2015
DOI: 10.1007/s12355-015-0394-x
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COI Gene-based Species Diagnostic Kit for Sugarcane Scale Insect, Melanaspis glomerata (Green) (Homoptera: Diaspididae)

Abstract: Cytochrome c oxidase I (COI) gene-based DNA barcode was generated for sugarcane scale insect, Melanaspis glomerata (Green). The generated DNA barcode would certainly serve as an ideal diagnostic kit for M. glomerata. The barcode developed by us (GenBank Accession Number KR153875) would probably be the first for this species. The amino acid sequence of the M. glomerata COI fragment did not have any stop codon, and the uninterrupted open reading frame confirmed the quality of the DNA barcode. The extent of ident… Show more

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Cited by 6 publications
(7 citation statements)
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References 13 publications
(14 reference statements)
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“…North America, Africa, Europe) require the use of keys that are increasingly out-of-date (Balachowsky 1953(Balachowsky , 1954(Balachowsky , 1958Ferris 1942;Hall 1946). Given the training, library, and labor required for the morphological identification of scale insects, there has been a great deal of interest in their molecular identification (Campbell et al 2014;Ramasubramanian et al 2015;Rugman-Jones et al 2009).…”
Section: Introductionmentioning
confidence: 99%
“…North America, Africa, Europe) require the use of keys that are increasingly out-of-date (Balachowsky 1953(Balachowsky , 1954(Balachowsky , 1958Ferris 1942;Hall 1946). Given the training, library, and labor required for the morphological identification of scale insects, there has been a great deal of interest in their molecular identification (Campbell et al 2014;Ramasubramanian et al 2015;Rugman-Jones et al 2009).…”
Section: Introductionmentioning
confidence: 99%
“…viburni (Signoret))、葡萄绵粉蚧、 扶桑绵粉蚧 [59] 、 康氏粉蚧(Ps. comstocki (Kuwana)) [48] 、 无花果蜡蚧 [67] 、Melanaspis glomerata (Green) [65] 等的 种特异性 PCR 检测方法. 值得关注的是, Beltrà 等 人 [68] [70] 以及陈哲等 人 [71] 的研究发现, 扶桑绵粉蚧存在 2 个进化支系, 入 侵我国的扶桑绵粉蚧仅为其中的一个谱系.…”
Section: 在介壳虫类昆虫研究中的应用unclassified
“…1 ) [ 22 ]. Stage-specific taxonomic keys, phenotypic variability in key characteristics, and damaged adult specimens further complicate the identification process [ 23 , 24 ]. Although morphological identification complemented by DNA barcoding can be employed, this method demands taxonomic expertise, is time consuming, and is constrained by the scope and accuracy of the existing DNA database [ 25 ].…”
Section: Introductionmentioning
confidence: 99%