Siphoninus finitimus Silvestri (Hemiptera: Aleyrodidae), "mosquita blanca del olivo" en Arica-Chile

In this note are given background on the morphometric differences, in the genitalia of adults and the puparium of aleyrodidae populations associated with olive, pear and pomegranate in the region of Arica-Parinacota, Chile. The significant differences (p < 0.01) found in the dimension, and in the morphology of the structures studied between the different populations of whitelfly that attack to olive trees with regard to the pear and the pomegranate allow to establish that in Arica the whitefly of the olive tree is Siphoninus finitimus Silvestri and that S. phillyreae, it is associated with pear and pomegranate.Se ent regan antecedentes sobr e las diferencias morfométricas en distintas estructuras de adultos y del pupoide de las poblaciones de aleyródidos asociados a olivo, peral y granado en la región de Arica- Parinacota, Chile. Las significativas diferencias (p < 0,01) encontradas en las dimensiones y en la morfología de las estructuras estudiadas entre las distintas poblaciones de mosquitas blancas que atacan a olivos respecto del peral y del granado, permiten establecer que en Arica la mosquita blanca del olivo es Siphoninus finitimus Silvestri y que S. phillyreae, está asociada a peral y granado

Simultaneous Analysis of Multiple Mycobacterium tuberculosis Knockdown Mutants In Vitro and In Vivo

Mycobacterium tuberculosis (Mtb) represents one of the most persistent bacterial threats to human health and new drugs are needed to limit its impact. Conditional knockdown mutants can help validate new drug targets, but the analysis of individual mutants is laborious and time consuming. Here, we describe quantitative DNA tags (qTags) and their use to simultaneously analyze conditional Mtb knockdown mutants that allowed silencing the glyoxylate and methylcitrate cycles (via depletion of isocitrate lyase, ICL), the serine protease Rv3671c, and the core subunits of the mycobacterial proteasome, PrcB and PrcA. The impact of gene silencing in multi-strain cultures was determined by measuring the relative abundance of mutant-specific qTags with real-time PCR. This achieved accurate quantification over a broad range of qTag abundances and depletion of ICL, Rv3671c, or PrcBA resulted in the expected impairment of growth of Mtb with butyrate as the primary carbon source, survival during oxidative stress, acid stress and starvation. The impact of depleting ICL, Rv3671c, or PrcBA in multi-strain mouse infections was analyzed with two approaches. We first measured the relative abundance of mutant-specific qTags in total chromosomal DNA isolated from bacteria that were recovered from infected lungs on agar plates. We then developed a two-step amplification procedure, which allowed us to measure the abundances of individual mutants directly in infected lung tissue. Both strategies confirmed that inactivation of Rv3671c and PrcBA severely reduced persistence of Mtb in mice. The multi-strain infections furthermore suggested that silencing ICL not only prevented growth of Mtb during acute infections but also prevented survival of Mtb during chronic infections. Analyses of the ICL knockdown mutant in single-strain infections confirmed this and demonstrated that silencing of ICL during chronic infections impaired persistence of Mtb to the extent that the pathogen was cleared from the lungs of most mice