Caitlin E. Older, Bradley M. Richardson, Monica Wood, Geoffrey C. Waldbieser, Cynthia Ware, Matt J. Griffin, Brian D. Ott
In the United States, catfish are primarily farmed in earthen ponds, resulting in an aquatic environment influenced both by management practices and natural ecological processes. Profiling pond water microbiota can be useful for understanding what conditions may lead to microbial communities associated with production issues and could inform management practices. The aim of this study was to identify appropriate methods for bacterial community profiling of catfish pond water with nanopore sequencing of the 16S rRNA gene. To this end, two forward primers, two reverse primers, and three different polymerase chain reaction (PCR) cycle numbers were tested on a mock community consisting of aquaculture-relevant bacteria. The optimized protocol was applied to water samples obtained from three experimental catfish ponds sampled in May, June, August, and September 2020. Applying these methods to pond samples allowed for the identification of 1488 genera, primarily within four dominating phyla: Actinobacteriota, Bacteroidota, Cyanobacteria, and Firmicutes. High variation was observed between individual ponds and sampling timepoints; only 18 of the 1488 genera were found in relative abundances ≥1% in all ponds from at least one sampling point. Despite this variation, consistent results could be observed. Samples obtained from the month of September had the highest number of observed genera, and samples from June had the lowest. Overall, these data demonstrated individual ponds represent distinct microcosms composed of unique bacterial communities, although this pond effect was secondary to the influence of sampling month on pond community composition.
{"title":"Evaluating nanopore sequencing for microbial community characterization in catfish pond water","authors":"Caitlin E. Older, Bradley M. Richardson, Monica Wood, Geoffrey C. Waldbieser, Cynthia Ware, Matt J. Griffin, Brian D. Ott","doi":"10.1111/jwas.13002","DOIUrl":"10.1111/jwas.13002","url":null,"abstract":"<p>In the United States, catfish are primarily farmed in earthen ponds, resulting in an aquatic environment influenced both by management practices and natural ecological processes. Profiling pond water microbiota can be useful for understanding what conditions may lead to microbial communities associated with production issues and could inform management practices. The aim of this study was to identify appropriate methods for bacterial community profiling of catfish pond water with nanopore sequencing of the 16S rRNA gene. To this end, two forward primers, two reverse primers, and three different polymerase chain reaction (PCR) cycle numbers were tested on a mock community consisting of aquaculture-relevant bacteria. The optimized protocol was applied to water samples obtained from three experimental catfish ponds sampled in May, June, August, and September 2020. Applying these methods to pond samples allowed for the identification of 1488 genera, primarily within four dominating phyla: Actinobacteriota, Bacteroidota, Cyanobacteria, and Firmicutes. High variation was observed between individual ponds and sampling timepoints; only 18 of the 1488 genera were found in relative abundances ≥1% in all ponds from at least one sampling point. Despite this variation, consistent results could be observed. Samples obtained from the month of September had the highest number of observed genera, and samples from June had the lowest. Overall, these data demonstrated individual ponds represent distinct microcosms composed of unique bacterial communities, although this pond effect was secondary to the influence of sampling month on pond community composition.</p>","PeriodicalId":17284,"journal":{"name":"Journal of The World Aquaculture Society","volume":"55 1","pages":"289-301"},"PeriodicalIF":2.8,"publicationDate":"2023-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jwas.13002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43371378","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
An acute infectious disease of northern sheatfish (Silurus soldatovi) was found in a commercial aquaculture pond in Tianjin, China. Herein, two dominant bacterial strains were isolated from naturally diseased northern sheatfish and identified as Aeromonas veronii and Vibrio cholerae. Seven healthy and seven naturally diseased fish that were collected from the pond were used for the gut microbiota analysis by high-throughput 16S rRNA gene sequencing. The α-diversity indices (ACE, Chao 1, and Shannon) did not differ significantly between diseased and healthy fish (p > 0.05), but a significant separation was observed between them when β-diversity analysis of the bacterial population was performed. The diseased fish demonstrated a significant elevation in the relative abundances of Aeromonas, Vibrio, Blautia, and Megamonas and a decrease in Cetobacterium, Bacteroides, Chryseolinea, Ralstonia, and Pseudomonas compared with healthy fish (p < 0.05). Linear discriminant analysis effect size showed that microbial marker species in the diseased fish were in the order Aeromonadales, the family Aeromonadaceae, and the genus Aeromonas. The functional profiles of the microbial community that were predicted using the PICRUSt2 indicated that the disturbance of gut microbiota caused the alteration of its functional profiles in the diseased fish.
{"title":"Changes in the intestinal microbiota of farmed northern sheatfish (Silurus soldatovi) associated with natural bacterial infection","authors":"Zhongjie Zan, Qing Mao, Zhuoran Han, Jingfeng Sun","doi":"10.1111/jwas.13000","DOIUrl":"10.1111/jwas.13000","url":null,"abstract":"<p>An acute infectious disease of northern sheatfish (<i>Silurus soldatovi</i>) was found in a commercial aquaculture pond in Tianjin, China. Herein, two dominant bacterial strains were isolated from naturally diseased northern sheatfish and identified as <i>Aeromonas veronii</i> and <i>Vibrio cholerae</i>. Seven healthy and seven naturally diseased fish that were collected from the pond were used for the gut microbiota analysis by high-throughput 16S rRNA gene sequencing. The α-diversity indices (ACE, Chao 1, and Shannon) did not differ significantly between diseased and healthy fish (<i>p</i> > 0.05), but a significant separation was observed between them when β<i>-</i>diversity analysis of the bacterial population was performed. The diseased fish demonstrated a significant elevation in the relative abundances of <i>Aeromonas</i>, <i>Vibrio</i>, <i>Blautia</i>, and <i>Megamonas</i> and a decrease in <i>Cetobacterium</i>, <i>Bacteroides</i>, <i>Chryseolinea</i>, <i>Ralstonia</i>, and <i>Pseudomonas</i> compared with healthy fish (<i>p</i> < 0.05). Linear discriminant analysis effect size showed that microbial marker species in the diseased fish were in the order Aeromonadales, the family Aeromonadaceae, and the genus <i>Aeromonas</i>. The functional profiles of the microbial community that were predicted using the PICRUSt2 indicated that the disturbance of gut microbiota caused the alteration of its functional profiles in the diseased fish.</p>","PeriodicalId":17284,"journal":{"name":"Journal of The World Aquaculture Society","volume":"54 6","pages":"1575-1591"},"PeriodicalIF":2.8,"publicationDate":"2023-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jwas.13000","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44499306","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-07-01Epub Date: 2022-09-28DOI: 10.4103/ajts.ajts_38_21
Mohd Faeiz Yusop, Norlida Mohamad Tahir, Sharifah Mai Sarah Syed Azim, Ameera Ashyila Kamaruzaman, Nur Raihan Mohd Hata, Arvend Kugaan, Mohd Fairuz Osman, Tengku Norita Tengku Yazid, Suryati Mokhtar, Haniza Omar, Ahmad Suhaimi Amir
Background: Liver transplantation (LT) is a complicated surgical procedure with high risk for massive intraoperative blood loss due to pre-existing coagulopathy, portosystemic shunts with collateral circulations, and splenomegaly. The transfusion service will direct most of their resources toward LT programs with great impact on cost. The purpose of this study was to evaluate single center transfusion strategies and to identify the risk factors associated with the intraoperative blood loss and blood transfusion.
Methods: The study includes 18 patients who underwent LT at Hospital Selayang between January 2020 and December 2020. Retrospective analysis of data included preoperative assessment of coagulopathy, intraoperative blood loss, and blood component transfusion.
Results: The mean age in the study group was 36.4 ± 12.68 years. The mean intraoperative blood loss was 4450 ± 1646 ml requiring 4.17 ± 3.3 packed red blood cell (PRBC) units, 7.56 ± 5.5 platelet units, and 9.50 ± 6.0 fresh-frozen plasma units. The independent risk factor for high blood loss (HBL) group was lower preoperative platelet count and it is statistically significant (P = 0.024). The HBL group is associated with higher usage of PRBC (P = 0.024) and platelet units (P = 0.031) and it is statistically significant. The length of stay (LOS) in intensive care unit (ICU) averaging 8.6 ± 4.95 days, and there is no significant differences comparing the HBL and LBL group (P = 0.552). The mortality <90 days for all recipients was 22.2%.
Conclusion: The preoperative platelet count for is the most important factor associated with HBL in LT procedure. The usage of PRBC and platelet units was statistically higher in the HBL group. Comparing HBL and LBL patients, there is no difference in terms of the LOS in ICU postoperatively. A larger sample size would be needed in view of relatively small sample size.
{"title":"Intraoperative blood loss and blood transfusion requirement among liver transplant recipients: A national single-center experience 2020.","authors":"Mohd Faeiz Yusop, Norlida Mohamad Tahir, Sharifah Mai Sarah Syed Azim, Ameera Ashyila Kamaruzaman, Nur Raihan Mohd Hata, Arvend Kugaan, Mohd Fairuz Osman, Tengku Norita Tengku Yazid, Suryati Mokhtar, Haniza Omar, Ahmad Suhaimi Amir","doi":"10.4103/ajts.ajts_38_21","DOIUrl":"10.4103/ajts.ajts_38_21","url":null,"abstract":"<p><strong>Background: </strong>Liver transplantation (LT) is a complicated surgical procedure with high risk for massive intraoperative blood loss due to pre-existing coagulopathy, portosystemic shunts with collateral circulations, and splenomegaly. The transfusion service will direct most of their resources toward LT programs with great impact on cost. The purpose of this study was to evaluate single center transfusion strategies and to identify the risk factors associated with the intraoperative blood loss and blood transfusion.</p><p><strong>Methods: </strong>The study includes 18 patients who underwent LT at Hospital Selayang between January 2020 and December 2020. Retrospective analysis of data included preoperative assessment of coagulopathy, intraoperative blood loss, and blood component transfusion.</p><p><strong>Results: </strong>The mean age in the study group was 36.4 ± 12.68 years. The mean intraoperative blood loss was 4450 ± 1646 ml requiring 4.17 ± 3.3 packed red blood cell (PRBC) units, 7.56 ± 5.5 platelet units, and 9.50 ± 6.0 fresh-frozen plasma units. The independent risk factor for high blood loss (HBL) group was lower preoperative platelet count and it is statistically significant (<i>P</i> = 0.024). The HBL group is associated with higher usage of PRBC (<i>P</i> = 0.024) and platelet units (<i>P</i> = 0.031) and it is statistically significant. The length of stay (LOS) in intensive care unit (ICU) averaging 8.6 ± 4.95 days, and there is no significant differences comparing the HBL and LBL group (<i>P</i> = 0.552). The mortality <90 days for all recipients was 22.2%.</p><p><strong>Conclusion: </strong>The preoperative platelet count for is the most important factor associated with HBL in LT procedure. The usage of PRBC and platelet units was statistically higher in the HBL group. Comparing HBL and LBL patients, there is no difference in terms of the LOS in ICU postoperatively. A larger sample size would be needed in view of relatively small sample size.</p>","PeriodicalId":17284,"journal":{"name":"Journal of The World Aquaculture Society","volume":"35 1","pages":"251-255"},"PeriodicalIF":0.6,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10807514/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85723136","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This study was conducted to investigate the effects of dietary black cumin (Nigella sativa L.) oil on growth performance, hemato-biochemical, and histopathology of cypermethrin-intoxicated Nile tilapia. After determining the LC50 (96 h) value of cypermethrin, cypermethrin was added to the water at a ratio of 1:20 of this concentration, and the fish were fed for 42 days. To reduce the effects of cypermethrin, 1% black cumin oil was added to the fish feed as a potential protectant. Growth parameters, hematology, blood biochemistry, and histopathological changes of Nile tilapia were examined after the feeding period. In this study, the best growth was observed in the group fed with feed containing 1% black cumin oil, while the worst growth performance was observed in the group fed with water containing cypermethrin and without black cumin oil in the feed. As a result of the study, it was observed that black cumin oil added to the fish diet reduced the negative effects of water-borne cypermethrin on growth, hematology, blood biochemistry, and histopathological parameters of Nile tilapia.
{"title":"Effects of dietary black cumin (Nigella sativa L.) oil on growth performance, hemato-biochemical and histopathology of cypermethrin-intoxicated Nile tilapia (Oreochromis niloticus)","authors":"Mustafa Öz, Enes Üstüner, Ferhan Bölükbaş","doi":"10.1111/jwas.13005","DOIUrl":"10.1111/jwas.13005","url":null,"abstract":"<p>This study was conducted to investigate the effects of dietary black cumin (<i>Nigella sativa</i> L.) oil on growth performance, hemato-biochemical, and histopathology of cypermethrin-intoxicated Nile tilapia. After determining the LC<sub>50</sub> (96 h) value of cypermethrin, cypermethrin was added to the water at a ratio of 1:20 of this concentration, and the fish were fed for 42 days. To reduce the effects of cypermethrin, 1% black cumin oil was added to the fish feed as a potential protectant. Growth parameters, hematology, blood biochemistry, and histopathological changes of Nile tilapia were examined after the feeding period. In this study, the best growth was observed in the group fed with feed containing 1% black cumin oil, while the worst growth performance was observed in the group fed with water containing cypermethrin and without black cumin oil in the feed. As a result of the study, it was observed that black cumin oil added to the fish diet reduced the negative effects of water-borne cypermethrin on growth, hematology, blood biochemistry, and histopathological parameters of Nile tilapia.</p>","PeriodicalId":17284,"journal":{"name":"Journal of The World Aquaculture Society","volume":"55 1","pages":"273-288"},"PeriodicalIF":2.8,"publicationDate":"2023-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jwas.13005","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41323613","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
<p>Aquatic genetic resources (AqGR) include DNA, tissues, gametes, embryos, and other early life stages, wild and farmed individuals, and communities of organisms of actual or potential value for food and aquaculture. Monitoring the AqGR at national, regional, and global levels would not only help to improve production traits, enhance disease resistance, and ensure the long-term sustainability of aquatic species but also provide valuable information on the state of rare or endangered aquatic species. While the importance of monitoring and reporting of AqGR is becoming more and more apparent among different stakeholders, efforts to date are still insufficient (FAO, <span>2022</span>).</p><p>A common method to estimate the AqGR is genotyping, which is a process of determining the genotype at positions within the genome of an individual and comparing it to other individuals' sequences. It is often used to understand association between genotype and phenotype. Sequence variations like single-nucleotide polymorphisms (SNPs) or microsatellite loci are applied as markers in linkage and association studies to determine genes relevant to specific traits. SNPs are the most common sequence variant widely used in genome-wide association studies (GWAS). With more and more SNPs being discovered, SNP genotyping technologies have been greatly promoted and include low-throughput and high-throughput methods. Nowadays, demands of high-throughput SNP genotyping are increasing, especially for hybridization-based SNP arrays and various next-generation sequencing (NGS)-enabled genotyping methods, such as genotyping-by-sequencing (GBS).</p><p>Besides genotyping AqGR, related molecular methods have also been wildly used in pathogen diagnosis in aquaculture. For farmers, early detection of pathogens can help to prevent spread of disease and minimize economic losses due to disease outbreaks. Rapid, pond-side methods allow for quick and efficient diagnosis of diseases, which can lead to more timely and effective treatment options. Furthermore, effective disease management can help to minimize the use of antibiotics and other treatments, thus reducing the risk of antimicrobial resistance and promoting more sustainable aquaculture practices.</p><p>Both good management of AqGR and disease control are key elements of sustainable aquaculture. Here, we summarize the methods used for genotyping AqGR and detecting disease by molecular diagnosis with an emphasis on high-throughput and onsite solutions.</p><p>The common laboratory procedure for genotyping involves sample collection, DNA extraction, PCR, and subsequent detection of genetic variation. For example, tissue samples are collected from fish, usually by taking a small piece of tissue such as a fin clip. DNA is extracted from the tissue sample using standard laboratory techniques, such as phenol-chloroform extraction or commercial DNA extraction kits. Then, specific molecular markers may need to be designed for detecting any
水生遗传资源包括对食品和水产养殖具有实际或潜在价值的DNA、组织、配子、胚胎和其他早期生命阶段、野生和养殖个体以及生物群落。在国家、区域和全球各级监测水生遗传资源不仅有助于改善生产性状、增强抗病性和确保水生物种的长期可持续性,而且还可提供有关稀有或濒危水生物种状况的宝贵信息。虽然监测和报告水生遗传资源的重要性在不同利益攸关方之间变得越来越明显,但迄今为止的努力仍然不足(粮农组织,2022年)。估计AqGR的一种常用方法是基因分型,这是一个确定个体基因组中位置的基因型并将其与其他个体的序列进行比较的过程。它经常被用来理解基因型和表型之间的关系。序列变异如单核苷酸多态性(snp)或微卫星位点被用作连锁和关联研究中的标记,以确定与特定性状相关的基因。SNPs是全基因组关联研究(GWAS)中最常用的序列变异。随着越来越多的SNP被发现,SNP基因分型技术得到了极大的推广,包括低通量和高通量两种方法。目前,对高通量SNP基因分型的需求正在增加,特别是基于杂交的SNP阵列和各种支持下一代测序(NGS)的基因分型方法,如测序基因分型(GBS)。除AqGR基因分型外,相关分子方法也广泛应用于水产养殖病原体诊断。对农民来说,早期发现病原体有助于防止疾病传播,并最大限度地减少疾病爆发造成的经济损失。快速的池边方法允许快速和有效地诊断疾病,这可以导致更及时和有效的治疗方案。此外,有效的疾病管理有助于最大限度地减少抗生素和其他治疗方法的使用,从而减少抗微生物药物耐药性的风险,促进更可持续的水产养殖做法。良好的水生遗传资源管理和疾病控制都是可持续水产养殖的关键要素。本文综述了AqGR基因分型和分子诊断检测疾病的方法,重点介绍了高通量和现场解决方案。基因分型的常见实验室程序包括样本收集、DNA提取、PCR和随后的遗传变异检测。例如,从鱼身上收集组织样本,通常是取一小块组织,比如鱼鳍夹。使用标准实验室技术从组织样本中提取DNA,如苯酚-氯仿提取或商业DNA提取试剂盒。然后,可能需要设计特定的分子标记来检测任何遗传变异;一个例子是线粒体细胞色素氧化酶亚基1 (COI)基因。微卫星标记可用于基因分型,但SNP标记现在更常用于基因分型,因为可以从基因组SNP数据中提取更多的位点和更多的信息。SNP基因分型可以使用多种方法进行,如限制性片段长度多态性(RFLP)、单链构象多态性(SSCP)或测序。RFLP和SSCP基于SNP变异导致的DNA片段的大小和/或形状差异,而测序提供了核苷酸序列的直接信息。与高通量基因分型相比,传统方法通常效率较低,耗时较长,并且可能需要大量的起始材料。传统的基因分型方法也可能有较高的错误率,对低频变异不太敏感。此外,传统方法可能无法像高通量方法那样同时对许多位点进行基因分型,这限制了它们在某些应用中的实用性,例如全基因组关联研究。随着下一代测序(NGS)技术的快速发展,许多高通量基因分型方法被开发出来,主要分为SNP阵列和测序(GBS)方法的基因分型(Scheben et al., 2017)。后者有各种相关方法,如全基因组重测序(WGR)和减少代表性测序(RRS),包括序列捕获、限制性位点相关DNA测序(RAD-seq)、千位基因分型测序(GT-seq)等。控制水生疾病的最佳方法是预防,但发现问题和及时治疗同样重要。一种快速的池边病原体检测方法对水产养殖业的疾病控制至关重要。
{"title":"High-throughput genotyping in estimating genetic resources and detecting pathogens in aquaculture","authors":"Chenhong Li, Junlong Jiang","doi":"10.1111/jwas.12996","DOIUrl":"10.1111/jwas.12996","url":null,"abstract":"<p>Aquatic genetic resources (AqGR) include DNA, tissues, gametes, embryos, and other early life stages, wild and farmed individuals, and communities of organisms of actual or potential value for food and aquaculture. Monitoring the AqGR at national, regional, and global levels would not only help to improve production traits, enhance disease resistance, and ensure the long-term sustainability of aquatic species but also provide valuable information on the state of rare or endangered aquatic species. While the importance of monitoring and reporting of AqGR is becoming more and more apparent among different stakeholders, efforts to date are still insufficient (FAO, <span>2022</span>).</p><p>A common method to estimate the AqGR is genotyping, which is a process of determining the genotype at positions within the genome of an individual and comparing it to other individuals' sequences. It is often used to understand association between genotype and phenotype. Sequence variations like single-nucleotide polymorphisms (SNPs) or microsatellite loci are applied as markers in linkage and association studies to determine genes relevant to specific traits. SNPs are the most common sequence variant widely used in genome-wide association studies (GWAS). With more and more SNPs being discovered, SNP genotyping technologies have been greatly promoted and include low-throughput and high-throughput methods. Nowadays, demands of high-throughput SNP genotyping are increasing, especially for hybridization-based SNP arrays and various next-generation sequencing (NGS)-enabled genotyping methods, such as genotyping-by-sequencing (GBS).</p><p>Besides genotyping AqGR, related molecular methods have also been wildly used in pathogen diagnosis in aquaculture. For farmers, early detection of pathogens can help to prevent spread of disease and minimize economic losses due to disease outbreaks. Rapid, pond-side methods allow for quick and efficient diagnosis of diseases, which can lead to more timely and effective treatment options. Furthermore, effective disease management can help to minimize the use of antibiotics and other treatments, thus reducing the risk of antimicrobial resistance and promoting more sustainable aquaculture practices.</p><p>Both good management of AqGR and disease control are key elements of sustainable aquaculture. Here, we summarize the methods used for genotyping AqGR and detecting disease by molecular diagnosis with an emphasis on high-throughput and onsite solutions.</p><p>The common laboratory procedure for genotyping involves sample collection, DNA extraction, PCR, and subsequent detection of genetic variation. For example, tissue samples are collected from fish, usually by taking a small piece of tissue such as a fin clip. DNA is extracted from the tissue sample using standard laboratory techniques, such as phenol-chloroform extraction or commercial DNA extraction kits. Then, specific molecular markers may need to be designed for detecting any ","PeriodicalId":17284,"journal":{"name":"Journal of The World Aquaculture Society","volume":"54 3","pages":"558-565"},"PeriodicalIF":2.8,"publicationDate":"2023-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jwas.12996","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46302178","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Cheng-Han Chuang, Uei-Chen Chiu, Chang-Wen Huang, Kuan Y. Chang
Maintaining proper green water is important for a fish farming pond. However, it remains unclear how to translate this important rule into specific water quality characteristics to associate or even forecast changes in water color. To address this issue, we conducted a study based on daily monitoring of six grouper ponds in Fangliao Township, Pingtung, Taiwan, from March to December 2018. We investigated the relationships between changes in water color and anomalies in water temperature, salinity, and pH, as these three parameters had the most complete records. We employed a long-short-term memory model to detect water quality anomalies by computing residual values. Our findings indicate that changes in water color were associated with anomalies in these parameters, with water temperature anomalies being the best indicator for early detection. In fact, the top 5% of water temperature anomalies could predict over 40% of the water color changes. Additionally, pH anomalies occurred immediately after the color changes. This rule-to-physicochemical-parameter paradigm that we developed for grouper ponds could be applied to other aquaculture farms. We anticipate that with the help of advanced environmental surveillance models, such as the one we used, the prospect of autonomous fish farming will be realized.
{"title":"Associations of anomalous water temperature, salinity, and pH with change in water color of fish farming ponds","authors":"Cheng-Han Chuang, Uei-Chen Chiu, Chang-Wen Huang, Kuan Y. Chang","doi":"10.1111/jwas.12991","DOIUrl":"10.1111/jwas.12991","url":null,"abstract":"<p>Maintaining proper green water is important for a fish farming pond. However, it remains unclear how to translate this important rule into specific water quality characteristics to associate or even forecast changes in water color. To address this issue, we conducted a study based on daily monitoring of six grouper ponds in Fangliao Township, Pingtung, Taiwan, from March to December 2018. We investigated the relationships between changes in water color and anomalies in water temperature, salinity, and pH, as these three parameters had the most complete records. We employed a long-short-term memory model to detect water quality anomalies by computing residual values. Our findings indicate that changes in water color were associated with anomalies in these parameters, with water temperature anomalies being the best indicator for early detection. In fact, the top 5% of water temperature anomalies could predict over 40% of the water color changes. Additionally, pH anomalies occurred immediately after the color changes. This rule-to-physicochemical-parameter paradigm that we developed for grouper ponds could be applied to other aquaculture farms. We anticipate that with the help of advanced environmental surveillance models, such as the one we used, the prospect of autonomous fish farming will be realized.</p>","PeriodicalId":17284,"journal":{"name":"Journal of The World Aquaculture Society","volume":"54 6","pages":"1563-1574"},"PeriodicalIF":2.8,"publicationDate":"2023-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jwas.12991","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43567396","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Peikui Yang, Yuzhong Zheng, Xianghui Zou, Yanjie Sun, Yaqun Liu
In recent years, bullfrog (Lithobates catesbeianus) has become one of the most commercially important amphibians for aquaculture in China, and its annual production has grown rapidly. However, bacterial diseases caused by Citrobacter freundii infection have resulted in enormous economic losses. The present study used RNA sequencing technology to analyze the transcriptomic profile and differentially expressed genes (DEGs) in the bullfrog liver and spleen post C. freundii infection. De novo assembly resulted in the generation of 77,556 L. catesbeianus transcripts, and 49,421 of these genes were successfully annotated to the databases. Overall, 1487 DEGs were identified in the liver group, including 788 upregulated and 709 downregulated DEGs. A total of 799 DEGs, including 311 upregulated and 488 downregulated genes, were detected in the spleen groups. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses revealed significantly enriched pathways, including pathways involved in metabolism and immune responses. The processes in which the DEGs were enriched were those related to metabolic activities, including the lipid metabolism pathway, amino acid pathway, immune-related pathway, and inflammatory responses. The results of this study provide insight into the response of bullfrogs against C. freundii at the transcriptome level and reveal the mechanism of the immune response against C. freundii.
{"title":"Comparative transcriptomic analysis of gene expression profiles in the liver and spleen of American bullfrog (Lithobates catesbeianus) in response to Citrobacter freundii infection","authors":"Peikui Yang, Yuzhong Zheng, Xianghui Zou, Yanjie Sun, Yaqun Liu","doi":"10.1111/jwas.12999","DOIUrl":"10.1111/jwas.12999","url":null,"abstract":"<p>In recent years, bullfrog (<i>Lithobates catesbeianus</i>) has become one of the most commercially important amphibians for aquaculture in China, and its annual production has grown rapidly. However, bacterial diseases caused by <i>Citrobacter freundii</i> infection have resulted in enormous economic losses. The present study used RNA sequencing technology to analyze the transcriptomic profile and differentially expressed genes (DEGs) in the bullfrog liver and spleen post <i>C. freundii</i> infection. De novo assembly resulted in the generation of 77,556 <i>L. catesbeianus</i> transcripts, and 49,421 of these genes were successfully annotated to the databases. Overall, 1487 DEGs were identified in the liver group, including 788 upregulated and 709 downregulated DEGs. A total of 799 DEGs, including 311 upregulated and 488 downregulated genes, were detected in the spleen groups. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses revealed significantly enriched pathways, including pathways involved in metabolism and immune responses. The processes in which the DEGs were enriched were those related to metabolic activities, including the lipid metabolism pathway, amino acid pathway, immune-related pathway, and inflammatory responses. The results of this study provide insight into the response of bullfrogs against <i>C. freundii</i> at the transcriptome level and reveal the mechanism of the immune response against <i>C. freundii</i>.</p>","PeriodicalId":17284,"journal":{"name":"Journal of The World Aquaculture Society","volume":"55 1","pages":"353-372"},"PeriodicalIF":2.8,"publicationDate":"2023-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jwas.12999","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47979591","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The experiment was conducted to study the effect of different dietary supplementation of alanyl-glutamine dipeptide (AGD) and/or vitamin E (VE) on the growth performance, antioxidant indexes, and the expression of glutathione peroxidase (GPx) and peroxisome proliferator-activated receptor α (PPARⱭ) genes in juvenile marine medaka (Oryzias melastigma) in seawater acidification. Seven groups of juvenile marine medaka in triplicate were studied in an ecosystem. One of them was in normal seawater (pH 8.1, pH control), and the others were in seawater acidification (pH 7.7) regulated by carbon dioxide (CO2). The juveniles were separately fed for 10 weeks using one of six different diets. The six diets were one control diet (basic feed) without supplements and the other diets with different amounts of additional AGD and/or VE. The juveniles were sampled randomly for analysis of a whole fish in week 0 and week 10. The results showed that different dietary supplementation of AGD and/or VE could considerably promote the growth performance, antioxidant indexes, and the expression of GPx and PPARα genes of juvenile marine medaka in seawater acidification. The optimal diet was D4, with additional AGD 5 g and VE 50 IU per kg of dried feed.
{"title":"Growth performance, antioxidant indexes, and the expression of genes were considerably promoted by dietary supplementation of alanyl-glutamine and vitamin E in juvenile marine medaka in seawater acidification by carbon dioxide","authors":"Weifeng Li, Youqing Xu, Fujuan Liu, Qian Zhang, Ni Tang, Yimin Zheng, Zhaokun Ding","doi":"10.1111/jwas.12997","DOIUrl":"10.1111/jwas.12997","url":null,"abstract":"<p>The experiment was conducted to study the effect of different dietary supplementation of alanyl-glutamine dipeptide (AGD) and/or vitamin E (VE) on the growth performance, antioxidant indexes, and the expression of glutathione peroxidase (GPx) and peroxisome proliferator-activated receptor α (PPAR<sub>Ɑ</sub>) genes in juvenile marine medaka (<i>Oryzias melastigma</i>) in seawater acidification. Seven groups of juvenile marine medaka in triplicate were studied in an ecosystem. One of them was in normal seawater (pH 8.1, pH control), and the others were in seawater acidification (pH 7.7) regulated by carbon dioxide (CO<sub>2</sub>). The juveniles were separately fed for 10 weeks using one of six different diets. The six diets were one control diet (basic feed) without supplements and the other diets with different amounts of additional AGD and/or VE. The juveniles were sampled randomly for analysis of a whole fish in week 0 and week 10. The results showed that different dietary supplementation of AGD and/or VE could considerably promote the growth performance, antioxidant indexes, and the expression of GPx and PPARα genes of juvenile marine medaka in seawater acidification. The optimal diet was D4, with additional AGD 5 g and VE 50 IU per kg of dried feed.</p>","PeriodicalId":17284,"journal":{"name":"Journal of The World Aquaculture Society","volume":"54 6","pages":"1592-1606"},"PeriodicalIF":2.8,"publicationDate":"2023-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jwas.12997","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42741248","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This study investigated the effect of replacing a portion of fish meal with unfermented and/or fermented soybean meal in juvenile coho salmon (Oncorhynchus kisutch). Four groups of juveniles (initial weight 110.31 ± 3.12 g) in triplicate were fed for 90 days on four different iso-nitrogen and iso-lipid diets. The G0 diet comprised 28% fish meal protein (control group). In the other three diets (G1, G2, and G3), 10% of the fish meal protein was replaced with unfermented and/or fermented soybean meal protein. The main results were: Compared with G0, the WGR, SGR, CF; the contents of GLU, TP, ALB, T-CHO, and T-AOC, the activities of AKP, CAT, SOD, GST, GSH-PX, O2·-CR, OH·-CR, and GSH and the expressions of SOD, GSH-PX, GST, CAT, and Nrf2 genes of juvenile coho salmon in G3 were significantly (p < 0.05) increased, However, the FCR, HSI, the content of MDA, and the expressions of TNF-α and IL-6 genes of juvenile coho salmon in G3 were significantly (p < 0.05) decreased. There was no significant effect (p > 0.05) of diet on their survival rate (SR). In conclusion, the fermented soybean meal in the juvenile coho salmon diet can replace 10% of the fish meal protein.
{"title":"Effect of replacing a portion of fish meal with unfermented and/or fermented soybean meal on the growth performance, antioxidant and immunity capacity and related gene expression in juvenile Coho Salmon, Oncorhynchus kisutch","authors":"Qin Zhang, Jiajing Wang, Qiuyue Yang, Lixiao Xu, Jian Xu, Yongqiang Liu, Tong Tong","doi":"10.1111/jwas.12998","DOIUrl":"10.1111/jwas.12998","url":null,"abstract":"<p>This study investigated the effect of replacing a portion of fish meal with unfermented and/or fermented soybean meal in juvenile coho salmon (<i>Oncorhynchus kisutch</i>). Four groups of juveniles (initial weight 110.31 ± 3.12 g) in triplicate were fed for 90 days on four different iso-nitrogen and iso-lipid diets. The G0 diet comprised 28% fish meal protein (control group). In the other three diets (G1, G2, and G3), 10% of the fish meal protein was replaced with unfermented and/or fermented soybean meal protein. The main results were: Compared with G0, the WGR, SGR, CF; the contents of GLU, TP, ALB, T-CHO, and T-AOC, the activities of AKP, CAT, SOD, GST, GSH-PX, O<sub>2</sub>·-CR, OH·-CR, and GSH and the expressions of SOD, GSH-PX, GST, CAT, and Nrf2 genes of juvenile coho salmon in G3 were significantly (<i>p <</i> 0.05) increased, However, the FCR, HSI, the content of MDA, and the expressions of TNF-α and IL-6 genes of juvenile coho salmon in G3 were significantly (<i>p <</i> 0.05) decreased. There was no significant effect (<i>p</i> > 0.05) of diet on their survival rate (SR). In conclusion, the fermented soybean meal in the juvenile coho salmon diet can replace 10% of the fish meal protein.</p>","PeriodicalId":17284,"journal":{"name":"Journal of The World Aquaculture Society","volume":"55 1","pages":"223-239"},"PeriodicalIF":2.8,"publicationDate":"2023-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jwas.12998","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136066078","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Imtiaz Ahmed, Younis Mohd Khan, Anzar Lateef, Kousar Jan, Aamir Majeed, Manzoor A. Shah
A 12-week growth experiment was conducted to evaluate the suitability of Azolla cristata as a fish meal (FM) substitute in diets for Cyprinus carpio var. communis fingerlings. Six iso-nitrogenous and isocaloric (16.17 kJ/g GE) diets were formulated to contain 42% crude protein and each treatment had three replicates. The mean initial weight of the fish was 3.4 ± 0.2 g. Graded levels of A. cristata 0, 10, 20, 30, 40, and 50% in the diets were fed to the fish in triplicate groups, respectively. No significant (p > 0.05) differences in growth performance of fish-fed diets containing 10% and control (0%) inclusion levels were seen. However, further increase in Azolla meal (AM) supplementation resulted in gradual decline in growth performance of fish in terms of live weight gain, specific growth rate, feed conversion ratio, and protein efficiency ratio. All hematological parameters had a linear declining trend as the proportion of AM in diet was increased. Protein content of fish was found significantly (p < 0.05) reduced in fish-fed higher inclusion of AM. Serum biochemical parameters were also noted to reduce with increasing inclusion of AM, except for glucose, cholesterol, alanine aminotransferase (ALT), and aspartate aminotransferase (AST). On the basis of results obtained in the present study, it is recommended that 10% Azolla meal can be included in the practical diets for C. carpio var. communis fingerlings as partial replacement for fishmeal without affecting their growth, feed efficiency, and fish quality for the intensive culture of this fish species.
{"title":"Effect of fish meal replacement by Azolla meal on growth performance, hemato-biochemical and serum parameters in the diet of scale carp, Cyprinus carpio var. communis","authors":"Imtiaz Ahmed, Younis Mohd Khan, Anzar Lateef, Kousar Jan, Aamir Majeed, Manzoor A. Shah","doi":"10.1111/jwas.12995","DOIUrl":"10.1111/jwas.12995","url":null,"abstract":"<p>A 12-week growth experiment was conducted to evaluate the suitability of <i>Azolla cristata</i> as a fish meal (FM) substitute in diets for <i>Cyprinus carpio</i> var<i>. communis</i> fingerlings. Six iso-nitrogenous and isocaloric (16.17 kJ/g GE) diets were formulated to contain 42% crude protein and each treatment had three replicates. The mean initial weight of the fish was 3.4 ± 0.2 g. Graded levels of <i>A</i>. <i>cristata</i> 0, 10, 20, 30, 40, and 50% in the diets were fed to the fish in triplicate groups, respectively. No significant (<i>p</i> > 0.05) differences in growth performance of fish-fed diets containing 10% and control (0%) inclusion levels were seen. However, further increase in <i>Azolla</i> meal (AM) supplementation resulted in gradual decline in growth performance of fish in terms of live weight gain, specific growth rate, feed conversion ratio, and protein efficiency ratio. All hematological parameters had a linear declining trend as the proportion of AM in diet was increased. Protein content of fish was found significantly (<i>p</i> < 0.05) reduced in fish-fed higher inclusion of AM. Serum biochemical parameters were also noted to reduce with increasing inclusion of AM, except for glucose, cholesterol, alanine aminotransferase (ALT), and aspartate aminotransferase (AST). On the basis of results obtained in the present study, it is recommended that 10% <i>Azolla</i> meal can be included in the practical diets for <i>C. carpio</i> var. <i>communis</i> fingerlings as partial replacement for fishmeal without affecting their growth, feed efficiency, and fish quality for the intensive culture of this fish species.</p>","PeriodicalId":17284,"journal":{"name":"Journal of The World Aquaculture Society","volume":"54 5","pages":"1301-1316"},"PeriodicalIF":2.8,"publicationDate":"2023-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jwas.12995","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49632568","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}