Bacterial vaginosis (BV) is the most common vaginal infection in women of reproductive age and has been associated with serious health complications, mainly in pregnant women. It is characterized by a decrease in the number of species in the healthy vaginal microbiota and an overgrowth of strict and facultative anaerobic bacteria that develop a polymicrobial biofilm. Despite over 60 years of research investigating BV, its etiology is not fully understood. spp. is a crucial microorganism that contributes to the formation of the biofilm and the development of BV, but the role of other BV-associated bacteria is not clear. Nevertheless, (previously known as ) is a highly specific species for BV, and co-colonization with is thought to be a very specific diagnostic marker. The diagnosis of BV still presents some limitations, since currently used methods often fail to accurately detect BV. This work aims to develop a novel peptide nucleic acid (PNA) probe targeting . This probe was further validated in a multiplex assay, which included a specific PNA probe, as a possible method for diagnosis of BV, and was compared with quantification by qPCR. The new PNA probe showed excellent sensitivity and specificity and could discriminate - biofilms, confirming the potential to be used for the detection of BV-associated pathogens.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637528 | PMC |
http://dx.doi.org/10.3389/fcimb.2021.779376 | DOI Listing |
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