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李明, 王崇, 汪建国, 喻达辉, 王文博, 戈贤平, 徐跑, 谢骏, 龚小宁. 鲩肠袋虫18S rDNA的扩增、测序与分析[J]. 水生生物学报, 2011, 35(2): 203-209. DOI: 10.3724/SP.J.1035.2011.00203
引用本文: 李明, 王崇, 汪建国, 喻达辉, 王文博, 戈贤平, 徐跑, 谢骏, 龚小宁. 鲩肠袋虫18S rDNA的扩增、测序与分析[J]. 水生生物学报, 2011, 35(2): 203-209. DOI: 10.3724/SP.J.1035.2011.00203
LI Ming, WANG Chong, WANG Jian-Guo, YU Da-Hui, WANG Wen-Bo, GE Xian-Ping, XU Pao, XIE Jun, GONG Xiao-Ning. PCR AMPLIFICATION, SEQUENCING AND ANALYSIS OF 18S rDNA OF|BALANTIDIUM CTENOPHARYNGODONI INHABITING GRASS CARP[J]. ACTA HYDROBIOLOGICA SINICA, 2011, 35(2): 203-209. DOI: 10.3724/SP.J.1035.2011.00203
Citation: LI Ming, WANG Chong, WANG Jian-Guo, YU Da-Hui, WANG Wen-Bo, GE Xian-Ping, XU Pao, XIE Jun, GONG Xiao-Ning. PCR AMPLIFICATION, SEQUENCING AND ANALYSIS OF 18S rDNA OF|BALANTIDIUM CTENOPHARYNGODONI INHABITING GRASS CARP[J]. ACTA HYDROBIOLOGICA SINICA, 2011, 35(2): 203-209. DOI: 10.3724/SP.J.1035.2011.00203

鲩肠袋虫18S rDNA的扩增、测序与分析

PCR AMPLIFICATION, SEQUENCING AND ANALYSIS OF 18S rDNA OF|BALANTIDIUM CTENOPHARYNGODONI INHABITING GRASS CARP

  • 摘要: 研究测定了寄生于草鱼肠道的鲩肠袋虫的18S rDNA序列。鲩肠袋虫的18S rDNA基因序列包括1638个碱基。分别用3种分析方法(邻接法、最大简约法、贝叶斯法)构建了毛口亚纲的系统发育树,得到结果如下:均支持毛口亚纲为单系发生且内分前庭目、内毛目和澳大利亚枝3个类群(100%Bay、100%MP、100%NJ);均支持内毛目(100%Bay、98%MP、93%NJ)、澳大利亚枝(100%Bay、97%MP、99%NJ)的单系性和前庭目的并系性。3种构树方法都支持鲩肠袋虫与澳大利亚枝聚类(100%Bay、100%MP、100%NJ),而后与"内毛目+前庭目(部分)"构成姊妹群(100%Bay、85%MP、72%NJ);而结肠小袋纤毛虫与"澳大利亚枝+鲩肠袋虫"以及"内毛目+前庭目(部分)"分枝并列,共同构成毛口亚纲(100%Bay、100%MP、100%NJ)。这暗示了肠袋虫类群在系统发育上的并系性和其分类阶元的提升。

     

    Abstract: Balantidium ctenopharyngodoni, an obligatory intestinal symbiont and possibly opportunistic parasite ofgrass carp (Ctenopharyngodon idella), was first discovered and named by Chen (1955). It mainly inhabits the cream-likeluminal contents and spaces between mucosal folds of the hindgut. In the present study, twenty two or three-summergrass carp were bought from Wuhan Fruit-Lake Market in March 2009 and transported alive to the laboratory for furtherexamination. All fish samples were dissected and the intestines were cut to collect the luminal contents into Petri dishesfor examination. Then 0.65% saline solution was added to the contents and waited for a few minutes to allow B. ctenopharyngodoniswim free of luminal contents. The ciliates were collected with Pasteur micropipette and washed twice indistilled water. The parasite gDNA was isolated by proteinase K digestion overnight at 37℃, followed by phenol-chloroform protein extraction and ethanol precipitation. Its 18S rDNA was then sequenced, which contains 1638base pairs. Phylogenetic trees were also constructed by the neighbour joining method, the maximum parsimony methodand the Bayesian method, respectively. The results indicated that the subclass Trichostomatia was monophyletic andcomposed of the order Entodiniomorphida, Vestibuliferida and Australian clade (100% Bay; 100% MP; 100% NJ). Theoder Entodiniomorphida (100% Bay; 98% MP; 93% NJ) and Australian clade (100% Bay; 97% MP; 99% NJ) showedtheir monophyletic while the order Vestibuliferida showed its paraphyly. As to the phylogenetic position, B. ctenopharyngodonifirst clustered with the Australian clade with higher bootstrap values (100% Bay; 100% MP; 100% NJ).Then they formed a sister clade to “Entodiniomorphida+ Vestibuliferida” (100% Bay; 85% MP; 72% NJ). B. coli, as anisolated taxon, was joined together with “Australian clade + B. ctenopharyngodoni” and “Entodiniomorphida + Vestibuliferida(part)” to form the subclass Trichostomatia (100% Bay; 100% MP; 100% NJ). It also suggested that the genusBalantidium should be recognized as a higher taxon.

     

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