Staphylococcus epidermidis
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| Staphylococcus epidermidis | ||||||||||||||
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| Staphylococcus epidermidis |
Description and significance
Staphylococcus epidermidis is a gram positive coccus, nonpigmented, bacterium. This organism, usually 0.5 to 1.5 mm in diameter, is a normal inhabitant of the human skin that grows in clusters. Research studies reveal that S. epidermidis lives in close association with S. aureus, a very destructive pathogen.
Even though a coagulase-negative gram bacterium, S. epidermidis has been lately classified among the most important pathogens responsible for divers nosocomial infections. Most strains are highly resistant to multiple antibiotics, such as penicillin, tetracycline, methicillin and many more, which makes it very difficult to treat the infections resulting from these bacteria. According to the Centers for Disease Control and Prevention's National Nosocomial infection surveillance system, S. epidermidis is responsible for 33.5% of nosocomial blood stream infections.
Genome structure
Among all the S. epidermidis strains, the genome sequence of only 2 strains has been completely described: S. epidermidis RP62a with a genome length of 2,616,530 bp and S. epidermids ATCC12228, 2,499,279 bp. RP62a encodes 2585 protein genes, 61 tRNA and 19 rRNA; whereas the ATCC12228 strain contains a number of 2381 protein coding genes, 60tRNA and 16rRNA. The low G+C content (32.1% for both strains) stands for the virulence and the high resistance of S. epidermidis. The genomic elements, which include, the genome islands, the insertions sequences, the composite transposons and the integrated plasmids, constitute more or less 9% of the genome. Studies have shown that a high level of genetic diversity exists within S. epidermidis at the level of a single locus as a result of adaption to different environment in hospitals and communities..[1]
Cell structure and metabolism
As a gram-positive bacterium, S. epidermidis has a cell wall made of a large concentration of peptidoglycan layer but no outer membrane. The cell-wall anchored(CWA)proteins of these bacteria are part of a family of surface-exposed proteins that interact with targets in the host. These CWA proteins possess an N-terminal secretion signal sequence (S) required for sec-dependent secretion, followed by a non-repeat A domain that contains the ligand-binding site. These interactions are particular important because they are involved in bacterial adherence and escape from the host defense systems. No mechanism is known to explain the virulence of S. epidermidis, but it is thought that the cell wall proteins are potential factors that must be involved.
S.epidermis requires mannitol as the carbon source to grow in aerobic conditions; however, this organism also survives anaerobically when placed in a standardized complex medium of glucose. It is non-motile and has no endospores. Since it is a pathogen of the human skin, S. epidermidis grows best at 37°C (mesophilic), the optimal temperature for the human body.
Pathology
Most infections caused by S. epidermidis affect hospital patients because these organisms develop structures called biofilms on the surface of implanted medical devices. These biofilms result from the agglomeration of bacterial cells that are contained in an exopolysaccharide matrix, the slime, to produce a very dense and protected environment from the host defense systems and antibiotics. They not only provide protection from the host but they also result in the damage of surrounding tissues of the host.
Skin and tissues infections, post-surgical wounds are the common points of entry for infection by S. epidermis. This bacterium accounts for most catheter-related infections, joint replacement infections, the majority of prosthetic cardiac valve infections and infections following post-neurosurgical procedures.In addition, studies have reported that S. epidermidis is highly predominant in the milk and feces of breast-fed infants compared to formula-fed ones. However, whether or not the presence of these bacteria can cause infections in these children have not been determined.
Moreover, S. epidermis plays a significant role in some external ocular diseases, such as chronic blepharitis and suppurative keratitis. Fortunately, these infections are treatable; and ciprofloxacin is considered the best drug in the cure of bacterial keratitis. Interestingly, methicillin-resistant S. epidermidis was identified in the cause of nosocomial meningitis when prosthetic devices were used in a trauma case in 2003. Even though, the antibiotic, vancomycin, was the treatment of choice, it was not successful in the recovery of the patient. Instead, better results were obtained with the use of linezolid. Due to their high resistance to antimicrobial agents, other techniques have been employed to prevent the staphylococcal infections which imply mechanical cleaning, the stopping of biofilm growth by the removal of essential nutrients, the inhibition of microbial attachments to surfaces, and biomass detachment.
Application to Biotechnology
The pulse-field gel electrophoresis is the most common method used to study methicillin-resistant S.epidermidis. It allows scientists to determine the cause of nosocomial infections and the means of transmission of this bacterium. Because S. epidermidis does not release toxins, it is very difficult to trace the infections, but some molecular genetics technologies, such as the automated culture system BacT/ALERT™ in Canada and the Real-Time Reverse Transcriptase Polymerase Chain Reaction (PCR) Assay,have been employed in the testing of bacterial contamination of blood platelets. Moreover, multilocus sequence typing (MLST) is implemented to study the phylogenetic relationships of divers bacterial pathogens, including S. epidermidis and S. aureus.
Current Research
Two decades ago, S. epidermidis was considered a nonsignificant, simple Gram positive bacterium. However, there has been lately a growing interest in the study of this organism due to its high level of pathogenicity in nosocomial infections. A lot of research is in progress at Baylor College of Medicine in the determination of the genome sequence of different strains, such as S. epidermidis M23864:W2, S. epidermidis CONS. Besides, more studies are currently implemented so as to reveal the mechanisms of virulence and transmission at the molecular and cellular level. There is also a great focus on the research of more effective preventive inventions agaisnt these infections. Because S. epidermidis is highly resistant to most antibiotics and lightly resistant to only vancomycin, it is very difficult to treat the nosocomial infections. But a class of antimicrobial agents, the cationic antimicrobial peptides (AMPs), are actually under study,which are thought to kill the microbial cell by pore formation or cell disruption.
References
[3]↑http://mic.sgmjournals.org/cgi/reprint/151/5/1453. Identification and preliminary characterization of cell-wall-anchored proteins of Staphylococcus epidermidis. Microbiology. DOI 10.1099/mic.0.27534-0. Retrieved on 2009-04-20.
[9]↑http://jmm.sgmjournals.org/cgi/reprint/50/7/582.pdf. Staphylococcus epidermidis Biofilms: importance and implications. Journal of Microbiology.ISSN 0022-2615. Retrieved on 2009-04-21.]
[10]↑ Method for detection of Staphylococcus epidermidis. Microbiology. DOI 10.1099/mic.0.28165-0. Retrieved on 2009-04-21.]
- ↑ Miragaia, M (2007). "Inferring a Population Structure for Staphylococcus epidermidis from Multilocus Sequence Typing Data". Journal of Bacteriology 189 (6): 2540-2552. Retrieved on 2009-04-20.