Life-history parameters (juvenile development time, adult longevity, host instar preference and rate of parasitism) of four parasitoids of Bemisia argentifolii (two strains of Encarsia formosa (D and B), Eretmocerus eremicus and Eretmocerus mundus) were studied in the laboratory. At 15°C juvenile development time was the shortest for E. formosa B (48 days), longest for E. eremicus (79.3 days) and intermediate for E. formosa D (62.8 days) and E. mundus (64 days) at 15°C. With increase in temperature, development time decreased to around 14 days for all species/strains at 32°C. The lower developmental threshold for development was 11.5, 8.1, 13.0 and 11.5°C for E. formosa D, E. formosa B, E. eremicus and E. mundus, respectively. E. formosa D and B, and E. mundus all appeared to prefer to parasitize 3rd instar nymphs. The presence of hosts shortened adult longevity in most of the parasitoids, with the exception of E. formosa B, which lived longer than other species/strains irrespective of the presence of hosts. At 15°C daily parasitism was very low by all parasitoids. The two Encarsia strains had a constant, but low rate of reproduction during adult life, while the two Eretmocerus species had a very high rate of reproduction when one-day old, which then decreased very quickly. Lifetime fecundity, estimated using a non-linear model, indicated that it was higher for the two Encarsia strains than for the Eretmocerus species. Life history parameters reported in the literature for the four parasitoids are reviewed and compared with our results. Finally, the potential value for the biological control of whiteflies on greenhouse crops of parasitoids having either a high reproductive rate over a short period (Eretmocerus spp.) or a low rate of reproduction over a long period (Encarsia spp.) is discussed.
Stable reference genes (RGs) determine the reliability of quantitative polymerase chain reaction (qPCR) analyses and it is recommended that different reference genes are used for different types of DNA and tissues. The present study aimed to screen for stable RGs for the qPCR analysis of the immune responses of the whitefly Bemisia tabaci to the Wolbachia wMel strain from Drosophila melanogaster. A total of eight candidate RGs were evaluated using five different methods, i.e., Coefficient of Variation analysis, GeNorm, NormFinder, BestKeeper and ΔCt. The stability of these RGs was assessed for both genomic DNA (gDNA) and complementary DNA (cDNA). The results indicate that β-actin (Actin) and elongation factor 1 alpha (EF-1α) were the most stable RGs for gDNA, whereas 18S rRNA (18S) and glyceraldehyde phosphate dehydrogenase (GAPDH) were the least stable; in contrast, Actin and GAPDH were the most stable for cDNA, whereas RPL29 and ATPase were the least stable. The effectiveness of the most stable RGs was then validated against the least stable using qPCR analysis of the titre of wMel (gDNA) and the transcriptional responses of the antimicrobial peptide Alo-3-like and the phosphatidylinositol-bisphosphate 3-kinase catalytic subunit delta isoform (cDNA) to wMel transfection. The results support the notion that reliable RGs are essential for a qPCR analysis of samples of both gDNA and cDNA.