Capillary electromigration techniques can be understood as the ones used to separate neutral compounds, solvated ions and ionized species, considering the differentiated migration among them when an electrical field is applied within a capillary column filled with a background electrolyte. Several existing capillary electrophoresis setups provide the possibility of developing reliable quantitative assays of inorganic ions, organic acids, fatty acids, amino acids, carbohydrates, nucleic acids, proteins, hormones, vitamins, macromolecules, and more. Therefore, given the chemical complexity of bodily fluid matrices, capillary electrophoresis (CE) and its variations present themselves as an advantageous strategy for enhancing traditional clinical diagnostic methods and for the development of new ones. The recent advances in the study of the human metabolome associated with technological improvements towards medical applications make CE a very useful and versatile technique for clinical laboratory assays. Within this context, this review has the purpose of presenting some traditional methods used for exams of blood, urine, saliva, feces, and sweat, and how CE can be implemented as a real alternative to enable faster, automated, and cost-effective analysis with a comprehensive perspective that shall result in better diagnostic possibilities for patients, being a powerful tool for helping physicians on the precision medicine achievements. compounds species electrolyte acids carbohydrates proteins hormones vitamins macromolecules more Therefore matrices (CE context blood urine saliva feces sweat faster automated costeffective cost effective patients achievements

ABSTRACT: This study performed a molecular detection and characterization of Giardia duodenalis infecting pigs, goats and sheep in rural and peri-urban communities in the state of Piauí, northeastern Brazil, and proposed phylogenetic relationships among the characterized parasites. We assessed 52 fecal samples from pigs, 13 from goats, and 10 from sheep. A fragment of the β-giardin locus was PCR-amplified and sequenced. Overall, PCR-based G. duodenalis positivity was 11/52 (21.2%) in pigs, 2/13 (15.4%) in goats, and 2/10 (20%) in sheep. Seven out of 15 successfully amplified samples could be sequenced: three from pigs, two from goats, and two from sheep. Parasites from different hosts were found to belong to sub-assemblage AII. The phylogenetic analyses of the original G. duodenalis AII β-giardin sequences obtained from distinct host species and sequences of G. duodenalis recovered from humans available in GenBank suggest that the parasites are genetically related, supporting a local scenario of cross-host transmission.

RESUMO: Este estudo teve como objetivo detectar e caracterizar geneticamente amostras de Giardia duodenalis recuperadas de suínos, caprinos e ovinos em comunidades rurais do estado do Piauí, no nordeste do Brasil, propondo relações filogenéticas entre os parasitas caracterizados. Foram estudadas 52 amostras fecais de suínos, 13 de caprinos e 10 de ovinos. Uma região (560 pb) do lócus codificante da β-giardina foi amplificada por PCR e submetida a sequenciamento nucleotídico. A positividade para G. duodenalis pela PCR foi 11/52 (21,2%) em suínos, 2/13 (15,4%) em caprinos e 2/10 (20%) em ovinos. De 15 amostras amplificadas, sete puderam ser sequenciadas: três obtidas de suínos, dois de caprinos e dois de ovinos. Todas foram caracterizadas como pertencentes à subassemblage AII. Análises filogenéticas de amostras de G. duodenalis AII identificadas em diferentes hospedeiros, incluindo sequências de parasitas recuperadas de humanos e obtidas no GenBank, sugerem que os isolados têm alto grau de homologia. Os resultados apontam para um cenário de transmissão cruzada entre diferentes espécies de hospedeiros.