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Analysis of the Molecular Diversity Among Cronobacter Species Isolated From Filth Flies Using Targeted PCR, Pan Genomic DNA Microarray, and Whole Genome Sequencing Analyses.
Jang, Hyein; Chase, Hannah R; Gangiredla, Jayanthi; Grim, Christopher J; Patel, Isha R; Kothary, Mahendra H; Jackson, Scott A; Mammel, Mark K; Carter, Laurenda; Negrete, Flavia; Finkelstein, Samantha; Weinstein, Leah; Yan, QiongQiong; Iversen, Carol; Pagotto, Franco; Stephan, Roger; Lehner, Angelika; Eshwar, Athmanya K; Fanning, Seamus; Farber, Jeffery; Gopinath, Gopal R; Tall, Ben D; Pava-Ripoll, Monica.
Afiliación
  • Jang H; Center of Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD, United States.
  • Chase HR; Center of Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD, United States.
  • Gangiredla J; Center of Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD, United States.
  • Grim CJ; Center of Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD, United States.
  • Patel IR; Center of Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD, United States.
  • Kothary MH; Center of Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD, United States.
  • Jackson SA; Center of Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD, United States.
  • Mammel MK; Center of Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD, United States.
  • Carter L; Center of Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD, United States.
  • Negrete F; Center of Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD, United States.
  • Finkelstein S; Center of Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD, United States.
  • Weinstein L; Center of Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD, United States.
  • Yan Q; WHO Collaborating Centre for Cronobacter, University College Dublin, Dublin, Ireland.
  • Iversen C; UCD Centre for Food Safety, School of Public Health, Physiotherapy and Population Science, University College Dublin, Dublin, Ireland.
  • Pagotto F; WHO Collaborating Centre for Cronobacter, University College Dublin, Dublin, Ireland.
  • Stephan R; UCD Centre for Food Safety, School of Public Health, Physiotherapy and Population Science, University College Dublin, Dublin, Ireland.
  • Lehner A; Food Directorate, Bureau of Microbial Hazards, Health Canada, Ottawa, ON, Canada.
  • Eshwar AK; Institute for Food Safety and Hygiene, University of Zürich, Zurich, Switzerland.
  • Fanning S; Institute for Food Safety and Hygiene, University of Zürich, Zurich, Switzerland.
  • Farber J; Institute for Food Safety and Hygiene, University of Zürich, Zurich, Switzerland.
  • Gopinath GR; WHO Collaborating Centre for Cronobacter, University College Dublin, Dublin, Ireland.
  • Tall BD; UCD Centre for Food Safety, School of Public Health, Physiotherapy and Population Science, University College Dublin, Dublin, Ireland.
  • Pava-Ripoll M; Department of Food Science, University of Guelph, Guelph, ON, Canada.
Front Microbiol ; 11: 561204, 2020.
Article en En | MEDLINE | ID: mdl-33101235
Cronobacter species are opportunistic pathogens capable of causing life-threatening infections in humans, with serious complications arising in neonates, infants, immuno-compromised individuals, and elderly adults. The genus is comprised of seven species: Cronobacter sakazakii, Cronobacter malonaticus, Cronobacter turicensis, Cronobacter muytjensii, Cronobacter dublinensis, Cronobacter universalis, and Cronobacter condimenti. Despite a multiplicity of genomic data for the genus, little is known about likely transmission vectors. Using DNA microarray analysis, in parallel with whole genome sequencing, and targeted PCR analyses, the total gene content of two C. malonaticus, three C. turicensis, and 14 C. sakazaki isolated from various filth flies was assessed. Phylogenetic relatedness among these and other strains obtained during surveillance and outbreak investigations were comparatively assessed. Specifically, microarray analysis (MA) demonstrated its utility to cluster strains according to species-specific and sequence type (ST) phylogenetic relatedness, and that the fly strains clustered among strains obtained from clinical, food and environmental sources from United States, Europe, and Southeast Asia. This combinatorial approach was useful in data mining for virulence factor genes, and phage genes and gene clusters. In addition, results of plasmidotyping were in agreement with the species identity for each strain as determined by species-specific PCR assays, MA, and whole genome sequencing. Microarray and BLAST analyses of Cronobacter fly sequence datasets were corroborative and showed that the presence and absence of virulence factors followed species and ST evolutionary lines even though such genes were orthologous. Additionally, zebrafish infectivity studies showed that these pathotypes were as virulent to zebrafish embryos as other clinical strains. In summary, these findings support a striking phylogeny amongst fly, clinical, and surveillance strains isolated during 2010-2015, suggesting that flies are capable vectors for transmission of virulent Cronobacter spp.; they continue to circulate among United States and European populations, environments, and that this "pattern of circulation" has continued over decades.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Microbiol Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Microbiol Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza