Strain-resolved microbiome sequencing reveals mobile elements that drive bacterial competition on a clinical timescale

• Published in: Genome medicine 2020-05, Vol.12 (1), p.50-50, Article 50
• Main Authors: Zlitni, Soumaya, Bishara, Alex, Moss, Eli L, Tkachenko, Ekaterina, Kang, Joyce B, Culver, Rebecca N, Andermann, Tessa M, Weng, Ziming, Wood, Christina, Handy, Christine, Ji, Hanlee P, Batzoglou, Serafim, Bhatt, Ami S
• Format: Article
• Language: English
• Subjects: Anti-infective agents; Anti-Infective Agents - pharmacology; Antibiotic resistance; Antibiotics; Antimicrobial agents; Azacitidine - pharmacology; Azithromycin - pharmacology; Bacteria; Bacteria - classification; Bacteria - drug effects; Bacteria - genetics; Bacteria - isolation & purification; Case studies; Ciprofloxacin - pharmacology; Comparative analysis; Deoxyribonucleic acid; Diet; Digestive system; DNA; DNA sequencing; DNA, Bacterial; Drug resistance; Ethanol; Feces - microbiology; Gastrointestinal Microbiome - drug effects; Gastrointestinal Microbiome - genetics; Genes; Genetic diversity; Genome, Bacterial; Genomes; Genomics; Gut microbiome; Hematopoietic Stem Cell Transplantation; Humans; Immunosuppressive agents; Immunosuppressive Agents - pharmacology; Intestinal microflora; Library collections; Male; Medical research; Metagenome; Metagenomics; Microbial drug resistance; Microbiomes; Microbiota; Middle Aged; Mutation; Myelodysplastic Syndromes - microbiology; Myelodysplastic Syndromes - therapy; Patients; Population; Primary Myelofibrosis - microbiology; Primary Myelofibrosis - therapy; Read cloud assembly; Ribonucleic acid; RNA; RNA sequencing; RNA-Seq; Sequence Analysis, DNA; Sequencing; Strain diversity; Strains (organisms); Transplantation; Whole genome sequencing
• ISSN: 1756-994X; 1756-994X
• DOI: 10.1186/s13073-020-00747-0

Populations of closely related microbial strains can be simultaneously present in bacterial communities such as the human gut microbiome. We recently developed a de novo genome assembly approach that uses read cloud sequencing to provide more complete microbial genome drafts, enabling precise differentiation and tracking of strain-level dynamics across metagenomic samples. In this case study, we present a proof-of-concept using read cloud sequencing to describe bacterial strain diversity in the gut microbiome of one hematopoietic cell transplantation patient over a 2-month time course and highlight temporal strain variation of gut microbes during therapy. The treatment was accompanied by diet changes and administration of multiple immunosuppressants and antimicrobials. We conducted short-read and read cloud metagenomic sequencing of DNA extracted from four longitudinal stool samples collected during the course of treatment of one hematopoietic cell transplantation (HCT) patient. After applying read cloud metagenomic assembly to discover strain-level sequence variants in these complex microbiome samples, we performed metatranscriptomic analysis to investigate differential expression of antibiotic resistance genes. Finally, we validated predictions from the genomic and metatranscriptomic findings through in vitro antibiotic susceptibility testing and whole genome sequencing of isolates derived from the patient stool samples. During the 56-day longitudinal time course that was studied, the patient's microbiome was profoundly disrupted and eventually dominated by Bacteroides caccae. Comparative analysis of B. caccae genomes obtained using read cloud sequencing together with metagenomic RNA sequencing allowed us to identify differences in substrain populations over time. Based on this, we predicted that particular mobile element integrations likely resulted in increased antibiotic resistance, which we further supported using in vitro antibiotic susceptibility testing. We find read cloud assembly to be useful in identifying key structural genomic strain variants within a metagenomic sample. These strains have fluctuating relative abundance over relatively short time periods in human microbiomes. We also find specific structural genomic variations that are associated with increased antibiotic resistance over the course of clinical treatment.