Literature DB >> 32104157

Clostridioides difficile Spores: Bile Acid Sensors and Trojan Horses of Transmission.

Aimee Shen1.   

Abstract

The Gram-positive, spore-forming bacterium, Clostridioides difficile is the leading cause of healthcare-associated infections in the United States, although it also causes a significant number of community-acquired infections. C. difficile infections, which range in severity from mild diarrhea to toxic megacolon, cost more to treat than matched infections, with an annual treatment cost of approximately $6 billion for almost half-a-million infections. These high-treatment costs are due to the high rates of C. difficile disease recurrence (>20%) and necessity for special disinfection measures. These complications arise in part because C. difficile makes metabolically dormant spores, which are the major infectious particle of this obligate anaerobe. These seemingly inanimate life forms are inert to antibiotics, resistant to commonly used disinfectants, readily disseminated, and capable of surviving in the environment for a long period of time. However, upon sensing specific bile salts in the vertebrate gut, C. difficile spores transform back into the vegetative cells that are responsible for causing disease. This review discusses how spores are ideal vectors for disease transmission and how antibiotics modulate this process. We also describe the resistance properties of spores and how they create challenges eradicating spores, as well as promote their spread. Lastly, environmental reservoirs of C. difficile spores and strategies for destroying them particularly in health care environments will be discussed. © Thieme Medical Publishers.

Entities:  

Keywords:  Clostridioides difficile; disinfection; germination; resistance; spore

Year:  2020        PMID: 32104157      PMCID: PMC7042012          DOI: 10.1055/s-0040-1701230

Source DB:  PubMed          Journal:  Clin Colon Rectal Surg        ISSN: 1530-9681


  98 in total

1.  Emergence of Clostridium difficile infection due to a new hypervirulent strain, polymerase chain reaction ribotype 078.

Authors:  Abraham Goorhuis; Dennis Bakker; Jeroen Corver; Sylvia B Debast; Celine Harmanus; Daan W Notermans; Aldert A Bergwerff; Frido W Dekker; Ed J Kuijper
Journal:  Clin Infect Dis       Date:  2008-11-01       Impact factor: 9.079

2.  A new strategy for the prevention of Clostridium difficile infection.

Authors:  Amber Howerton; Manomita Patra; Ernesto Abel-Santos
Journal:  J Infect Dis       Date:  2013-02-18       Impact factor: 5.226

3.  General methods for the analysis of metabolic profiles of bile acids and related compounds in feces.

Authors:  K D Setchell; A M Lawson; N Tanida; J Sjövall
Journal:  J Lipid Res       Date:  1983-08       Impact factor: 5.922

4.  Environmental transmission of Clostridioides difficile ribotype 027 at a long-term care facility; an outbreak investigation guided by whole genome sequencing.

Authors:  Bradley T Endres; Kierra M Dotson; Kelley Poblete; Jacob McPherson; Chris Lancaster; Eugénie Bassères; Ali Memariani; Sandi Arnold; Shawn Tupy; Conner Carlsen; Bonnie Morehead; Sophia Anyatonwu; Christa Cook; Khurshida Begum; M Jahangir Alam; Kevin W Garey
Journal:  Infect Control Hosp Epidemiol       Date:  2018-09-26       Impact factor: 3.254

5.  Effect of the Synthetic Bile Salt Analog CamSA on the Hamster Model of Clostridium difficile Infection.

Authors:  Amber Howerton; Cale O Seymour; Senthil K Murugapiran; Zhenlin Liao; Jacqueline R Phan; Alan Estrada; Adam J Wagner; Chrisabelle C Mefferd; Brian P Hedlund; Ernesto Abel-Santos
Journal:  Antimicrob Agents Chemother       Date:  2018-09-24       Impact factor: 5.191

Review 6.  A review of Clostridioides [Clostridium] difficile occurrence through the food chain.

Authors:  Carmen Candel-Pérez; Gaspar Ros-Berruezo; Carmen Martínez-Graciá
Journal:  Food Microbiol       Date:  2018-08-22       Impact factor: 5.516

7.  Changes in Colonic Bile Acid Composition following Fecal Microbiota Transplantation Are Sufficient to Control Clostridium difficile Germination and Growth.

Authors:  Alexa R Weingarden; Peter I Dosa; Erin DeWinter; Clifford J Steer; Megan K Shaughnessy; James R Johnson; Alexander Khoruts; Michael J Sadowsky
Journal:  PLoS One       Date:  2016-01-20       Impact factor: 3.240

8.  Chemical and Stress Resistances of Clostridium difficile Spores and Vegetative Cells.

Authors:  Adrianne N Edwards; Samiha T Karim; Ricardo A Pascual; Lina M Jowhar; Sarah E Anderson; Shonna M McBride
Journal:  Front Microbiol       Date:  2016-10-26       Impact factor: 5.640

9.  Intestinal calcium and bile salts facilitate germination of Clostridium difficile spores.

Authors:  Travis J Kochan; Madeline J Somers; Alyssa M Kaiser; Michelle S Shoshiev; Ada K Hagan; Jessica L Hastie; Nicole P Giordano; Ashley D Smith; Alyxandria M Schubert; Paul E Carlson; Philip C Hanna
Journal:  PLoS Pathog       Date:  2017-07-13       Impact factor: 6.823

10.  Pathogenicity Locus, Core Genome, and Accessory Gene Contributions to Clostridium difficile Virulence.

Authors:  Brittany B Lewis; Rebecca A Carter; Lilan Ling; Ingrid Leiner; Ying Taur; Mini Kamboj; Erik R Dubberke; Joao Xavier; Eric G Pamer
Journal:  mBio       Date:  2017-08-08       Impact factor: 7.867

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