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BackgroundIn captive breed turtles and tortoises conjunctival disease is common. Our aim was to investigate the bacterial and fungal flora present in the eyes of healthy and pathological chelonians and to compare findings in turtles with those in tortoises.ResultsSamples were taken from the conjunctival sacs of 34, diseased and healthy, chelonians (18 tortoises and 16 turtles) and submitted to bacterial and fungal investigation. All samples showed bacterial growth. Thirteen animals (38%), harboured a single bacterial species as sole isolate and twenty-one animals (62%) harboured more than one species. Detection of multiple bacterial infection was clearly greater in tortoises compared to turtles. Most frequently isolated bacterial species were Bacillus spp. (13 isolates), Staphylococcus xylosus (10 isolates), Sphingomonas paucimobilis (6 isolates), Staphylococcus sciuri and Aeromonas hydrophila/caviae (each 5 isolates), Ochrobactrum anthropi (3 isolates), Citrobacter freundii, Enterobacter cloacae and Pseudomonas luteola (each 2 isolates). Only one isolate of Kocuria varians/rosea, Staphylococcus aureus, Staphylococcus auricularis, Staphylococcus haemolyticus, Staphylococcus lentus, Morganella morganii, Pasteurella multocida, Pasteurella pneumotropica/haemolytica, Proteus spp., Pseudomonas putida, Salmonella enterica ssp. arizonae, Stenotrophomonas maltophilia and Vibrio parahaemolyticus was evidenced. The presence in 8 animals of Mycoplasma spp. and in 1 animal with severe conjunctivitis of Chlamydia spp. was detected by PCR. Candida spp. was also isolated from two healthy animals.ConclusionsA clear predominance of Gram positive isolates in tortoises and Gram negative isolates in turtles was found. However, we cannot ascribe the observed difference to the diversity of animal species, as other factors, including especially different characteristics of the living environments, may play a role. Almost all bacterial species isolated may have clinical significance, mostly as opportunistic pathogens, both for humans and animals. That chelonians are often carrier of bacteria with zoonotic potential is a well-known fact, in particular with regard to Salmonella spp. Therefore, it is not surprising the detection of a strain of Salmonella enterica ssp. arizonae in the eye of one of the animals tested. Worthy of note is the finding of Chlamydia spp. in a severe case of conjunctivitis, though we cannot epidemiologically assess a cause-effect relationship between presence of chlamydia and disease.Electronic supplementary materialThe online version of this article (doi:10.1186/s12917-015-0405-x) contains supplementary material, which is available to authorized users.

Most drugs are delivered as crystalline solids, but some widely used pharmaceutical ingredients cannot be crystallized at ambient conditions: propofol, one of the most widely used anesthetic agents in the world is a liquid. Here we stabilize propofol in a crystalline phase by cocrystallization, and we thoroughly characterize the structural and thermodynamic properties of the new materials. Ternary solubility diagrams of a liquid pharmaceutical ingredient cocrystallized with a solid coformer are presented and analyzed for the first time. It is shown that, when equilibrated with the solid cocrsytal, the concentration of propofol in water is kept constant in a wide range of starting compositions.

The bacterium Pseudomonas aeruginosa (PA) and the yeast Candida albicans (CA) are pathogens that cohabit the mucosa of the respiratory tracts of animals and humans. Their virulence is largely determined by chemical communication driven by quorum sensing systems (QS), and the cross perception of their quorum sensing molecules (QSM) can modulate the prevalence of one microorganism over the other. Aiming to investigate whether some of the protein components dissolved in the mucus layering the respiratory mucosa might interfere with virulence and cross-communication of these, and eventually other microorganisms, ligand binding assays were carried out to test the scavenging potential of the bovine and porcine forms of the Lipocalin odorant binding protein (OBP) for several QSMs (farnesol, and acylhomoserine lactones), and for pyocyanin, a toxin produced by PA. In addition, the direct antimicrobial activity of the OBPs was tested by time kill assay (TKA) against CA, PA and other bacteria and yeasts. The positivity of all the ligand binding assays and the antimicrobial activity determined for CA, and for some of the other microorganisms tested, let hypothesize that vertebrate OBPs might behave as humoral components of innate immunity, active against pathogenic bacteria and fungi. In addition, TKAs with mutants of bovine OBP with structural properties different from those of the native form, and with OBP forms tagged with histidines at the amino terminal, provided information about the mechanisms responsible of their antimicrobial activity and suggested possible applications of the OBPs as alternative or co-adjuvants to antibiotic therapeutic treatments.

Sb2Se3, (ASe) thin-films were deposited as the absorber layers in photovoltaic solar cells using the radio frequency magnetron sputtering deposition technique. Starting from a binary target, high quality crystallization and good vertical alignment of Sb4Se6 ribbons were attained at growth temperatures below 300 °C, and use of an additional selenization process was unnecessary for compensating Se loss. By the structural characterization of films grown on different substrates, a strong dependence of the ribbon orientation on the substrate type was verified. This study clearly confirms that the ribbon alignment is the key factor for enhancing the performance of Sb2Se3 solar cells, in particular the short circuit current density (J sc). A photovoltaic efficiency of 0.24% and a J sc of 5 mA cm−2 were obtained by depositing ASe on Mo, in a CuInGaSe2-like solar cell structure (Al:ZnO/ZnO/CdS/ASe/Mo/Glass), while the J sc was boosted up to 27 mA cm−2 when the ASe solar cells were fabricated in superstrate configuration with an Au/ASe/CdS/FTO architecture, leading to an efficiency of 2.36%.