp; Bhagiya, B. K. (2025). Time-course nutrient uptake efficiency of intertidal red seaweeds in shrimp farm effluent: a sustainable bioremediation approach. <em>Blue Biotechnology, 2</em>(1), Article 23. <a href="https://doi.org/10.1186/s44315-025-00044-8" rel="noopener noreferrer">https://doi.org/10.1186/s44315-025-00044-8</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1186/s44315-025-00044-8" rel="noopener noreferrer">10.1186/s44315-025-00044-8</a></p>
<p><strong>Keywords:</strong> bioremediation, seaweed, shrimp aquaculture, nutrient uptake, eutrophication, red algae, Gracilaria corticata, Sarconema filiforme, IMTA, coastal pollution, sustainable aquaculture, wastewater treatment</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">212483</post-id>	</item>
		<item>
		<title>Shrimp-Killing Vibrio Genomes Reveal Toxin and Secretion Weaponry Are Not Directly Linked</title>
		<link>https://scienmag.com/shrimp-killing-vibrio-genomes-reveal-toxin-and-secretion-weaponry-are-not-directly-linked/</link>
		
		<dc:creator><![CDATA[Juliet Wilcox]]></dc:creator>
		<pubDate>Wed, 23 Sep 2026 21:09:55 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[AHPND]]></category>
		<category><![CDATA[AHPND bacterial genomes]]></category>
		<category><![CDATA[aquaculture disease outbreaks]]></category>
		<category><![CDATA[bacterial toxin secretion mechanisms]]></category>
		<category><![CDATA[bacterial virulence]]></category>
		<category><![CDATA[bacterial virulence factors]]></category>
		<category><![CDATA[BMC Genomics]]></category>
		<category><![CDATA[genomic analysis of shrimp pathogens]]></category>
		<category><![CDATA[genomic studies in marine bacteria]]></category>
		<category><![CDATA[molecular weapons in bacterial pathogens]]></category>
		<category><![CDATA[phylogenetics]]></category>
		<category><![CDATA[pirAB]]></category>
		<category><![CDATA[PirAB toxin plasmid]]></category>
		<category><![CDATA[plasmid]]></category>
		<category><![CDATA[shrimp aquaculture]]></category>
		<category><![CDATA[shrimp disease]]></category>
		<category><![CDATA[shrimp farm bacterial infections]]></category>
		<category><![CDATA[T6SS]]></category>
		<category><![CDATA[type VI secretion system]]></category>
		<category><![CDATA[type VI secretion system in bacteria]]></category>
		<category><![CDATA[Vibrio bacteria]]></category>
		<category><![CDATA[Vibrio campbellii]]></category>
		<category><![CDATA[Vibrio parahaemolyticus]]></category>
		<category><![CDATA[whole genome sequencing]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=210317</guid>

					<description><![CDATA[A large-scale genomic analysis of Philippine shrimp farm isolates and over 800 public Vibrio genomes finds that the apparent link between the PirAB toxin plasmid and type VI secretion systems reflects shared bacterial lineage rather than a direct functional association.]]></description>
										<content:encoded><![CDATA[<p>A devastating bacterial disease that has wiped out shrimp farms across Asia and the Americas may not be as genetically straightforward as scientists once believed. Acute Hepatopancreatic Necrosis Disease, known throughout the aquaculture world simply as AHPND, has been blamed almost entirely on a single binary toxin called PirAB, carried on a plasmid of roughly 70 kilobases inside certain strains of Vibrio bacteria. But a new genomic study suggests that the story of what makes these bacteria lethal is more complicated, and that one of the most feared molecular weapons in the bacterial arsenal, the type VI secretion system, may have been unfairly implicated by a statistical illusion.</p>
<p>The research, published in BMC Genomics by Jenz C. Contante and colleagues at the Philippine Department of Agriculture&#8217;s National Fisheries Research and Development Institute, together with the Southeast Asian Fisheries Development Center, set out to test a widely repeated claim: that the type VI secretion system, or T6SS, occurs exclusively in AHPND-causing strains of Vibrio parahaemolyticus. If true, this molecular machine, which functions as a spring-loaded spear that bacteria use to kill rivals and attack host cells, could be a genuine contributor to shrimp disease. If false, its apparent association with the deadly strains might simply reflect shared ancestry rather than shared function.</p>
<p>To answer the question, the team combined freshly generated genomic data with a massive public dataset. They sequenced four new bacterial isolates recovered from Philippine shrimp farms that had experienced documented mortality outbreaks: two strains of Vibrio parahaemolyticus, designated PH1339 and PH1273, and two strains of a related species, Vibrio campbellii, designated PH1401 and PH1409. These were then analyzed alongside 807 publicly available genomes, giving the researchers a dataset large enough to distinguish genuine biological associations from coincidental patterns of inheritance.</p>
<p>The technical analysis revealed a surprisingly rich repertoire of secretion machinery. Among the newly sequenced strains, the researchers identified three distinct type VI secretion system gene clusters, which they labeled T6SS1, T6SS2, and T6SS3. T6SS1 was found in the AHPND-causing strains PH1339 and PH1401, but also, critically, in the non-AHPND strain PH1409, a finding that immediately weakened the idea that this cluster is a signature of disease-causing ability. T6SS2 was present in all four newly sequenced strains, regardless of whether they carried the toxin plasmid or caused disease. T6SS3, by contrast, appeared exclusively in Vibrio campbellii, marking it as a species-specific feature in this collection.</p>
<p>When the researchers widened their view to the full genomic dataset, a consistent pattern emerged at first glance. Every strain carrying the pirAB toxin genes also encoded both T6SS1 and T6SS2, and the pirAB-positive strains of Vibrio campbellii additionally carried T6SS3. On its face, this looked like strong evidence for a functional partnership: the toxin plasmid and the secretion systems appearing together, as if the secretion machinery were helping deliver the PirAB toxin or otherwise supporting the disease process. Earlier studies had drawn exactly this kind of conclusion from similar observations.</p>
<p>But the Philippine team applied a more rigorous statistical approach, one that accounted for the evolutionary relationships among the bacterial strains. This phylogeny-aware co-occurrence analysis changed the picture entirely. Once the researchers controlled for the fact that closely related bacteria tend to share genes simply by descent, the apparent association between pirAB and the T6SS gene clusters dissolved. There was no statistically significant link between the toxin plasmid and any of the secretion system clusters. The co-occurrence that had seemed so meaningful was, in fact, a reflection of lineage dependence: certain bacterial lineages happen to carry both features because they inherited them from common ancestors, not because the genes work together to cause disease.</p>
<p>This distinction matters enormously for how scientists understand and combat AHPND. The type VI secretion system is a conserved bacterial nanomachine found across many Gram-negative pathogens, where it serves dual roles in interbacterial competition, allowing bacteria to inject toxic effectors into rival microbes, and in host virulence, delivering effectors directly into the cells of infected organisms. In principle, such a weapon could plausibly contribute to the rapid tissue destruction that characterizes AHPND, in which the shrimp&#8217;s hepatopancreas, the organ responsible for digestion and nutrient absorption, undergoes catastrophic necrosis within hours of infection. The new findings do not rule out such a role, but they remove the genomic evidence that had been cited in its favor.</p>
<p>The study also carries practical implications for disease surveillance in aquaculture. If T6SS presence had genuinely marked AHPND-causing strains, then screening for secretion system genes could have served as a diagnostic shortcut, allowing farm managers and laboratories to identify dangerous bacteria without waiting for the slow process of isolating and challenging shrimp with each suspect strain. The new analysis shows that such a shortcut would produce false alarms, since non-pathogenic strains like PH1409 carry T6SS1, and would miss nothing useful, since the toxin plasmid itself remains the reliable genetic marker of AHPND potential. Diagnostic efforts should therefore continue to focus on pirAB detection.</p>
<p>Beyond the immediate question of diagnostics, the research provides something the field has lacked: a comprehensive genomic framework for the distribution of T6SS clusters across AHPND-associated Vibrio lineages. By cataloguing where T6SS1, T6SS2, and T6SS3 appear across more than 800 genomes, and by demonstrating which patterns survive proper evolutionary scrutiny, the study gives future investigators a solid foundation for experimental work. The authors are careful to frame their conclusions this way, noting that their findings clarify the distribution of these gene clusters and provide a basis for further investigation of their potential roles in AHPND pathogenesis, rather than closing the door on any functional involvement.</p>
<p>For an industry that has suffered severe and sustained economic losses from AHPND worldwide, the study is a reminder that genomic correlations can mislead as easily as they inform. The PirAB toxin plasmid remains the central villain in acute hepatopancreatic necrosis disease, and controlling its spread remains the priority. But the bacterial weapons that surround it, including the remarkable type VI secretion systems that these Vibrio strains carry in multiple copies, must now be evaluated on their own experimental merits rather than assumed to be accomplices. As shrimp farming expands in the face of warming waters and intensifying disease pressure, that kind of genomic rigor, separating inheritance from function, may prove as valuable as any single discovery about the pathogen itself.</p>
<p><strong>Subject of Research:</strong> Genomic distribution of type VI secretion systems and the pirAB toxin plasmid in AHPND-associated Vibrio parahaemolyticus and Vibrio campbellii</p>
<p><strong>Article Title:</strong> Distribution of the type VI secretion systems and the plasmid encoding pirAB genes in Vibrio parahaemolyticus and Vibrio campbellii</p>
<p><strong>Article References:</strong> Contante, J. C., Tabesora, R. M. D., Hinolan, M. A. V., Prieto, R. G., de la Peña, L. D., &amp; Santos, M. N. M. (2026). Distribution of the type VI secretion systems and the plasmid encoding pirAB genes in Vibrio parahaemolyticus and Vibrio campbellii. <em>BMC Genomics</em>. <a href="https://doi.org/10.1186/s12864-026-13380-9" rel="noopener noreferrer">https://doi.org/10.1186/s12864-026-13380-9</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1186/s12864-026-13380-9" rel="noopener noreferrer">10.1186/s12864-026-13380-9</a></p>
<p><strong>Keywords:</strong> AHPND, Vibrio parahaemolyticus, Vibrio campbellii, pirAB, type VI secretion system, T6SS, shrimp aquaculture, whole-genome sequencing, plasmid, bacterial virulence, phylogenetics, BMC Genomics</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">210317</post-id>	</item>
	</channel>
</rss>
