“Nocardia”的意思、由来-开放百科全书

Nocardia is a genus of weakly staining Gram-positive, catalase-positive, rod-shaped bacteria. It forms partially acid-fast beaded branching filaments (acting as fungi, but being truly bacteria). It contains a total of 85 species. Some species are nonpathogenic, while others are responsible for nocardiosis.^[1] Nocardia species are found worldwide in soil rich in organic matter. In addition, they are oral microflora found in healthy gingiva, as well as periodontal pockets. Most Nocardia infections are acquired by inhalation of the bacteria or through traumatic introduction.

Culture and staining

Nocardia colonies have a variable appearance, but most species appear to have aerial hyphae when viewed with a dissecting microscope, particularly when they have been grown on nutritionally limiting media. Nocardia grow slowly on nonselective culture media, and are strict aerobes with the ability to grow in a wide temperature range. Some species are partially acid-fast (meaning a less concentrated solution of sulfuric or hydrochloric acid should be used during the staining procedure) due to the presence of intermediate-length mycolic acids in their cell wall. Majority of strains possess the cord factor (trehalose 6-6' dimycolate), an important virulence factor.

They are catalase positive and can grow easily on the most commonly used media with colonies becoming evident in 3–5 days. However, prolonged incubation periods (2–3 weeks) are sometimes needed.

Virulence

The various species of Nocardia are pathogenic bacteria with low virulence; therefore clinically significant disease most frequently occurs as an opportunistic infection in those with a weak immune system, such as small children, the elderly, and the immunocompromised (most typically, HIV). Nocardial virulence factors are the enzymes catalase and superoxide dismutase (which inactivate reactive oxygen species that would otherwise prove toxic to the bacteria), as well as a "cord factor" (which interferes with phagocytosis by macrophages by preventing the fusion of the phagosome with the lysosome).

Clinical disease and microbiological diagnosis

The most commonly encountered species are Nocardia brasiliensis, Nocardia cyriacigeorgica, Nocardia farcinica, and Nocardia nova. Nocardia asteroides is most frequently found species causing noncutaneous invasive disease. Most cases occur as an opportunistic infection in immunocompromised patients. N. brasiliensis is the most common species causing cutaneous nocardiosis. N. caviae is another species of medical interest. The genus is acid-fast to some degree, it stains only weakly Gram positive.

The most common form of human nocardial disease is a slowly progressive pneumonia, the common symptoms of which include cough, dyspnea (shortness of breath), and fever. It is not uncommon for this infection to spread to the pleura or chest wall. Pre-existing pulmonary disease, especially pulmonary alveolar proteinosis, increases the risk of contracting a Nocardia pneumonia. Every organ can be affected if a systemic spread takes place.

Nocardia species are deeply involved in the process of endocarditis as one of its main pathogenic effects. In about 25–33% of people Nocardia infection takes the form of encephalitis and/or brain abscess formation. Nocardia may also cause a variety of cutaneous infections such as actinomycetoma (especially N. brasiliensis), lymphocutaneous disease, cellulitis, and subcutaneous abscesses.

Nocardia isolation from biological specimens can be performed using an agar medium enriched with yeast extract and activated charcoal (BCYE), the same used for Legionella species. Selective media for mycobacteria or fungi can also be inoculated. The most suitable specimens are the sputum, or when clinically necessary, bronchoalveolar lavage or biopsy. Further biochemical tests for species identification are not routinely performed. Serological or cutaneous tests are not available.

Treatment

Antibiotic therapy is continued for six months (in immunocompetent people) to a year (in immunosuppression), and may need to be continued indefinitely.^[2] Proper wound care is also critical.

Genetics

Although Nocardia has interesting and important features such as production of antibiotics and aromatic compound-degrading or -converting enzymes, the genetic study of this organism has been hampered by the lack of genetic tools. However, practical Nocardia–E. coli shuttle vectors have been developed recently.^[7]

The genera Nocardia and Rhodococcus have been found to be closely related, supported by two conserved signature indels consisting of a one-amino-acid deletion in the alpha subunit of acetyl coenzyme A carboxylase (ACC), and a three-amino-acid insertion in a conserved region of an ATP-binding protein that are specifically shared by species from these two genera. In addition, 14 hypothetical conserved signature proteins have been identified which are unique to the genera Nocardia and Rhodococcus.^[8]

Name

The genus was named for Edmond Nocard, a 19th-century veterinarian and biologist.

References

1. ^{{cite book | author = Ryan KJ; Ray CG (editors) | title = Sherris Medical Microbiology | pages = 460–2 | edition = 4th | publisher = McGraw Hill | year = 2004 | isbn = 0-8385-8529-9 }}
2. ^¹²{{cite web |url=http://prod.hopkins-abxguide.org/pathogens/bacteria/aerobic_gram_positive_bacillus/nocardia.html |title=Nocardia |author=Bartlett JG |date=October 5, 2007 |work=Point-of-Care Information Technology ABX Guide |publisher=Johns Hopkins University |deadurl=yes |archiveurl=https://web.archive.org/web/20091201183311/http://prod.hopkins-abxguide.org/pathogens/bacteria/aerobic_gram_positive_bacillus/nocardia.html |archivedate=December 1, 2009 |df= }} Retrieved on January 3, 2009. Freely available with registration.
3. ^{{cite journal |vauthors=Muñoz P, Muñoz RM, Palomo J, Rodríguez-Creixéms M, Muñoz R, Bouza E |title=Pneumocystis carinii infection in heart transplant recipients. Efficacy of a weekend prophylaxis schedule |journal=Medicine (Baltimore) |volume=76 |issue=6 |pages=415–22 |date=November 1997 |pmid=9413427 |doi=10.1097/00005792-199711000-00004}}
4. ^{{cite journal |vauthors=Peleg AY, Husain S, Qureshi ZA, etal |title=Risk factors, clinical characteristics, and outcome of Nocardia infection in organ transplant recipients: a matched case-control study |journal=Clin Infect Dis |volume=44 |issue=10 |pages=1307–14 |date=May 2007 |pmid=17443467 |doi=10.1086/514340 |laysummary=http://www.docguide.com/news/content.nsf/news/852571020057ccf6852572b2004cf6a2 |laysource=Doctor's Guide}}
5. ^{{cite journal |vauthors=Khan BA, Duncan M, Reynolds J, Wilkes DS |title=Nocardia infection in lung transplant recipients |journal=Clin Transplant |volume=22 |issue=5 |pages=562–6 |year=2008 |pmid=18435787 |pmc=3755737 |doi=10.1111/j.1399-0012.2008.00824.x}}
6. ^{{cite journal |vauthors=Jodlowski TZ, Melnychuk I, Conry J |title=Linezolid for the treatment of Nocardia spp. infections |journal=Ann Pharmacother |volume=41 |issue=10 |pages=1694–9 |date=October 2007 |pmid=17785610 |doi=10.1345/aph.1K196}}
7. ^{{cite journal |vauthors=Chiba K, Hoshino Y, Ishino K, Kogure T, Mikami Y, Uehara Y, Ishikawa J |title=Construction of a Pair of Practical Nocardia-Escherichia coli Shuttle Vectors |journal=Jpn J Infect Dis |volume=60 |issue=1 |pages=45–7 |year=2007 |url=http://www.nih.go.jp/niid/JJID/60/45.html |pmid=17314425 |deadurl=yes |archiveurl=https://web.archive.org/web/20070817111052/http://www.nih.go.jp/niid/JJID/60/45.html |archivedate=2007-08-17 |df= }}
8. ^{{Cite journal | last1 = Gao | first1 = B. | last2 = Gupta | first2 = R. S. | doi = 10.1128/MMBR.05011-11 | title = Phylogenetic Framework and Molecular Signatures for the Main Clades of the Phylum Actinobacteria | journal = Microbiology and Molecular Biology Reviews | volume = 76 | issue = 1 | pages = 66–112 | year = 2012 | pmid = 22390973| pmc =3294427 }}