Romero-Ricardo Luis, Lastre-Meza Natalia, Pérez-Doria Alveiro, Bejarano Eduar E
Investigaciones Biomédicas, Universidad de Sucre, Sincelejo, Sucre, Colombia.
Investigaciones Biomédicas, Universidad de Sucre, Sincelejo, Sucre, Colombia.
Acta Trop. 2016 Jul;159:125-31. doi: 10.1016/j.actatropica.2016.03.017. Epub 2016 Mar 15.
Identification of the species of phlebotomine sand flies present in each focus of leishmaniasis is necessary to incriminate vectors and implement vector control strategies. Although the cytochrome oxidase I (COI) gene has been proposed as a barcode for the identification of animal species, less than 20% of New World phlebotomines have been characterized to date. In this study DNA barcoding was used to identify phlebotomine species of the mixed leishmaniasis focus in the Colombian Caribbean by means of three evolutionary models: Kimura's two parameter (K2P) nucleotide substitution model, that of (Tamura and Nei, 1993) (TN93) and proportional sequence divergence (p-distances). A 681bp sequence of the COI gene was obtained from 66 individuals belonging to 19 species of the genus Lutzomyia (Lu. abonnenci, Lu. atroclavata, Lu. bicolor, Lu. carpenteri, Lu. cayennensis cayennensis, Lu. dubitans, Lu. evansi, Lu. gomezi, Lu. gorbitzi, Lu. longipalpis, Lu. micropyga, Lu. migonei, Lu. panamensis, Lu. (Psathyromyia) sp., Lu. rangeliana, Lu. serrana, Lu. shannoni, Lu. trinidadensis and Lu. venezuelensis) and one of Brumptomyia (B. mesai). The genetic divergence values for TN93 among individuals of the same species fluctuated up to 3.2% (vs. 2.9% for K2P and 2.8% for p-distances), while the values between species ranged from 8.8-43.7% (vs. 6.8-19.6% for K2P and 6.6-17.4% for p-distances). A dendrogram constructed by means of the Neighbor-Joining method grouped phlebotomines into 20 clusters according to species, with bootstrap values of up to 100% in those with more than one individual. However, loss of the phylogenetic signal of the gene COI was observed at the supraspecific level as a consequence of substitutional saturation. In conclusion, irrespective of the evolutionary model selected, all phlebotomines were correctly assigned to species, showing 100% concordance with morphological identification.
确定利什曼病各疫源地存在的白蛉种类对于确认病媒和实施病媒控制策略至关重要。尽管细胞色素氧化酶I(COI)基因已被提议作为识别动物物种的条形码,但迄今为止,新大陆的白蛉中只有不到20%得到了鉴定。在本研究中,利用三种进化模型,即木村二参数(K2P)核苷酸替代模型、(Tamura和Nei,1993)(TN93)模型以及比例序列差异(p距离),通过DNA条形码技术鉴定了哥伦比亚加勒比地区混合利什曼病疫源地的白蛉种类。从属于19种罗蛉属(罗.阿博南西、罗.黑锁骨、罗.双色、罗.卡彭特丽、罗.卡宴卡宴、罗.可疑、罗.埃万斯、罗.戈麦兹、罗.戈尔比齐、罗.长须、罗.微臀、罗.米戈内、罗.巴拿马、罗.(拟沙罗蛉)种、罗.兰热利亚纳、罗.塞拉纳、罗.香农尼、罗.特立尼达和罗.委内瑞拉)和一种布鲁姆普托蛉(布.梅赛)的66个个体中获得了一段681bp的COI基因序列。同一物种个体之间TN93的遗传差异值波动高达3.2%(K2P为2.9%,p距离为2.8%),而不同物种之间的值在8.8 - 43.7%之间(K2P为6.8 - 19.6%,p距离为6.6 - 17.4%)。通过邻接法构建的系统发育树根据物种将白蛉分为20个簇,在有多个个体的簇中自展值高达100%。然而,由于替代饱和,在超种水平上观察到COI基因的系统发育信号丧失。总之,无论选择哪种进化模型,所有白蛉都能正确地按物种分类,与形态学鉴定的一致性达100%。