Posttransfusion Sepsis Attributable to Bacterial Contamination in Platelet Collection Set Manufacturing Facility, United States
Ian Kracalik, Alyssa G. Kent, Carlos H. Villa, Paige Gable, Pallavi Annambhotla, Gillian McAllister, Deborah Yokoe, Charles R. Langelier, Kelly Oakeson, Judith Noble-Wang, Orieji Illoh, Alison Laufer Halpin, Anne F. Eder, and Sridhar V. Basavaraju
Author affiliations: Centers for Disease Control and Prevention, Atlanta, Georgia, USA (I. Kracalik, A.G. Kent, P. Gable, P. Annambhotla, G. McAllister, J. Noble-Wang, A.L. Halpin, S.V. Basavaraju); Food and Drug Administration, Silver Spring, Maryland, USA (C.H. Villa, O. Illoh, A.F. Eder); University of California San Francisco School of Medicine, San Francisco, California, USA (D. Yokoe, C.R. Langelier); Utah Department of Health, Salt Lake City, Utah, USA (K. Oakeson)
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Figure 4
Figure 4. Public ACBC shown with study isolates from investigation of bacterial contamination of platelet blood products, United States, 2018–2022. Shown is a RaxML (https://cme.h-its.org)‒generated phylogeny based on core genes of genomes from ACBC isolates from this study compared with all A. calcoaceticus, A. lactucae, and A. seifertii and a subsampled set of A. baumannii, A. nosocomialis, and A. pittii genomes from the National Center for Biotechnology Information RefSeq (https://www.ncbi.nlm.nih.gov/refseq) database, along with all Staphylococcus saprophyticus from the RefSeq database. Isolate location, isolate source, and species from National Center for Biotechnology Information database along with all S. saprophyticus isolates or by average nucleotide identity were layered onto the phylogeny. Pink and green indicate the 2 clusters from Figure 3, panel B. Black circles on branches indicate 100% support for the branch of 100 bootstraps. US states are identified by 2-letter postal codes. Scale bar indicates nucleotide substitutions per site. ACBC, Acinetobacter calcoaceticus-baumannii; DR, Dominican Republic.
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