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BACKGROUND: Immune response of triatomines plays an important role in the success or failure of transmission of T. cruzi. Studies on parasite-vector interaction have shown the presence of trypanolytic factors and have been observed to be differentially expressed among triatomines, which affects the transmission of some T. cruzi strains or DTUs (Discrete Typing Units). METHODOLOGY/PRINCIPAL FINDINGS: Trypanolytic factors were detected in the hemolymph and saliva of R. prolixus against epimastigotes and trypomastigotes of the Y strain (T. cruzi II). To identify the components of the immune response that could be involved in this lytic activity, a comparative proteomic analysis was carried out, detecting 120 proteins in the hemolymph of R. prolixus and 107 in R. colombiensis. In salivary glands, 1103 proteins were detected in R. prolixus and 853 in R. colombiensis. A higher relative abundance of lysozyme, prolixin, nitrophorins, and serpin as immune response proteins was detected in the hemolymph of R. prolixus. Among the R. prolixus salivary proteins, a higher relative abundance of nitrophorins, lipocalins, and triabins was detected. The higher relative abundance of these immune factors in R. prolixus supports their participation in the lytic activity on Y strain (T. cruzi II), but not on Dm28c (T. cruzi I), which is resistant to lysis by hemolymph and salivary proteins of R. prolixus due to mechanisms of evading oxidative stress caused by immune factors. CONCLUSIONS/SIGNIFICANCE: The lysis resistance observed in the Dm28c strain would be occurring at the DTU I level. T. cruzi I is the DTU with the greatest geographic distribution, from the south of the United States to central Chile and Argentina, a distribution that could be related to resistance to oxidative stress from vectors. Likewise, we can say that lysis against strain Y could occur at the level of DTU II and could be a determinant of the vector inability of these species to transmit T. cruzi II. Future proteomic and transcriptomic studies on vectors and the interactions of the intestinal microbiota with parasites will help to confirm the determinants of successful or failed vector transmission of T. cruzi DTUs in different parts of the Western Hemisphere.

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Chagas is an endemic disease in tropical regions of Latin America, caused by the parasite Trypanosoma cruzi. High intraspecies variability and genome complexity have been challenges to assemble high quality genomes needed for studies in evolution, population genomics, diagnosis and drug development. Here we present a chromosome-level phased assembly of a TcI T. cruzi strain (Dm25). While 29 chromosomes show a large collinearity with the assembly of the Brazil A4 strain, three chromosomes show both large heterozygosity and large divergence, compared to previous assemblies of TcI T. cruzi strains. Nucleotide and protein evolution statistics indicate that T. cruzi Marinkellei separated before the diversification of T. cruzi in the known DTUs. Interchromosomal paralogs of dispersed gene families and histones appeared before but at the same time have a more strict purifying selection, compared to other repeat families. Previously unreported large tandem arrays of protein kinases and histones were identified in this assembly. Over one million variants obtained from Illumina reads aligned to the primary assembly clearly separate the main DTUs. We expect that this new assembly will be a valuable resource for further studies on evolution and functional genomics of Trypanosomatids.

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The primary objective of this study is to develop a novel experimental nanofluid based on surfactant-nanoparticle-brine tuning, subsequently evaluate its performance in the laboratory under reservoir conditions, then upscale the design for a field trial of the nanotechnology-enhanced surfactant injection process. Two different mixtures of commercial anionic surfactants (SA and SB) were characterized by their critical micelle concentration (CMC), density, and Fourier transform infrared (FTIR) spectra. Two types of commercial nanoparticles (CNA and CNB) were utilized, and they were characterized by SBET, FTIR spectra, hydrodynamic mean sizes (dp50), isoelectric points (pHIEP), and functional groups. The evaluation of both surfactant-nanoparticle systems demonstrated that the best performance was obtained with a total dissolved solid (TDS) of 0.75% with the SA surfactant and the CNA nanoparticles. A nanofluid formulation with 100 mg·L-1 of CNA provided suitable interfacial tension (IFT) values between 0.18 and 0.15 mN·m-1 for a surfactant dosage range of 750-1000 mg·L-1. Results obtained from adsorption tests indicated that the surfactant adsorption on the rock would be reduced by at least 40% under static and dynamic conditions due to nanoparticle addition. Moreover, during core flooding tests, it was observed that the recovery factor was increased by 22% for the nanofluid usage in contrast with a 17% increase with only the use of the surfactant. These results are related to the estimated capillary number of 3 × 10-5, 3 × 10-4, and 5 × 10-4 for the brine, the surfactant, and the nanofluid, respectively, as well as to the reduction in the surfactant adsorption on the rock which enhances the efficiency of the process. The field trial application was performed with the same nanofluid formulation in the two different injection patterns of a Colombian oil field and represented the first application worldwide of nanoparticles/nanofluids in enhanced oil recovery (EOR) processes. The cumulative incremental oil production was nearly 30,035 Bbls for both injection patterns by May 19, 2020. The decline rate was estimated through an exponential model to be -0.104 month-1 before the intervention, to -0.016 month-1 after the nanofluid injection. The pilot was designed based on a production increment of 3.5%, which was successfully surpassed with this field test with an increment of 27.3%. This application is the first, worldwide, to demonstrate surfactant flooding assisted by nanotechnology in a chemical enhanced oil recovery (CEOR) process in a low interfacial tension region.

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The main objective of this study is to evaluate the effect of the textural properties and surface chemical nature of silica nanoparticles obtained from different synthesis routes and silicon precursors, on their interactions with asphaltenes and further viscosity reduction of heavy crude oil (HO). Four different SiO2 nanoparticles were used, namely, commercial fumed silica nanoparticles (CSNs) and three in-house-synthesized nanoparticles (named based on the silicon source) modifying the silicon precursor: sodium silicate (SNSS), tetraethylorthosilicate (TEOS) (SNT), and rice husk (SNRH). The nanomaterials were characterized through dynamic light scattering (DLS), transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy, N2 physisorption (S BET), atomic force microscopy (AFM), and X-ray photoelectron (XP) spectroscopy (XPS). The adsorption of asphaltenes over the different nanoparticles was evaluated at a concentration of 1000 mg·L-1 in toluene. The asphaltene-nanoparticle interactions are closely related to several textural properties, such as roughness, surface area, and hydrodynamic diameter, as well as the surface chemical nature of the materials. The results in the textural characterization exhibited that the sizes of the nanoparticles from TEM ranged between 6.9 and 11.5 nm. Nevertheless, the standard deviation of the measurements showed that the sizes are statistically similar. Inversely, the hydrodynamic diameter changed, affecting the surface silanol group's availability due to a hindering effect on functional groups as the hydrodynamic size of the material increased. The rheological measurements were performed at a fixed nanoparticle dosage of 1000 mg·L-1 and showed that the trend of the degree of viscosity reduction (DVR) was CSN > SNT > SNSS > SNRH with the highest value yielding at 30%. The results of DVR are in accordance with the nanoparticles' adsorptive capacity as higher values were obtained with the material that leads to a higher amount of adsorbed asphaltenes. Also, the oxygen amount related to silanol groups, estimated by the XPS analysis, showed a direct relation regarding adsorption capacity and further HO viscosity reduction.

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Para el control de Rhipicephalus microplus, garrapata común de los bovinos, se usan compuestos piretroides entre otros. El estudio de los mecanismos de resistencia hacia piretroides en esta garrapata ha demostrado la presencia de mutaciones en el gen del canal del sodio, sitio blanco del acaricida. El presente estudio tuvo como objetivo principal detectar el polimorfismo T2134A en el gen del canal del sodio que ha sido relacionado con resistencia a piretroides en individuos portadores. Para ello se recolectaron 182 garrapatas R. microplus en dos fincas con historial de resistencia a este tipo de acaricidas y se sometieron a una prueba de inmersión de hembras en una solución de cipermetrina preparada a la dosis recomendada para uso en campo, obteniendo seis individuos susceptibles, 92 resistentes y 84 medianamente resistentes. Se extrajo el ADN de todos los especímenes utilizando QIAamp DNA Mini Kit® y se procesó por PCR convencional empleando cebadores alelo específicos para amplificar un segmento del dominio IIIS6 del gen del canal del sodio. Los amplicones resultantes se detectaron por electroforesis en geles de agarosa al 2 % teñidos con GelRed® y se visualizaron con luz ultravioleta. De igual manera se efectuó el secuenciamiento de 20 muestras obtenidas en los tres fenotipos susceptible, medianamente resistente y resistente y las secuencias resultantes fueron alineadas mediante el programa Mega 7 y comparadas con secuencias almacenadas en el GenBank®. Los análisis mostraron que la población de R. microplus estudiada no presentaba la mutación esperada sino una mutación diferente en el sitio 2 134. Se observó la sustitución de una timina pero por una citosina, T2134C, que a la traducción genera el cambio de una fenilalanina por una leucina, a diferencia de la mutación previamente identificada, que genera el cambio de una fenilalanina por una isoleucina. Esto demuestra la presencia de un polimorfismo que no ha sido reportado en esta especie de garrapata y que generaría un nuevo marcador molecular de resistencia a piretroides para poblaciones de este ácaro.

For the control of Rhipicephalus microplus, cattle tick, pyrethroid compounds are used among others. The study of the mechanisms of resistance to pyrethroids in this tick has shown the presence of mutations in the sodium channel gen, the target site of acaricide. The main objective of the present study was to detect the T2134A polymorphism in the sodium channel gene that has been related to pyrethroid resistance in carriers. To do so, 182 ticks R. microplus were collected in two farms with a history of resistance to this type of acaricide and were subjected to a dip test of females in a cypermethrin solution prepared at the recommended dose for field use, obtaining six susceptible, 92 resistants and 84 moderately resistants. DNA is extracted from all specimens using QIAamp DNA Mini Kit® and processed by conventional PCR using allele-specific primers to amplify a segment of domain IIIS6 of the sodium channel gene. The resulting amplicons were detected by electrophoresis in 2 % agarose gels stained with GelRed® and visualized with ultraviolet light. In the same way, 20 samples were sequenced of the three susceptible phenotypes, moderately resistant and resistant and the resulting sequences were aligned through the Mega 7 program and compared with the sequences stored in the GenBank®. The information of the population of R. Microplus studied did not show the expected mutation but a different mutation in the site 2134. We also observed the substitution of a thymine but by a cytosine, T2134C, which changes to a phenylalanine by a leucine, a difference from the previously identified mutation, that the change from phenylalanine to isoleucine. This shows the presence of a polymorphism that has not been reported in this species of tick and that would generate a new molecular marker of pyrethroid resistance for populations of this mite.

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OBJECTIVE: The aim of this study was to measure the impact of osteoarthritis on the functioning and health status of individuals living in a low-income urban community in Mexico. METHODS: We conducted a cross-sectional, community-based study from December 2014 to November 2015, using the Community Oriented Program for Control of Rheumatic Diseases methodology to identify cases of musculoskeletal disease in a sample of adults older than 18 years in Pueblo Nuevo, Apodaca, Mexico. Two rheumatologists confirmed all cases of osteoarthritis (OA) using predefined criteria. Functioning was evaluated through (a) self-report of difficulty doing personal care, work, and leisure activities; (b) the modified Stanford Health Assessment Questionnaire-Disability Index; and (c) the Timed Up and Go test. Health status was evaluated using the EuroQoL 5 Dimensions. Statistical analyses were performed using χ tests and logistic regression models. RESULTS: Four hundred thirty-nine individuals with a mean age of 45.2 years were included, and 83 cases of OA were confirmed. The presence of OA was not significantly associated with having difficulties to do personal care, work, or leisure activities, but it was significantly associated with a higher Health Assessment Questionnaire-Disability Index score, longer time to complete the Timed Up and Go, and lower health status. CONCLUSIONS: Osteoarthritis is associated with having higher disability and worse health status in the community studied. A disability paradox was detected as some individuals perceived disability for doing standard activities but did not present disability performing their real-life activities. This underlies the importance of addressing the mental dimension during the management of this population.

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Leptospira interrogans has been identified to cause leptospirosis, a widespread zoonotic disease that has been identified in domestic and wild animals. This work analyzed kidneys from two species of wild rodents from the state of Campeche, Mexico. Analyses were made by PCR using specific primers for detection of Leptospira interrogans DNA. The rodent species that tested positive were Heteromys gaumeri and Ototylomys phyllotis, both of which are new hosts for the bacteria in Southeastern Mexico. These records provide new insights into the disease's transmission that should be studied carefully in order to identify other potential host species, including humans, which are at risk of becoming infected if they are in contact with infected wildlife.

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Parasites are important in the management of the health of primate populations. We examined 36 fecal samples from Peruvian red uakari monkeys (Cacajao calvus ucayalii) collected from wild animals in the northeastern Peruvian Amazon. Samples were positive for helminth infection. Nematodes egg: Strongyloididae, Trypanoxyuris sp., Spirurid, and a cestode egg were identified.

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Human ether à-go-go 1 (Eag1) potassium channels are potential tumor markers and therapeutic targets for several types of malignancies, including cervical cancer. Estrogens and human papilloma virus oncogenes regulate Eag1 gene expression, suggesting that Eag1 may already be present in pre-malignant lesions. Therefore, Eag1 could be used as an early marker and/or a potential risk indicator for cervical cancer. Consequently, we studied Eag1 protein expression by immunochemistry in cervical cancer cell lines, normal keratinocytes, cervical cytologies from intraepithelial lesions, biopsies from cervical intraepithelial neoplasias (CIN 1, 2 and 3) and in normal smears from patients taking or not taking estrogens. Two hundred and eighty-six samples obtained by liquid-based cytology and fifteen CIN biopsies were studied. We observed Eag1 protein expression in the cervical cancer cell lines, as opposed to normal keratinocytes. Eag1 was found in 67% of the cervical cytologies from low-grade intra-epithelial lesions and in 92% of the samples from high-grade intraepithelial lesions, but only in 27% of the normal samples. Noteworthy, morphologically normal cells obtained from dysplastic samples also exhibited Eag1 expression. In CIN biopsies we found that the higher the grade of the lesion, the broader the Eag1 protein distribution. Almost 50% of the normal patients taking estrogens displayed Eag1 expression. We suggest Eag1 as a potential marker of cervical dysplasia and a risk indicator for developing cervical lesions in patients taking estrogens. Eag1 detection in cervical cancer screening programs should help to improve early diagnosis and decrease mortality rates from this disease.

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