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Background: Flow-Diverter (FD) porosity has been pointed as a critical factor in the occlusion of cerebral aneurysms after treatment. Objective: Verification and Validation of computational models in terms of predictive capacity, relating FD porosity and occlusion after cerebral aneurysms treatment. Methods: Sixty-four aneurysms, with pre-treatment and follow-up images, were considered. Patient demographics and aneurysm morphological information were collected. The computational simulation provided by ANKYRAS provided FD porosity, expansion, and mesh angle. FD occlusion was assessed and recorded from follow-up images. Multiple regression Logit and analysis of covariance (ANCOVA) models were used to model the data with both categorical and continuous models. Results: Occlusion of the aneurysm after 12 months was affected by aneurysm morphology but not by FD mesh morphology. A Time-To-Occlusion (TTO) of 6.92 months on average was observed with an SE of 0.24 months in the aneurysm population surveyed. TTO was estimated with statistical significance from the resulting model for the data examined and was capable of explaining 92% of the data variation. Conclusions: Porosity was found to have the most correction power when assessing TTO, proving its importance in the process of aneurysm occlusion. Still, further Verification and Validation (V&V) of treatment simulation in more extensive, multi-center, and randomized databases is required.

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Cattle maintaining a low proviral load (LPL) status after bovine leukaemia virus (BLV) infection have been recognized as BLV controllers and non-transmitters to uninfected cattle in experimental and natural conditions. LPL has been associated with host genetics, mainly with the BoLA class II DRB3 gene. The aim of this work was to study the kinetics of BLV and the host response in Holstein calves carrying different BoLA-DRB3 alleles. Twenty BLV-free calves were inoculated with infected lymphocytes. Two calves were maintained uninfected as controls. Proviral load, total leukocyte and lymphocyte counts, anti-BLVgp51 titres and BLVp24 expression levels were determined in blood samples at various times post-inoculation. The viral load peaked at 30 days post-inoculation (dpi) in all animals. The viral load decreased steadily from seroconversion (38 dpi) to the end of the study (178 dpi) in calves carrying a resistance-associated allele (*0902), while it was maintained at elevated levels in calves with *1501 or neutral alleles after seroconversion. Leukocyte and lymphocyte counts and BLVp24 expression did not significantly differ between genetic groups. Animals with < 20 proviral copies/30 ng of DNA at 178 dpi or < 200 proviral copies at 88 dpi were classified as LPL, while calves with levels above these limits were considered to have high proviral load (HPL) profiles. All six calves with the *1501 allele progressed to HPL, while LPL was attained by 6/7 (86%) and 2/6 (33%) of the calves with the *0902 and neutral alleles, respectively. One calf with both *0902 and *1501 developed LPL. This is the first report of experimental induction of the LPL profile in cattle.

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The critical factor in restoration and conservation of urban streams and their catchments is the human population, however the most of studies of urban ecosystems do not present social descriptors as concrete variables of analysis. The objective of this study is to perform an environmental diagnosis from a social-ecological perspective by considering both ecological and urban development descriptors of an urban basin. We selected 12 sampling sites of the Langueyú upper basin where social and ecological descriptors were determined. We arranged sampling sites according to their physicochemical characteristics (pre-urban, urban and post-urban sites). An ecological index was defined from habitat and biological descriptors: vegetation cover, richness and total density of invertebrates and organic matter. The index determined that urban and post-urban sites showed similar characteristics, and pre-urban sites presented the best habitat and biological conditions. An urbanisation index was defined from urban development descriptors: distance to the stormwater drainage network, number of industries, distance to a house without sewage, impervious surface and housing density. The results showed that the pre-urban and post-urban sites share a greater similarity in relation to the urban descriptors but with different impact in ecological quality. The headwaters in the hills (pre-urban zone) still presents a very good ecological condition (although threatened by urbanisation and tourism); however, once it crosses the dense urban area, no >5 km distance, the environmental degradation is alarming. We were able to determine that the structural measures associated with greater urbanisation, added to illegally connected sewer pipes and illegally industrial connections, produce the ecological degradation of the stream. This environmental diagnosis allowed us a deep understanding of the urbanisation impact on the ecological integrity of an urban stream in a developing country which, like many others, doesn't have monitoring programs or an integrated vision of water resources.

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The objective of this work was assessing the sensitivity of leeches to several water quality attributes in lowlands streams. We used occupancy modelling that account explicitly for detectability, to estimate the influence of four variables (dissolved oxygen, 5-days biochemicals oxygen demand, conductivity, and dissolved inorganic nitrogen) affecting nine species. We described the sensitivity as a change in the occupancy along the range of water quality attributes. We found at least one species of Helobdella in 81% of sites and Helobdella, as genus, was detected along the entire gradient of each attribute. However, differences in the sensitivity were observed between species. For example, if we analyse the sensitivity of the genus Helobdella to dissolved oxygen, we can say that it is very tolerant. However, if we analyse the response to dissolved oxygen of each one of the species of Helobdella, we will realize that H. michaelseni, and H. simplex showed a high occupancy at high levels of dissolved oxygen; while H. hyalina and H. triserialis lineata showed high occupancy at low levels. Describe the sensitivity of the species in terms of occupancy, offers a new methodology to understand how the species behave along a stressor gradient.

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High proviral load (HPL) profile in bovine leukemia virus infected animals poses increased risk of transmission, and development of HPL or low proviral load (LPL) profile may be attributed to host genetics. Genetic resistance and susceptibility has been mapped to the Major Histocompatibility Complex class II DRB3 gene (BoLA DRB3). The aim of this work was to determine the effect of Mycobacterium bovis infection on certain virological and host immunological parameters of BLV experimental infection. Twenty-six Argentinian Holstein calves carrying the resistance-associated marker allele BoLA DRB3*0902, susceptibility-associated marker allele BoLA DRB3*1501, or neutral BoLA DRB3 alleles, exposed to M. bovis were used. Twenty calves were inoculated with BLV, three were naturally infected and other three were BLV-negative. Seven from twenty six (27%) of the animals resulted positive to the PPD test. The proviral load, absolute leukocyte and lymphocyte counts, time to seroconversion, antibody titer against BLV, and viral antigen expression in vitro at various times post inoculation were determined and compared between PPD+ and PPD- animals. From a total of 23 BLV positive animals (naturally and experimentally infected), 13 (56.5%) developed HPL, and 10 (43.5%) developed LPL. None of the investigated parameters were affected by infection with M. bovis. We concluded that the ability of cattle carrying resistance-associated marker to control BLV and to progress towards a LPL phenotype was not altered by M. bovis co-infection.

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Environmental samples were taken from ground, cattle water troughs, and feeders from a dairy farm with different STEC prevalence between animal categories (weaning calves, rearing calves, and dairy cows). Overall, 23 % of samples were positive for stx genes, stx(2) being the most prevalent type. Isolates were analyzed by PCR monoplex to confirm generic E. coli and by two multiplex PCR to investigate the presence of stx(1), stx(2), eae, saa, ehxA, and other putative virulence genes encoded in STEC plasmids: katP, espP, subA, and stcE. The toxin genes were subtyped and the strains were serotyped. The ground and the environment of the rearing calves were the sites with the highest number of STEC-positive samples; however, cattle water troughs and the environment of cows were the places with the greater chance of finding stx(2EDL933) which is a subtype associated with serious disease in humans. Several non-O157 STEC serotypes were detected. The serotypes O8:H19; O26:H11; O26:H-; O118:H2; O141:H-; and O145:H- have been asociated with human illness. Furthermore, the emergent pathogen STEC O157:H- (stx(1)-ehxA-eae) was detected in the environment of the weaning calves. These results emphasize the risk that represents the environment as source of STEC, a potential pathogen for human and suggest the importance of developing control methods designed to prevent contaminations of food products and transmission from animal to person.

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