Back

Kairos infers in situ horizontal gene transfer in longitudinally sampled microbiomes through microdiversity-aware sequence analysis

Brown, C. L.; Cheung, Y. F.; Song, H.; Snead, D.; Vikesland, P. L.; Pruden, A.; Zhang, L.

2023-10-27 bioinformatics
10.1101/2023.10.24.563791 bioRxiv
Show abstract

Horizontal gene transfer (HGT) occurring within microbiomes is linked to complex environmental and ecological dynamics that are challenging to replicate in controlled settings. Consequently, most extant studies of microbiome HGT are either simplistic experimental settings with tenuous relevance to real microbiomes or correlative studies that assume that HGT potential is a function of the relative abundance of mobile genetic elements (MGEs), the vehicles of HGT. Here we introduce Kairos as a bioinformatic tool deployed in nextflow for detecting HGT events "in situ," i.e., within a microbiome, through analysis of time-series metagenomic sequencing data. The in-situ framework proposed here leverages available metagenomic data from a longitudinally sampled microbiome to assess whether the chronological occurrence of potential donors, recipients, and putatively transferred regions could plausibly have arisen due to HGT over a range of defined time periods. The centerpiece of the Kairos workflow is a novel competitive read alignment method that enables discernment of even very similar genomic sequences, such as those produced by MGE-associated recombination. A key advantage of Kairos is its reliance on assemblies rather than metagenome assembled genomes (MAGs), which avoids systematic exclusion of accessory genes associated with the binning process. In an example test-case of real world data, use of assemblies directly produced a 264-fold increase in the number of antibiotic resistance genes included in the analysis of HGT compared to analysis of MAGs with MetaCHIP. Further, in silico evaluation of contig taxonomy was performed to assess the accuracy of classification for both chromosomally- and MGE-derived sequences, indicating a high degree of accuracy even for conjugative plasmids up to the level of class or order. Thus, Kairos enables the analysis of very recent HGT events, making it suitable for studying rapid prokaryotic adaptation in environmental systems without disturbing the ornate ecological dynamics associated with microbiomes. Current versions of the Kairos workflow are available here: https://github.com/clb21565/kairos.

Matching journals

The top 3 journals account for 50% of the predicted probability mass.

1
Microbiome
139 papers in training set
Top 0.1%
37.4%
2
Nature Communications
4913 papers in training set
Top 18%
10.0%
3
Nature Biotechnology
147 papers in training set
Top 0.9%
8.3%
50% of probability mass above
4
mSystems
361 papers in training set
Top 2%
6.2%
5
Bioinformatics
1061 papers in training set
Top 5%
3.6%
6
Cell Reports Methods
141 papers in training set
Top 0.9%
3.6%
7
Nucleic Acids Research
1128 papers in training set
Top 7%
2.7%
8
Cell Systems
167 papers in training set
Top 5%
2.6%
9
PLOS Computational Biology
1633 papers in training set
Top 15%
1.9%
10
Genome Biology
555 papers in training set
Top 4%
1.7%
11
Frontiers in Microbiology
375 papers in training set
Top 6%
1.6%
12
Bioinformatics Advances
184 papers in training set
Top 3%
1.3%
13
mSphere
281 papers in training set
Top 4%
1.3%
14
Microbial Genomics
204 papers in training set
Top 1%
1.3%
15
Advanced Science
249 papers in training set
Top 14%
1.2%
16
eLife
5422 papers in training set
Top 54%
0.9%
17
ISME Communications
103 papers in training set
Top 2%
0.9%
18
Nature Microbiology
133 papers in training set
Top 4%
0.8%
19
Methods in Ecology and Evolution
160 papers in training set
Top 2%
0.8%
20
PLOS ONE
4510 papers in training set
Top 70%
0.7%
21
Frontiers in Bioinformatics
45 papers in training set
Top 1%
0.6%
22
Nature Computational Science
50 papers in training set
Top 2%
0.6%
23
Metabolites
50 papers in training set
Top 2%
0.6%