Insect chemosensory systems, such as smell and taste, are mediated by chemosensory receptor and non-receptor protein families. In the last decade, many studies have focused on discovering these families in Tephritidae species of agricultural importance. However, to date, there is no information on the Mexican fruit fly Anastrepha ludens Loew, a priority pest of quarantine importance in Mexico and other countries. This work represents the first effort to identify, classify and characterize the six chemosensory gene families by analyzing two head transcriptomes of sexually immature and mature adults of A. ludens from laboratory-reared and wild populations, respectively. We identified 120 chemosensory genes encoding 31 Odorant-Binding Proteins (OBPs), 5 Chemosensory Proteins (CSPs), 2 Sensory Neuron Membrane Proteins (SNMPs), 42 Odorant Receptors (ORs), 17 Ionotropic Receptors (IRs), and 23 Gustatory Receptors (GRs). The 120 described chemosensory proteins of the Mexican fruit fly significantly contribute to the genetic databases of insects, particularly dipterans. Except for some OBPs, this work reports for the first time the repertoire of olfactory proteins for one species of the genus Anastrepha, which provides a further basis for studying the olfactory system in the family Tephritidae, one of the most important for its economic and social impact worldwide.

The pepper weevil Anthonomus eugenii is one of the most damaging pests to the pepper crop. To offer alternative management strategies to insecticides, several studies have identified the semiochemicals that are involved in the pepper weevil’s aggregation and mating behavior; however, there is no information on its perireceptor molecular mechanism, to date. In this study, bioinformatics tools were used to functionally annotate and characterize the A. eugenii head transcriptome and their probable coding proteins. We identified twenty-two transcripts belonging to families related to chemosensory processes, seventeen corresponding to odorant-binding proteins (OBP), and six to chemosensory proteins (CSP). All results matched with closely related Coleoptera: Curculionidae homologous proteins. Likewise, twelve OBP and three CSP transcripts were experimentally characterized by RT-PCR in different female and male tissues. The results by sex and tissue display the different expression patterns of the AeugOBPs and AeugCSPs; some are present in both sexes and all tissues, while others show expressions with higher specificity, which suggests diverse physiological functions in addition to chemo-detection. This study provides information to support the understanding of odor perception in the pepper weevil.

The Mediterranean fruit fly (Ceratitis capitata Wiedemann, medfly) is a highly invasive agricultural pest with a considerable threat to global fruit production. Its olfactory system, mediated by odorant-binding proteins (OBPs), plays a fundamental role in key behaviors such as host localization, mate recognition, and oviposition site selection. This study presents a comprehensive homologation and systematic reclassification of CcapOBPs through comparative genomic analyses with the model organism Drosophila melanogaster Meigen and 8 Tephritidae species (tribes Dacini, Toxotrypanini, and Trypetini), supported by Bayesian phylogenetic inference. By integrating 2 genome assemblies (Ccap_2.1 and EGII-3.2.1), additional GenBank entries, a de novo head transcriptome from sexually mature wild males, and comparative analyses with D. melanogaster orthologs, we consolidated 156 candidate sequences into a homologized repertoire of 48 CcapOBPs. RT-PCR validation of 21 representative CcapObps confirmed their expression in male heads and highlighted how the de novo transcriptome recovered genes missing from individual genome assemblies, demonstrating consistency across all data sources. Phylogenetic reconstruction of CcapOBP and tephritid species revealed clustering patterns consistent with the established evolutionary relationships within the family, enabling the identification of ortholog genes, lineage-specific diversification events, gene duplications, expansions in C. capitata. However, limitations were identified in datasets for the other fruit fly species, and the need for nomenclature adjustments based on chromosomal localization. This study represents the most comprehensive OBP homologation in medfly to date, providing a robust framework for understanding the molecular evolution of chemosensory systems in Tephritidae and supporting the development of species-specific and environmentally sustainable pest management strategies.

The round-headed pine beetle Dendroctonus adjunctus, whose dispersion and colonization behaviors are linked to a communication system mediated by semiochemicals, is one of the five most critical primary pests in forest ecosystems in Mexico. This study provides the first head transcriptome analysis of D. adjunctus and the identification of the nonreceptor olfactory genes involved in the perception of odors. De novo assembly yielded 44,420 unigenes, and GO annotations were similar to those of antennal transcriptomes of other beetle species, which reflect metabolic processes related to smell and signal transduction. A total of 36 new transcripts of nonreceptor olfactory genes were identified, of which 27 encode OBPs, 7 encode CSPs, and 2 encode SNMP candidates, which were subsequently compared to homologous proteins from other bark beetles and Coleoptera species by searching for sequence motifs and performing phylogenetic analyses. Our study provides information on genes encoding nonreceptor proteins in D. adjunctus and broadens the knowledge of olfactory genes in Coleoptera and bark beetle species, and will help to understand colonization and aggregation behaviors for the development of tools that complement management strategies.

In the indigenous communities of central Veracruz, herds of creole sheep have been established and managed through traditional practices of crossing, but their genetic characteristics have never been examined in order to evaluate their state of endogamy, and to help the management programs to protect this genetic resource. The objective of the present study was to characterize the genetic diversity of three populations of creole sheep managed by indigenous communities in the central region of Veracruz, Mexico. Indigenous family producers of creole sheep were located and blood samples taken from 90 individual sheep from the municipalities of Tehuipango, Astacinga and Tlaquilpa, Veracruz. In the laboratory, the genomic DNA was extracted and genetic diversity characterized using four microsatellites (ILSTS11, ILSTS5, SRCRSP9 and OarFCB128) amplified by PCR and visualized on polyacrylamide gels. The four microsatellites were highly informative (PIC = 85%) and presented values of 0.6 to 0.81 of heterozygosity, with an average number of 16 alleles. According to the Hardy–Weinberg equilibrium model, three of the loci were not significant (p < 0.05), presumably this means that they do not deviate significantly from H–W predictions and there was slight genetic differentiation (F_ST = 0.025), along with a slight decrease in homozygotes (F_IS = −0.021). According to the analysis of variance, 99% of the total variation was hosted at the individual level. It is concluded that the three creole sheep populations still present genetic diversity at the four loci and non-random pairings have occurred.

La identificación precisa del complejo gallina ciega es complicada y no se cuenta con claves dicotómicas de las especies potencialmente nocivas, presentes en la zona de producción de caña de azúcar que permita una rápida identificación de éstas especies. Por lo que se propuso elaborar una clave dicotómica ilustrada de machos con los caracteres diagnósticos de las especies de Phyllophaga presentes en Morelos. Se realizaron colectas con trampas tipo embudo con luz blanca dentro del cultivo de caña de azúcar y capturas manuales en zonas aledañas, en el periodo marzo 2013 a julio 2015. La separación a subgéneros, grupos, y complejos de especies fue principalmente con base en las características de las mesotibias, uñas, cobertura setífera, y segmentos antenales, en tanto que la morfología de la genitalia permitió la separación de especies. De cada especie se realizó una lámina con las fotografías de los caracteres diagnósticos. Finalmente, se elaboró una clave dicotómica ilustrada para los machos del género Phyllophaga encontrados en la zona. Accurate identification of the grub species complex potentially harmful to sugarcane is complicated, and lacks a dichotomous key for a rapid identification. A dichotomous key for Phyllophaga male species of Morelos is presented. Adults were hand-collected and in funnel traps in sugarcane fields and surrounding areas between March 2013 and July 2015. The separation of subgenres, groups, and species complexes was based in the characteristics of mesotibias, nails, setifera coverage, and antennal segments, while the morphology of the genitalia allowed for the separation of species. Photographs of the diagnostic characteristics of each species are presented. An illustrated dichotomous key for Phyllophaga males found in Morelos was developed.