Transcultural adaptation of the who oral health questionnaire and its validation in chilean children

Indexación: Scopus.Introduction: The last edition of the WHO "Oral Health Questionnaire for Children" was published in 2013. This is an only-English version, and as such it requires linguistic adaptation and validation to be applied in the Chilean population. Objectives: To translate and adapt the WHO Oral Health Questionnaire for Children to Spanish and validate it in a Chilean population. Methods: A translation and back translation of the original instrument from English to Spanish was carried out by four translators. The questionnaire was self-reported as a pilot test in ten individuals. A sample was subsequently selected for convenience taking into account the population distribution, resulting in a final sample of 103 individuals. The internal consistency was calculated with Cronbach's alpha, criterion validity with Pearson's correlation coefficient and construct validity with Exploratory Factor Analysis. Results: A conceptual and semantic equivalence of the instrument was obtained. Women and men accounted for 43.69% and 56.31% of the sample, respectively. Cronbach's alpha coefficient was 0.62, while criterion validity was slightly positive between the total dimensions and the DMFT (r=0.13, p-value= 0.20). The Exploratory Factor Analysis yielded a total of 11 factors that explain 70% of the variability in the data. Conclusions: The oral health questionnaire has been appropriately adapted to Spanish, having conceptual as well as semantic equivalence to the original version, being reliable and valid to be used in a population of 12-year-old Chilean children. © 2018, Universidad de Concepcion. All rights reserved.http://joralres.com/index.php/JOR/article/view/432/43

On the formation and physical properties of the Intra-Cluster Light in hierarchical galaxy formation models

We study the formation of the Intra-Cluster Light (ICL) using a semi-analytic model of galaxy formation, coupled to merger trees extracted from N-body simulations of groups and clusters. We assume that the ICL forms by (1) stellar stripping of satellite galaxies and (2) relaxation processes that take place during galaxy mergers. The fraction of ICL in groups and clusters predicted by our models ranges between 10 and 40 per cent, with a large halo-to-halo scatter and no halo mass dependence. We note, however, that our predicted ICL fractions depend on the resolution: for a set of simulations with particle mass one order of magnitude larger than that adopted in the high resolution runs used in our study, we find that the predicted ICL fractions are ~30-40 per cent larger than those found in the high resolution runs. On cluster scale, large part of the scatter is due to a range of dynamical histories, while on smaller scale it is driven by individual accretion events and stripping of very massive satellites, $M_{*} \gtrsim 10^{10.5} M_{\odot}$, that we find to be the major contributors to the ICL. The ICL in our models forms very late (below $z\sim 1$), and a fraction varying between 5 and 25 per cent of it has been accreted during the hierarchical growth of haloes. In agreement with recent observational measurements, we find the ICL to be made of stars covering a relatively large range of metallicity, with the bulk of them being sub-solar.Comment: Accepted for Publication in MNRAS, 19 pages, 13 figures, 1 tabl

On extending actions of groups

Problems of dense and closed extension of actions of compact transformation groups are solved. The method developed in the paper is applied to problems of extension of equivariant maps and of construction of equivariant compactifications

Groundwater-dependent ecosystems: Recent insights from satellite and field-based studies

© 2015 Author(s). Groundwater-dependent ecosystems (GDEs) are at risk globally due to unsustainable levels of groundwater extraction, especially in arid and semi-arid regions. In this review, we examine recent developments in the ecohydrology of GDEs with a focus on three knowledge gaps: (1) how do we locate GDEs, (2) how much water is transpired from shallow aquifers by GDEs and (3) what are the responses of GDEs to excessive groundwater extraction? The answers to these questions will determine water allocations that are required to sustain functioning of GDEs and to guide regulations on groundwater extraction to avoid negative impacts on GDEs. We discuss three methods for identifying GDEs: (1) techniques relying on remotely sensed information; (2) fluctuations in depth-to-groundwater that are associated with diurnal variations in transpiration; and (3) stable isotope analysis of water sources in the transpiration stream. We then discuss several methods for estimating rates of GW use, including direct measurement using sapflux or eddy covariance technologies, estimation of a climate wetness index within a Budyko framework, spatial distribution of evapotranspiration (ET) using remote sensing, groundwater modelling and stable isotopes. Remote sensing methods often rely on direct measurements to calibrate the relationship between vegetation indices and ET. ET from GDEs is also determined using hydrologic models of varying complexity, from the White method to fully coupled, variable saturation models. Combinations of methods are typically employed to obtain clearer insight into the components of groundwater discharge in GDEs, such as the proportional importance of transpiration versus evaporation (e.g. using stable isotopes) or from groundwater versus rainwater sources. Groundwater extraction can have severe consequences for the structure and function of GDEs. In the most extreme cases, phreatophytes experience crown dieback and death following groundwater drawdown.We provide a brief review of two case studies of the impacts of GW extraction and then provide an ecosystem-scale, multiple trait, integrated metric of the impact of differences in groundwater depth on the structure and function of eucalypt forests growing along a natural gradient in depth-to-groundwater. We conclude with a discussion of a depth-to-groundwater threshold in this mesic GDE. Beyond this threshold, significant changes occur in ecosystem structure and function

The ability of four strains of Streptococcus uberis to induce clinical mastitis after intramammary inoculation in lactating cows

AIM: To compare the ability of four strains of Streptococcus uberis at two doses to induce clinical mastitis in lactating dairy cows after intramammary inoculation in order to evaluate their usefulness for future experimental infection models. MATERIALS AND METHODS: Four field strains of Streptococcus uberis (26LB, S418, and S523 and SR115) were obtained from cows with clinical mastitis in the Wairarapa and Waikato regions of New Zealand. Twenty-four crossbred lactating cows, with no history of mastitis and absence of major pathogens following culture of milk samples, were randomly allocated to four groups (one per strain) of six cows. Each cow was infused (Day 0) in one quarter with approximately 104 cfu and in the contralateral quarter with approximately 106 cfu of the same strain. The other two quarters remained unchallenged. All four quarters were then inspected for signs of clinical mastitis, by palpation and observation of the foremilk, twice daily from Days 0–9, and composite milk samples were collected from Days 0–8 for analysis of somatic cell counts (SCC). Quarters were treated with penicillin when clinical mastitis was observed. Duplicate milk samples were collected and cultured on presentation of each clinical case and on Day 4 from challenged quarters with no clinical signs. RESULTS: Clinical mastitis was diagnosed in 26/48 (54%) challenged quarters. Challenge with strain S418 resulted in more cases of mastitis (12/12 quarters) than strains SR115 (7/12), 26LB (6/12) or S523 (1/12), and the mean interval from challenge to first diagnosis of mastitis was shorter for S418 than the other strains (p<0.001). The proportion of quarters from which S. uberis could be isolated after challenge was less for strain 26LB (1/6) than SR115 (6/7) (p<0.05), and SCC following challenge was lower for strain S523 than the other strains (p<0.05). CONCLUSIONS: There were significant differences between the strains in the proportion of quarters developing clinical mastitis, the interval to mastitis onset, SCC following challenge and the proportion of clinical cases from which S. uberis could be isolated. These results illustrate the difference in the ability of S. uberis strains to cause mastitis and the severity of the infections caused. CLINICAL RELEVANCE: Experimental challenge models can be used to compare infectivity and pathogenicity of different strains of mastitis-causing bacteria, the efficacy of pharmaceutical products and host-responses in a cost-effective manner.S Notcovich, G deNicolo, NB Williamson, A Grinberg, N Lopez-Villalobos, KR Petrovsk

A family of thermostable fungal cellulases created by structure-guided recombination

SCHEMA structure-guided recombination of 3 fungal class II cellobiohydrolases (CBH II cellulases) has yielded a collection of highly thermostable CBH II chimeras. Twenty-three of 48 genes sampled from the 6,561 possible chimeric sequences were secreted by the Saccharomyces cerevisiae heterologous host in catalytically active form. Five of these chimeras have half-lives of thermal inactivation at 63°C that are greater than the most stable parent, CBH II enzyme from the thermophilic fungus Humicola insolens, which suggests that this chimera collection contains hundreds of highly stable cellulases. Twenty-five new sequences were designed based on mathematical modeling of the thermostabilities for the first set of chimeras. Ten of these sequences were expressed in active form; all 10 retained more activity than H. insolens CBH II after incubation at 63°C. The total of 15 validated thermostable CBH II enzymes have high sequence diversity, differing from their closest natural homologs at up to 63 amino acid positions. Selected purified thermostable chimeras hydrolyzed phosphoric acid swollen cellulose at temperatures 7 to 15°C higher than the parent enzymes. These chimeras also hydrolyzed as much or more cellulose than the parent CBH II enzymes in long-time cellulose hydrolysis assays and had pH/activity profiles as broad, or broader than, the parent enzymes. Generating this group of diverse, thermostable fungal CBH II chimeras is the first step in building an inventory of stable cellulases from which optimized enzyme mixtures for biomass conversion can be formulated