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Many sampling protocols have been established to successfully retrieve human DNA from archaeological remains, however the systematic detection of ancient pathogens remains challenging. Here, we present a first assessment of the intra-bone variability of metagenomic composition in human skeletal remains and its effect on the sampling success for Mycobacterium tuberculosis (MTB) and human endogenous DNA. For this purpose, four bone samples from published peer-reviewed studies with PCR-based evidence for ancient MTB DNA were selected. Two bone samples of a Neolithic individual from Halberstadt, Germany and two ribs of two 18th-century Hungarian church mummies were sampled at multiple locations for equal amounts, followed by DNA extraction and library construction. Shotgun sequencing data was generated for taxonomic profiling as well as quantitative and qualitative evaluation of MTB and human endogenous DNA. Despite low variance in microbial diversity within and across samples, intra-bone variability of up to 36.45- and 62.88-fold for authentic ancient MTB and human reads, respectively, was detected. This study demonstrates the variable sampling success for MTB and human endogenous DNA within single skeletal samples despite relatively consistent microbial composition and highlights how a multisampling approach can facilitate the detection of hotspots with highly concentrated pathogen and human endogenous DNA.
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http://dx.doi.org/10.1016/j.tube.2023.102392 | DOI Listing |
PLoS Pathog
September 2025
Centre for Molecular Inflammation Research (CEMIR), Norwegian University of, Science and Technology (NTNU), Trondheim, Norway.
Drosophila melanogaster (Drosophila) is one of the most extensively studied animal models we have, with a broad, advanced, and organized research community. Yet, Drosophila has barely been exploited to understand the underlying mechanisms of mycobacterial infections, which cause some of the deadliest infectious diseases humans are currently battling. Here, we identified mycobacterial genes required for the pathogen's growth during Drosophila infection.
View Article and Find Full Text PDFAlveolar macrophages (AMs) are the first immune cells to encounter Mycobacterium tuberculosis (Mtb) in the lungs, but they frequently fail to eliminate this causative agent of tuberculosis (TB), allowing Mtb to persist or replicate. Interstitial macrophages (IMs) are recruited to restrict Mtb growth and limit immune evasion. While IMs have been implicated in the control of acute Mtb infection, their role during latent tuberculosis infection (LTBI) has not yet been explored.
View Article and Find Full Text PDFDiabetologia
September 2025
Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.
Aims/hypothesis: The aim of this study was to investigate whether basic fibroblast growth factor (bFGF) can restore the proliferation and migration capacities of adipose-derived stem cells (ASCs), which are impaired by type 2 diabetes, and improve vascular remodelling.
Methods: ASCs obtained from individuals with or without diabetes were cultured with 10 ng/ml bFGF for 9 days. The ASCs were phenotypically characterised and functionally tested for proliferation capacity.
Stud Health Technol Inform
September 2025
MOLIT Institute, Heilbronn, Germany.
Introduction: In the context of precision oncology, patients often have complex conditions that require treatment based on specific and up-to-date knowledge of guidelines and research. This entails considerable effort when preparing such cases for molecular tumor boards (MTBs). Large language models (LLMs) could help to lower this burden if they could provide such information quickly and precisely on demand.
View Article and Find Full Text PDFMath Biosci Eng
July 2025
Departamento de Matemáticas y Estadística, Universidad de Nariño, Calle 18-Cra 50, Pasto 520002, Colombia.
Tuberculosis stands as the leading cause of death worldwide, driven by infection from a single bacterial agent, and has been recognized as a global public health concern by the World Health Organization. Recent studies highlight that the innate immune response has a central role in controlling the initial spread of (Mtb) within the host, and triggers adaptive immune response. We developed and analyzed a model examining the interactions among macrophages, innate cells, and Mtb to determine whether the infection is controlled by the innate immune response or whether a specific adaptive response is triggered.
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