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The unusual bacterial pneumonias described in this chapter are caused by agents that are phylogenetically diverse and reside in a wide variety of locations, ranging from extracellular Mycoplasma attached to respiratory epithelium to obligately intracellular organisms. The obligately intracellular agents range from Rickettsia and Orientia, living in the cytosol of endothelial cells, to Chlamydia, Ehrlichia, and Anaplasma, living in modified cytoplasmic vacuoles. Coxiella, a facultatively intracellular bacterium, lives in acidic cytoplasmic phagolysosomes of macrophages. Transmission varies from person-to-person communicability (Mycoplasma, C. trachomatis, C. pneumoniae) to vectorborne inoculation by ticks ( Rickettsia, Ehrlichia, and Anaplasma ), lice or fleas (Rickettsia), and mites ( Orientia and Rickettsia ). The organisms themselves vary from gram-negative bacteria with cell walls containing lipopolysaccharide (LPS) and peptidoglycan (Rickettsia), cell walls containing LPS but no peptidoglycan (Chlamydia), cell walls containing neither LPS nor peptidoglycan ( Orientia, Ehrlichia, and Anaplasma ), to bacteria lacking a cell wall altogether (Mycoplasma). Although generally having small genomes due to selective genome reduction, these organisms are highly adapted to their individual ecologic niches. Their composition and interaction with the host, including the particular target cells in the lung, determine the pulmonary pathology that they cause.
For some of these diseases, such as Mycoplasma and chlamydial pneumonias and Q fever, fatality and biopsy are exceedingly rare. Clinical microbiology laboratories seldom undertake cultivation of these agents from respiratory samples, if even at all. Thus recognizing the pathologic lesions and establishing an etiologic diagnosis are challenging.
Lower respiratory tract infection and inflammatory consolidation caused by Mycoplasma pneumoniae
One of the most common community-acquired pneumonias
A fatal outcome is rare
Highest incidence in 5- to 20-year-olds
9% of community-acquired pneumonia isolates in patients younger than 5 years, 51% in 5- to 9-year-olds, 74% in 9- to 15-year-olds, and 3.3% to 18% in adults; in university students, 11% of clinically diagnosed pneumonias and 22% of radiologically confirmed pneumonias
Gradual onset of headache, malaise, fever, sore throat, and cough
Mycoplasma tracheobronchitis occurs 30 times more frequently than pneumonia
Similar incidence of productive cough, rales, and diarrhea as community-acquired pneumococcal or Legionella pneumonia, but with more frequent upper respiratory symptoms, normal leukocyte count, and younger age
Bronchopneumonia usually involving a single lobe, subsegmental atelectasis, peribronchial thickening, and streaky interstitial densities
High-resolution computerized tomography shows centrilobular consolidation, acinar shadows less than 1 cm in diameter, air bronchograms and bronchiolograms, and thickening of the bronchovascular bundle
Usually self-limited
The duration of illness, but not Mycoplasma carriage, is shortened by oral ambulatory treatment with doxycycline, erythromycin, clarithromycin, or azithromycin for 5 days; levofloxacin or moxifloxacin for 14 to 21 days
Because Mycoplasma pneumonia is rarely fatal, the gross pathologic lesions are not well described
Limited human autopsy and biopsy materials and similar observations in a hamster model show peribronchial, peribronchiolar, and interstitial infiltrates of macrophages, CD4 and CD8 T-lymphocytes, B-lymphocytes, and plasma cells
Airway lumens contain mucus, fibrin, polymorphonuclear leukocytes, and detached respiratory epithelial cells, which frequently cause obstruction leading to segmental and subsegmental atelectasis
In some cases, combinations of bronchiolitis obliterans, organizing pneumonia, and interstitial fibrosis occur rather than resolution
An immunohistochemical method for detection of Mycoplasma pneumoniae has been developed
Experimental studies of animals have demonstrated attachment of M. pneumoniae to the cell surface of respiratory epithelial cells between cilia by a specialized tip structure
Cilia are shed, intercellular junctions are disrupted, and the respiratory epithelial cells detach from the basement membrane
Influenza A and B, parainfluenza 1–4 pneumonia, respiratory syncytial virus pneumonia, and chlamydial pneumonias (C. trachomatis, C. pneumoniae, C. psittaci)
Mycoplasma pneumonia is among the most common lower respiratory infections worldwide. Its pathologic features reflect the secretion of peroxide by bacteria attached to the respiratory epithelium and the response of the host defenses ( Figs. 15.1 and 15.2 ).
Lower respiratory tract infection and inflammatory consolidation caused by Chlamydia trachomatis
C. trachomatis is the etiologic agent of 25% to 36% of the cases of pneumonia requiring hospitalization in 1- to 3-month-old infants
Of infants born to mothers harboring C. trachomatis genital infection, 17% to 22% develop chlamydial pneumonia
Usually a prolonged self-limited illness, C. trachomatis can cause severe pneumonia in low-birth-weight neonates
Infection is usually acquired intrapartum, with onset of symptoms at 4 to 12 weeks of age
Pneumonia caused by C. trachomatis is rare in adults, even immunocompromised persons
Typical onset is characterized by afebrile, staccato cough, tachypnea, rales, hypoxemia, and mild peripheral eosinophilia
Chlamydial conjunctivitis is present in only 50% at the presentation with pneumonia
Chest radiographs reveal hyperexpansion and diffuse or patchy interstitial infiltrates
Rarely fatal
Infants are treated with erythromycin (12.5 mg/kg four times daily for 2 weeks), azithromycin (20 mg/kg once daily for 3 days), or trimethoprim-sulfamethoxazole (5 mg/kg two times daily for 2 weeks).
Lower respiratory tract infection and inflammatory consolidation caused by Chlamydia pneumoniae
C. pneumoniae is the fourth most common cause of infectious pneumonia, responsible for 6% to 12% of cases
Based on the detection of antibodies in half of the adult population, C. pneumoniae infection is likely nearly universal with frequent reinfections
Generally a mild or asymptomatic infection (90%), it is more severe in older patients
Rarely fatal
Persons of all ages greater than 5 years may become infected
Infected children younger than 11 years of age are more likely to develop bronchitis, otitis media, and rhinitis than asymptomatic infection, pneumonia, pharyngitis, laryngitis, tonsillitis, or croup
Initially presenting with pharyngitis, infection gradually proceeds to cough and pneumonia over days to a week
Adults manifest cough (61%) that is productive of sputum (44%), rales (61%), and fever (56%)
Primary C. pneumoniae pneumonia in adults causes alveolar infiltrates on admission more frequently than interstitial infiltrates, but interstitial infiltrates occur more often with reinfection
More than half of cases develop pleural effusions
Infection is self-limited
Doxycycline (tetracycline), erythromycin for 14 days, azithromycin for 5 days, or clarithromycin for 10 days or levofloxacin moxifloxacin for 7 days
Lower respiratory tract infection and inflammatory consolidation caused by Chlamydia psittaci
Although more than 813 cases of psittacosis were reported to the Centers for Disease Control and Prevention from 1988–1998, only 10 to 24 cases were registered annually in 2001–2004
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