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Although antimicrobial use is a key selector for antimicrobial resistance, recent studies have suggested that the ecological context in which antimicrobials are used might provide important factors for the prediction of the emergence and spread of antimicrobial resistance.

Water-borne viral diseases are a significant concern for public health. In particular, they threaten the health of people and animals in countries that lack proper water treatment facilities. Novel water treatment technology may efficiently improve water quality and prevent the spread of waterborne viral pathogens. Laser-induced graphene (LIG) has been shown to inactivate viruses and bacteria with its photothermal properties, electrochemical reaction, and rough surface texture. However, LIG's activity to prevent virus transmission via contaminated water has not been fully explored. Here, we demonstrated that enveloped and non-enveloped viruses in seawater could be rapidly inactivated by LIG technology. After being activated by 3 V of electricity, the LIG electrodes inactivated both types of viruses spiked in water within 30 min. In addition, the electrolyzed seawater exhibited virucidal effects even after the cessation of the electrical charge. The generation of different oxidants, such as chlorine, chlorine dioxide, and hydrogen peroxide, may play an essential role in the antiviral mechanism of the LIG electrodes. Furthermore, after 10 min of electrolysis, the pH of the seawater dropped from approximately 8–5, which may also have contributed to the virucidal effects of the LIG technology. The virucidal activity of LIG technology highlighted its potential for preventing the spread of viral infections via seawater systems which may have public health implications in areas where seawater is used in the sewage system. It may also have applications in aquaculture, where viral diseases do not have treatments and can cause high fish mortality.

Doente de 83 anos, sexo feminino, com antecedentes de artrite reumatoide há 10 anos, foi internada por infecção do trato urinário com lesão renal aguda em doença renal crónica e insuficiência cardíaca descompensada de etiologia não esclarecida. Ecocardiograma transesofágico (ETE) com vegetação apensa ao folheto posterior da válvula mitral, colocando‐se a hipótese de endocardite infeciosa, tendo‐se iniciado antibioterapia empírica. Repetição de ecocardiograma transesofágico após antibioterapia com manutenção da vegetação referida e menção a outra de menores dimensões, sendo colocada a hipótese de endocardite trombótica não bacteriana. A investigação clínica não evidenciou qualquer processo infecioso. Após hipocoagulação durante dois meses, foi repetido o ecocardiograma transesofágico com desaparecimento das vegetações anteriormente apresentadas.

The Sphingomonas paucimobilis β-glucosidase Bgl1 is encoded by the bgl1 gene, associated with an 1308bp open reading frame. The deduced protein has a potential signal peptide of 24 amino acids in the N-terminal region, and experimental evidence is consistent with the processing and export of the Bgl1 protein through the inner membrane to the periplasmic space. A His6-tagged 44.3kDa protein was over-produced in the cytosol of Escherichia coli from a recombinant plasmid, which contained the S. paucimobilis bgl1 gene lacking the region encoding the putative signal peptide. Mature β-glucosidase Bgl1 is specific for aryl-β-glucosides and has no apparent activity with oligosaccharides derived from cellulose hydrolysis and other saccharides. A structure-based alignment established structural relations between S. paucimobilis Bgl1 and other members of the glycoside hydrolase (GH) family 1 enzymes. At subsite —1, the conserved residues required for catalysis by GH1 enzymes are present in Bgl1 with only minor differences. Major differences are found at subsite +1, the aglycone binding site. This alignment seeded a sequence-based phylogenetic analysis of GH1 enzymes, revealing an absence of horizontal transfer between phyla. Bootstrap analysis supported the definition of subfamilies and revealed that Bgl1, the first characterized β-glucosidase from the genus Sphingomonas, represents a very divergent bacterial subfamily, closer to archaeal subfamilies than to others of bacterial origin.

We studied the clonality of medullary thyroid carcinomas (MTC) from 16 female patients by determining X chromosome inactivation by polymerase chain reaction (PCR) amplification of a CAG repeat in exon 1 of the human androgen-receptor gene. One patient with sporadic medullary thyroid carcinoma (MTC) was homozygous for this microsatellite and was not considered for the assessment of clonality. Sixteen tumor samples from the informative 15 patients were studied: 11 were from sporadic cases and 5 were from familial cases (3 cases of multiple endocrine neoplasia type 2A [MEN 2A]; 1 case of familial medullary thyroid carcinoma [FMTC]). Fourteen tumor samples (10/11 sporadic, 3/4 MEN 2A and 1/1 FMTC) were clearly monoclonal with allelic cleavage ratios between 2.5 and 49.1. Sixty-four percent of these cases (9/14) had the preferential amplification of the shorter allele while 36 percent (5/14) had the preferential amplification of the longer allele. Two frozen tumor samples (1 sporadic and 1 MEN 2A) were polyclonal. However, the corresponding tumor embedded in paraffin from the sporadic case was monoclonal. The other polyclonal tumor was found in the right thyroid lobe of a patient with MEN 2A who had a monoclonal tumor in the left lobe. Our results clearly demonstrate that MTC have a monoclonal origin in the majority of the cases.