Stenotrophomonas maltophilia and species of the Burkholderia cepacia complex are opportunistic pathogens that cause infections in immunocompromised hosts. They are associated with nosocomial infections from medical equipment and solutions. Transmission between cystic fibrosis patients has also been observed. Accurate diagnosis and antibiotic susceptibility testing are important due to their high intrinsic antibiotic resistance. Treatment often involves combination therapy with trimethoprim-sulfamethoxazole or other agents shown to have in vitro activity. Strict infection control and water supply surveillance are needed to prevent nosocomial outbreaks.
Stenotrophomonas maltophilia and species of the Burkholderia cepacia complex are opportunistic pathogens that cause infections in immunocompromised hosts. They are associated with nosocomial infections from medical equipment and solutions. Transmission between cystic fibrosis patients has also been observed. Accurate diagnosis and antibiotic susceptibility testing are important due to their high intrinsic antibiotic resistance. Treatment often involves combination therapy with trimethoprim-sulfamethoxazole or other agents shown to have in vitro activity. Strict infection control and water supply surveillance are needed to prevent nosocomial outbreaks.
Stenotrophomonas maltophilia and species of the Burkholderia cepacia complex are opportunistic pathogens that cause infections in immunocompromised hosts. They are associated with nosocomial infections from medical equipment and solutions. Transmission between cystic fibrosis patients has also been observed. Accurate diagnosis and antibiotic susceptibility testing are important due to their high intrinsic antibiotic resistance. Treatment often involves combination therapy with trimethoprim-sulfamethoxazole or other agents shown to have in vitro activity. Strict infection control and water supply surveillance are needed to prevent nosocomial outbreaks.
Stenotrophomonas maltophilia and species of the Burkholderia cepacia complex are opportunistic pathogens that cause infections in immunocompromised hosts. They are associated with nosocomial infections from medical equipment and solutions. Transmission between cystic fibrosis patients has also been observed. Accurate diagnosis and antibiotic susceptibility testing are important due to their high intrinsic antibiotic resistance. Treatment often involves combination therapy with trimethoprim-sulfamethoxazole or other agents shown to have in vitro activity. Strict infection control and water supply surveillance are needed to prevent nosocomial outbreaks.
Burkholderia cepacia complex (BCC) are opportunistic gram-negative pathogens that cause a variety of clinical infections in various immunocompromised hosts including individuals with host genetic defects and individuals with weakened immune systems. Epidemiology • S. maltophilia has had increasing rates of isolation worldwide and has caused nosocomial infections associated with medical equipment and solutions. It also is known to cause invasive infections in patients with cancer and has been increasing in frequency in patients with cystic fibrosis (CF). • BCC species have caused nosocomial outbreaks associated with contaminated solutions and can cause significant morbidity and mortality in patients with CF and chronic granulomatous disease. Burkholderia cenocepacia and Burkholderia multivorans are two of the major species that are found to cause disease in patients with CF. Patient-topatient transmission has been demonstrated in patients with CF. Microbiology • S. maltophilia and BCC spp. are gram- negative aerobic bacteria that are motile. • As free-living organisms, they reside in a broad range of environments including aquatic environments. • They are catalase-positive, they do not ferment glucose, and many BCC members are oxidase-positive. • BCC spp. comprise a number of phenotypically similar but genotypically distinct species; currently there are at least 20 species in the BCC. • S. maltophilia is found worldwide and has significant genetic diversity among isolates. Diagnosis • Accurate diagnosis is critical, as these pathogens have high levels of intrinsic antibiotic resistance. Newer methods have been used for successful identification of both BCC members and S. maltophilia including 16S ribosomal RNA sequencing and matrix- assisted desorption/ ionization time-of- flight mass spectrometry. Therapy • Given that both pathogens have high levels of intrinsic resistance to antibiotics, choice of antibiotics should be driven by antibiotic susceptibility testing. • Trimethoprim-sulfamethoxazole is the preferred antibiotic for both S. maltophilia and BCC, although resistance has been reported and is increasing in certain areas. Combination therapy is frequently used. • Fluoroquinolones such as moxifloxacin show activity in S. maltophilia, but resistance has been reported during single-drug therapy. • Other drugs that have been shown to have in vitro and in vivo activity in both pathogens include minocycline, ceftazidime, and newer agents such as ceftazidime-avibactam. Carbapenems have activity in BCC, and ticarcillin- clavulanate and ampicillin-sulbactam can retain activity in S. maltophilia. Prevention • Nosocomial outbreaks require strict infection control measures including isolation measures. • Surveillance of hospital water supplies is important f