This study reports a case of
Staphylococcus warneri
dissemination in the hair of ICU/ER doctors. Eleven of 23 doctors in the first survey and
11 of 24
doctors in the second survey, which were conducted after 6 months, carried S. warneri, while hair contamination of other coagulase-negative staphylococci was only sporadic. Chromosomal DNA analysis with PFGE revealed that 7 S. warneri strains isolated in the first survey and 7 strains isolated in the second survey showed similar PFGE patterns, suggesting that a cross-infection with a S. warneri strain continued over 6 months among the ICU doctors.
<i>Staphylococcus warneri</i> ICU Doctor PFGE1. Introduction
Coagulase-negative staphylococcal species (CNS) constitute a major component of the normal flora of the human skin. Their role in causing opportunistic infections, however, has been recognized in recent years. Infections caused by CNS involve indwelling catheters and artificial devices and are sometimes life-threatening. Kawamura identified 1230 staphylococcal strains from human clinical specimens with DNA-DNA hybridization, the most reliable method for the determination of staphylococcal species, and found that the isolation frequencies of CNS species were in the order of Staphylococcus epidermidis, S. haemolyticus, S. caprae, S. simulans, S. hominis, S. capitis, S. saprophyticus, S. warneri, and S. lugdunensis [1] . CNS colonizing on the hair and in the skin niche of patients is probably the source of infection and those colonizing on the hair and the skin of doctors and nurses can also be the source of infection in compromised patients. We therefore investigated the colonization of staphylococci on the hair of doctors working in the surgical ICU/ER of a university hospital, and found the dissemination of a S. warneri strain among the ICU doctors.
2. Materials and Methods2.1. Samplings and Identification of Bacteria
A bunch of head hair was removed without contamination from each of the 36 ICU doctors at a university hospital in July 2011, January 2012, and April 2012. The second survey was conducted without informing the examinees of the results of the first survey; however, the third survey in April 2012 was conducted 2 weeks after informing the examinees of the previous results.
A 10-cm-long hair from each examinee was used for bacterial examination. The hair was homogenized with a glass homogenizer (Iwaki Sci Tech, AGC, Japan) in 0.2 mL sterilized distilled water and 20 μL of the supernatant was inoculated on a mannitol salt agar plate (Nissui Pharmaceutical Co., Ltd., Tokyo, Japan). After 48 h of incubation at 37˚C, colonies on the plate were gram-stained, and suspected colonies were applied to a VITEK 2 automated system with a GP card (bioMerieux Inc., Durham, NC, USA) for identification. Identified staphylococci were then amplified in Tryptic Soy Broth (BD Japan, Tokyo, Japan) and stored at −80˚C until use. This study was approved as the approved number 59 by the institutional ethics committee, Sugiyama Jogakuen University School of Nursing, Nagoya, Japan. All subjects provided informed consent prior to enrollment in the study.
2.2. DNA Fingerprinting
DNA fingerprinting of S. warneri chromosomal DNA was performed by pulsed-field gel electrophoresis (PFGE) as described previously, with some modifications [2] [3] . In brief, the bacteria were spread from the −80˚C stock on LB agar and cultured overnight at 37˚C. The colonies were collected and suspended in TE8 buffer (10 mM Tris-HCl and 1 mM EDTA, pH 8.0). The suspension was mixed with an equal volume of 1.2% Seaken Gold Agarose (Cambrex Bio Science Rockland, Inc., Rockland, ME, USA) and allowed to solidify in a CHEF disposable plug mold (Bio-Rad Laboratories, Inc., Hercules, CA, USA). The gel block was incubated for 24 h at 37˚C in a lysis solution [1 M NaCl, 0.1 M EDTA, 6 mM Tris-HCl, pH 8.0, 0.2% deoxycholate, 0.5% Na-N-do- decylsarcosine, supplemented with lysozyme (3 mg/mL, Sigma-Aldrich Japan, Tokyo, Japan) and lysostaphin (60 IU/mL, Wako Pure Chemical Industries, Ltd., Osaka, Japan)]. The block was then incubated at 55˚C for 20 h in a proteinase K solution [0.5 M EDTA, 3 % Na-N-dodecylsarcosine, pH 8.0, supplemented with proteinase K (1 mg/mL, Wako Pure Chemical Industries, Ltd.)] and washed with TE8 buffer for more than 8 h. A thinly sliced section of the block was digested with 10 units of SmaI (Takara Bio Inc., Shiga, Japan) overnight at 30˚C and then electrophoresed at 6 V/cm for pulse times ranging from 1 to 40 s through 1% agarose gel in TBE buffer (50 mM Tris-HCl, 50 mM boric acid, 1 mM EDTA, pH 8.0), supplemented with 50 μM thiourea (Wako Pure Chemical Industries, Ltd.) at 14˚C for 20 h with the CHEF-DRII system (Bio-Rad Laboratories, Inc.). Thereafter, the gel was stained with ethidium bromide, washed with distilled water, and photographed. A yeast chromosome PFGE marker (New England Biolabs Japan, Inc., Tokyo, Japan) was used as the size standard. Chromosomal patterns were digitally analyzed with Finger Print II (Bio-Rad) to generate a dendrogram based on Dice coefficients.
3. Results and Discussion
An aliquot of the supernatant of the hair-homogenate was cultured on mannitol salt agar plates and bacterial colonies on the plates were gram-stained. Colonies of probable staphylococci were further identified with a VITEK 2 automated system/GP card. As shown in Table 1, most identified species of the strains that colonized on the hair of the ICU doctors were CNS, and among these, S. warneri was dominant. Eleven of 23 doctors in the first survey and 11 of 24 doctors in the second survey carried S. warneri. Other identified species were S. aureus, S. epidermidis, and S. kristinae. None of the examined doctors in the third survey carried staphylococci in their hair.
Chromosomal DNA fragment analysis with PFGE presented in Figure 1 and Figure 2 revealed two lineages
PFGE analysis of Staphylococcus warneri strains. Chromosomal DNA of S. warneri strains sw1-sw22 digested with SmaI was analyzed with PFGE. M, Yeast chromosome size standard
Dendrogram of PFGE results based on the Dice coefficients and schematic representation of the SmaI restriction pulsotype of S. warneri strains
A and B of S. warneri strains. A group of sw9, sw19, sw10, and sw16 showed an almost identical pattern and the patterns of a group of sw1, sw2, sw7, and sw8 were almost identical, suggesting that cross-infections with S. warneri strains existed among the ICU doctors. S. warneri sw1, sw2, sw5, sw7, sw8, sw9, and sw10 isolated from the hair of different doctors in the first survey, and sw14, sw16, sw18, sw19, sw20, sw21, and sw22 iso-
Isolation of staphylococci from the hair of ICU/ER doctors
Examinee*1)
First survey (July 2011)
Second survey (January 2012)
Third survey (April 2012)
1
S. warneri (sw1)
ND*2)
ND
2
S. aureus
3
S. warneri (sw2)
ND
4
S. epidermidis
ND
ND
5
S. warneri (sw3)
ND
ND
6
S. kristinae
ND
ND
7
S. epidermidis
ND
ND
10
S. warneri (sw4)
ND
ND
11
ND
ND
ND
13
S. warneri (sw5)
S. warneri (sw12)
ND
14
S. warneri (sw6)
S. warneri (sw13)
ND
15
ND
S. warneri (sw14)
ND
16
ND
S. warneri (sw15)
ND
17
ND
S. warneri (sw16)
ND
18
S. warneri (sw7)
S. warneri (sw17)
ND
19
ND
ND
20
S. warneri (sw8)
S. warneri (sw18)
21
S. warneri (sw9)
S. epidermidis
ND
22
ND
ND
23
ND
ND
ND
24
S. warneri (sw10)
ND
25
S. warneri (sw19)
ND
26
ND
27
ND
28
ND
ND
29
S. warneri (sw11)
ND
30
ND
ND
31
ND
ND
32
ND
ND
33
S. warneri (sw20)
ND
34
S. warneri (sw21)
ND
35
ND
ND
36
S. warneri (sw22)
ND
*1) ICU/ER doctor. *2) ND, no staphylococci was isolated.
*Corresponding author.
Although S. warneri represents only 1% of the skin staphylococci in normal individuals [5] , it may be associated with various human infections such as septicemia, endocarditis, meningitis, conjunctivitis, and wound infections [5] - [8] . According to previous reports, S. warneri infections were most frequently associated with indwelling devices in patients with underlying immunosuppressive illnesses [7] [8] . All postoperative patients in ICU are in high-risk conditions with indwelling catheters after severely invasive treatments. S. warneri may cause serious infections, including blood stream infections and endocarditis, in these patients. This study therefore emphasizes the importance of the eradication of S. warneri from the hair of ICU doctors.
Conflict of Interest Statement
The authors have no conflict of interest to report.
Funding
This study was supported by Grants-in-aid for Scientific Research (C)-24593262 and (C)-24593541 from the Ministry of Education and Culture, Sports, Science and Technology-Japan.
Cite this paper
IkueShamoto,YukaIshihara,AkikoSato,HisaeUsami,NaoyukiMatsuda,MichioOhta, (2015) Dissemination of Staphylococcus warneri in the Hair of ICU Doctors. Advances in Microbiology,05,599-603. doi: 10.4236/aim.2015.58062
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