RESUMEN
There have been numerous changes in the nomenclature of species of Dendroctonus. The case of Dendroctonus parallelocollis Chapuis and Dendroctonus approximatus Dietz has been particularly noteworthy. These bark beetles colonize pine trees but are not aggressive species. The high morphological similarity, their overlapping geographical distribution, and the limited knowledge of these species have resulted in taxonomic confusion. The aim of the present study was to assess morphological characters reported in the literature and to scrutinize new characters that might be useful for the separation of these species. We evaluated 26 morphological attributes and performed geometric morphometrics analysis of the antenna, pronotum, spermatheca, and seminal rod to test if the variations in the shape of these structures allow the recognition of additional discrete characters to differentiate them. Our results show that five double-state characters of external morphology are useful to identify these species, and the shape of antenna, spermatheca, and seminal rod.
Asunto(s)
Gorgojos/anatomía & histología , Gorgojos/clasificación , Animales , Femenino , Guatemala , Honduras , Masculino , MéxicoRESUMEN
The distribution range of the western pine beetle Dendroctonus brevicomis LeConte (Coleoptera: Curculionidae) is supported only by scattered records in the northern parts of Mexico, suggesting that its populations may be marginal and rare in this region. In this study, we review the geographical distribution of D. brevicomis in northern Mexico and perform a geometric morphometric analysis of seminal rod shape to evaluate its reliability for identifying this species with respect to other members of the Dendroctonus frontalis Zimmermann (Coleoptera: Curculionidae) complex. Our results provide 30 new records, with 26 distributed in the Sierra Madre Occidental and 4 in the Sierra Madre Oriental. These records extend the known distribution range of D. brevicomis to Durango and Tamaulipas states in northern Mexico. Furthermore, we find high geographic variation in size and shape of the seminal rod, with conspicous differences among individuals from different geographical regions, namely west and east of the Great Basin and between mountain systems in Mexico.
Asunto(s)
Distribución Animal , Gorgojos/clasificación , Gorgojos/fisiología , Animales , Masculino , México , Pinus , Gorgojos/anatomía & histologíaRESUMEN
BACKGROUND: Helicobacter pylori (H. pylori) is associated with gastroduodenal diseases. Virulence of clinical isolates is related to clinical outcome. Moreover, with microdiversity studies in clinical isolates from a single patient, but from a different origin (antrum or corpus), it is possible to demonstrate that there are simultaneous mixed infections. AIMS: To genotype H. pylori strains with multiplex PCR, according to their clinical virulence, and in this manner know the frequency of each genotype and relate it to clinical outcome in order to prevent the development of severe diseases. METHODS: A total of 210 patients with gastric alterations were studied. Virulence classification of H. pylori strains was carried out with multiplex PCR and 127 strains were identified as H. pylori by PCR (glmM and cagE). Genotype and clinical outcome were evaluated with the Fisher's exact test. In addition, RAPD-PCR was performed as a fingerprinting method to analyze mixed infections. RESULTS: The cagA, vacAs1, and vacAm1 genes were detected in all the clinical isolates. Strains were classified as: type i, 40.15% (51/127); type ii, 22.04% (28/127); and type iii, 28.4% (36/127), but two new different genotypes were also detected: (1) babA2+, cagA+, vacAs1+, 6.29% (8/127) and (2) babA2+, cagA-, vacAs2/m2+, 3.14% (4/127). The cagE gene was detected in type i strains. CONCLUSIONS: The Fisher's exact test did not support a significant association between clinical outcome and genotype. The main circulating genotypes in the Mexican population studied were: cagA+, vacAs1, and vacAm1. Multiplex PCR can be used as a screening test for H. pylori strains. Furthermore, the cagE gene is a good marker for identifying cag-PAI positive strains.