Sustainable Management of Aquatic Animal Health: Advances in Immunology, Pathogenesis, and Innovative Disease Control Strategies

A special issue of Biology (ISSN 2079-7737). This special issue belongs to the section "Immunology".

Deadline for manuscript submissions: 31 December 2025 | Viewed by 446

Special Issue Editors

School of Fisheries, Aquaculture and Aquatic Sciences, Auburn University, Auburn, AL 36849, USA
Interests: fish breeding and physiology; genome editing; transgenics; applied bioinformatics and genomics; gene function and characterization; mucosal immunity
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Guest Editor
School of Marine Biology and Fisheries/Breeding and Multiplication (Sanya Institute of Breeding and Multiplication), Hainan University, Haikou 570228, China
Interests: aquatic animal immunology; genetics of disease resistance; pathogenic microbiology

Special Issue Information

Dear Colleagues,

Aquatic animal health is a critical factor influencing the sustainability and productivity of aquaculture. The increasing scale and intensification of aquaculture have led to more frequent and severe disease outbreaks caused by various pathogens, resulting in substantial economic losses and raising concerns about animal welfare. As a response, recent progress in immunology, molecular biology, and genomics has deepened our understanding of the immune systems of aquatic species and the mechanisms behind disease development. These advancements have opened up new avenues for improving disease detection, prevention, and treatment, enabling more precise and targeted approaches to aquacultural health management.

A better understanding of the innate and adaptive immune responses in aquatic animals has facilitated the identification of key immune-related genes and pathways involved in host defense against various pathogens. Studies focusing on pattern recognition receptors (PRRs), signaling cascades, and effector molecules have provided insights into how aquatic organisms recognize and respond to infections. Furthermore, transcriptomic and proteomic analyses have revealed the dynamics of immune responses under different environmental and pathogenic stresses, highlighting the complex interplay between host and pathogen.

On the technological front, molecular diagnostics have evolved rapidly, offering new tools for the early and accurate detection of pathogens. Traditional methods such as PCR and next-generation sequencing (NGS) are now complemented by CRISPR-based detection technologies, which offer faster, more sensitive, and field-deployable solutions for monitoring aquatic diseases. CRISPR/Cas systems, including CRISPR/Cas9, Cas12a, Cas13a, base editing, prime editing, CRISPRi/a, and multiplex genome editing, have demonstrated remarkable potential in detecting viral and bacterial pathogens with high precision, making them invaluable in disease surveillance and control.

Additionally, genome editing technologies, particularly CRISPR/Cas9, are being leveraged to enhance the disease resistance of farmed aquatic species. Targeted gene knockouts and insertions have shown promise in creating strains with improved immunity and better growth performance, reducing the reliance on antibiotics and other chemical treatments. Beyond improving productivity, these genetic advancements contribute to the welfare of aquatic species by minimizing disease burden and stress.

This Special Issue will provide a platform for disseminating research on these topics, aiming to promote a holistic and integrated approach to aquatic animal health. By highlighting advances in pathogen detection, immune response mechanisms, CRISPR-based innovations, next-generation sequencing, and welfare-orientated strategies, this Special Issue will foster collaboration among researchers, veterinarians, and aquaculture practitioners, ultimately contributing to sustainable aquaculture development.

Dr. Baofeng Su
Dr. Dongdong Zhang
Guest Editors

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Keywords

  • aquatic animal health
  • immunology
  • pathogenesis
  • CRISPR-based innovations
  • sustainable aquaculture

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Published Papers (2 papers)

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Research

16 pages, 9628 KiB  
Article
Bactericidal Effect and Mechanism of Polyhexamethylene Biguanide (PHMB) on Pathogenic Bacteria in Marine Aquaculture
by Lanting Wu, Chunyuan Wang, Yingeng Wang, Yongxiang Yu, Zheng Zhang, Cuiping Ma, Xiaojun Rong, Ling Chen, Meijie Liao and Yapeng Yang
Biology 2025, 14(5), 470; https://doi.org/10.3390/biology14050470 - 25 Apr 2025
Viewed by 115
Abstract
Guanidine disinfectants are cationic polymers recognized for their effective sterilization properties and their ability to prevent bacterial resistance. As a result, they are widely utilized in medical, healthcare, household, and animal husbandry settings. However, the bactericidal effects and mechanisms of guanidine in marine [...] Read more.
Guanidine disinfectants are cationic polymers recognized for their effective sterilization properties and their ability to prevent bacterial resistance. As a result, they are widely utilized in medical, healthcare, household, and animal husbandry settings. However, the bactericidal effects and mechanisms of guanidine in marine aquaculture systems remain unclear due to the polymeric nature of guanidine ions and the complexity of marine environments. The inhibitory effects and bactericidal mechanisms of polyhexamethylene biguanide (PHMB) on key pathogens and probiotics are examined in this study. It was shown that PHMB had inhibitory effects on Vibrio parahaemolyticus (VP), Photobacterium damselae subsp. damselae (PDD), Bacillus subtilis (BS), Escherichia coli (EPEC), and Staphylococcus aureus (SAU), with minimum inhibitory concentrations (MICs) ranging from 3.91 to 125.0 µg/mL, and minimum bactericidal concentrations (MBCs) from 15.63 to 250.0 µg/mL. A stronger bactericidal effect of PHMB on marine bacteria compared to EPEC and SAU was exhibited. It was shown in ion interference experiments that the addition of calcium ions reduced the bactericidal effectiveness of PHMB against VP and PDD by 87.73% and 53.35%, respectively. At a PHMB concentration of 62.50 µg/mL, minor changes in cell surface potential energy (CSPE) were exhibited by Gram-positive bacteria (SAU and BS), while more significant alterations were shown by Gram-negative pathogens. It was revealed by propidium iodide staining and scanning electron microscopy (SEM) analysis that the bacterial cell membrane was directly disrupted by PHMB. DNA and RNA release analysis further revealed that following PHMB treatment, changes in membrane permeability were exhibited by Gram-negative pathogens, with a significant increase in extracellular DNA content as PHMB concentration increased. No such effect was observed in Gram-positive bacteria. Additional evidence was provided by the findings that PHMB effectively inhibits bacterial pathogens in mariculture systems, with a significantly stronger inhibitory effect on Gram-negative pathogens than on Gram-positive bacteria. These results indicated that PHMB could serve as a new antimicrobial agent in mariculture. Full article
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15 pages, 5654 KiB  
Article
Development of a Real-Time Enzymatic Recombinase Amplification Assay (RT-ERA) and an ERA Combined with a Lateral Flow Dipstick (LFD) Assay (ERA-LFD) for Enteric Microsporidian (Enterospora epinepheli) in Grouper Fishes
by Minqi Chen, Yongcan Zhou, Shifeng Wang, Jian Luo, Weiliang Guo, Hengwei Deng, Pei Zheng, Zhihong Zhong, Baofeng Su, Dongdong Zhang and Zhi Ye
Biology 2025, 14(4), 330; https://doi.org/10.3390/biology14040330 - 25 Mar 2025
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Abstract
Enterospora epinepheli poses a severe threat to grouper aquaculture due to the absence of effective prevention and treatment strategies. To address this challenge, we developed and validated two isothermal diagnostic tools, the real-time enzymatic recombinase amplification (RT-ERA) assay and the enzymatic recombinase amplification [...] Read more.
Enterospora epinepheli poses a severe threat to grouper aquaculture due to the absence of effective prevention and treatment strategies. To address this challenge, we developed and validated two isothermal diagnostic tools, the real-time enzymatic recombinase amplification (RT-ERA) assay and the enzymatic recombinase amplification combined with a lateral flow dipstick (ERA-LFD) assay, targeting the 18S rDNA gene of the parasite. These assays operate under isothermal conditions at ≤40 °C and offer rapid detection, with RT-ERA yielding results in 14~20 min and ERA-LFD in approximately 10 min. The RT-ERA assay demonstrated a strong linear relationship between plasmid copy numbers and cycle threshold (Ct) values (y = −2.1226x + 19.562, R2 = 0.9915), enabling accurate quantification. Both methods displayed a detection limit of 2 × 100 copies/μL and no cross-reactivity with other aquaculture pathogens. Validation using grouper tissue and water samples from Hainan, China, demonstrated 100% concordance rates with basic ERA and outperformed compared to conventional PCR. These assays provide sensitive, specific, and rapid detection tools for effective monitoring and pathogen load assessment of E. epinepheli, with broad applicability to pathogen detection in aquaculture systems. Full article
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