White spot syndrome virus endogenous viral elements (EVE) revealed by circular viral copy DNA (cvcDNA) in shrimp
Issued Date
2024-04-01
Resource Type
eISSN
23525134
Scopus ID
2-s2.0-85188213994
Journal Title
Aquaculture Reports
Volume
35
Rights Holder(s)
SCOPUS
Bibliographic Citation
Aquaculture Reports Vol.35 (2024)
Suggested Citation
Taengchaiyaphum S., Srisala J., Wongkhaluang P., Sukthaworn S., Macias J., Udin I.I., Chokkara M.B., Athikkavil M.M., Alday-Sanz V., Flegel T.W., Sritunyalucksana K. White spot syndrome virus endogenous viral elements (EVE) revealed by circular viral copy DNA (cvcDNA) in shrimp. Aquaculture Reports Vol.35 (2024). doi:10.1016/j.aqrep.2024.102003 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/97758
Title
White spot syndrome virus endogenous viral elements (EVE) revealed by circular viral copy DNA (cvcDNA) in shrimp
Corresponding Author(s)
Other Contributor(s)
Abstract
Circular, viral copy DNA (cvcDNA) can reveal the existence of endogenous viral elements (EVE) in shrimp genomic DNA. Here we describe isolation and sequencing of cvcDNA from a breeding stock of the whiteleg shrimp Penaeus vannamei. The stock was developed by onward breeding and selection for white spot syndrome virus (WSSV)-free individual survivors of white spot disease outbreaks. The stock exhibits high tolerance to WSSV. A pool of DNA extracted from 10 shrimp from this stock was subjected to cvcDNA isolation and amplification followed by high throughput sequencing. This revealed DNA fragments corresponding to locations covering much of the 300,000 bp WSSV genome. However, high frequency-read-fragments (HFRF) mapped to a surprisingly small region of approximately 1400 bp. We hypothesized that the HFRF reflected their selection due to provision of tolerance to WSSV. Four PCR primer sets were designed to cover the 1365 bp mapped region. One pair (Set 1) targeted the whole 1365 bp mapped region, while another 3 primer sets (Set 2–4), targeted regions within the 1365 bp target. All 4 primer sets were used with DNA samples from each of 36 shrimp from the same breeding stock (including the 10 used for cvcDNA preparation). Individual positive PCR results varied from shrimp to shrimp, ranging from only 1 primer set up to 4 primer sets. Only 1 specimen gave an amplicon of 1365 bp, while others gave single to multiple positive amplicons in both continuous and discontinuous regions. This indicated that the amplicons did not arise from contiguous targets and might vary in insertion length. The results also confirmed that none of the shrimp were infected with WSSV. Sequencing of the PCR amplicons of expected sizes revealed sequence identity to extant WSSV genomes. This data will be used to screen the breeding stock for EVE that provide WSSV tolerance.