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Discovery: Antibiotics and the Rise of the Superbug

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Abstract

“I see resistant staph all the time,” says nurse practitioner Maggie G. Her enormous blue eyes convey both the compassion and the weariness of someone who has seen it all. Over the course of 25 years, the Western Massachusetts nurse has treated farmers, hill-town hippies, and teens seeking treatment for STDs and fevers, as well as men, women, and children who walk for miles and wait patiently with festering wounds and suppurating tumors in the Sierra Leone clinic that she visits once a year. One constant throughout all of Maggie’s experiences is methicillin-resistant staph, or MRSA. Back in the late eighties, when Maggie was just finishing nursing school, MRSA was rare. But over the years she has witnessed the rise of this drug-resistant bug, tending to countless cases—one of the most memorable involved a young camp counselor whose infected toe turned into a life-threatening hole in her heart. When we spoke, Maggie was working with recovering addicts at a psych hospital. MRSA spreads so easily in needle-using addict populations through needle sharing or festering open wounds that Maggie says addicts are often treated “presumptively”—meaning the staff doesn’t always test but assumes drug resistance. It’s a reasonable assumption. In some places, nearly 50 percent of the needle-using population may be positive for community-acquired MRSA.

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Notes

  1. 1.

    For more about the history and treatment of MRSA, see: Maryn McKenna, Superbug: The Fatal Menace of MRSA (New York: Free Press, 2010), 1–288; A. El-Sharif and H. M. Ashour, “Community-Acquired Methicillin-Resistant Staphylococcus aureus (CA-MRSA) Colonization and Infection in Intravenous and Inhalational Opiate Drug Users,” Experimental Biology and Medicine 233 (July 2008): 874–80, doi:10.3181/0711-RM-294. (“Maggie G.” is a pseudonym.)

  2. 2.

    Centers for Disease Control and Prevention, Antibiotic Resistance Threats in the United States 2013 (Washington, DC: US Department of Health and Human Services, 2013), 16; see also www.cdc.gov/abcs/reports-findings/survivereports/mrsa12.html.

  3. 3.

    Aidan Hollis and Ziana Ahmed, “Preserving Antibiotics, Rationally,” New England Journal of Medicine 396 (December 2013): 2474–76.

  4. 4.

    Evan Snitkin et al., “Tracking a Hospital Outbreak of a Carbapenam-Resistant Klebsiella Pneumonia with Whole-Genome Sequencing,” Science Translational Medicine 4 (August 2012): 148ra116, doi:10.1126/scitranslmed.3004129.

  5. 5.

    Dennis Pitt and Jean-Michel Aubin, “Joseph Lister: Father of Modern Surgery,” Canadian Journal of Surgery 55 (October 2012): 1–3, doi: 10.1503/cjs007112.

  6. 6.

    George Sternbach, “The History of Anthrax,” Journal of Emergency Medicine 24 (May 2003): 463–67.

  7. 7.

    Klaus Strebhardt and Axel Ullrich, “Paul Ehrlich’s Magic Bullet Concept: 100 Years of Progress,” Nature Reviews 8 (June 2008): 473–80.

  8. 8.

    Amanda Yarnell, “Salvarsan,” Chemical and Engineering News 83 (June 2005), http://pubs.acs.org/cen/coverstory/83/8325/8325salvarsan.html.

  9. 9.

    Sebastian Amyes, Magic Bullets, Lost Horizons: The Rise and Fall of Antibiotics (London: Taylor and Francis, 2001), 8.

  10. 10.

    Yarnell, “Salvarsan.” Interestingly, why Salvarsan zeros in on syphilis remains a mystery.

  11. 11.

    N. Svartz, “Gerhard Domagk, Presentation Ceremony Speech,” in Nobel Lectures, Physiology or Medicine 1922–1941 (Amsterdam: Elsevier Publishing Company, 1965), www.nobelprize.org/nobel_prizes/medicine/laureates/1939/press.html.

  12. 12.

    Alexander Fleming, “On the Antibacterial Action of Cultures of a Penicillium,” British Journal of Experimental Pathology 10 (1929): 226–36, www.ncbi.nlm.nih.gov/pmc/articles/PMC2566493/pdf/11545337.pdf.

  13. 13.

    Dave Gilyeat, “Norman Heatley, the Unsung Hero Who Developed Penicillin,” BBC, http://news.bbc.co.uk/local/oxford/hi/people_and_places/history/newsid_8828000/8828836.stm (last modified July 20, 2010).

  14. 14.

    Alexander Fleming, “Penicillin: Nobel Lecture,” Nobelprize.org, http://nobelprize.org/nobel_prizes/medicine/laureates/1945/fleming-lecture.pdf.

  15. 15.

    H. Chambers and F. DeLeo, “Waves of Resistance, Staphylococcus aureus in the Antibiotic Era,” Nature Reviews Microbiology 7 (September 2009): 629–41.

  16. 16.

    John Lesch, The First Miracle Drug (Oxford: Oxford University Press, 2007), 236.

  17. 17.

    Maureen Ogle, “Riots, Rage, and Resistance: A Brief History of How Antibiotics Arrived on the Farm,” Scientific American (blog), September 3, 2013, http://blogs.scientificamerican.com/guest-blog/2013/09/03/riots-rage-and-resistance-a-brief-history-of-how-antibiotics-arrived-on-the-farm/.

  18. 18.

    E. T. Cetin and O. Ang, “Staphylococci Resistant to Methicillin (‘Celbenin’),” British Medical Journal 52 (July 7, 1962), 51–52.

  19. 19.

    Fred F. Barrett, MD, Read F. McGehee Jr., MD, and Maxwell Finland, MD, “Methicillin-Resistant Staphylococcus aureus at Boston City Hospital—Bacteriology and Epidemiologic Observations,” New England Journal of Medicine 279 (August 1968): 441–48.

  20. 20.

    Centers for Disease Control and Prevention, “Antibiotic Resistance,” 11.

  21. 21.

    Michael M. Mwangi et al., “Tracking the In Vivo Evolution of Multidrug Resistance in Staphylococcus aureus by Whole Genome Sequencing,” Proceedings of the National Academy of Science 22 (2007): 9451–56.

  22. 22.

    Julian Davies, “Microbes Have the Last Word. A Drastic Reevaluation of Antimicrobial Treatment Is Needed to Overcome the Threat of Antibiotic-Resistant Bacteria,” EMBO Reports 8 (2007): 616–21; S. Mitsuhashi et al., “On the Drug-Resistance of Enteric Bacteria,” Japan Journal of Experimental Medicine 31 (1961): 47–52.

  23. 23.

    Julian Davies, “Vicious Circles: Looking Back on Resistance Plasmids,” Genetics 139 (1995): 1465–68.

  24. 24.

    For a review, see: Davies, “Microbes Have the Last Word”; also see: Davies, “Vicious Circles.”

  25. 25.

    Davies, “Vicious Circles.”

  26. 26.

    Bacteria can acquire new genes by engaging in the processes of transformation, transduction, and conjugation. Transformation refers to the direct uptake of DNA from the environment (say, from a neighbor recently broken apart by penicillin). Perhaps for obvious reasons—it is not yet considered a major route for sharing resistance genes. Transduction is the transfer of DNA into bacteria by bacterial viruses or bacteriophages (phages). For example, bacterial viruses carrying resistance were recently isolated from river water and from sewage water, leading some to suggest that phages could serve as an environmental reservoir of resistance genes. For more, see: Marta Colomer-Lluch, Juan Jofre, and Maite Munieasa, “Antibiotic Resistance Genes in the Bacteriophage DNA Fraction of Environmental Samples,” PLoS ONE 6 (March 2011): e17549, doi:10.1371/journal.pone.0017549.

  27. 27.

    Eugene Koonin and Yuri Wolf, “Dynamics of Bacteria and Archaea: The Emerging Dynamic View of the Prokaryotic World,” Nucleic Acids Research 36 (2008): 6688–719.

  28. 28.

    Kirandeep Bhullar et al., “Antibiotic Resistance Is Prevalent in an Isolated Cave Microbiome,” PLoS ONE 7 (April 2012): e34953, doi:10.1371/journal.pone.0034953.

  29. 29.

    Julian Davies, “Are Antibiotics Naturally Antibiotics?” Journal of Industrial Microbiology and Biotechnology 33 (March 2006): 496–99.

  30. 30.

    Another, more complicated role for antibiotics production may be to enable cooperation within a bacterial population—rather than as a benefit to the individual bacterium. Just as our society is composed of warriors and nonviolent members who require protection, so, too, are populations of bacteria composed of antibiotic-producing bacteria and resistant bacteria—suggesting a kind of bacterial “social unit.” For more, see: Helene Morlon, “Bacterial Cooperative Warfare,” Science 337 (2012): 1184–85; and Otto X. Cordero et al., “Ecological Populations of Bacteria Act as Socially Cohesive Units of Antibiotic Production and Resistance,” Science 337 (September 2012): 1228–31.

  31. 31.

    Julian Davies (professor emeritus in the Department of Microbiology & Immunology, University of British Columbia, Vancouver, Canada) in discussion with the author, October 2012. Note: All quoted material attributed to Julian Davies in this chapter is from this same discussion.

  32. 32.

    Michael Gillings and H. W. Stokes, “Are Humans Increasing Bacterial Evolvability?” Trends in Ecology and Evolution 27 (March 2012): 346–52.

  33. 33.

    Julian Davies, letter to the editor, Globe and Mail, April 10, 2012, http://www.theglobeandmail.com/globe-debate/april-10-letters-to-the-editor/article4098926/.

  34. 34.

    Karen Bush et al., “Tackling Antibiotic Resistance,” Nature Reviews Microbiology 9 (December 2011): 894–96.

  35. 35.

    S. Y. Chen et al., “Health-Care-Associated Measles Outbreak in the United States after an Importation: Challenges and Economic Impact,” Journal of Infectious Disease 203 (June 2011): 1517–25.

  36. 36.

    T. H. Dellit et al., “Infectious Diseases Society of America and the Society for Healthcare Epidemiology of America Guidelines for Developing an Institutional Program to Enhance Antimicrobial Stewardship,” Clinical Infectious Diseases 44 (2007): 159–77.

  37. 37.

    Arjun Srinivasan, Associate Director for Healthcare and Associated Infection Prevention Programs, Division of Healthcare Quality Promotion, audio transcript for “Get Smart about Antibiotics Week 2012,” United States Centers for Disease Control and Prevention, www.cdc.gov/media/dpk/2013/docs/getsmart/dpk-antibiotics-week-Arjun-Srinivasan’s-audio-transcript.pdf.

  38. 38.

    Srinivasan, audio transcript.

  39. 39.

    American Academy of Microbiology, Antibiotic Resistance: An Ecological Perspective on an Old Problem (Washington, DC: American Academy of Microbiology, 2009), 11, http://academy.asm.org/images/stories/documents/antibioticresistance.pdf.

  40. 40.

    Dr. Arjun Srinivasan (Associate Director for Healthcare-Associated Infection Prevention Programs in the Division of Healthcare Quality Promotion at the Centers for Disease Control and Prevention) in discussion with the author, December 2013.

  41. 41.

    Carol Cogliani, Herman Goossens, and Christina Greko, “Restricting Antimicrobial Use in Food Animals: Lessons from Europe,” Microbe 6 (2011): 274–79.

  42. 42.

    “FDA’s Strategy on Antimicrobial Resistance—Questions and Answers,” United States Food and Drug Association, www.fda.gov/AnimalVeterinary/GuidanceComplianceEnforcement/GuidanceforIndustry/ucm216939.htm, accessed November 2012.

  43. 43.

    “Protecting Employees Who Protect Our Environment,” FDA Strategy Memos, PEER, www.peer.org/assets/docs/fda/10_17_12_FDA_strategy_memos.pdf, accessed November 2012.

  44. 44.

    For more about antibiotic use and resistance in the United States, state by state, see: The Centers for Disease Dynamics and Disease Policy, “Resistance Map” project, www.cddep.org/map.

  45. 45.

    H. Brotz-Oesterhelt and P. Sass, “Postgenomic Strategies in Antibacterial Drug Discovery,” Future Microbiology 5 (October 2010): 1553–79.

  46. 46.

    Bush et al., “Tackling Antibiotic Resistance.”

  47. 47.

    Srinivasan, audio transcript.

  48. 48.

    “Antimicrobial Resistance: Global Report on Surveillance,” World Health Organization, www.who.int/drugresistance/documents/surveillancereport/en, 3, accessed May 2014.

  49. 49.

    B. J. Culliton, “Emerging Viruses, Emerging Threat,” Science 247 (January 1990): 279–80.

  50. 50.

    The role of indigenous bacteria in health is becoming increasingly important. Illness caused by the bacterium Clostridium difficile, for example, afflicts an estimated 250,000, of whom 14,000 die annually. Antibiotics are a major contributing factor by clearing out the good bacteria, leaving individuals susceptible to infection by C. dif. For more, see: Centers for Disease Control and Prevention, “Antibiotic Resistance.” Also, recent attempts to cure some illness by recolonizing patients with gut bacteria are proving effective. For more, see: “Quick, Inexpensive and a 90% Cure Rate,” For Medical Professionals (blog), Mayo Clinic, www.mayoclinic.org/medical-professionals/clinical-updates/digestive-diseases/quick-inexpensive-90-percent-cure-rate, accessed March 2014.

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© 2015 Emily Monosson

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Monosson, E. (2015). Discovery: Antibiotics and the Rise of the Superbug. In: Unnatural Selection. Island Press, Washington, DC. https://doi.org/10.5822/978-1-61091-500-7_2

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