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Caro-Castro, J.

Publications and source records attributed to Caro-Castro, J..

2 recordsLinked to original sources

Klebsiella pneumoniae isolated from the intestines of Tenebrio molitor larvae (Coleoptera: Tenebrionidae) that consume expanded polystyrene

Plastics such as polystyrene are resistant to biodegradation, pollute the environment, and negatively impact the health of living organisms. However, several organisms, such as the larvae of Tenebrio molitor (Coleoptera: Tenebrionidae) and their associated gut microbiome, contribute to its degradation. The aim of this research was to determine the efficiency of expanded polystyrene (EPS) degradation by gut bacteria isolated from T. molitor larvae. To achieve this, a set of EPS-degrading bacteria was selected based on the time required to utilize the polymer as a carbon and energy source. Additionally, EPS degradation efficiency was compared, and the most efficient degrading bacterium was identified at the molecular level. Results showed that 95.13% of the bacteria isolated on nutrient agar and 86.57% of those isolated on McConkey agar were able to grow on EPS, with five bacteria being selected that utilized the polymer after 36 hours of incubation. The efficiency of EPS degradation, expressed as the percentage of weight loss by the degrading bacteria, ranged from 5.29% to 12.68%, with a reduction rate of 0.0005 to 0.0013 g per day and a half-life of 533.15 to 1386.20 days. Finally, 16S rRNA gene analysis identified the bacterium as Klebsiella pneumoniae. Cultivable gut bacteria from T. molitor larvae have demonstrated potential as candidates for EPS degradation, and biotechnological techniques can further enhance the efficiency of the degradation process.

microbiology↗

Evaluation of Loop-Mediated Isothermal Amplification (LAMP) for Rapid Detection of Campylobacter jejuni

In recent years, the worldwide incidence of diarrheal diseases caused by Campylobacter jejuni has been increasing, causing large-scale outbreaks in developing countries, which added to the capacity of the microorganism to cause Guillain-Barre syndrome (GBS), increasing the need for rapid and timely diagnosis to stop and prevent outbreaks. In this study, a loop-mediated isothermal amplification (LAMP) assay based on the cdtC gene was developed and evaluated for the rapid detection of C. jejuni, using 91 strains for the standardization and validation. The LAMP assay was compared to whole-genome sequencing as the gold standard. The LAMP assay for C. jejuni showed a sensitivity of 100% (CI: 90.94 - 100%), a specificity of 100% (CI: 89.56 - 100%), a positive predictive value of 100% (CI: 90.94 - 100%) and a negative predictive value of 100% (CI: 89.56 - 100%). The assay demonstrated strong agreement between the LAMP assay and genomic sequencing (kappa value = 1). The LAMP assay based on the cdtC gene is a method that provides reliable and rapid results, with high sensitivity and specificity for the identification of C. jejuni, and is considered a suitable alternative for the diagnosis of diarrheal infections by this pathogen in low-income countries.

molecular biology↗