Abstract

• The size of mitogenome sequences in T. absoluta varied among individuals from different geographical locations. • The differences in the lengths of intergenic spacer were contributed to the size difference of mitogenomes among different populations. • cox2 , atp6 , nad1 and nad5 genes were sensitive mitochondrial gene markers for population genetics in T. absoluta . Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae) is a devastating invasive pest worldwide, causing severe damage to tomatoes. Recently, it has been recorded in the northwestern and southwestern parts of China. Here, the mitogenomes and genetic variation of two newly invaded T. absoluta populations in Xinjiang and Yunnan, were determined. The results showed that the complete mitogenome size of T. absoluta is 15298 bp for the individual from Xinjiang and 15296 bp for the individual from Yunnan, which were both longer than the reported mitogenome from Spain (15290 bp). The mitogenome sequences of individuals collected from three locations showed high levels of sequence similarity, except for 8 polymorphic sites, which were in genes cox2 (1 site), cox3 (2 sites), cob (1 site) , atp6 (1 site), nad1 (2 sites) and nad5 (1 site). Tuta absoluta mitogenomes share many features with other 6 Gelechiidae mitogenomes, except for several differences in the start and stop codons of protein-coding genes and the length of intergenic spacers. Seven partial mitochondrial genes ( cox1 , cox2 , cox3 , atp6 , cob , nad1 , and nad5 ) were used for genetic variation analysis, and significant population differentiation was found between the two populations based on cox2 , atp6 , nad1 , and nad5 . The complete mitogenomes and sensitive mitochondrial gene markers reported here provide useful data for further population genetics study of this pest.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.