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Journal of Clinical Microbiology, December 2000, p. 4640-4642, Vol. 38, No. 12
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Apparent Culture-Negative Prosthetic Valve
Endocarditis Caused by Peptostreptococcus magnus
Eric R.
van der
Vorm,1,*
Arjen M.
Dondorp,2
Ruud J.
van
Ketel,1 and
Jacob
Dankert1
Department of Medical
Microbiology1 and Department of
Intensive Care,2 Academic Medical Center,
University of Amsterdam, Amsterdam, The Netherlands
Received 10 July 2000/Returned for modification 6 August
2000/Accepted 13 September 2000
 |
ABSTRACT |
In two patients with prosthetic valve endocarditis due to
Peptostreptococcus magnus, blood cultures in the BacT/Alert
and BACTEC 9240 systems were signal negative. The capability of the BacT/Alert system to detect various Peptostreptococcus
species was assessed. P. magnus and P. anaerobius could not be detected, and subcultures remained
negative. The growth in conventional media of these two species and
other Peptostreptococcus species was similar.
 |
TEXT |
Gram-positive anaerobic cocci (GPAC)
are commonly present in clinical specimens and are often mixed with
other anaerobic or aerobic bacteria. GPAC can be involved in chronic
infections of the upper respiratory tract, ears, mastoid, sinuses and
teeth, intra-abdominal and female pelvic regions, subcutaneous and soft tissue abscesses, and diabetic foot ulcers, as well as in osteomyelitis and arthritis (2, 3, 7). Peptostreptococcus
magnus, one of the GPAC species, is part of the normal flora of
the human mucocutaneous surfaces. Although P. magnus is the
most frequently isolated GPAC from clinical specimens, as well as in
pure culture and from normally sterile sites, it has been scarcely
reported as a cause of septicemia or native- or prosthetic-valve
endocarditis (7, 8). Automated blood culture systems are
developed in order to culture a broad variety of microorganisms. The
anticipated pitfall of these systems is the inability to recover
fastidious microorganisms with low CO2 production, such as
Brucella species (12). Recently, however,
false-negative cultures in an automated blood system were also reported
for Pseudomonas aeruginosa as well (5). We report
here two cases of prosthetic-valve endocarditis due to P. magnus which was recovered after culturing the surgically removed
infected valve, whereas BacT/Alert blood cultures, incubated for
14 days, remained negative. Therefore, we assessed the
capability of the BacT/Alert system to detect GPAC bacteremia.
Case 1.
The first case was a 65-year-old man who suffered from
a mitral valve incompetence due to degenerative changes. The patient was scheduled for mitral valvuloplasty and a venous single graft coronary bypass on the posterior descending branch. Routine
preoperative screening for infectious dental foci was negative.
During the operation, valvuloplasty appeared to give insufficient
results, so the mitral valve was excised and replaced with a prosthetic heart valve (Medtronic Hall number 29). The patient received
cefamandole as routine surgical prophylaxis for 2 days. The
postoperative course was unremarkable, and the patient was discharged
19 days after surgery. On day 23 the patient was admitted to local
hospital A because of a high-grade fever (39.2°C) with cold chills.
On physical examination he was hemodynamically stable and clear clicks of the prosthetic valve were present without any murmurs. The wound of
the venectomy on the left leg was slightly inflamed. C-reactive-protein
(CRP) levels were increased up to 157 U/liter, there was a mild
normocytic anemia of 5.6 mmol/liter, and there was an increased
leukocyte count of 34.2 × 109/liter, with band
forms. In total, 14 blood culture sets were taken and
incubated in the BACTEC 9240 system. All cultures remained negative
after incubation for 2 weeks. A culture taken from the venectomy wound
revealed Staphylococcus aureus, and flucloxacillin was
started (6,000 mg/24 h). Despite treatment, the patient remained febrile. On day 33 after surgery, the patient developed a sudden, rapidly progressive pulmonary congestion and was referred to our hospital. On transesophageal echocardiography (TEE), a severe paravalvular leakage of the prosthetic mitral valve was demonstrated due to an almost complete dehiscence. On this valve, vegetations were
observed. Two blood culture sets were taken and incubated in the
BacT/Alert system, used in our laboratory. At reoperation the infected
prosthetic valve was removed, the infected area was surgically cleaned,
and a new Medtronic Hall prosthetic mitral valve was implanted. The
removed valve was immediately transported to our laboratory in a
sterile container. Several impression smears were made. Gram staining
showed some destructed cells and no bacteria. Histopathologic
preparations showed only degenerative changes and no bacteria. Valve
parts were ground and cultured on Columbia blood agar (Oxoid,
Basingstoke, England), on chocolate agar (GC Agar Base; Oxoid), and in
BBL Thioglycollate Medium (Becton Dickinson, Cockeysville, Md.).
Incubation was done at 5% CO2 and anaerobically at 37°C
for up to 7 days. The patient was treated with vancomycin (2,000 mg/24
h), gentamicin (240 mg/24 h), and rifampin (1,200 mg/24 h). Despite
maximal support, the patient died 2 days later because of untreatable
cardiogenic shock. On autopsy, a dilated hypertrophic left and right
ventricle was found with signs of an old infarction in the posterior
wall with recent extension to the lateral side of the septum. The
grafts on the posterior descending branch and the descending
anterior branch were patent. There was no dehiscence of the
reimplanted prosthetic heart valve. In the BacT/Alert system no growth
was detected after incubation for 14 days. Subcultures of the four
BacT/Alert bottles on Columbia blood agar and chocolate agar were also
negative. Anaerobic culture of the removed infected heart valve yielded
a few colonies of large gram-positive cocci after 48 h of
incubation on blood agar. Also, the Thioglycollate Medium showed
growth after 48 h. The cocci were biochemically inert,
sensitive for kanamycin, and resistant for sodium
polyanethol sulfonate (SPS) and were identified as P. magnus. The identification was confirmed by 16S rRNA sequencing (National Institute of Public Health, Bilthoven, The Netherlands).
Case 2.
The second case was a 39-year-old male who underwent
an aortic valve replacement because of severe aortic
regurgitation. Routine preoperative screening for infectious
dental foci was negative. Two months after the operation
dehiscence of the prosthetic valve was seen on TEE with paravalvular
leakage. A few months later there were progression of the dehiscence
and valvular vegetations, and aortic root abscesses could be detected
by TEE. Blood cultures collected at local hospital B and incubated in
the BACTEC 9240 remained negative, and no antibiotic therapy was
started. The patient was referred to our hospital for a second aortic
valve (Sorin 29) replacement. On admission, the CRP level was elevated (104 U/liter), and blood cultures were obtained. The removed valve was
handled according to standard operating procedures as described above
(case 1). The Gram staining of impression smears showed some leukocytes
and sporadic gram-positive cocci. Empirical treatment was started with
vancomycin (2,000 mg/24 h) and gentamicin (240 mg/24 h). Seven blood
culture sets incubated for 14 days in the BacT/Alert system remained
negative. P. magnus grew after 96 h of culture of the
valve vegetations on blood agar and in Thioglycollate Medium. The
patient was started on penicillin G (12,000,000 U/24 h) and
metronidazole (1,500 mg/24 h). A few days later a third operation was
necessary because of the presence of abscesses detected by TEE. A
bioprosthesis (Freestyle) was inserted. The postoperative period was
without complications, and the patient recovered completely. After 6 weeks of treatment, the CRP level was normal (<3 U/liter), and the
antibiotics were discontinued.
The findings of these two cases prompted us to the question whether
P. magnus could be detected in the BACTEC and BacT/Alert automated blood culture systems. Since we use the BacT/Alert system, assessment was done in this system. We compared the growth of P. magnus and other GPAC, including a more fastidious species (P. anaerobius) in blood culture media. The isolates from
the patients (G9g1, G11a2), other isolates from our own collection, and
strains from the American Type Culture Collection (ATCC) were used
(Table 1). After 48 h of anaerobic
growth a colony of GPAC was taken from a subculture, diluted in
phosphate-buffered saline (Merck), and then further diluted in horse
blood. Aerobic (FA) and anaerobic (FN) BacT/Alert FAN bottles were
seeded with 5 ml of horse blood containing 103 to
104 GPAC CFU per ml and incubated as recommended by the
manufacturer (Organon Teknika, Durham, N.C.). Simultaneously (for
quantity control), 10 µl of the blood sample was plated on blood
agar, and colonies were counted after 48 h of anaerobic growth.
Bacterial growth in these bottles was compared with that in
Thioglycollate Medium and Columbia Broth (Becton Dickinson,
Cockeysville, Md.), daily spotted by eye. Subcultures from
culture-negative bottles were made on days 3, 7, and 14 on blood agar
and incubated anaerobically for up to 96 h.
View this table:
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TABLE 1.
Growth of peptostreptococci in BacT/Alert FAN anaerobic
and aerobic blood culture media, Thioglycollate Medium, and Columbia
Broth supplemented with 5 ml of horse blood
|
|
P. micros,
P. asaccharolyticus, and
P. productus (recently renamed as
Ruminococcus productus)
grew readily in the anaerobic
BacT/Alert FAN bottles and were routinely
detected via CO
2 production.
Some
P. micros and
P. asaccharolyticus isolates also grew in the
vented aerobic
BacT/Alert FAN bottle (two of six isolates automatically
detected and
one of six isolates after subculture; Table
1).
P. magnus
and
P. anaerobius were not detected by the BacT/Alert
FAN
system, and subcultures remained negative (Table
1).
P. magnus grew readily in Thioglycollate Medium and Columbia Broth.
Repeated
seeding experiments in BacT/Alert FAN bottles (FN) with
inocula
of
P. magnus isolates ranging from 10
3
to 10
5 CFU/ml remained signal negative. Subcultures only
revealed growth
for the G9g1 isolate at an inoculum of 10
5
CFU/ml. There was no increase in CFU after incubation for 3 days,
and
subcultures after days 7 and 14 were negative. Thus, survival
in the
BacT/Alert system seems possible at high inocula for a
limited time.
The lack of growth of
P. magnus in the BacT/Alert
system has
not been described previously to our knowledge. SPS
cannot account for
this finding, because the
P. magnus isolates
were tested for
susceptibility to SPS and proved to be resistant.
The reason for the
inability to grow in the BacT/Alert system
for
P. magnus,
remains unclear. Strains of
P. anaerobius are known
to be
sensitive for SPS. Their inability to grow in the BacT/Alert
system is
probably due to SPS. However, some
P. anaerobius strains
have been detected in the routine use of the BacT/Alert system
(
11).
At local hospital A, where patient 1 was originally treated, 28 blood
culture bottles had been taken. No growth was detected
in the routine
setting by their BACTEC system. When the cultures
of the valve became
positive, 16 bottles were still available
for prolonged incubation (up
to 28 days) and subculture. In only
two bottles was
P. magnus detected after subculture. Thus, in
the BACTEC system
P. magnus also does not grow readily and at
least cannot be
automatically detected, probably due to insufficient
CO
2 production.
Endocarditis caused by GPAC remains a rare event.
P. micros,
P. magnus, and
P. anaerobius are the
species that have been described
in case reports so far (
6,
7,
8,
10). Anaerobic bacteria
are recovered from 3 to 8% of the
positive blood cultures in comparative
studies of various automated
blood culture systems (
1,
4,
9,
11,
13).
Clostridium and
Bacteroides species are the
predominant clinical relevant anaerobic species isolated.
P. micros is the most common GPAC isolate cultured from automated
blood
systems, probably because of its ability to produce
CO
2. The frequency
of
P. magnus in such systems
may be underestimated, based on our
findings. Since we were able to
culture the organism from the
excised valve in a case of apparent
culture-negative endocarditis,
P. magnus may be the
etiological agent in other cases of culture-negative
endocarditis and
has to be taken into account when selecting empirical
treatment.
Remarkably, in an earlier report of prosthetic valve
endocarditis,
P. magnus also was only detected after culture of
the
infected valve (
8).
In cases of bacteremia and native- or prosthetic-valve endocarditis,
automated blood culture sets may be not sensitive enough
to detect
microorganisms such as
P. magnus. Therefore, we recommend
the use of additional media, such as conventional Thioglycollate
Medium, for blood cultures from patients suspected for such
infections.
 |
FOOTNOTES |
*
Corresponding author. Mailing address: Laboratory
of Public Health, P.O. Box 30039, 9700 RM Groningen, The
Netherlands. Phone: 31 (0) 50-521-5100. Fax: 31 (0) 50-527-1488. E-mail: ervandervorm{at}hotmail.com.
 |
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Journal of Clinical Microbiology, December 2000, p. 4640-4642, Vol. 38, No. 12
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.