In silico mining of microsatellites and analysis of genetic diversity among inter- and intra-generic aphids of the subfamily Aphidinae

• Published in: Entomologia experimentalis et applicata Vol. 160; no. 2; pp. 179 - 187
• Main Authors: Vaddi, Sridhar, Thiruvengadam, Venkatesan, Joshi, Sunil, Jalali, Sushil Kumar, Chinnappareddy, Lakshmana Reddy Dhoranalapalli, Nimmakayala, Padma, Tomason, Yan, Vajja, Gopinath, Reddy, Umesh K.
• Format: Journal Article
• Language: English
• Published: Amsterdam Blackwell Publishing Ltd 01-08-2016; Wiley Subscription Services, Inc
• Subjects: Acyrthosiphon pisum; Aphididae; Aphis gossypii; cross-amplification; Hemiptera; phenogram; polymorphism; tribe
• ISSN: 0013-8703; 1570-7458
• DOI: 10.1111/eea.12460

Nearly 5 000 aphid species damage crops, either by sucking plant sap or as disease‐transmitting vectors. Microsatellites are used for understanding molecular diversity and eco‐geographical relationships among aphid species. Expressed sequence tag (EST)‐microsatellite motifs were identified through an in silico approach using inbuilt simple sequence repeat mining tools in aphid EST dataset. Microsatellite mining revealed one in every five aphid genes as containing a repeat motif, and out of 9 290 EST microsatellites mined from Aphis gossypii Glover and Acyrthosiphon pisum (Harris) (both Hemiptera: Aphididae), 80% were of A and/or T (AT, ATA, AAT, AATA, and ATTT) motifs, and the rest contained G and/or C motifs. All microsatellite sequences were annotated using BLAST. Primers for EST microsatellites were designed using the Primer 3.0 tool. 106 primer pairs of both dinucleotide repeats (DNRs) and trinucleotide repeats (TNRs), representing open reading frames (ORFs) and untranslated regions (UTRs), were synthesized to amplify 15 aphid species belonging to the subfamily Aphidinae, collected from diverse hosts. Four hundred forty‐five polymorphic alleles were amplified. Fifty TNR and 23 DNR microsatellites amplified across the species studied. Polymorphism information content values of microsatellites ranged from 0.23 to 0.91, amplifying 2–16 alleles. Genetic similarity indices were estimated using the ‘NTSYS‐pc’ software package. Unweighted pair group with arithmetic mean and principal component analysis resolved taxonomic relationships of the aphid species studied. The new aphid microsatellites developed will provide valuable information to researchers to study Indian aphid species diversity and genetic relationships.