Background: Monitoring trends in multiple infections with SARS-CoV-2, following several pandemic waves, provides insight into the biological characteristics of new variants, but also necessitates methods to understand the risk of multiple reinfections.
Objectives: We generalised a catalytic model designed to detect increases in the risk of SARS-CoV-2 reinfection, to assess the population-level risk of multiple reinfections.
Methods: The catalytic model assumes the risk of reinfection is proportional to observed infections and uses a Bayesian approach to fit model parameters to the number of nth infections among individuals that occur at least 90 days after a previous infection. Using a posterior draw from the fitted model parameters, a 95% projection interval of daily nth infections is calculated under the assumption of a constant nth infection hazard coefficient. An additional model parameter was incorporated for the increased reinfection risk detected during the Omicron wave. The generalised model's performance was then assessed using simulation-based validation.
Key Findings: No additional increase in the risk of third infection was detected after the increase detected during the Omicron wave. Using simulation-based validation, we show that the model can successfully detect increases in the risk of third infections under different scenarios.
Limitations: Even though the generalised model is intended to detect the risk of nth infections, it is validated specifically for third infections, with its applicability for four or more infections being unconfirmed. Furthermore, the method's sensitivity to low counts of nth infections, limits application in settings with small epidemics, limited testing coverage or early in an outbreak.
Conclusions: The catalytic model was successfully adapted to detect increases in the risk of nth infections, enhancing our capacity to identify future changes in the risk of nth infections by SARS-CoV-2 or other similar pathogens.
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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0315476 | PLOS |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11694959 | PMC |
PLoS One
January 2025
South African DSI-NRF Centre of Excellence in Epidemiological Modelling and Analysis (SACEMA), Stellenbosch University, Stellenbosch, South Africa.
Background: Monitoring trends in multiple infections with SARS-CoV-2, following several pandemic waves, provides insight into the biological characteristics of new variants, but also necessitates methods to understand the risk of multiple reinfections.
Objectives: We generalised a catalytic model designed to detect increases in the risk of SARS-CoV-2 reinfection, to assess the population-level risk of multiple reinfections.
Methods: The catalytic model assumes the risk of reinfection is proportional to observed infections and uses a Bayesian approach to fit model parameters to the number of nth infections among individuals that occur at least 90 days after a previous infection.
Acta Pharm Sin B
September 2024
NHC Key Laboratory of Systems Biology of Pathogens, National Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Viruses often manipulate ubiquitination pathways to facilitate their replication and pathogenesis. CUL2 known as the substrate receptor of cullin-2 RING E3 ligase, is bound by SARS-CoV-2 ORF10 to increase its E3 ligase activity, leading to degradation of IFT46, a protein component of the intraflagellar transport (IFT) complex B. This results in dysfunctional cilia, which explains certain symptoms that are specific to COVID-19.
View Article and Find Full Text PDFAntimicrob Agents Chemother
October 2024
Laboratory for Drug Discovery and Disease Research, Shionogi & Co., Ltd., Toyonaka, Japan.
Treatment of infection is challenging due to its intrinsic and acquired antibiotic resistance. As the number of current therapeutic options for infections is limited, developing novel treatments against the pathogen is an urgent clinical priority. The suppression of virulence of could be a new therapeutic option, and the type III secretion system (T3SS), which enables the bacteria to translocate various kinds of toxins into host cells and inhibits cellular functions, is considered as one possible target.
View Article and Find Full Text PDFBiofilm
December 2024
Department of Microbiology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
biofilm is correlated with pathogenesis, antibiotic resistance, and relapsing cases of melioidosis, leading to challenges in clinical management. There is increasing interest in employing biofilm dispersal agents as adjunctive treatments for biofilm-associated infections. Methionine (Met) has shown promise as an anti-biofilm agent by inducing bacterial DNase production, resulting in the degradation of extracellular DNA (eDNA) and dispersion of bacterial biofilm.
View Article and Find Full Text PDFPLoS Comput Biol
March 2024
Institute of ecology and environmental sciences of Paris (iEES-Paris, UMR 7618), Sorbonne Université, CNRS, UPEC, IRD, INRAE, Paris, France.
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