Author/Authors :
Wang, Jingjing Tianjin Key Laboratory of Industrial Biological Systems and Process Engineering - Tianjin Institute of Industrial Biotechnology - Chinese Academy of Sciences, China , Zhao, Wei Tianjin Key Laboratory of Industrial Biological Systems and Process Engineering - Tianjin Institute of Industrial Biotechnology - Chinese Academy of Sciences, China , Liang, Yajie Tianjin Key Laboratory of Industrial Biological Systems and Process Engineering - Tianjin Institute of Industrial Biotechnology - Chinese Academy of Sciences, China , Han, Yifan Tianjin Key Laboratory of Industrial Biological Systems and Process Engineering - Tianjin Institute of Industrial Biotechnology - Chinese Academy of Sciences, China , Wang, Xingbiao Tianjin Key Laboratory of Industrial Biological Systems and Process Engineering - Tianjin Institute of Industrial Biotechnology - Chinese Academy of Sciences, China , Zhang, Xiaoxia Tianjin Key Laboratory of Industrial Biological Systems and Process Engineering - Tianjin Institute of Industrial Biotechnology - Chinese Academy of Sciences, China , Ma, Xiaomei Tianjin Key Laboratory of Industrial Biological Systems and Process Engineering - Tianjin Institute of Industrial Biotechnology - Chinese Academy of Sciences, China , Zhang, Demin School of Marine Sciences - Ningbo University, China , Huang, Zhiyong Tianjin Key Laboratory of Industrial Biological Systems and Process Engineering - Tianjin Institute of Industrial Biotechnology - Chinese Academy of Sciences, China
Abstract :
Many reports have shown that the composition of the bacterioplankton community can serve as a biological indicator to evaluate the occurrence of shrimp diseases. However, the distribution, diversity, and function of planktonic actinobacteria in shrimp ponds are still poorly understood. In this study, a prototype of a 16S rRNA gene-based taxonomic microarray was developed and evaluated for monitoring of planktonic actinobacteria in shrimp ponds. The prototype microarray is composed of 30 probes that target ten dominant families of planktonic actinobacteria found in shrimp ponds. The specificity of the actinobacterial microarray was validated by a set of control hybridizations with 16S rRNA genes clones. The prototype microarray was subsequently tested with two seawater samples from ponds with diseased shrimp populations (PDS) and ponds with healthy shrimp populations (PHS). The actinobacteria hybridization profiles revealed a lower abundance of Microbacteriaceae and a higher abundance of Mycobacteriaceae in PDS than in PHS. The changes in planktonic actinobacterial communities were validated by pyrosequencing data. These results support the utility of the microarray for monitoring planktonic actinobacteria in shrimp ponds and aquaculture environments.
Keywords :
Microarray , Planktonic actinobacteria , Shrimp ponds , 16S rRNA gene , Aquaculture environment
