跳到主要內容區塊

以次世代定序解析臺灣養殖文蛤之轉錄體及相關遺傳分析

  • 日期:107-02-20
  • 計畫編號:107農科-9.5.1-水-A1(5)
  • 年度:2018
  • 領域:漁業科技研發
  • 主持人:黃慶輝
  • 研究人員:吳嘉哲

     近年臺灣文蛤人工養殖技術逐漸完備並推廣至民間業者,然而隨著養殖規模的 擴大,如生長停滯、偶發及季節性的大量死亡等問題也持續發生,是近年文蛤產量 不甚穩定的主因,如105年8月於雲林縣臺西麥寮一帶養殖文蛤大量暴斃事件,其育 成率由原先的6至7成銳減為3成不到。前述問題初步推測可能原因為:季節轉換氣溫 變化劇烈、養殖密度過高造成之水質環境惡化;目前市面上可見之養殖文蛤大致有 五物種,臺灣文蛤 (Meretrix meretrix) 、麗文蛤 (Meretrix lusoria) 、 韓國 文蛤(Meretrix lamarckii ) 、 中華文蛤(Meretrix petechialis) 、 皺肋文蛤( Meretrix lyrata) ,根據前導試驗結果,前述五物種文蛤均可在臺灣各地發現;為 更有效率地釐清何者為臺灣目前主要養殖物種,本計畫使用次世代定序技術(NGS)作 為本研究基因遺傳分析之主要工具,並針對最主要之養殖文蛤物種之轉錄基因體展 開研究,期能改善目前文蛤養殖遭遇之相關問題,執行成果說明如下:

1. 本計畫以PCR擴增產於雲林臺西、嘉義東石52文蛤個體之COI(母系來源)序列,結 果其中有49個體屬同一系群(系群A),3個體屬另一系群(系群B)。本結果可瞭解臺 灣養殖文蛤養殖系群(母系)之大致分布情形,供後續次世代定序對象個體挑選參 考。

2.  完成次世代定序的文蛤轉錄體序列,經由Function Annotator pipeline進行序列 註解(annotation),再由NCBI Blastx等進行序列比對之結果,文蛤轉錄體 (transcriptome)其序列與現有相關軟體動物之序列資料相似度較低,最接近之大 西洋牡蠣亦僅有33.6%之相似度,另經由比較不同溫度下之文蛤轉錄體樣本其相關 序列之表現量差異,目前篩選出11個可能與耐溫相關之候選基因,惟仍須進一步 測試以確認。

研究報告摘要(英)


     Hard clam, Meretrix spp. , are widely commercial aquaculture species in Asia. Various breeding programs, such as mass selection, family selection, and hybridization between different geographic populations, have been used in hard clam. Their growth and survival are often influenced by environmental factors, pathogens or genetic defect. However, the production of hard clam farming declined recently in Taiwan. There are five major aquaculture species in Taiwan: Meretrix meretrix, M. lusoria, M. lamarckii, M. petechialis, M. lyrata. Next-generation sequencing (NGS) can allow us to collect gene data and establish gene library much more quickly and cheaply than previous methods. In this project, genetic samples of Meretrix spp. from major farming area in Taiwan will be analyzed by NGS for species detection and gene variation to explore the causes of declined production:

In this project:

1. The COI sequence of 52 hard clam individuals from Taishi, Yunlin and DongShih, Chiayi were amplified by PCR.  In sequence alignment and phylogenetic tree analysis, 49 individuals belonged  to one clade and 3 individuals belong to another clade. These results showed the clade distribution of aquacultured hard clam and the sample picking of NGS experiments.

2. Assembled sequences of hard clams transcriptome were annotated with Function Annotator pipeline. Several methods were used to infer their potential functions. Briefly, assembled sequences were aligned to NCBI nr database with blastx program and potential coding regions were predicted with TransCoder program. The transcriptome of hard clam showed lower similarity of mRNA sequences of other Mollusca species, the highest is Pacific oyster with 33.6% by taxonomic distribution analysis. 11 candidates of temperature-tolerant genes were picked by sequence expression comparison between hard calms individuals cultured in different temperatures. More tests and experiments are needed for confirmation.