Whole genome resequencing data enables a targeted SNP panel for conservation and aquaculture of Oreochromis cichlid fishes
Research output: Contribution to journal › Article › peer-review
Standard Standard
In: Aquaculture, Vol. 548, No. Part 2, 737637, 15.02.2022, p. 737637.
Research output: Contribution to journal › Article › peer-review
HarvardHarvard
APA
CBE
MLA
VancouverVancouver
Author
RIS
TY - JOUR
T1 - Whole genome resequencing data enables a targeted SNP panel for conservation and aquaculture of Oreochromis cichlid fishes
AU - Ciezarek, A.
AU - Ford, Antonia G.P.
AU - Etherington, Graham J.
AU - Kasozi, Nasser
AU - Malinsky, Milan
AU - Mehta, Tarang K.
AU - Penso-Dolfin, Luca
AU - Ngatunga, Benjamin P.
AU - Shechonge, Asilatu
AU - Tamatamah, Rashid
AU - Haerty, Wilfried
AU - Palma, Federica Di
AU - Genner, Martin J.
AU - Turner, George F.
N1 - © 2021 The Authors.
PY - 2022/2/15
Y1 - 2022/2/15
N2 - Cichlid fish of the genus Oreochromis form the basis of the global tilapia aquaculture and fisheries industries. Broodstocks for aquaculture are often collected from wild populations, which in Africa may be from locations containing multiple Oreochromis species. However, many species are difficult to distinguish morphologically, hampering efforts to maintain good quality farmed strains. Additionally, non-native farmed tilapia populations are known to be widely distributed across Africa and to hybridize with native Oreochromis species, which themselves are important for capture fisheries. The morphological identification of these hybrids is particularly unreliable. Here, we describe the development of a single nucleotide polymorphism (SNP) genotyping panel from whole-genome resequencing data that enables targeted species identification in Tanzania. We demonstrate that an optimized panel of 96 genome-wide SNPs based on FST outliers performs comparably to whole genome resequencing in distinguishing species and identifying hybrids. We also show this panel outperforms microsatellite-based and phenotype-based classification methods. Case studies indicate several locations where introduced aquaculture species have become established in the wild, threatening native Oreochromis species. The novel SNP markers identified here represent an important resource for assessing broodstock purity in hatcheries and helping to conserve unique endemic biodiversity.
AB - Cichlid fish of the genus Oreochromis form the basis of the global tilapia aquaculture and fisheries industries. Broodstocks for aquaculture are often collected from wild populations, which in Africa may be from locations containing multiple Oreochromis species. However, many species are difficult to distinguish morphologically, hampering efforts to maintain good quality farmed strains. Additionally, non-native farmed tilapia populations are known to be widely distributed across Africa and to hybridize with native Oreochromis species, which themselves are important for capture fisheries. The morphological identification of these hybrids is particularly unreliable. Here, we describe the development of a single nucleotide polymorphism (SNP) genotyping panel from whole-genome resequencing data that enables targeted species identification in Tanzania. We demonstrate that an optimized panel of 96 genome-wide SNPs based on FST outliers performs comparably to whole genome resequencing in distinguishing species and identifying hybrids. We also show this panel outperforms microsatellite-based and phenotype-based classification methods. Case studies indicate several locations where introduced aquaculture species have become established in the wild, threatening native Oreochromis species. The novel SNP markers identified here represent an important resource for assessing broodstock purity in hatcheries and helping to conserve unique endemic biodiversity.
KW - Tilapia
KW - Tanzania
KW - Fisheries
KW - Hybridization
U2 - 10.1016/j.aquaculture.2021.737637
DO - 10.1016/j.aquaculture.2021.737637
M3 - Article
C2 - 35177872
VL - 548
SP - 737637
JO - Aquaculture
JF - Aquaculture
SN - 0044-8486
IS - Part 2
M1 - 737637
ER -