Identification of genes associated with resistance trait to VPAHPND in Pacific white shrimp (Litopenaeus vannamei) using Bulk Segregation Analysis (BSA)

Vibrio parahaemolyticus harboring the PirA/PirB toxin (VPAHPND) is regarded as one of the main pathogens that caused Acute hepatopancreatic necrosis disease (AHPND) in the Pacific white shrimp Litopenaeus vannamei (L. vannamei). Breeding new varieties resistant to VPAHPND is considered to be the mos...

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Main Authors: Zhenning Bao, Yang Yu, Pengfei Lin, Fuhua Li
Format: Article
Language:English
Published: Elsevier 2025-09-01
Series:Aquaculture Reports
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Online Access:http://www.sciencedirect.com/science/article/pii/S2352513425002881
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author Zhenning Bao
Yang Yu
Pengfei Lin
Fuhua Li
author_facet Zhenning Bao
Yang Yu
Pengfei Lin
Fuhua Li
author_sort Zhenning Bao
collection DOAJ
description Vibrio parahaemolyticus harboring the PirA/PirB toxin (VPAHPND) is regarded as one of the main pathogens that caused Acute hepatopancreatic necrosis disease (AHPND) in the Pacific white shrimp Litopenaeus vannamei (L. vannamei). Breeding new varieties resistant to VPAHPND is considered to be the most effective way to reduce the economic losses in shrimp aquaculture. Identification of genes and SNP markers associated with resistance trait could accelerate the breeding efficiency by application of marker assisted selection and genomic selection. In the present study, a Bulk Segregation Analysis coupled to whole genome sequencing method was employed to identify SNPs and genes associated with resistance trait to VPAHPND in L. vannamei. The DNA of susceptible and resistant individuals was pooled separately. ED (Euclidean distance) and the chi-square test were applied to calculate the allele frequency and genotype frequency differences between susceptible and resistant individuals. A total of 2238 SNPs and 97 genes were identified to be associated with resistance trait to VPAHPND. KEGG enrichment analysis showed that these genes were significantly enriched in PPAR signaling pathway, PI3K-Akt signaling pathway, NLR pathway and O-Antigen nucleotide sugar biosynthesis pathway. The acyl-CoA delta-9 desaturase gene, 14–3–3 epsilon-like gene, retrovirus-related Pol polyprotein gene, enzymatic polyprotein gene in these pathways were considered as candidate genes associated with resistance trait to VPAHPND of shrimp. This study demonstrated that BSA based on whole genome re-sequencing was a cost-effective method for identifying disease resistant genes in aquaculture animals. These data will not only provide useful information for understanding the genetic basis of shrimp resistance trait to VPAHPND, but also offer a source of SNPs for marker-assisted selection and genomic selection in shrimp breeding.
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spelling doaj-art-2b2dd822bf724353ba28f8b26487915b2025-08-20T03:45:12ZengElsevierAquaculture Reports2352-51342025-09-014310290210.1016/j.aqrep.2025.102902Identification of genes associated with resistance trait to VPAHPND in Pacific white shrimp (Litopenaeus vannamei) using Bulk Segregation Analysis (BSA)Zhenning Bao0Yang Yu1Pengfei Lin2Fuhua Li3State Key Laboratory of Breeding Biotechnology and Sustainable Aquaculture, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266000, China; University of Chinese Academy of Sciences, Beijing 100049, ChinaState Key Laboratory of Breeding Biotechnology and Sustainable Aquaculture, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266000, China; Laboratory for Marine Biology and Biotechnology, Qingdao Marine Science and Technology Center, Qingdao 266071, China; University of Chinese Academy of Sciences, Beijing 100049, China; Corresponding authors at: State Key Laboratory of Breeding Biotechnology and Sustainable Aquaculture, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266000, China.State Key Laboratory of Breeding Biotechnology and Sustainable Aquaculture, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266000, China; University of Chinese Academy of Sciences, Beijing 100049, ChinaState Key Laboratory of Breeding Biotechnology and Sustainable Aquaculture, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266000, China; Laboratory for Marine Biology and Biotechnology, Qingdao Marine Science and Technology Center, Qingdao 266071, China; University of Chinese Academy of Sciences, Beijing 100049, China; Corresponding authors at: State Key Laboratory of Breeding Biotechnology and Sustainable Aquaculture, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266000, China.Vibrio parahaemolyticus harboring the PirA/PirB toxin (VPAHPND) is regarded as one of the main pathogens that caused Acute hepatopancreatic necrosis disease (AHPND) in the Pacific white shrimp Litopenaeus vannamei (L. vannamei). Breeding new varieties resistant to VPAHPND is considered to be the most effective way to reduce the economic losses in shrimp aquaculture. Identification of genes and SNP markers associated with resistance trait could accelerate the breeding efficiency by application of marker assisted selection and genomic selection. In the present study, a Bulk Segregation Analysis coupled to whole genome sequencing method was employed to identify SNPs and genes associated with resistance trait to VPAHPND in L. vannamei. The DNA of susceptible and resistant individuals was pooled separately. ED (Euclidean distance) and the chi-square test were applied to calculate the allele frequency and genotype frequency differences between susceptible and resistant individuals. A total of 2238 SNPs and 97 genes were identified to be associated with resistance trait to VPAHPND. KEGG enrichment analysis showed that these genes were significantly enriched in PPAR signaling pathway, PI3K-Akt signaling pathway, NLR pathway and O-Antigen nucleotide sugar biosynthesis pathway. The acyl-CoA delta-9 desaturase gene, 14–3–3 epsilon-like gene, retrovirus-related Pol polyprotein gene, enzymatic polyprotein gene in these pathways were considered as candidate genes associated with resistance trait to VPAHPND of shrimp. This study demonstrated that BSA based on whole genome re-sequencing was a cost-effective method for identifying disease resistant genes in aquaculture animals. These data will not only provide useful information for understanding the genetic basis of shrimp resistance trait to VPAHPND, but also offer a source of SNPs for marker-assisted selection and genomic selection in shrimp breeding.http://www.sciencedirect.com/science/article/pii/S2352513425002881Litopenaeus vannameiBulk Segregation Analysis (BSA)Resistance to VPAHPNDSingle nucleotide polymorphisms (SNPs)Sliding window algorithm
spellingShingle Zhenning Bao
Yang Yu
Pengfei Lin
Fuhua Li
Identification of genes associated with resistance trait to VPAHPND in Pacific white shrimp (Litopenaeus vannamei) using Bulk Segregation Analysis (BSA)
Aquaculture Reports
Litopenaeus vannamei
Bulk Segregation Analysis (BSA)
Resistance to VPAHPND
Single nucleotide polymorphisms (SNPs)
Sliding window algorithm
title Identification of genes associated with resistance trait to VPAHPND in Pacific white shrimp (Litopenaeus vannamei) using Bulk Segregation Analysis (BSA)
title_full Identification of genes associated with resistance trait to VPAHPND in Pacific white shrimp (Litopenaeus vannamei) using Bulk Segregation Analysis (BSA)
title_fullStr Identification of genes associated with resistance trait to VPAHPND in Pacific white shrimp (Litopenaeus vannamei) using Bulk Segregation Analysis (BSA)
title_full_unstemmed Identification of genes associated with resistance trait to VPAHPND in Pacific white shrimp (Litopenaeus vannamei) using Bulk Segregation Analysis (BSA)
title_short Identification of genes associated with resistance trait to VPAHPND in Pacific white shrimp (Litopenaeus vannamei) using Bulk Segregation Analysis (BSA)
title_sort identification of genes associated with resistance trait to vpahpnd in pacific white shrimp litopenaeus vannamei using bulk segregation analysis bsa
topic Litopenaeus vannamei
Bulk Segregation Analysis (BSA)
Resistance to VPAHPND
Single nucleotide polymorphisms (SNPs)
Sliding window algorithm
url http://www.sciencedirect.com/science/article/pii/S2352513425002881
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