Publications by authors named "Shankha Nath"

Article Synopsis
  • In India, 13% of newborns are preterm, contributing to a significant portion (23.4%) of global preterm births.
  • A study was conducted analyzing 600 high vaginal swab samples from pregnant women across all trimesters to compare microbiome differences between those who delivered at term and those with preterm births.
  • The research identified specific microbial signatures linked to term and preterm births and developed a simple dipstick assay for quick identification of preterm-associated bacteria in low-resource settings.
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The role of the upper respiratory tract (URT) microbiome in predicting lung health has been documented in several studies. The dysbiosis in COVID patients has been associated with disease outcomes by modulating the host immune system. However, although it has been known that different SARS-CoV-2 variants manifest distinct transmissibility and mortality rates in human populations, their effect on the composition and diversity of the URT microbiome has not been studied to date.

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Background: Diabetic foot ulcer (DFU) is a major complication of diabetes often impacted by polymicrobial infection in the wound site. Diabetic patients are immunocompromised in nature and hence vulnerable to infection once the skin barrier is breached. Microbiological culture-based methods show that Staphylococcus aureus (SA) is the most frequently isolated bacteria from the DFU wounds.

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Atopic Dermatitis (AD) has been associated with the loss of function (LoF) mutations in Filaggrin () gene and increase in relative abundance of specific microbes in the lesional skin, predominantly in Caucasians. Our study aims to determine, in Indian AD patients, (a) the prevalence of LoF and missense mutations, and (b) the nature and extent of dysbiosis and altered microbial pathways with and without mutations in . AD patients ( = 34) and healthy controls ( = 54) were recruited from India in this study and shotgun sequencing was carried out in a subset of samples with adequate microbiome DNA concentration.

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