Physiological Responses in Fishes

A special issue of Animals (ISSN 2076-2615). This special issue belongs to the section "Aquatic Animals".

Deadline for manuscript submissions: closed (28 February 2022) | Viewed by 16570

Special Issue Editors


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Guest Editor
Department of Biology, University of Crete, 70013 Heraklion, Greece
Interests: allostasis; cortisol response; fish physiology; fish endocrinology; stress physiology; welfare

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Guest Editor
Department of Research & Development, Nireus Aquaculture SA, 341 00 Chalkida, Greece
Interests: aquaculture; nutrition; finfish production; fish physiology

Special Issue Information

Dear Colleagues,

Fish are a diverse group of animals that comprise the vast majority of vertebrate species. The variability of their physiological adaptations and responses to stimuli are unique and often inadequately studied, especially in species of no or low commercial interest. On the other hand, fish are being widely used by humans in activities such as fisheries, aquaculture, and recreational fishing, as pets, and recently in science as laboratory animals. In this demanding scheme, fish show a variety of physiological responses in order to cope with the different challenges—physiological responses that are unique and in many cases species specific.

The aim of this Special Issue is to publish manuscripts that cover the physiological responses of fish. Manuscripts that address responses to environment, husbandry, and feeding (in terms of farmed and pet fish), and social challenges are invited in this Special Issue. Contributions addressing the responses of wild, farmed, and pet fish are welcome.

Dr. Athanasios Samaras
Dr. Arkadios Dimitroglou
Guest Editors

Manuscript Submission Information

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Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2400 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • addressing challenges
  • gene expression
  • farmed fish
  • fish
  • fisheries
  • feeding
  • husbandry
  • ornamental fish
  • physiology
  • responses
  • stress
  • welfare
  • wild fish

Published Papers (5 papers)

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Research

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14 pages, 1602 KiB  
Article
Biometric Indices, Physio-Metabolic Responses and Carcass Quality in Rohu (Labeo rohita) during Feed Deprivation
by Sona Yengkokpam, Narottam Prasad Sahu, Asim Kumar Pal, Dipesh Debnath, Kamal Kant Jain, Rishikesh Subhashrao Dalvi, Petr Slama, Kavindra Kumar Kesari and Shubhadeep Roychoudhury
Animals 2022, 12(6), 769; https://doi.org/10.3390/ani12060769 - 18 Mar 2022
Cited by 1 | Viewed by 1947
Abstract
Understanding changes in biometric indices and metabolism in fish exposed to feed deprivation may be useful in aquaculture. The present study elucidates the effect of feed deprivation on physio-biochemical responses, such as changes in biometric indices, nutrient mobilization patterns, and enzyme activities in [...] Read more.
Understanding changes in biometric indices and metabolism in fish exposed to feed deprivation may be useful in aquaculture. The present study elucidates the effect of feed deprivation on physio-biochemical responses, such as changes in biometric indices, nutrient mobilization patterns, and enzyme activities in rohu (Labeo rohita). Experimental fish (av. wt. 3.41 ± 0.07 g) were deprived of feed and sampled at intervals of 0, 15, 30, 45, and 60 days to measure weight, length, body composition, and the activities of enzymes involved in digestion, metabolism, and antioxidation. A decrease in body weight, condition factor (CF), hepatosomatic index (HSI), and gastrosomatic index (GSI) was observed during the initial stage of feed deprivation (15 to 30 days) but remained unchanged thereafter. The total carbohydrate and lipid content also decreased rapidly up until 30 days, then stabilized. However, the reduction in tissue protein content (% wet weight) continued gradually with the duration of feed deprivation from 12.85 ± 0.36 at 0 days to 10.04 ± 0.67 at 15 days, 8.79 ± 0.59 at 30 days, 6.95 ± 0.69 at 45 days, and 6.16 ± 0.8 at 60 days, which was lower, compared to the other two body constituents. Amylase, protease. and lipase activities significantly reduced up until 30 days, but then stabilized. Although G6PDH enzyme activity decreased, gluconeogenic (LDH, AST, and ALT) and antioxidative (SOD and catalase) enzyme activities increased during initial feed deprivation (up to 30 days). A tissue-specific difference in amino acid metabolism with a major role of ALT in liver and AST in muscle was observed. This study revealed that rohu fingerlings adapted well to feed deprivation up until 30 days, beyond which there was an overall deterioration in the metabolic functions. Full article
(This article belongs to the Special Issue Physiological Responses in Fishes)
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15 pages, 3982 KiB  
Article
Molecular Characterization and Response of Prolyl Hydroxylase Domain (PHD) Genes to Hypoxia Stress in Hypophthalmichthys molitrix
by Xiaohui Li, Meidong Zhang, Chen Ling, Hang Sha, Guiwei Zou and Hongwei Liang
Animals 2022, 12(2), 131; https://doi.org/10.3390/ani12020131 - 06 Jan 2022
Cited by 7 | Viewed by 1678
Abstract
As an economically and ecologically important freshwater fish, silver carp (Hypophthalmichthys molitrix) is sensitive to low oxygen tension. Prolyl hydroxylase domain (PHD) proteins are critical regulators of adaptive responses to hypoxia for their function of regulating the hypoxia inducible factor-1 alpha [...] Read more.
As an economically and ecologically important freshwater fish, silver carp (Hypophthalmichthys molitrix) is sensitive to low oxygen tension. Prolyl hydroxylase domain (PHD) proteins are critical regulators of adaptive responses to hypoxia for their function of regulating the hypoxia inducible factor-1 alpha subunit (HIF-1α) stability via hydroxylation reaction. In the present study, three PHD genes were cloned from H. molitrix by rapid amplification of cDNA ends (RACE). The total length of HmPHD1, HmPHD2, and HmPHD3 were 2981, 1954, and 1847 base pair (bp), and contained 1449, 1080, and 738 bp open reading frames (ORFs) that encoded 482, 359, and 245 amino acids (aa), respectively. Amino acid sequence analysis showed that HmPHD1, HmPHD2, and HmPHD3 had the conserved prolyl 4-hydroxylase alpha subunit homolog domains at their C-termini. Meanwhile, the evaluation of phylogeny revealed PHD2 and PHD3 of H. molitrix were more closely related as they belonged to sister clades, whereas the clade of PHD1 was relatively distant from these two. The transcripts of PHD genes are ubiquitously distributed in H. molitrix tissues, with the highest expressional level of HmPHD1 and HmPHD3 in liver, and HmPHD2 in muscle. After acute hypoxic treatment for 0.5 h, PHD genes of H. molitrix were induced mainly in liver and brain, and different from HmPHD1 and HmPHD2, the expression of HmPHD3 showed no overt tissue specificity. Furthermore, under continued hypoxic condition, PHD genes exhibited an obviously rapid but gradually attenuated response from 3 h to 24 h, and upon reoxygenation, the transcriptional expression of PHD genes showed a decreasing trend in most of the tissues. These results indicate that the PHD genes of H. molitrix are involved in the early response to hypoxic stress, and they show tissue-specific transcript expression when performing physiological regulation functions. This study is of great relevance for advancing our understanding of how PHD genes are regulated when addressing the hypoxic challenge and provides a reference for the subsequent research of the molecular mechanisms underlying hypoxia adaptation in silver carp. Full article
(This article belongs to the Special Issue Physiological Responses in Fishes)
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21 pages, 45972 KiB  
Article
Genetics Responses to Hypoxia and Reoxygenation Stress in Larimichthys crocea Revealed via Transcriptome Analysis and Weighted Gene Co-Expression Network
by Yibo Zhang, Jie Ding, Cheng Liu, Shengyu Luo, Xinming Gao, Yuanjie Wu, Jingqian Wang, Xuelei Wang, Xiongfei Wu, Weiliang Shen and Junquan Zhu
Animals 2021, 11(11), 3021; https://doi.org/10.3390/ani11113021 - 20 Oct 2021
Cited by 5 | Viewed by 2387
Abstract
The large yellow croaker (Larimichthys crocea) is an important marine economic fish in China; however, its intolerance to hypoxia causes widespread mortality. To understand the molecular mechanisms underlying hypoxia tolerance in L. crocea, the transcriptome gene expression profiling of three [...] Read more.
The large yellow croaker (Larimichthys crocea) is an important marine economic fish in China; however, its intolerance to hypoxia causes widespread mortality. To understand the molecular mechanisms underlying hypoxia tolerance in L. crocea, the transcriptome gene expression profiling of three different tissues (blood, gills, and liver) of L. crocea exposed to hypoxia and reoxygenation stress were performed. In parallel, the gene relationships were investigated based on weighted gene co-expression network analysis (WGCNA). Accordingly, the Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis showed that several pathways (e.g., energy metabolism, signal transduction, oxygen transport, and osmotic regulation) may be involved in the response of L. crocea to hypoxia and reoxygenation stress. In addition, also, four key modules (darkorange, magenta, saddlebrown, and darkolivegreen) that were highly relevant to the samples were identified by WGCNA. Furthermore, some hub genes within the association module, including RPS16, EDRF1, KCNK5, SNAT2, PFKL, GSK-3β, and PIK3CD, were found. This is the first study to report the co-expression patterns of a gene network after hypoxia stress in marine fish. The results provide new clues for further research on the molecular mechanisms underlying hypoxia tolerance in L. crocea. Full article
(This article belongs to the Special Issue Physiological Responses in Fishes)
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18 pages, 2206 KiB  
Article
Multi-Approach Assessment for Stress Evaluation in Rainbow Trout Females, Oncorhynchus mykiss (Walbaum, 1792) from Three Different Farms during the Summer Season
by Paul Uiuiu, Călin Lațiu, Tudor Păpuc, Cristina Craioveanu, Andrada Ihuț, Alexandru Sava, Camelia Răducu, Cosmin Șonea, Radu Constantinescu, Daniel Cocan and Vioara Mireșan
Animals 2021, 11(6), 1810; https://doi.org/10.3390/ani11061810 - 17 Jun 2021
Cited by 9 | Viewed by 2159
Abstract
Blood biochemistry parameters are valuable tools for monitoring fish health. Their baseline values are still undefined for a multitude of farmed fish species. In this study, changes in the blood profile of rainbow trout females (Oncorhynchus mykiss) from three farms were [...] Read more.
Blood biochemistry parameters are valuable tools for monitoring fish health. Their baseline values are still undefined for a multitude of farmed fish species. In this study, changes in the blood profile of rainbow trout females (Oncorhynchus mykiss) from three farms were investigated using different biomarkers during the summer season. In the given context, the main water physicochemical parameters were investigated and twelve biochemical parameters were measured from blood samples of rainbow trout reared in the Fiad, Șoimul de Jos, and Strâmba farms. We selected these farms because the genetic background of the rainbow trout is the same, with all studied specimens coming from the Fiad farm, which has an incubation station. Forty-five samples were collected monthly (May to August) throughout summer to observe the changes in the blood profile of rainbow trout. Principal component analysis showed a clear separation both among the studied farms and months. Furthermore, significant correlations (p < 0.05) between the majority of the biochemical parameters were found, indicating that the environmental parameters can influence several blood parameters at the same time. The present study provides several useful norms for assessing the welfare of rainbow trout, indicating that the relationships among different parameters are important factors in interpreting the blood biochemical profiles. Full article
(This article belongs to the Special Issue Physiological Responses in Fishes)
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Review

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19 pages, 979 KiB  
Review
Toxic Effects on Bioaccumulation, Hematological Parameters, Oxidative Stress, Immune Responses and Tissue Structure in Fish Exposed to Ammonia Nitrogen: A Review
by Zhenkun Xu, Jie Cao, Xiaoming Qin, Weiqiang Qiu, Jun Mei and Jing Xie
Animals 2021, 11(11), 3304; https://doi.org/10.3390/ani11113304 - 19 Nov 2021
Cited by 81 | Viewed by 7319
Abstract
Ammonia nitrogen is the major oxygen-consuming pollutant in aquatic environments. Exposure to ammonia nitrogen in the aquatic environment can lead to bioaccumulation in fish, and the ammonia nitrogen concentration is the main determinant of accumulation. In most aquatic environments, fish are at the [...] Read more.
Ammonia nitrogen is the major oxygen-consuming pollutant in aquatic environments. Exposure to ammonia nitrogen in the aquatic environment can lead to bioaccumulation in fish, and the ammonia nitrogen concentration is the main determinant of accumulation. In most aquatic environments, fish are at the top of the food chain and are most vulnerable to the toxic effects of high levels of ammonia nitrogen exposure. In fish exposed to toxicants, ammonia-induced toxicity is mainly caused by bioaccumulation in certain tissues. Ammonia nitrogen absorbed in the fish enters the circulatory system and affects hematological properties. Ammonia nitrogen also breaks balance in antioxidant capacity and causes oxidative damage. In addition, ammonia nitrogen affects the immune response and causes neurotoxicity because of the physical and chemical toxicity. Thence, the purpose of this review was to investigate various toxic effects of ammonia nitrogen, including oxidative stress, neurotoxicity and immune response. Full article
(This article belongs to the Special Issue Physiological Responses in Fishes)
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