Evaluation of the 16S and 12S rRNA genes as universal markers for the identification of commercial fish species in South Africa

被引:54
作者
Cawthorn, Donna-Maree [1 ]
Steinman, Harris Andrew [2 ]
Witthuhn, R. Corli [1 ]
机构
[1] Univ Stellenbosch, Dept Food Sci, ZA-7602 Matieland, South Africa
[2] FACTS, ZA-7435 Milnerton, South Africa
关键词
Marine fishes; Mitochondrial DNA; Ribosomal genes; Sequence analysis; Species authentication; Species identification; PCR-RFLP ANALYSIS; MITOCHONDRIAL; 12S; MOLECULAR-IDENTIFICATION; RESTRICTION ANALYSIS; SEQUENCE-ANALYSIS; ANIMAL ORIGIN; DNA; AUTHENTICATION; FOOD; AMPLIFICATION;
D O I
10.1016/j.gene.2011.09.009
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The development of DNA-based methods for the identification of fish species is important for fisheries research and control, as well as for the detection of unintentional or fraudulent species substitutions in the marketplace. The aim of this study was to generate a comprehensive reference database of DNA sequences from the mitochondrial 16S and 12S ribosomal RNA (rRNA) genes for 53 commercial fish species in South Africa and to evaluate the applicability of these genetic markers for the identification of fish at the species level. The DNA extracted from all target species was readily amplified using universal primers targeting both rRNA gene regions. Sequences from the 16S and 12S rRNA genes were submitted to GenBank for the first time for 34% and 53% of the fish species, respectively. Cumulative analysis of the 16S rRNA gene sequences revealed mean conspecific, congeneric and confamilial Kimura two parameter (K2P) distances of 0.03%, 0.70% and 5.10% and the corresponding values at the 12S level were 0.03%, 1.00% and 5.57%. K2P neighbour-joining trees based on both sequence datasets generally clustered species in accordance with their taxonomic classifications. The nucleotide variation in both the 16S and 12S sequences was suitable for identifying the large majority of the examined fish specimens to at least the level of genus, but was found to be less useful for the explicit differentiation of certain congeneric fish species. It is recommended that one or more faster-evolving DNA regions be analysed to confirm the identities of closely-related fish species in South Africa. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:40 / 48
页数:9
相关论文
共 60 条
[1]   Identification of alfonsino and related fish species belonging to the genus Beryx with mitochondrial 16S rRNA gene and its application on their pelagic eggs [J].
Akimoto, S ;
Kinoshita, S ;
Sezaki, K ;
Mitani, I ;
Watabe, S .
FISHERIES SCIENCE, 2002, 68 (06) :1242-1249
[2]  
[Anonymous], 2009, Step-by-step guide for implementing national adaptation programmes of action, P1
[3]  
[Anonymous], FISH SADC REG SEL CO
[4]   DNA barcoding for conservation and management of Amazonian commercial fish [J].
Ardura, Alba ;
Linde, Ana Rosa ;
Moreira, Josino C. ;
Garcia-Vazquez, Eva .
BIOLOGICAL CONSERVATION, 2010, 143 (06) :1438-1443
[5]   Species identification by means of pyrosequencing the mitochondrial 12S rRNA gene [J].
Balitzki-Korte, B ;
Anslinger, K ;
Bartsch, C ;
Rolf, B .
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 2005, 119 (05) :291-294
[6]  
BARTLETT SE, 1992, BIOTECHNIQUES, V12, P408
[7]   Taxonomists are an endangered species in Europe [J].
Buyck, B .
NATURE, 1999, 401 (6751) :321-321
[8]   Comparative study of different methods for the extraction of DNA from fish species commercially available in South Africa [J].
Cawthorn, Donna-Maree ;
Steinman, Harris Andrew ;
Witthuhn, R. Corli .
FOOD CONTROL, 2011, 22 (02) :231-244
[9]  
Céspedes A, 1998, J FOOD SCI, V63, P206
[10]   Molecular identification of five commercial flatfish species by PCR-RFLP analysis of a 12S rRNA gene fragment [J].
Comesaña, AS ;
Abella, P ;
Sanjuan, A .
JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 2003, 83 (08) :752-759