Abstract

To compare environmental and culture-derived microbial communities, we performed 16S metabarcoding of uncultured samples and their culture-derived bacterial lawns. Microbial communities were obtained from freshwater river samples representative of an anthropization gradient along a river stream. Their culture-derived bacterial lawns were obtained by growing aliquots of the samples on a broad range medium and on two different semi-selective media. The V3–V4 16S rRNA region was amplified and sequenced. The bacterial diversity of water samples decreased from the upper to lower stream sampling sites and, as expected, these differences were mostly suppressed by the culture step. Overall, the diversity of cultured-derived bacterial communities reflected selectivity of each tested medium. Comparison of treatments indicated that the culture selected both detected and rare undetected environmental species. Accurate detection of rare environmental bacteria of the Pectobacterium genus by 16S metabarcoding of the culture lawn was demonstrated. Interestingly, for abundant taxa, such as those of the Pseudomonas genus, the culture/environment ratio varied between sampled sites, indicating the difficulty of comparing cultured-derived taxa abundance between environmental sites. Finally, our study also highlighted media specificity and complementarity: bacterial communities grown on the two selective media, while selecting a small set of specific species, were mostly a subset of the bacterial community observed on the broad range medium.

Highlights

  • Advances in culture independent methodologies have revolutionized our understanding of microbial diversity

  • Sampling of surface water was performed at three sites along the Durance River chosen for their differential altitudes and surrounding land uses and, respectively, called the Upper Durance sampling site (UD) (Upper Durance), Middle Durance sampling site (MD) (Medium Durance), and Lower Durance sampling site (LD) (Lower Durance) (Figure 1)

  • These results suggest that dissolved organic matter (DOM) in the MD site could be less bioavailable than in the UD and LD sites

Read more

Summary

Introduction

Advances in culture independent methodologies have revolutionized our understanding of microbial diversity. The 16S rRNA gene is currently the most commonly used target in the analysis of bacterial diversity [1]. When combined with high throughput sequencing (HTS), the 16S rRNA gene offers the opportunity to rapidly, and efficiently describe a bacterial community in a given environment [2]. The number of bacterial species identified through 16S rRNA gene sequence analysis is far greater than the number of bacterial species identified on a given culture medium. A large number of bacterial groups are only known as operational taxonomic units (OTUs), and their ecological role and physiology are difficult to study. Culturing microorganisms opens the possibility of studying the ecological role and physiology of cultured bacteria including their potential virulence as suspected pathogens. To complete 16S-driven approaches of microbial diversity, culture-based approaches are necessary

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.