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A study was carried out during a three-year period (2006 to 2008) in traditional olive groves in the Terra Quente region of north-eastern Portugal to evaluate the potential of two commercially available traps for predicting infestations by olive fly,Bactrocera oleae(Rossi). We used yellow sticky traps baited with pheromone, and McPhail traps baited with diammonium phosphate. The results show that the variation in infestation is explained by captures of adults in both traps. Thus, even if infestation has changed significantly between years as well as groves and olive tree varieties, captures obtained by both types of trap can be valuable indicators of fruit infestation in Terra Quente, and probably in other regions that have a continental Mediterranean climate. The information obtained can enable growers and consultants to time treatments, and so avoid the use of more labour-intensive visual sampling methods. [ABSTRACT FROM PUBLISHER]

The European grapevine moth (Lobesia botrana; Denis and Schiffermüller, 1775) is considered a key pest for grapevine (Vitis vinifera L.) in the Douro Region, Portugal. The phenology of both the grapevine and the pest has changed in the last decades due to the increase in temperature. Here, we assess the potential impact of climate change on the (a)synchrony of both species. The results show that the phenological stages (budburst, flowering and veraison) undergo an advancement throughout the region (at an ~1 km resolution) under a climate change scenario (Representative Concentration Pathways, RCP8.5) for the period 2051–2080, with respect to the historic period (1989–2015). For cv. Touriga Nacional and Touriga Franca, the budburst advances up to 14 days, whereas for flowering and veraison the advancements are up to 10 days (mainly at low elevations along the Douro River). For the phenology of Lobesia botrana, earliness was also verified in the three flights (consequently there may be more generations per year), covering the entire region. Furthermore, the third flight advances further compared to the others. For both varieties, the interaction between the third flight (beginning and peak) and the veraison date is the most relevant modification under the future climate change scenario (RCP8.5, 2051–2080). The aforementioned outcomes from the phenology models help to better understand the possible shifts of both trophic levels in the region under future climate, giving insights into their future interactions. [ABSTRACT FROM AUTHOR]

From 2006 to 2008, we studied the natural mortality of olive fly, Bactrocera oleae (Rossi), eggs and larvae as collected in fruit on the tree, in two to five ‘traditional’ olive groves of Trás-os-Montes (north-eastern Portugal), per year. We also studied the fate of 2044 puparia that were buried in the soil from November to May for two seasons, by using exclusion cages to estimate predation. Mortality of eggs inside the fruit was estimated as between 5.4±2.4 and 16.6±6.1%, and as 10.7±2.1 and 100.0% for young larvae. Similarly, the estimated mortality of mature larvae was between 0 and 66.7±33.3%. The highest mortality levels for young larvae could reach 100% during August, and 47.4% during the first fortnight of December, coincident with high temperatures in summer or low temperatures at the end of autumn and early winter. Mortality (winter disappearance) of puparia was estimated at up to 98.5% of the population. Predation of eggs was low, at 0.6±0.3 to 6.3±4.0% in 2006, 0 to 4.1±1.1% in 2007, and 0 to 3.6±3.6% in 2008. Parasitism was insignificant during the study, and only one parasitoid was identified, the eulophid Pnigalio agraules (Walker). We also surveyed entomopathogenic fungi associated with the insect in 12 olive groves, and evaluated three of the latter against larvae, puparia, and adult B. oleae in the laboratory. Of the 15 fungal species identified from immature stages, three were considered to be entomopathogenic (i.e. Cordyceps bassiana, Penicillium corylophilum and Mucor hiemalis). We observed up to 20.0±3.2% and 94.0±2.5% mortality of larvae and puparia, respectively when treated with P. corylophilum and up to 32.5±11.1% of adults when treated with M. hiemalis. [ABSTRACT FROM AUTHOR]

Accurate HIV-2 plasma viral load quantification is crucial for adequate HIV-2 patient management and for the proper conduct of clinical trials and international cohort collaborations. This study compared the homogeneity of HIV-2 RNA quantification when using HIV-2 assays from ACHI(E)V(2E) study sites and either in-house PCR calibration standards or common viral load standards supplied to all collaborators. Each of the 12 participating laboratories quantified blinded HIV-2 samples, using its own HIV-2 viral load assay and standard as well as centrally validated and distributed common HIV-2 group A and B standards (http://www.hiv.lanl.gov/content/sequence/HelpDocs/subtypes-more.html). Aliquots of HIV-2 group A and B strains, each at 2 theoretical concentrations (2.7 and 3.7 log(10) copies/ml), were tested. Intralaboratory, interlaboratory, and overall variances of quantification results obtained with both standards were compared using F tests. For HIV-2 group A quantifications, overall and interlaboratory and/or intralaboratory variances were significantly lower when using the common standard than when using in-house standards at the concentration levels of 2.7 log(10) copies/ml and 3.7 log(10) copies/ml, respectively. For HIV-2 group B, a high heterogeneity was observed and the variances did not differ according to the type of standard used. In this international collaboration, the use of a common standard improved the homogeneity of HIV-2 group A RNA quantification only. The diversity of HIV-2 group B, particularly in PCR primer-binding regions, may explain the heterogeneity in quantification of this strain. Development of a validated HIV-2 viral load assay that accurately quantifies distinct circulating strains is needed.