Genome-based characterization of AHPND and non-AHPND Vibrio campbellii isolates from Republic of Korea

With mounting evidence that <i>Vibrio campbellii</i> can act as a causative agent, acute hepatopancreatic necrosis disease (AHPND) represents a serious threat to global shrimp aquaculture. In this study, we present a comparative genomic analysis of 101 <i>V. campbellii</i> strains, including the recently isolated pathogenic and non-pathogenic strains, <i>V. campbellii</i> HJ-2023 and <i>V. campbellii</i> HJ-2023n, from the Republic of Korea. Whole-genome sequencing revealed that the pathogenic strain harbors three plasmids and carries the canonical AHPND toxin genes <i>pirA</i> and <i>pirB</i>, along with an expanded repertoire of virulence and secretion system genes. Pan-genome and insertion sequence analyses showed that pathogenic strains tend to cluster based on shared mobile genetic elements, particularly transposases located near toxin genes, underscoring the role of horizontal gene transfer in virulence acquisition. Although all strains displayed a broad distribution of antibiotic-resistance genes, pathogenicity did not consistently correlate with their presence. Similarly, carbohydrate-active enzyme (CAZyme) profiles were largely conserved, although certain enzymes, such as chitinases, may contribute accessory functions in host invasion. Notably, the AHPND-associated <i>V. campbellii</i> HJ-2023 strain contained multiple copies of key <i>T6SS</i> and <i>T1SS</i> genes, suggesting an increased potential for toxin delivery. These findings suggest that pathogenic potential in <i>V. campbellii</i> likely arises not only from the presence of toxins but also from the complex interplay of mobile elements, secretion systems, and genomic architecture. This study provides an essential genomic framework for understanding the emergence of AHPND in <i>V. campbellii</i> and offers insights to enhance molecular diagnostics, strengthen biosecurity, and improve disease control strategies in shrimp aquaculture.

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Journal
Frontiers in Microbiology
Published
2026-01-26
DOI
https://doi.org/10.3389/fmicb.2026.1724818
Primary Topic
Invertebrate Immune Response Mechanisms
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article
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article

Genome-based characterization of AHPND and non-AHPND Vibrio campbellii isolates from Republic of Korea

Jun Soung Kwak, Yue Jai KANG, Jaeyoung Choi, Seonhyun Lee et al.
Frontiers in Microbiology
Invertebrate Immune Response Mechanisms
article

Genome-based characterization of AHPND and non-AHPND Vibrio campbellii isolates from Republic of Korea

Jun Soung Kwak, Yue Jai KANG, Jaeyoung Choi, Seonhyun Lee, So-Young Lee, Hee-Jae Choi, Sung-Chul Hong
article en

Abstract

With mounting evidence that <i>Vibrio campbellii</i> can act as a causative agent, acute hepatopancreatic necrosis disease (AHPND) represents a serious threat to global shrimp aquaculture. In this study, we present a comparative genomic analysis of 101 <i>V. campbellii</i> strains, including the recently isolated pathogenic and non-pathogenic strains, <i>V. campbellii</i> HJ-2023 and <i>V. campbellii</i> HJ-2023n, from the Republic of Korea. Whole-genome sequencing revealed that the pathogenic strain harbors three plasmids and carries the canonical AHPND toxin genes <i>pirA</i> and <i>pirB</i>, along with an expanded repertoire of virulence and secretion system genes. Pan-genome and insertion sequence analyses showed that pathogenic strains tend to cluster based on shared mobile genetic elements, particularly transposases located near toxin genes, underscoring the role of horizontal gene transfer in virulence acquisition. Although all strains displayed a broad distribution of antibiotic-resistance genes, pathogenicity did not consistently correlate with their presence. Similarly, carbohydrate-active enzyme (CAZyme) profiles were largely conserved, although certain enzymes, such as chitinases, may contribute accessory functions in host invasion. Notably, the AHPND-associated <i>V. campbellii</i> HJ-2023 strain contained multiple copies of key <i>T6SS</i> and <i>T1SS</i> genes, suggesting an increased potential for toxin delivery. These findings suggest that pathogenic potential in <i>V. campbellii</i> likely arises not only from the presence of toxins but also from the complex interplay of mobile elements, secretion systems, and genomic architecture. This study provides an essential genomic framework for understanding the emergence of AHPND in <i>V. campbellii</i> and offers insights to enhance molecular diagnostics, strengthen biosecurity, and improve disease control strategies in shrimp aquaculture.

Frontiers in MicrobiologyVol. 17
Kunsan National University (KR), Kongju National University (KR), Kyung Hee University (KR), National Pension Service (KR), National Fisheries University (JP)
National Research Foundation, National Research Foundation of Korea, Ministry of Science and ICT, South Korea
Life below water
Openalex Percentile: Top 77%
Invertebrate Immune Response Mechanisms
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