Enrichment dynamics of Listeria monocytogenes and the associated microbiome from naturally contaminated ice cream linked to a listeriosis outbreak

被引:120
作者
Ottesen, Andrea [1 ]
Ramachandran, Padmini [1 ]
Reed, Elizabeth [1 ]
White, James R. [2 ]
Hasan, Nur [3 ]
Subramanian, Poorani [3 ]
Ryan, Gina [1 ]
Jarvis, Karen [4 ]
Grim, Christopher [4 ]
Daquiqan, Ninalynn [4 ]
Hanes, Darcy [4 ]
Allard, Marc [1 ]
Colwell, Rita [3 ]
Brown, Eric [1 ]
Chen, Yi [1 ]
机构
[1] Ctr Food Safety & Appl Nutr Food & Drug Adm, Off Regulatory Sci, 5001 Campus Dr, College Pk, MD 20740 USA
[2] Resphera Biosci, 1529 Lancaster St, Baltimore, MD 21231 USA
[3] CosmosID, 155 Gibbs St, Rockville, MD 20850 USA
[4] Ctr Food Safety & Appl Nutr Food & Drug Adm, Off Appl Res & Safety Assessment, 8301 Muirkirk Rd, Laurel, MD 20708 USA
关键词
Listeria monocytogenes; Enrichment; Ice cream; Microbiota; Co-enriching bacteria; 16S rRNA; Shotgun metagenomics; Next-generation sequencing; NGS; ISO; FDA; USDA; Buffered Listeria enrichment broth (BLEB); Half-Fraser broth (HFB); Fraser broth (FB); University of Vermont modified broth (UVM); 16S RIBOSOMAL-RNA; LAG-PHASE; TEMPERATURE; ALIGNMENT;
D O I
10.1186/s12866-016-0894-1
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Microbiota that co-enrich during efforts to recover pathogens from foodborne outbreaks interfere with efficient detection and recovery. Here, dynamics of co-enriching microbiota during recovery of Listeria monocytogenes from naturally contaminated ice cream samples linked to an outbreak are described for three different initial enrichment formulations used by the Food and Drug Administration (FDA), the International Organization of Standardization (ISO), and the United States Department of Agriculture (USDA). Enrichment cultures were analyzed using DNA extraction and sequencing from samples taken every 4 h throughout 48 h of enrichment. Resphera Insight and CosmosID analysis tools were employed for high-resolution profiling of 16S rRNA amplicons and whole genome shotgun data, respectively. Results: During enrichment, other bacterial taxa were identified, including Anoxybacillus, Geobacillus, Serratia, Pseudomonas, Erwinia, and Streptococcus spp. Surprisingly, incidence of L. monocytogenes was proportionally greater at hour 0 than when tested 4, 8, and 12 h later with all three enrichment schemes. The corresponding increase in Anoxybacillus and Geobacillus spp. indicated these taxa co-enriched in competition with L. monocytogenes during early enrichment hours. L. monocytogenes became dominant after 24 h in all three enrichments. DNA sequences obtained from shotgun metagenomic data of Listeria monocytogenes at 48 h were assembled to produce a consensus draft genome which appeared to have a similar tracking utility to pure culture isolates of L. monocytogenes. Conclusions: All three methods performed equally well for enrichment of Listeria monocytogenes. The observation of potential competitive exclusion of L. mono by Anoxybacillus and Geobacillus in early enrichment hours provided novel information that may be used to further optimize enrichment formulations. Application of Resphera Insight for high-resolution analysis of 16S amplicon sequences accurately identified L. monocytogenes. Both shotgun and 16S rRNA data supported the presence of three slightly variable genomes of L. monocytogenes. Moreover, the draft assembly of a consensus genome of L. monocytogenes from shotgun metagenomic data demonstrated the potential utility of this approach to expedite trace-back of outbreak-associated strains, although further validation will be needed to confirm this utility.
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页数:11
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