2019
DOI: 10.1016/j.ijbiomac.2018.12.186
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The complete mitochondrial genome of Bactrocera biguttula (Bezzi) (Diptera: Tephritidae) and phylogenetic relationships with other Dacini

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Cited by 17 publications
(16 citation statements)
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“…The ML phylogenetic analysis with the complete Bactrocera mitochondrial sequences (six generated in the present study and 20 from GenBank) ( Supplementary Table S1) conducted with MEGA software (Figure 2) resulted in almost identical tree topology to the one inferred by the IQ-Tree ML algorithm (data not shown). Topologies were very similar to other recent analyses also using data of complete mitogenomes to explore phylogenetic relationships within the Bactrocera genus [54,58,63,82,83,91,92] and confirmed the very close relationship of the B. dorsalis complex members. Within the complex (Figure 2B), the B. dorsalis sequences formed a highly supported clade, while all B. carambolae sequences, though not forming a single clade, were placed outside the B. dorsalis clade.…”
Section: Sequence Comparisons and Phylogenetic Analysissupporting
confidence: 85%
“…The ML phylogenetic analysis with the complete Bactrocera mitochondrial sequences (six generated in the present study and 20 from GenBank) ( Supplementary Table S1) conducted with MEGA software (Figure 2) resulted in almost identical tree topology to the one inferred by the IQ-Tree ML algorithm (data not shown). Topologies were very similar to other recent analyses also using data of complete mitogenomes to explore phylogenetic relationships within the Bactrocera genus [54,58,63,82,83,91,92] and confirmed the very close relationship of the B. dorsalis complex members. Within the complex (Figure 2B), the B. dorsalis sequences formed a highly supported clade, while all B. carambolae sequences, though not forming a single clade, were placed outside the B. dorsalis clade.…”
Section: Sequence Comparisons and Phylogenetic Analysissupporting
confidence: 85%
“…All PCR and sequencing primers were designed by the authors specifically for this study except for segment S03*, which was amplified and sequenced using arthropod universal DNA barcoding primers [44]. PCR was carried out in 25 μL total volume containing 75 mM Tris-HCl (pH 8.8), 20 mM (NH4)2SO4, 0.01% (v/v) Tween 20 (Fermentas), 3.0 mM MgCl2 (Fermentas), 0.5 mM of each dNTP (Fermentas), 25 [45], as well as completion and curation of published mitochondrial sequences [23]. However, the correct assembly of insect mitogenomes from NGS data can be hampered by lack of adequate reference sequences, particularly in groups where gene rearrangements are common (e.g., Hymenoptera), and complete mitogenomes for some subfamilies are not available (e.g., Opiinae).…”
Section: Sanger Sequencingmentioning
confidence: 99%
“…PCR was carried out in 25 PCR products were purified by treatment with ExonucleaseI (Fermentas) and Shrimp Alkaline Phosphatase (Fermentas), and Sanger-sequenced by Macrogen Europe (Amsterdam, The Netherlands). Mitochondrial DNA is usually overrepresented in Next Generation Sequencing (NGS) reads, allowing for easy retrieval of mitogenomes [45], as well as completion and curation of published mitochondrial sequences [23]. However, the correct assembly of insect mitogenomes from NGS data can be hampered by lack of adequate reference sequences, particularly in groups where gene rearrangements are common (e.g., Hymenoptera), and complete mitogenomes for some subfamilies are not available (e.g., Opiinae).…”
Section: Sanger Sequencingmentioning
confidence: 99%
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“…Sub-Saharan Africa has a rich assemblage of native insects associated with Oleaceae, including several species of olive fruit flies and olive flea beetles, and a diversity of parasitoid, hyperparasitoid and olive seed wasps [ 3 , 4 , 5 , 6 , 7 ]. Lace bugs feeding on Oleaceae are only found in sub-Saharan Africa: Catoplatus dilatatus Jakovlev (on Olea sp.…”
Section: Introductionmentioning
confidence: 99%