Staphylococcus Also see Staphylococcus in sludge biosolids
MRSA Studies and Statistics
Produces poisonous H2S gas and necrotizing infections
Pharmacological Approaches for Pediatric Patients With Osteomyelitis: Current Issues and Answers
By Amanda Geist, PharmD; Robert Kuhn, PharmD
ORTHOPEDICS 2009; 32:573
Osteomyelitis is an inflammatory process of the bone caused by bacterial or fungal infection. The overall incidence of
osteomyelitis in children in the United States is unknown; however, the incidence has been reported as approximately 1
per 5000 children, accounting for approximately 1% of all pediatric hospitalizations.3,4 Half of all cases of osteomyelitis
in children occur before 5 years of age.3 Boys are affected more commonly than girls, with a ratio of approximately 2:1.4
Signs and symptoms of osteomyelitis vary depending on the child’s age and the affected area. For example, an older
child may report pain and tenderness at the site of the infected area, but osteomyelitis in an infant who is unable to
verbalize pain may manifest as guarding of the involved extremity or irritability.5 Other signs and symptoms include
fever and swelling, warmth, and erythema of the infected area.5
The most common sites of involvement typically are long bones such as the tibia and femur, comprising approximately
20% to 30% of cases.6 Other less commonly infected sites include short bones, such as the ribs, clavicle, and scapula.
6 The most common pathogens implicated in osteomyelitis are bacterial in nature, and the etiology of osteomyelitis in
children is typically hematogenous spread, with infection caused by spread from trauma, surgery, or vascular
insufficiency occurring much less frequently.5,6 Several pathogens may be involved in osteomyelitis, and in children it
will vary depending on age and type of osteomyelitis involved. For example, the most common pathogens for children of
any age are S aureus and Streptococcus pyogenes; while Kingella kingae and Streptococcus pneumoniae are more
common in younger children.5,6
Recent studies have shown that osteomyelitis caused by CA-MRSA has increased complications compared with
infection caused by methicillin-sensitive Staphylococcus aureus (MSSA) or other pathogens.7,8 These complications
include increased need for surgical intervention, more febrile days, increased length of hospitalization, and increased
duration of antibiotics.7,8 A rise in the number of cases of culture-proven CA-MRSA also has a direct impact on clinical
case load and transition from the inpatient to outpatient setting.
1947 The 1st penicillin resistant strains of Staphylococcus aureus were reported.
(NG, 11/04, p.21)
1960 The new antibiotic methicillin was introduced. In 1961 strains of Staphylococcus aureus resistant to Methicillin
(MRSA) were first reported.
(SFC, 5/29/97, p.A4)(www.wellcome.ac.uk/doc_WTX026108.html)
1961 Strains of Staphylococcus aureus resistant to Methicillin (MRSA) were first reported. The antibiotic methicillin
had only become available in 1960.
(Econ, 11/5/05, p.87)(www.wellcome.ac.uk/doc_WTX026108.html)
Infections linked to cot deaths
In many cases, the infection was caused by Staphylococcus aureus, a particularly virulent bacteria, known to
produce potentially lethal toxins. Some experts believe toxins produced by these bacteria could trigger a
chemical storm, which overwhelms the baby, resulting in sudden death.
September 10, 2008 Flesh-eating superbug confounds the experts
SCIENTISTS are warning of a deadly flesh-eating superbug ``epidemic'' which has been blamed for the deaths of
healthy teenagers across the country. Known as the Queensland clone, a new mutation of the drug-resistant bacteria
kills one out of every two patients who acquire it, a medical summit has been told. It has been blamed for the
deaths of healthy teenagers and is reportedly on the verge of an outbreak.
EID Journal Home > Volume 13, Number 8–August 2007
Volume 13, Number 8–August 2007
Skin and Soft Tissue Infections Caused by Methicillin-Resistant Staphylococcus aureus USA300 Clone
Jennifer K. Johnson,* Tina Khoie,* Simone Shurland,* Kristen Kreisel,* O. Colin Stine,* and Mary-Claire Roghmann*†
*University of Maryland School of Medicine, Baltimore, Maryland, USA; and †Veterans Affairs Maryland Health Care
System, Baltimore, Maryland, USA
Until recently, methicillin-resistant Staphylococcus aureus (MRSA) has caused predominantly healthcare-associated
infections. We studied MRSA infections and overall skin and soft tissue infections (SSTIs) in outpatients receiving care
at the Baltimore Veterans Affairs Medical Center Emergency Care Service during 2001–2005. We found an increase in
MRSA infections, from 0.2 to 5.9 per 1,000 visits (p<0.01); most were community-associated SSTIs. Molecular typing
showed that >80% of MRSA infections were caused by USA300. In addition, SSTI visits increased from 20 to 61 per
1,000 visits (p<0.01). The proportion of SSTI cultures that yielded MRSA increased from 4% to 42% (p<0.01), while the
proportion that yielded methicillin-sensitive S. aureus remained the same (10% to 13%, p = 0.5). The increase in
community-associated MRSA infections and the overall increase in SSTIs in our population suggest that USA300 is
becoming more virulent and has a greater propensity to cause SSTIs.
suggested citation for this article: Bartels MD, Boye K, Larsen AR, Skov R, Westh H.
Rapid increase of genetically diverse methicillin-resistant Staphylococcus aureus, Copenhagen,
Denmark. Emerg Infect Dis. 2007 Oct; [Epub ahead of print]
Rapid Increase of Genetically Diverse Methicillin-Resistant Staphylococcus aureus, Copenhagen, Denmark
Mette Damkjær Bartels,* Kit Boye,* Anders Rhod Larsen,† Robert Skov,† and Henrik Westh*†
*Hvidovre Hospital, Hvidovre, Denmark; and †Statens Serum Institut, Copenhagen, Denmark
In Copenhagen, methicillin-resistant Staphylococcus aureus (MRSA) accounted for <15 isolates per year
during 1980–2002. However, since 2003 an epidemic increase has been observed, with 33 MRSA cases
in 2003 and 110 in 2004. We analyzed these 143 cases epidemiologically and characterized isolates by
pulsed-field gel electrophoresis, Staphylococcus protein A (spa) typing, multilocus sequence typing,
staphylococcal chromosome cassette (SCC) mec typing, and detection of Panton-Valentine leukocidin
(PVL) genes. Seventy-one percent of cases were community-onset MRSA (CO-MRSA); of these, 36%
had no identified risk factors. We identified 29 spa types (t) and 16 sequence types (STs) belonging to 8
clonal complexes and 3 ST singletons. The most common clonal types were t024/ST8-IV, t019/ST30-IV,
t044/ST80-IV, and t008/ST8-IV (USA300). A total of 86% of isolates harbored SCCmec IV, and 44% had
PVL. Skin and soft tissue infections dominated. CO-MRSA with diverse genetic backgrounds is rapidly
emerging in a low MRSA prevalence area.
For many years, methicillin-resistant Staphylococcus aureus (MRSA) has been a serious
and common nosocomial pathogen in hospitals outside the Nordic countries and the Netherlands
(1). Community-onset MRSA (CO-MRSA) was first reported in Western Australia in the early
1990s (2) and has, especially during the past 5 years, emerged as a global problem (1,3). COMRSA
in the United States has mostly been caused by the Panton-Valentine leukocidin (PVL)–
positive clones USA400 (sequence type [ST]1) and more recently by USA300 (ST8) (1,4–7). In
Europe the increase in CO-MRSA has mostly been attributed to the PVL-positive ST80 clone
Page 2 of 18
(3,8). In Denmark, since 1980, MRSA has accounted for <100 MRSA isolates per year
nationwide (www.danmap.org/pdffiles/danmap_2005.pdf). At our laboratory, MRSA has been
isolated from <15 patients per year until 2002. Approximately half of the MRSA cases found in
Denmark during these years were imported, i.e., through patients transferred from foreign
Since 2003 the number of MRSA-positive persons increased both nationally and in
Copenhagen. Nationally, the number increased from 50–105 new cases per year to 243 in 2003,
549 in 2004, and 864 in 2005. At Hvidovre Hospital, we found MRSA in 5 persons in 2001, 14
in 2002, 33 in 2003, 110 in 2004, and 170 in 2005. We describe the epidemiology of the
emergence of MRSA in Copenhagen in 2003 and 2004 and characterize the genetic background
of the isolates.
Staphylococci can cause a wide variety of diseases in humans and other animals either through toxin production or
invasion. Staphylococcal toxins are a common cause of food poisoning. The bacteria grow in improperly stored food.
Although the cooking process kills them, the enterotoxins are heat resistant and can survive boiling for several minutes.
Staphylococci can grow in foods with relatively low water activity (such as cheese and salami).
One pathogenic species is Staphylococcus aureus, which can infect wounds. These bacteria can survive on dry
surfaces, increasing the chance of transmission. Of this type, Methicillin-resistant Staphylococcus aureus (MRSA) has
recently become a major cause of hospital-acquired infections and is being recognized with increasing frequency in
community acquired infections. S. aureus is also implicated in toxic shock syndrome; during the 1980s some tampons
allowed the rapid growth of S. aureus, which released toxins that were absorbed into the bloodstream. Any S. aureus
infection can cause the staphylococcal scalded skin syndrome, a cutaneous reaction to exotoxin absorbed into the
bloodstream. It can also cause a type of septicaemia called pyaemia.
The coagulase positive Staphylococcus that inhabits and sometimes infects the skin of domestic dogs and cats is
Staphylococcus intermedius. This organism, too, can carry the genetic material that imparts multiple bacterial
resistance. It is rarely implicated in infections in humans, as a zoonosis.
S. epidermidis, a coagulase-negative staphylococcus species, is a commensal of the skin, but can cause severe
infections in immune suppressed patients and those with central venous catheters.
S. saprophyticus, another coagulase-negative species, is predominantly implicated in genitourinary tract infections in
sexually active young women.
In recent years several other Staphylococcus species have been implicated in human infections, notably S.
lugdunensis, S. schleiferi, and S. caprae.
Staphylococcus can also be found on the tips of the fingers. Most commonly it is found on the index finger as well as
the thumb. This infection is known as a felon. As are many other "staph" infections this is very painful and can be
treated with antibiotics.
Necrotizing fasciitis is the result of an invasive bacterial infection that destroys deep soft tissue .
Staphylococcus genus: S. aureus is a leading cause of soft tissue infections, as well as toxic shock syndrome (TSS)
and scalded skin syndrome. pathogenic effects of Staph are mainly asssociated with the toxins it produces. it is not
uncommon for an infected site to contain no viable Staph cells. The S. aureus enterotoxin causes quick onset food
poisoning which can lead to cramps and severe vomiting. microbes also secrete leukocidin, a toxin which destroys white
blood cells and leads to the formation of pus and acne. S. aureus has been found to be the causative agent in such
ailments as pneumonia, meningitis, boils, arthritis, and osteomyelitis (chronic bone infection).
S. epidermis is an opportunistic pathogen which is a normal resident of human skin. Those susceptible to infection by
the bacterium are IV drug users, newborns, elderly, and those using catheters or other artificial appliances
The results of Necrotizing infections are no a pretty sight
Am J Surg. 1977 Jul ;134 (1):52-7 327844 [Cited: 4]
Bacteriology of necrotizing fasciitis.
[My paper] A Giuliano , F Lewis Jr , K Hadley , F W Blaisdell
Sixteen patients with necrotizing fasciitis were observed under clinical and laboratory conditions for collection,
preservation, and culture that permitted optimal retrieval of anaerobes. The clinical observations of necrosis of fascia,
subcutaneous fat and skin with thrombosis of the microvasculature, and absence of myonecrosis were clearly apparent
in these patients. Two clear-cut groups of culture and gram stain results were found, suggesting that the clinical entity
of necrotizing fasciitis can occur after infection by different infecting organisms. The cultivation of Streptococcus
pyogenes (group A), either alone or in combination with staphylococcus, in three patients conforms to the culture
results found by Meleney  in his original description.