Molecular analysis of enteropathogenic Escherichia coli (EPEC) isolates from healthy food-producing animals and humans with diarrhoea.

Enteropathogenic Escherichia coli (EPEC) is a pathogen associated with acute diarrhoea in humans. To determine whether EPEC isolated from healthy food-producing animals possesses the same virulence gene repertoire as EPEC isolated from human with diarrhoea, we compared six typical EPEC (tEPEC) and 20 atypical EPEC (aEPEC) from humans with diarrhoea and 42 aEPEC from healthy animals (swine, sheep and buffaloes), using pulsed-field gel electrophoresis (PFGE), virulence markers, serotyping and subtyping of eae and tir genes. We found that human and animal isolates shared virulence genes, including nleB, nleE and nleF, which were associated with human diarrhoea. Serogroups and serotypes identified in isolates of food-producing animals such as O26:H11, O128:H2, O76:H7, O103, O108, O111 and O145, have previously been implicated in human disease. The subtypes eae and tir were also shared between human and animal isolates, being eae-γ1 and eae-ß1 the most prevalent in both groups, while the most common tir subtypes were α and ß. Despite PFGE analysis demonstrating that EPEC strains are heterogeneous and there was no prevalent clone identified, EPEC isolated from humans and food-producing animals shared some characteristics, such as virulence genes associated with human diarrhoea, indicating that food-producing animals could play a role as reservoirs for those genes.

A traceless linker for aliphatic amines that rapidly and quantitatively fragments after reduction.

Reduction sensitive linkers (RSLs) have the potential to transform the field of drug delivery due to their ease of use and selective cleavage in intracellular environments. However, despite their compelling attributes, developing reduction sensitive self-immolative linkers for aliphatic amines has been challenging due to their poor leaving group ability and high pK a values. Here a traceless self-immolative linker composed of a dithiol-ethyl carbonate connected to a benzyl carbamate (DEC) is presented, which can modify aliphatic amines and release them rapidly and quantitatively after disulfide reduction. DEC was able to reversibly modify the lysine residues on CRISPR-Cas9 with either PEG, the cell penetrating peptide Arg10, or donor DNA, and generated Cas9 conjugates with significantly improved biological properties. In particular, Cas9-DEC-PEG was able to diffuse through brain tissue significantly better than unmodified Cas9, making it a more suitable candidate for genome editing in animals. Furthermore, conjugation of Arg10 to Cas9 with DEC was able to generate a self-delivering Cas9 RNP that could edit cells without transfection reagents. Finally, conjugation of donor DNA to Cas9 with DEC increased the homology directed DNA repair (HDR) rate of the Cas9 RNP by 50% in HEK 293T cell line. We anticipate that DEC will have numerous applications in biotechnology, given the ubiquitous presence of aliphatic amines on small molecule and protein therapeutics.

Shigatoxigenic and atypical enteropathogenic Escherichia coli in fish for human consumption

ABSTRACT Shigatoxigenic and enteropathogenic Escherichia coli with virulence and multidrug resistance profile were isolated from Nile tilapia. This study finding is of great importance to public health because they help understand this pathogen epidemiology in fish and demonstrate how these animals can transmit E. coli related diseases to humans.

Shigatoxigenic and atypical enteropathogenic Escherichia coli in fish for human consumption.

Shigatoxigenic and enteropathogenic Escherichia coli with virulence and multidrug resistance profile were isolated from Nile tilapia. This study finding is of great importance to public health because they help understand this pathogen epidemiology in fish and demonstrate how these animals can transmit E. coli related diseases to humans.

Characterization and antimicrobial resistance patterns of Escherichia coli isolated from feces of healthy broiler chickens / Padrões da caracterização e resistência a antimicrobianos de Escherichia coli isolada das fezes de frangos de corte saudáveis

Avian pathogenic Escherichia coli (APEC) strains are isolated from lesions of poultry presenting colibacillosis, which is a disease that causes either systemic or localized clinical signs. Such strains share many characteristics with E. coli strains that cause extra-intestinal illness in humans. There is not a consensus on how to define the APEC pathotype with regard to the presence of virulence traits. On the other hand, in the past few years, five minimal predictors for APEC detection were proposed. The E. coli isolates in this work were tested through polymerase chain reaction (PCR) to the five proposed minimal predictors and cva C. The strains presenting them were categorized as potential APEC. The APEC and non-APEC categories showed high resistance (> 50%) to cephalotin, erythromycin, streptomycin, sulphametoxazol/trimethoprim, ampicillin, and amoxicillin. Potential APEC strains were significantly more resistant to cephalotin (p < 0.05) and neomcycin (p < 0.01) than non-APEC. These latter were significantly more resistant to tetracycline (p < 0.01) than the potential APEC strains. These results demonstrate that feces of poultry present E. coli strains with resistant features, showing or not the potential of causing colibacillosis in poultry. Because APEC and extra-intestinal illness in humans may be similar, these resistant strains are of interest to public health.(AU)

Cepas de Escherichia coli patogênica para aves (APEC) estão isoladas das lesões de frangos com colibacilose, uma doença que causa sinais clínicos sistêmicos ou localizados. As APEC compartilham algumas características com as cepas de Escherichia coli que produzem doenças extraintestinais nos seres humanos. Ainda não há um consenso sobre a definição de patotipos das cepas de APEC, no que diz respeito à presença das características de virulência. Entretanto, nos últimos anos, foram definidos cinco indicadores mínimos para a identificação de patotipos das cepas de APEC. Os isolados de E. coli utilizados neste trabalho foram testados por meio de reação em cadeia de polimerase (PCR) para os cinco indicadores mínimos e para cva C. Os isolados que possuíam os cinco indicadores mínimos foram definidos como potenciais cepas de APEC. As categorias APEC e não APEC apresentaram alta resistência (> 50%) à cefalotina, eritromicina, estreptomicina, sulfametoxazol mais trimetoprim, ampicilina e amoxicilina. Possíveis cepas de APEC foram significativamente mais resistentes à cefalotina (p < 0,05) e neomicina (p < 0,01) do que as cepas não-APEC. Estas foram significativamente mais resistentes à tetraciclina (p < 0,01) do que as possíveis cepas de APEC. Esses resultados demonstram que as fezes dos frangos de corte albergam cepas de E.coli com características de resistência, apresentando ou não potencialidade de causar colibacilose. Em função das características de similaridade entre APEC e doenças extraintestinais nos seres humanos, estas cepas resistentes são de interesse à saúde pública.(AU)

Detection of Shiga toxigenic (STEC) and enteropathogenic (EPEC) Escherichia coli in dairy buffalo.

Enteropathogenic (EPEC) and Shiga toxigenic (STEC) Escherichia coli are among the bacteria most associated with enteric diseases in man. The aims of this study were to determine the prevalence of STEC and EPEC in dairy buffalo and then characterize these isolates genetically. To determine the prevalence of these bacteria, samples were collected from the feces and milk of buffaloes. In total, 256 samples were collected in 3 samplings, of which 76 samples tested positive for either the stx1, stx2 or eae genes or a combination thereof. From the positive samples, 22 STEC and 11 atypical EPEC (aEPEC) isolates were obtained. The isolates showed 23 different genetic profiles. No profile was very frequent in STEC isolates. On the other hand, the profile eae+, ehxA+, iha+, efa1+, toxB+, paa+, lpfAO113+ was found in 45% of the aEPEC isolates. In addition to stx1, stx2 and eae, the genes ehxA, efa1, saa, lpfAO113, lpfAO157/OI-141, lpfAO157/OI-154, toxB and iha were present in the isolates. Serogroup O26 was found in 26% of the aEPEC. Other serogroups detected include O87, O145, O176 and O179. The isolates were sensitive to almost all drugs tested and some isolates shared the same fingerprint patterns by enterobacterial repetitive intergenic consensus sequence-PCR (ERIC-PCR). The results suggest that, besides major reservoirs of STEC, buffaloes are also aEPEC reservoirs. The detection of a serogroup (O26), and putative virulence genes (efa1 ehxA, paa and lpfAO113), previously associated with aEPEC isolated from humans with diarrhea in aEPEC from buffaloes should be studied further.

Shiga toxigenic and atypical enteropathogenic Escherichia coli in the feces and carcasses of slaughtered pigs.

Escherichia coli is a pathogen of major importance in swine and public health. To determine the prevalence of Shiga toxigenic E. coli (STEC) and enteropathogenic E. coli (EPEC), samples were collected from the feces and carcasses of swines. In total, 441 samples were collected in four samplings, of which 141 samples tested positive for either the stx1, stx2, and/or eae genes. From the positive samples, one STEC and 15 atypical EPEC (aEPEC) isolates were obtained, and all originated from the same sampling. In addition to eae, lpfA(O157/OI-141), ehxA, toxB, and lpfA(O113) were present in the aEPEC isolates. The only stx2-containing isolate carried stx2e and belonged to serotype O103:HNT. Resistance to four or more antimicrobials was found in almost half of the isolates, and some isolates shared the same fingerprint patterns by enterobacterial repetitive intergenic consensus-polymerase chain reaction (ERIC-PCR). The presence of certain virulence genes and the high level of resistance to antimicrobials, as well as the possible fecal contamination of carcasses showed that some of the isolates are of public health concern.