eMedicine Specialties > Emergency Medicine > Pulmonary

Pneumonia, Mycoplasma

Author: Michael J Bono, MD, FACEP, Professor of Emergency Medicine, Associate Director of Emergency Medicine Residency Program, Department of Emergency Medicine, Eastern Virginia Medical School
Contributor Information and Disclosures

Updated: Dec 14, 2009

Introduction

Background

Mycoplasma pneumoniae  is a common cause of community-acquired pneumonia, and, usually, the disease has a prolonged, gradual onset. M pneumoniae was first isolated in cattle with pleuropneumonia in 1898.

In 1938, Reimann described the first cases of mycoplasmal pneumonia in man. Reimann coined the term "primary atypical pneumonia" after observing 7 patients in Philadelphia with marked constitutional symptoms, upper and lower respiratory tract symptoms, and a protracted course with gradual resolution. Peterson discovered the phenomenon of cold agglutinin in 1943, and high titers of cold agglutinins in patients with this type of pneumonia were discovered accidentally. In 1944, Eaton was credited with discovering a specific agent, coined Eaton’s agent, as the principal cause of primary atypical pneumonia. First thought to be a virus, Eaton’s agent was proved to be a Mycoplasma species in 1961. The general characteristics of Mycoplasma species are presented in the image below.

General characteristics of <em>Mycoplasma</em> sp...

General characteristics of Mycoplasma species.

General characteristics of <em>Mycoplasma</em> sp...

General characteristics of Mycoplasma species.


Pathophysiology

The responsible organism, M pneumoniae, is a pleomorphic organism that, unlike bacteria, lacks a cell wall, and unlike viruses do not need a host cell for replication. The prolonged paroxysmal cough seen in this disease is thought to be due to the inhibition of ciliary movement. The organism has a remarkable gliding motility and specialized filamentous tips end that allows it to burrow between cilia within the respiratory epithelium, eventually causing sloughing of the respiratory epithelial cells.

The organism has two properties that seem to correlate well with its pathogenicity in humans. The first is a selective affinity for respiratory epithelial cells, and the second is the ability to produce hydrogen peroxide, which is thought to be responsible for much of the initial cell disruption in the respiratory tract and for damage to erythrocyte membranes.

The pathogenicity of M pneumoniae has been linked to the activation of inflammatory mediators, including cytokines. A recent study reported on a recent emergence of drug-resistant M pneumoniae infection; however, the study concluded that host immune maturity and not the virulence factor of the organism is a major determinant factor of disease severity.1

Frequency

United States

M pneumoniae is now recognized as one of the most common causes of community-acquired pneumonia in otherwise healthy patients younger than 40 years, with the highest rate in individuals aged 5-20 years. M pneumoniae causes upper and lower respiratory illness in all age groups, particularly in temperate climates, and in summer, may cause as many as 50% of all pneumonias.

Mycoplasmal pneumonia can occur at any time of the year, but large outbreaks tend to occur in the late summer and fall. The incubation period tends to be smoldering and averages 3 weeks, in contrast to that of influenza and other viral pneumonias, which is generally a few days. Epidemics of mycoplasmal pneumonia tend to occur every 4-8 years in the general population and tend to be more frequent within closed populations, such as in military and prison populations. Although M pneumoniae is a common cause of pneumonia, only 5-10% of infected patients actually develop pneumonia.

Mortality/Morbidity

In almost all patients, the pneumonia resolves without any serious complications. M pneumoniae can cause severe pneumonia in children and has recently been associated with acute chest syndrome in patients with sickle cell anemia.   

Race

No racial predilections are observed in mycoplasmal diseases.

Sex

No difference in disease frequency is observed between males and females, but illnesses are somewhat more severe in males.

Age

Mycoplasmal pneumonia is common in all age groups; however, it is most common in the first 2 decades of life and is rare in children younger than 5 years.

Clinical

History

Mycoplasmal pneumonia is a disease of gradual and insidious onset of several days to weeks. The patient's history may include the following:

  • Fever
  • Malaise
  • Persistent, slowly worsening dry cough; absence of cough makes the diagnosis of M pneumoniae unlikely
  • Headache
  • Chills, not rigors
  • Scratchy sore throat
  • Sore chest and tracheal tenderness (result of the protracted cough)
  • Pleuritic chest pain (rare)

Physical

Most cases of pneumonia due to M pneumoniae resolve after several weeks, although a dry cough can be present for as long as a month; some patients can have a protracted illness lasting as long as 6 weeks. Other findings may also include the following:

  • A nontoxic general appearance
  • Erythematous tympanic membranes or bullous myringitis in patients older than age 2 years, an uncommon but unique sign
  • Mild pharyngeal injection with minimal or no cervical adenopathy, but no exudate
  • Normal lung findings with early infection but rhonchi, rales, and/or wheezes several days later
  • Various exanthems including erythema multiforme and Stevens-Johnson syndrome

Causes

  • The causative agent is M pneumoniae, a bacterium lacking a cell wall, which belongs to the class Mollicutes, the smallest known free-living microorganisms.
  • Because the organism can be excreted from the respiratory tract for several weeks after the acute infection, isolation of the organism may not indicate acute infection.

More on Pneumonia, Mycoplasma

Overview: Pneumonia, Mycoplasma
Differential Diagnoses & Workup: Pneumonia, Mycoplasma
Treatment & Medication: Pneumonia, Mycoplasma
Follow-up: Pneumonia, Mycoplasma
Multimedia: Pneumonia, Mycoplasma
References

References

  1. Kamizono S, Ohya H, Higuchi S, Okazaki N, Narita M. Three familial cases of drug-resistant Mycoplasma pneumoniae infection. Eur J Pediatr. Nov 8 2009;[Medline].

  2. Blackmore TK, Reznikov M, Gordon DL. Clinical utility of the polymerase chain reaction to diagnose Mycoplasma pneumoniae infection. Pathology. Apr 1995;27(2):177-81. [Medline].

  3. Chen CJ, Hung MC, Kuo KL, Chung JL, Wu KG, Hwang BT, et al. The role of eosinophil cationic protein in patients with Mycoplasma pneumoniae infection. J Chin Med Assoc. Jan 2008;71(1):37-9. [Medline].

  4. American Hospital Formulary Service. Drug Information. 1998:250-1, 257-78, 397-406.

  5. Barone, MA. The Harriet Lane Handbook. 14th ed. 1996:26.

  6. Brown SM, Padley S, Bush A, et al. Mycoplasma pneumonia and pulmonary embolism in a child due to acquired prothrombotic factors. Pediatr Pulmonol. Feb 2008;43(2):200-2. [Medline].

  7. Cherry JD. Anemia and mucocutaneous lesions due to Mycoplasma pneumoniae infections. Clin Infect Dis. Aug 1993;17 Suppl 1:S47-51. [Medline].

  8. Chu HW, Campbell JA, Rino JG, et al. Inhaled fluticasone propionate reduces concentration of Mycoplasma pneumoniae, inflammation, and bronchial hyperresponsiveness in lungs of mice. J Infect Dis. Mar 15 2004;189(6):1119-27. [Medline].

  9. Di Marco E, Cangemi G, Filippetti M, et al. Development and clinical validation of a real-time PCR using a uni-molecular Scorpion-based probe for the detection of Mycoplasma pneumoniae in clinical isolates. New Microbiol. Oct 2007;30(4):415-21. [Medline].

  10. Drugs of choice for community-acquired bacterial pneumonia. Med Lett Drugs Ther. Jul 30 2007;49(1266):62-4. [Medline].

  11. Eaton MD, Meiklejohn G, VanHerick W. Studies on the etiology of primary atypical pneumonia: a filterable agent transmissible to cotton rats, hamsters, and chick embryos. J Exp Med. 1944;79:649-67.

  12. Fernald GW, Collier AM, Clyde WA Jr. Respiratory infections due to Mycoplasma pneumoniae in infants and children. Pediatrics. Mar 1975;55(3):327-35. [Medline].

  13. Gullsby K, Storm M, Bondeson K. Simultaneous detection of Chlamydophila pneumoniae and Mycoplasma pneumoniae by use of molecular beacons in a duplex real-time PCR. J Clin Microbiol. Feb 2008;46(2):727-31. [Medline].

  14. Koskiniemi M. CNS manifestations associated with Mycoplasma pneumoniae infections: summary of cases at the University of Helsinki and review. Clin Infect Dis. Aug 1993;17 Suppl 1:S52-7. [Medline].

  15. Llibre JM, Urban A, Garcia E, et al. Bronchiolitis obliterans organizing pneumonia associated with acute Mycoplasma pneumoniae infection. Clin Infect Dis. Dec 1997;25(6):1340-2. [Medline].

  16. McCormack WM. Infections due to Mycoplasmas. In: Kasper DL, Braunwald E, Fauci AS, et al, eds. Harrison's Principles of Internal Medicine. 16th ed. New York: McGraw-Hill; 2005:1008-1011/159.

  17. Milla E, Zografos L, Piguet B. Bilateral optic papillitis following mycoplasma pneumoniae pneumonia. Ophthalmologica. 1998;212(5):344-6. [Medline].

  18. Neumayr L, Lennette E, Kelly D, et al. Mycoplasma disease and acute chest syndrome in sickle cell disease. Pediatrics. Jul 2003;112(1 Pt 1):87-95. [Medline].

  19. Oermann C, Sockrider MM, Langston C. Severe necrotizing pneumonitis in a child with Mycoplasma pneumoniae infection. Pediatr Pulmonol. Jul 1997;24(1):61-5. [Medline].

  20. Peter G, ed. Mycoplasma pneumoniae infections. In: The Red Book, Report of the Committee on Infectious Diseases. 24th ed. 1997:370-2.

  21. Reimann HA. An acute infection of the respiratory tract with atypical pneumonia: a disease entity probably caused by a filtrable virus. JAMA. 1938;111:2377-2384.

  22. Reittner P, Muller NL, Heyneman L, et al. Mycoplasma pneumoniae pneumonia: radiographic and high-resolution CT features in 28 patients. AJR Am J Roentgenol. Jan 2000;174(1):37-41. [Medline].

  23. Venkatesan P, Patel V, Collingham KE, et al. Fatal thrombocytopenia associated with Mycoplasma pneumoniae infection. J Infect. Sep 1996;33(2):115-7. [Medline].

  24. Yang E, Altes T, Anupindi SA. Early Mycoplasma pneumoniae infection presenting as multiple pulmonary masses: an unusual presentation in a child. Pediatr Radiol. Apr 2008;38(4):477-80. [Medline].

Further Reading

Keywords

mycoplasma pneumonia, mycoplasmal pneumonia, Mycoplasma pneumoniae, M pneumoniae, CAP, community-acquired pneumonia, atypical pneumonia, sore chest, tracheal tenderness, dry cough, bullous myringitis, sore throat, treatment, diagnosis, symptoms

Contributor Information and Disclosures

Author

Michael J Bono, MD, FACEP, Professor of Emergency Medicine, Associate Director of Emergency Medicine Residency Program, Department of Emergency Medicine, Eastern Virginia Medical School
Michael J Bono, MD, FACEP is a member of the following medical societies: Alpha Omega Alpha, American College of Emergency Physicians, American Heart Association, Medical Society of Virginia, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Medical Editor

Joseph A Salomone III, MD, EMS Medical Director, Kansas City, Missouri; Associate Professor and Staff Physician, Truman Medical Centers/UMKC School of Medicine
Joseph A Salomone III, MD is a member of the following medical societies: American Academy of Emergency Medicine, National Association of EMS Physicians, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Paul Blackburn, DO, FACOEP, FACEP, Program Director, Department of Emergency Medicine, Maricopa Medical Center; Assistant Professor, Department of Surgery, University of Arizona
Paul Blackburn, DO, FACOEP, FACEP is a member of the following medical societies: American College of Emergency Physicians, American College of Osteopathic Emergency Physicians, American Medical Association, and Arizona Medical Association
Disclosure: Nothing to disclose.

CME Editor

John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Chief Editor

Robert E O'Connor, MD, MPH, Professor and Chair, Department of Emergency Medicine, University of Virginia Health System
Robert E O'Connor, MD, MPH is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American College of Physician Executives, American Heart Association, American Medical Association, Medical Society of Delaware, National Association of EMS Physicians, Society for Academic Emergency Medicine, and Wilderness Medical Society
Disclosure: Nothing to disclose.

 
 
HONcode

We subscribe to the
HONcode principles of the
Health On the Net Foundation

All material on this website is protected by copyright, Copyright© 1994- by Medscape.
This website also contains material copyrighted by 3rd parties.

DISCLAIMER: The content of this Website is not influenced by sponsors. The site is designed primarily for use by qualified physicians and other medical professionals. The information contained herein should NOT be used as a substitute for the advice of an appropriately qualified and licensed physician or other health care provider. The information provided here is for educational and informational purposes only. In no way should it be considered as offering medical advice. Please check with a physician if you suspect you are ill.