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Biology subjects

Cavadino, A.

Publications and source records attributed to Cavadino, A..

2 recordsLinked to original sources

Real-world testing of the durability claims of a commercially available spray-on surface biocide

Self-disinfecting biocidal surfaces have been proposed as a solution to prevent infections caused by the transmission of microorganisms from frequently touched surfaces in hospitals and other settings. For example, surface anchoring quaternary ammonium salt (SAQAS)-based biocides are purported to maintain their antimicrobial potency for up to 30 days and are available as spray-on formulations. We tested the 30-day potency claim of a commercially available spray-on SAQAS-based biocide ("SAQAS-A") under "real-world" conditions in a microbiology laboratory where regular cleaning is routine. To do this, we determined the background microbial burden on high-traffic floor areas, routinely used bench areas, frequently touched handles, and glass surfaces for 30 days before and after applying SAQAS-A. Experiments were repeated three times, and data was analysed using two Generalised Linear Mixed Models. We observed that for >80% of bench samples, the number of viable bacteria recovered was below the highest acceptable level of 2.5 CFU/cm2, with minimal reduction in CFU recovery observed after SAQAS-A treatment. In contrast, the number of floor and glass samples in which the microbial burden exceeded 2.5 CFU/cm2 was greater after biocide application (12.7 and 73%, respectively) than before (4.8 and 37%, respectively). Analysis of all data using two statistical models confirmed that the application of SAQAS-A had no antimicrobial effect. In conclusion, our results indicate that SAQAS-A was ineffective in preventing surface contamination over 30 days in a real-world scenario where routine cleaning occurs. ImportanceWe tested the claim that a commercially available spray-on biocide could protect surfaces from microbial contamination for 30 days. In the presence of routine disinfection, we found that spray-on applications of the surface anchoring quaternary ammonium salt-based biocide did not protect frequently touched surfaces in a working microbiology research lab for up to 30 days. Our data show that users of this type of product should be aware of the limitations of manufacturers claims of "continued protection", and manufacturers should consider formulations that more reliably attach to surfaces. Similarly, regulatory and consumer protection agencies should provide clear guidance for companies wishing to make durability and longevity claims for biocidal surface applications.

microbiology↗

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Birth weight (BW) variation is influenced by fetal and maternal genetic and non-genetic factors, and has been reproducibly associated with future cardio-metabolic health outcomes. These associations have been proposed to reflect the lifelong consequences of an adverse intrauterine environment. In earlier work, we demonstrated that much of the negative correlation between BW and adult cardio-metabolic traits could instead be attributable to shared genetic effects. However, that work and other previous studies did not systematically distinguish the direct effects of an individuals own genotype on BW and subsequent disease risk from indirect effects of their mothers correlated genotype, mediated by the intrauterine environment. Here, we describe expanded genome-wide association analyses of own BW (n=321,223) and offspring BW (n=230,069 mothers), which identified 278 independent association signals influencing BW (214 novel). We used structural equation modelling to decompose the contributions of direct fetal and indirect maternal genetic influences on BW, implicating fetal- and maternal-specific mechanisms. We used Mendelian randomization to explore the causal relationships between factors influencing BW through fetal or maternal routes, for example, glycemic traits and blood pressure. Direct fetal genotype effects dominate the shared genetic contribution to the association between lower BW and higher type 2 diabetes risk, whereas the relationship between lower BW and higher later blood pressure (BP) is driven by a combination of indirect maternal and direct fetal genetic effects: indirect effects of maternal BP-raising genotypes act to reduce offspring BW, but only direct fetal genotype effects (once inherited) increase the offsprings later BP. Instrumental variable analysis using maternal BW-lowering genotypes to proxy for an adverse intrauterine environment provided no evidence that it causally raises offspring BP. In successfully separating fetal from maternal genetic effects, this work represents an important advance in genetic studies of perinatal outcomes, and shows that the association between lower BW and higher adult BP is attributable to genetic effects, and not to intrauterine programming.

genetics↗