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The quality of air conditioning and ventilation systems in laboratories is vital to ensure optimum health of the users and guarantee the accuracy of experiments conducted. Moreover, recent studies show that the average quality of air conditioning and ventilation systems in labs can pose health risks to occupants. The study aims to examine the relationship between physical parameters and microbial pollutants in research laboratories' indoor air quality (IAQ) by quantifying and characterising the bacteria and fungi in the indoor environment of research laboratories using the settle plate method; whereby our Petri dishes containing media are exposed to the air for sample collection. This study was conducted over the course of 3 ​day ​at three different research laboratories: Virology Lab (VL), Genetic Lab (GL), and Aquatic Lab (AL). The physical parameters such as air temperature, humidity and carbon dioxide were measured using FLUKE 975 air meter, whereas the microbial parameters were assessed using the settle plate method with Tryptone Soya agar and Sabouraud Dextrose agar for the bacterial and fungal count, respectively. Our results showed that the high temperature and relative humidity, exceeded the standard threshold for temperature (23–26 ​°C) and relative humidity (40–70%) set by the Department of Occupational Safety and Health (DOSH). Additionally, because of poor air conditioning and ventilation system maintenance, there were high total bacterial counts in GL (CFU/m³ 234.34 ​± ​30.93) and total fungal counts in VL (CFU/m³ 589.34 ​± ​53.03). We also showed that the most commonly isolated bacteria and fungi in research laboratories were Staphylococcus spp. (72.2%) and Cladosporium spp. (76.7%). In conclusion, we reported that there was a correlation between the physical parameters and microbial pollutants in the research laboratories. Therefore, regular monitoring of indoor air quality (IAQ) parameters and maintenance of the air conditioning and ventilation system should be carried out to ensure a good and safe indoor environment in research laboratories. [ABSTRACT FROM AUTHOR]

The bifunctional alcohol/aldehyde dehydrogenase (AdhE) comprises both an N‐terminal aldehyde dehydrogenase (AldDH) and a C‐terminal alcohol dehydrogenase (ADH). In vivo, full‐length AdhE oligomerizes into long oligomers known as spirosomes. However, structural analysis of AdhE is challenging owing to the heterogeneity of the spirosomes. Therefore, the domains of AdhE are best characterized separately. Here, the structure of ADH from the pathogenic Escherichia coli O157:H7 was determined to 1.65 Å resolution. The dimeric crystal structure was confirmed in solution by small‐angle X‐ray scattering. [ABSTRACT FROM AUTHOR]

Genomic surveillance is crucial for tracking emergence and spread of novel variants of pathogens, such as SARS-CoV-2, to inform public health interventions and to enforce control measures. However, in some settings especially in low- and middle- income counties, where sequencing platforms are limited, only certain patients get to be selected for sequencing surveillance. Here, we show that patients with multiple comorbidities potentially harbour SARS-CoV-2 with higher mutation rates and thus deserve more attention for genomic surveillance. The relationship between the patient comorbidities, and type of amino acid mutations was assessed. Correlation analysis showed that there was a significant tendency for mutations to occur within the ORF1a region for patients with higher number of comorbidities. Frequency analysis of the amino acid substitution within ORF1a showed that nsp3 P822L of the PLpro protease was one of the highest occurring mutations. Using molecular dynamics, we simulated that the P822L mutation in PLpro represents a system with lower Root Mean Square Deviation (RMSD) fluctuations, and consistent Radius of gyration (Rg), Solvent Accessible Surface Area (SASA) values—indicate a much stabler protein than the wildtype. The outcome of this study will help determine the relationship between the clinical status of a patient and the mutations of the infecting SARS-CoV-2 virus. [ABSTRACT FROM AUTHOR]