Life stage and population density of Plutella xylostella affect the predation behavior of Euborellia annulipes

The diamondback moth (DBM), Plutella xylostella (L.) (Lepidoptera: Plutellidae), is the main pest of brassica crops worldwide. The ringlegged earwig, Euborellia annulipes (Lucas) (Dermaptera: Anisolabididae), has been reported as a potential predator of lepidopteran larvae, including this pest, and may therefore be used for biological control. Knowledge about predator–prey interactions is important to establish pest management strategies. Therefore, the objective of this work was to evaluate the influence of the developmental stage (larva and pupa) and density of P. xylostella on the preference and functional response of E. annulipes adult females. We used choice and no‐choice tests to evaluate the foraging behavior and preference of E. annulipes on DBM life stages and varied prey density to assess the type of functional response of the ringlegged earwig. Larvae were preferred over pupae, and the predator’s functional response was type II for both prey stages. Our results report the potential of E. annulipes as a biocontrol agent of P. xylostella. Understanding their interactions may help in decision‐making and optimization of integrated management strategies.     

Copy number variation (CNV) identification,interpretation, and database from Brazilian patients

Copy number variations (CNVs) constitute an important class of variation in the human genome and the interpretation of their pathogenicity considering different frequencies across populations is still a challenge for geneticists. Since the CNV databases are predominantly composed of European and non-admixed individuals, and Brazilian genetic constitution is admixed and ethnically diverse, diagnostic screenings on Brazilian variants are greatly difficulted by the lack of populational references. We analyzed a clinical sample of 268 Brazilian individuals, including patients with neurodevelopment disorders and/or congenital malformations. The pathogenicity of CNVs was classified according to their gene content and overlap with known benign and pathogenic variants. A total of 1,504 autosomal CNVs (1,207 gains and 297 losses) were classified as benign (92.9%), likely benign (1.6%), VUS (2.6%), likely pathogenic (0.2%) and pathogenic (2.7%). Some of the CNVs were recurrent and with frequency increased in our sample, when compared to populational open resources of structural variants: 14q32.33, 22q11.22, 1q21.1, and 1p36.32 gains. Thus, these highly recurrent CNVs classified as likely benign or VUS were considered non-pathogenic in our Brazilian sample. This study shows the relevance of introducing CNV data from diverse cohorts to improve on the interpretation of clinical impact of genomic variations.