Pierce's Disease
Research Updates

piercesdisease.cdfa.ca.gov

What is Pierce's Disease?

Pierce's Disease is a bacterial infection, which is spread by bugs that feed on grapevines, particularly the "glassy winged sharpshooter." Grapevines that become infected with PD can quickly become sick and die.

glassy-winged sharpshooter

DEVELOPMENT OF MOLECULAR DIAGNOSTIC MARKERS FOR GLASSY-WINGED AND SMOKETREE SHARPSHOOTERS FOR USE IN PREDATOR GUT CONTENT EXAMINATIONS


  • Author(s): Daane, Kent; de Le?n, Jesse; Fournier, Valarie; Hagler, James;
  • Abstract: To aid in identifying key predators of Proconiini sharpshooter species present in California, we developed and tested molecular diagnostic markers for the glassy-winged sharpshooter Homalodisca coagulata (Say) and smoke-tree sharpshooter Homalodisca liturata (Ball) (Homoptera: Cicadellidae: Proconiini). Two different types of markers were compared, those targeting single-copy sequence characterized amplified regions (SCAR) and mitochondrial markers targeting the multi-copy cytochrome oxidase subunit genes I (COI) and II (COII). A total of six markers were developed, two SCAR and four mitochondrial COI or COII markers. Specificity assays demonstrated that SCAR marker HcF5/HcR7 was H. coagulata-specific and HcF6/HcR9 was H. coagulata/H. liturata-specific. COI (HcCOI-F/R) and COII (HcCOII-F4/R4) markers were H. coagulata-specific, COII (G/S-COII-F/R) marker was H. coagulata/H. liturata-specific, and lastly, COII marker (Hl-COII-F/R) was H. liturata-specific. Sensitivity assays using genomic DNA showed the COI marker to be the most sensitive marker with a detection limit of 6 pg of DNA. This marker was 66-fold more sensitive than marker Hl-COII-F/R that showed a detection limit of 400 pg of DNA. In addition, the COI marker was 4.2-fold more sensitive than the COII marker. In predator gut assays, the COI and COII markers demonstrated significantly higher detection efficiency than the SCAR markers. Furthermore, the COI marker demonstrated slightly higher detection efficiency over the COII marker. Lastly, we describe the inclusion of an internal control (28S amplification) for predation studies performing predator gut analyses utilizing PCR. This control was critical in order to monitor reactions for PCR failures, PCR inhibitors, and for the presence of DNA.
  • Publication Date: Dec 2005
  • Journal: 2005 Pierce's Disease Research Symposium