Evidence map›Paper›PMID 40454365›Full record

ArticleFrontiers in microbiology2025

Comparative analysis of endophytic bacterial localization and microbiome diversity in plant varieties under varied growth conditions through microscopic imaging and sequencing techniques.

Mohd Shadab, Suman Kumar Samanta, Jilmil Baruah, Sujata Deka, Garima Raj, Narayan C Talukdar

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Article in Frontiers in microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Mohd ShadabFaculty of Science, Assam down town University, Guwahati, Assam, India.
Suman Kumar SamantaFaculty of Science, Assam down town University, Guwahati, Assam, India.
Jilmil BaruahLife Sciences Division, Institute of Advanced Study in Science and Technology, Guwahati, Assam, India.
Sujata DekaLife Sciences Division, Institute of Advanced Study in Science and Technology, Guwahati, Assam, India.
Garima RajLife Sciences Division, Institute of Advanced Study in Science and Technology, Guwahati, Assam, India.
Narayan C TalukdarFaculty of Science, Assam down town University, Guwahati, Assam, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Intracellular colonization by endophytic bacteria (EB) is a relatively new and less explored aspect of plant microbiome research. In this study, we investigated the presence and localization of EB in Methodology: Confocal Laser Scanning Microscopy (CLSM) was used to visualized bacterial localization, MitoTracker Deep Red (MDR) was used to confirm non- overlapping mitochondrial staining. Time-lapse imaging was employed to observe bacterial motility. For microbial community profiling next-generation sequencing (NGS) of the 16S rRNA gene was conducted to analyze bacterial diversity and composition. Results: Confocal laser scanning microscopy (CLSM) revealed S9-labelled live bacteria located close to the nucleus in Podali tissues and suspension cultures, while PI selectively stained dead cells. MitoTracker Deep Red (MDR) confirmed that there was no overlap with mitochondrial staining. Interestingly, time-lapse imaging captured the movement of bacteria within the cells, indicating possible bacterial motility. EB were observed in both in vitro and field-grown Podali plants, whereas they were detected only in field-grown Pratap plants. Next-generation sequencing revealed that Podali harbored a much higher bacterial diversity, with 37 bacterial families identified mainly from Conclusion: This study is among the first to report intracellular EB localization in these plant varieties and demonstrates how environmental conditions and growth methods can influence the composition of plant-associated microbiomes.

Indexed as

endophytic bacteriaintracellular colonizationmicrobiome diversitynext-generation sequencingplant-microbe interactions

Identifiers

PMID40454365
PMCPMC12122750

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