Literature DB >> 21346706

Fatal laboratory-acquired infection with an attenuated Yersinia pestis Strain--Chicago, Illinois, 2009.

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Abstract

On September 18, 2009, the Chicago Department of Public Health (CDPH) was notified by a local hospital of a suspected case of fatal laboratory-acquired infection with Yersinia pestis, the causative agent of plague. The patient, a researcher in a university laboratory, had been working along with other members of the laboratory group with a pigmentation-negative (pgm-) attenuated Y. pestis strain (KIM D27). The strain had not been known to have caused laboratory-acquired infections or human fatalities. Other researchers in a separate university laboratory facility in the same building had contact with a virulent Y. pestis strain (CO92) that is considered a select biologic agent; however, the pgm- attenuated KIM D27 is excluded from the National Select Agent Registry. The university, CDPH, the Illinois Department of Public Health (IDPH), and CDC conducted an investigation to ascertain the cause of death. This report summarizes the results of that investigation, which determined that the cause of death likely was an unrecognized occupational exposure (route unknown) to Y. pestis, leading to septic shock. Y. pestis was isolated from premortem blood cultures. Polymerase chain reaction (PCR) identified the clinical isolate as a pgm- strain of Y. pestis. Postmortem examination revealed no evidence of pneumonic plague. A postmortem diagnosis of hereditary hemochromatosis was made on the basis of histopathologic, laboratory, and genetic testing. One possible explanation for the unexpected fatal outcome in this patient is that hemochromatosis-induced iron overload might have provided the infecting KIM D27 strain, which is attenuated as a result of defects in its ability to acquire iron, with sufficient iron to overcome its iron-acquisition defects and become virulent. Researchers should adhere to recommended biosafety practices when handling any live bacterial cultures, even attenuated strains, and institutional biosafety committees should implement and maintain effective surveillance systems to detect and monitor unexpected acute illness in laboratory workers.

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Year:  2011        PMID: 21346706

Source DB:  PubMed          Journal:  MMWR Morb Mortal Wkly Rep        ISSN: 0149-2195            Impact factor:   17.586


  19 in total

1.  High-throughput, signature-tagged mutagenic approach to identify novel virulence factors of Yersinia pestis CO92 in a mouse model of infection.

Authors:  Duraisamy Ponnusamy; Eric C Fitts; Jian Sha; Tatiana E Erova; Elena V Kozlova; Michelle L Kirtley; Bethany L Tiner; Jourdan A Andersson; Ashok K Chopra
Journal:  Infect Immun       Date:  2015-03-09       Impact factor: 3.441

2.  Further characterization of a highly attenuated Yersinia pestis CO92 mutant deleted for the genes encoding Braun lipoprotein and plasminogen activator protease in murine alveolar and primary human macrophages.

Authors:  Christina J van Lier; Bethany L Tiner; Sadhana Chauhan; Vladimir L Motin; Eric C Fitts; Matthew B Huante; Janice J Endsley; Duraisamy Ponnusamy; Jian Sha; Ashok K Chopra
Journal:  Microb Pathog       Date:  2015-02-16       Impact factor: 3.738

3.  Development and Validation of Biosafety Climate Scale for Biological and Biomedical Science Laboratories in the United States.

Authors:  Sivarchana Mareedu-Boada; Torsten Alwin Hopp; Riten Mitra
Journal:  Appl Biosaf       Date:  2021-11-24

Review 4.  Plague gives surprises in the first decade of the 21st century in the United States and worldwide.

Authors:  Thomas Butler
Journal:  Am J Trop Med Hyg       Date:  2013-09-16       Impact factor: 2.345

5.  Intramuscular Immunization of Mice with a Live-Attenuated Triple Mutant of Yersinia pestis CO92 Induces Robust Humoral and Cell-Mediated Immunity To Completely Protect Animals against Pneumonic Plague.

Authors:  Bethany L Tiner; Jian Sha; Duraisamy Ponnusamy; Wallace B Baze; Eric C Fitts; Vsevolod L Popov; Christina J van Lier; Tatiana E Erova; Ashok K Chopra
Journal:  Clin Vaccine Immunol       Date:  2015-10-07

6.  Characterization of systemic and pneumonic murine models of plague infection using a conditionally virulent strain.

Authors:  Gabriela Mellado-Sanchez; Karina Ramirez; Cinthia B Drachenberg; Jovita Diaz-McNair; Ana L Rodriguez; James E Galen; James P Nataro; Marcela F Pasetti
Journal:  Comp Immunol Microbiol Infect Dis       Date:  2012-11-26       Impact factor: 2.268

Review 7.  Plague: Infections of Companion Animals and Opportunities for Intervention.

Authors:  Petra C F Oyston; Diane Williamson
Journal:  Animals (Basel)       Date:  2011-06-21       Impact factor: 2.752

Review 8.  Biologically hazardous agents at work and efforts to protect workers' health: a review of recent reports.

Authors:  Kyung-Taek Rim; Cheol-Hong Lim
Journal:  Saf Health Work       Date:  2014-04-05

9.  Risks and benefits of gain-of-function experiments with pathogens of pandemic potential, such as influenza virus: a call for a science-based discussion.

Authors:  Arturo Casadevall; Michael J Imperiale
Journal:  MBio       Date:  2014-08-01       Impact factor: 7.867

10.  Surveillance of laboratory exposures to human pathogens and toxins: Canada 2016.

Authors:  A Bienek; M Heisz; M Su
Journal:  Can Commun Dis Rep       Date:  2017-11-02
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