Staphylococcus lugdunensis

Staphylococcus lugdunensis
Scientific classification
Kingdom: Bacteria
Phylum: Firmicutes
Class: Bacilli
Order: Bacillales
Family: Staphylococcaceae
Genus: Staphylococcus
Species: S. lugdunensis
Binomial name
Staphylococcus lugdunensis
Freney et al. 1988

Staphylococcus lugdunensis is a coagulase-negative member of the genus Staphylococcus,[1] consisting of Gram-positive bacteria with spherical cells that appear in clusters.

History

It was first described in 1988 after being differentiated through DNA analysis. Its name comes from Lugdunum, the Latin name for Lyon, France, where the organism was first isolated.

Description

Colonies of S. lugdunensis are usually hemolytic, sticky, yellow or tan, and about 2–4 mm in diameter after a 48-hour incubation. They also can have a characteristic sweet, hay-like odor. S. lugdunensis may produce a bound coagulase (that is, the enzyme is bound to the cells), a property it shares with S. aureus, but unlike S. aureus, it does not produce a free coagulase. In the laboratory, it can give a positive slide-coagulase test but a negative tube-coagulase test. It is fairly easy to identify because, unlike the great majority of staphylococci, it decarboxylates ornithine and is positive for pyrrolidonyl arylamidase.

In the past, it was frequently misidentified as S. hominis, S. aureus, or other species. It occurs as a commensal on human skin, but has been recorded as a cause of serious human infections,[2][3] such as osteomyelitis, arthritis,[4] septicaemia, wound infections,[5] and aggressive endocarditis.[6] It is generally susceptible to antistaphylococcal antibiotics, but increasing penicillin resistance has been reported.

Acute postoperative endophthalmitis

Acute postoperative endophthalmitis caused by S. lugdunensis is infrequently reported in clinical studies. Five cases of acute postcataract surgery endophthalmitis were taken from a multicenter prospective study conducted in four university-affiliated hospitals in France (2004 to 2005). These cases were characterized by severe ocular inflammation occurring with a mean delay of 7.6 days after cataract surgery, severe visual loss (hand motions or less in three cases), and dense infiltration of the vitreous. Each of these patients was initially treated by using a standard protocol with intravitreal (vancomycin and ceftazidime), systemic, and topical antibiotics. Given the severity of the endophthalmitis, though bacteria were sensitive to intravitreal antibiotics, pars plana vitrectomy was needed in four cases. The final visual prognosis was complicated by severe retinal detachment in three cases. The microbiological diagnosis was reached by using conventional cultures with specific biochemical tests and eubacterial PCR amplification followed by direct sequencing.

Clinical features

S. lugdunensis has been associated with a wide variety of infections, including cardiovascular infections (severe native and prosthetic valve endocarditis, myocarditis, and infected myxoma), osteomyelitis and prosthetic/native joints infections, skin and soft-tissue infections (furuncles, cellulitis, and abscesses), central nervous infections, peritonitis, endocephalitis, and urinary tract infections.

See also

References

  1. Chu, Vivian H. "MD, MHS". Staphylococcus lugdunensis. Retrieved 28 August 2011.
  2. Klotchko, A.; Wallace, M. R.; Licitra, C.; Sieger, B. (2011). "Staphylococcus lugdunensis:". Southern Medical Journal. 104 (7): 509–514. doi:10.1097/SMJ.0b013e31821e91b1. PMID 21886051.
  3. Babu, E.; Oropello, J. (2011). "Staphylococcus lugdunensis: The coagulase-negative staphylococcus you don't want to ignore". Expert Review of Anti-infective Therapy. 9 (10): 901–907. doi:10.1586/eri.11.110. PMID 21973302.
  4. Mei-Dan, O.; Mann, G.; Steinbacher, G.; Ballester, S. J.; Cugat, R. B.; Alvarez, P. D. (2007). "Septic arthritis with Staphylococcus lugdunensis following arthroscopic ACL revision with BPTB allograft". Knee Surgery, Sports Traumatology, Arthroscopy. 16 (1): 15–18. doi:10.1007/s00167-007-0379-8. PMID 17684731.
  5. Papapetropoulos, N.; Papapetropoulou, M.; Vantarakis, A. (2012). "Abscesses and wound infections due to Staphylococcus lugdunensis: Report of 16 cases". Infection. 41 (2): 525–528. doi:10.1007/s15010-012-0381-z. PMID 23242962.
  6. Liu, P. Y.; Huang, Y. F.; Tang, C. W.; Chen, Y. Y.; Hsieh, K. S.; Ger, L. P.; Chen, Y. S.; Liu, Y. C. (2010). "Staphylococcus lugdunensis Infective Endocarditis: A Literature Review and Analysis of Risk Factors". Journal of Microbiology, Immunology and Infection. 43 (6): 478–484. doi:10.1016/S1684-1182(10)60074-6. PMID 21195974.

Further reading

  • Crompton, Marcus J.; Dunstan, R. Hugh; Macdonald, Margaret M.; Gottfries, Johan; von Eiff, Christof; Roberts, Timothy K.; Zhou, Dongsheng (8 April 2014). "Small Changes in Environmental Parameters Lead to Alterations in Antibiotic Resistance, Cell Morphology and Membrane Fatty Acid Composition in Staphylococcus lugdunensis". PLoS ONE. 9 (4): e92296. doi:10.1371/journal.pone.0092296. PMC 3979647. PMID 24714666.
  • Missineo, A.; Di Poto, A.; Geoghegan, J. A.; Rindi, S.; Heilbronner, S.; Gianotti, V.; Arciola, C. R.; Foster, T. J.; Speziale, P.; Pietrocola, G. (June 2014). "IsdC from Staphylococcus lugdunensis Induces Biofilm Formation under Low-Iron Growth Conditions". Infection and Immunity. 82 (6): 2448–2459. doi:10.1128/IAI.01542-14. PMC 4019187. PMID 24686057.
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