Two hundred and five Escherichia coli strains isolated from calves with diarrhea from mid-western Brazil were screened for the presence of virulence factors associated with bovine colibacillosis. One hundred and two (49.8%) of the E. coli strains produced toxins: Shiga toxins 1 (9.7%) and 2 (6.3%), α-hemolysin (9.7%), enterohemolysin (6.8%), Cytotoxic Necrotizing Factors type 1 (0.5%), and type 2 (4.4%), enterotoxins LT-II (8.3%) and STa (3.9%). No strain produced enterotoxin LT-I. Fimbrial adhesins F5 and F17 were produced by 7.3% and 4.8% of the strains, respectivly, and none expressed F41. Seven strains (3.4%) possessed the gene eae and belonged to serotypes O26:H-; O111:H-and O118:H16. These results suggest that calves in Brazil may be an important source of pathogenic E. coli for animals and humans.

The aim of this work was to test 101 strains of E. coli for virulence factors associated with enterotoxigenic and enterohemorrhagic pathotypes of E. coli isolated from diarrheic and non-diarrheic calves. The virulence factors of E. coli Stx1 (Shiga toxin), Stx2, Ehly (Enterohemolysin), the eae gene, LT-II (heat-labile enterotoxin), STa (heat-stable toxin), and adhesins K99 and F41 were detected by PCR. Serogroups were determined by serological methods and Stx production was observed by biological assays in Vero cells. The frequency of the eae gene was higher in isolates from diarrheic calves (35/58, 60.3%) than in non-diarrheic calves (8/43, 18.6%; P < 0.001). The gene for Stx1 occurred at high frequencies in the diarrheic strains (24/58, 41.3%) as well as in non-diarrheic (19/43, 44.2%) ones and all strains that were Stx positive by PCR showed cytotoxicity in Vero cells. Stx2 was found in ten strains, Ehly in eight strains, and LT-II in only two strains. Twenty-eight strains were negative for all of the PCR assays, including for F41 and K99 adhesins. The serogroups O7, O23, O4, O8, O153 and O156 were observed most frequently. Our results show that strains of E. coli isolated from cattle have similar virulence factors genes to strains isolated from cases of diseases in humans and may be a source of potentially pathogenic STEC for humans.KEY WORDS: Escherichia coli, diarrhea, cattle, PCR, shiga toxin. RESUMO DETECÇÃO DE GENES DE VIRULÊNCIA EM AMOSTRAS DE ESCHERICHIA COLI ISOLADAS DE FEZES DE BEZERROS COM E DIARREIA NO BRASIL. O objetivo deste trabalhofoi detectar em 101 amostras de E. coli isoladas de bezerros com e sem diarreia, fatores de virulência associados aos patotipos de E. coli enterotoxigênica e enterohemorrágica. Os fatores de virulência de E. coli Stx1 (Shiga toxina), Stx2, Ehly (Enterohemolisina), o gene eae, LT-II (enterotoxina termolábil), STa (toxina termo-estável), e adesinas K99 e F41 foram detectados por PCR. Os sorogrupos foram determinados por métodos sorológicos e a produção de Stx foi observada através de ensaios biológicos em células Vero. A frequência de detecção do gene eae foi maior nos isolados de bezerros com diarreia (35/58, 60,3%) do que em bezerros saudáveis (8/43, 18,6%; P < 0.001). O gene da toxina Stx1 foi detectado em alta frequência em amostras diarreicas (24/58, 40,3%), bem como em amostras não diarréicas (19/43, 44,2%) e todas as amostras positivas para toxina Stx em PCR mostraram citotoxicidade em células Vero. Stx2 foi encontrada em dez amostras, Ehly em oito amostras, e LT-II em duas amostras. Vinte e seis amostras foram negativas para todos os ensaios de PCR, incluindo para as adesinas F41 e K99. Os sorogrupos O7, O23, O4, O8, O153 e O156 foram detectados com maior frequência. O trabalho mostra que amostras de E. coli isoladas de bovinos apresentam fatores de virulência semelhantes à isolados de casos de doenças em humanos e possivelmente é uma fonte para STEC potencialmente patogênicas para humanos.

No abstract

No abstract

Arboviral diseases are a threat to global public health systems, with recent data suggesting that around 40% of the world’s population is at risk of contracting arboviruses. The use of mosquito repellents is an appropriate strategy to avoid humans coming into contact with vectors transmitting these viruses. However, the cost associated with daily applications of repellents can make their use unfeasible for the low-income populations that most need protection. Therefore, the development of effective formulations offers a way to expand access to this means of individual protection. Consequently, research efforts have focused on formulations with smaller quantities of active agents and sustained release technology, aiming to reduce re-applications, toxicity, and cost. The present study investigates the development of nanostructured lipid carriers (NLCs) loaded with a mixture of the compounds icaridin (synthetic) and geraniol (natural), incorporated in cellulose hydrogel. The NLCs were prepared by the emulsion/solvent evaporation method and were submitted to physicochemical characterization as a function of time (at 0, 15, 30, and 60 days). The prepared system presented an average particle size of 252 ± 5 nm, with encapsulation efficiency of 99% for both of the active compounds. The stability profile revealed that the change of particle size was not significant (p &gt; 0.05), indicating high stability of the system. Rheological characterization of the gels containing NLCs showed that all formulations presented pseudoplastic and thixotropic behavior, providing satisfactory spreadability and long shelf life. Morphological analysis using atomic force microscopy (AFM) revealed the presence of spherical nanoparticles (252 ± 5 nm) in the cellulose gel matrix. Permeation assays showed low fluxes of the active agents through a Strat-M® membrane, with low permeability coefficients, indicating that the repellents would be retained on the surface to which they are applied, rather than permeating the tissue. These findings open perspectives for the use of hybrid formulations consisting of gels containing nanoparticles that incorporate repellents effective against arthropod-borne virus. These systems could potentially provide improvements considering the issues of effectiveness, toxicity, and safety.