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Chandola, U.

Publications and source records attributed to Chandola, U..

2 recordsLinked to original sources

Combined in vivo and in situ genome-resolved metagenomics reveals novel symbiotic nitrogen fixing interactions between non-cyanobacterial diazotrophs and microalgae

BackgroundNon-cyanobacteria diazotrophs (NCDs) were shown to dominate in surface waters shifting the long-held paradigm of cyanobacteria dominance and raising fundamental questions on how these putative heterotrophic bacteria thrive in sunlit oceans. The absence of laboratory cultures of these bacteria significantly limits our ability to understand their behavior in natural environments and, consequently, their contribution to the marine nitrogen cycle. ResultsHere, we used a multidisciplinary approach and report an unprecedented finding in the diatom Phaeodactylum tricornutum (Pt) of NCDs in the phycosphere or the pelagic community sustaining its survival in the absence of bioavailable nitrogen. We sequenced the bacterial metacommunity associated with Pt and assembled several bacterial genomes, identifying multiple NCDs from the Rhizobiales order, including Bradyrhizobium, Mesorhizobium, Georhizobium and Methylobacterium. We demonstrated the nitrogen-fixing ability of PtNCDs through in silico identification of nitrogen fixation genes, or by using PCR, acetylene reduction, or 15N incorporation. We showed the wide occurrence of this type of interactions with the isolation of NCDs from other microalgae, their identification in the environment, and their predicted associations with photosynthetic microalgae. ConclusionsOur study underscores the importance of microalgae interactions with NCDs to permit and support nitrogen fixation. This work provides a unique model Pt-NCDs to study the ecology of this interaction advancing our understanding of the key drivers of global marine nitrogen fixation.

microbiology↗

High-risk human papillomavirus in oral cavity squamous cell carcinoma

PurposeThe prevalence of human papillomavirus (HPV) in oral cavity squamous cell carcinoma (OSCC) varies significantly based on assay sensitivity and patient geography. Accurate detection is essential to understand the role of HPV in disease prognosis and management of patients with OSCC.\n\nMethodsWe generated and integrated data from multiple analytes (HPV DNA, HPV RNA, and p16), assays (immunohistochemistry, PCR, qPCR and digital PCR) and molecular changes (somatic mutations and DNA methylation) from 153 OSCC patients to correlate p16 expression, HPV DNA, and HPV RNA with HPV incidence and patient survival.\n\nResultsHigh prevalence (33-58%) of HPV16/18 DNA did not correlate with the presence of transcriptionally active viral genomes (15%) in tumors. Eighteen percent of the tumors were p16 positive. and only 6% were both HPV DNA and RNA positive. Most tumors with relatively high-copy HPV DNA, and/or HPV RNA, but not with HPV DNA alone (irrespective of copy number), were wild-type for TP53 and CASP8 genes. In our study, p16 protein, HPV DNA and HPV RNA, either alone or in combinations, did not correlate with patient survival. Nine HPV-associated genes stratified the virus +ve from the -ve tumor group with high confidence (p<0.008) when HPV DNA copy number and/or HPV RNA were considered to define HPV positivity and not HPV DNA alone irrespective of their copy number (p < 0.2).\n\nConclusionsIn OSCC, the presence of both HPV RNA and p16 are rare. HPV DNA alone is not an accurate measure of HPV positivity and therefore not informative. Moreover, HPV DNA, RNA or p16 dont correlate with outcome.

cancer biology↗