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Journal of Clinical Microbiology, January 2000, p. 460-461, Vol. 38, No. 1
0095-1137/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Isolation of Pantoea agglomerans in Two
Cases of Septic Monoarthritis after Plant Thorn and Wood Sliver
Injuries
C.
De
Champs,1,*
S.
Le
Seaux,2
J. J.
Dubost,2
S.
Boisgard,3
B.
Sauvezie,2 and
J.
Sirot1
Service de
Bactériologie,1 Service de
Rhumatologie,2 and Service
d'Orthopédie-Traumatologie,3 CHRU BP
69, 63003 Clermont-Ferrand Cedex, France
Received 22 February 1999/Returned for modification 31 July
1999/Accepted 27 September 1999
 |
ABSTRACT |
Arthritis after plant injury is often apparently aseptic. We report
two cases due to Pantoea agglomerans. In one case, the bacterium was isolated only from the pediatric blood culture media, BACTEC Peds Plus, monitored in BACTEC 9240, and not from the other media inoculated with the joint fluid. This procedure could help improve the diagnosis of septic arthritis.
 |
CASE REPORTS |
Case 1.
A 13-year-old boy, 50 kg
in weight, was admitted to the hospital for sepsis with arthritis of
the right knee. One month before, he had run a thorn into his knee
after falling into a bush. Two days later, joint aspiration produced a
yellow inflammatory-looking fluid which was not analyzed. Twenty-three
days later, the knee had swollen again, and so a second aspiration was
performed. The fluid was clear and contained 4,000 leukocytes/mm3 with 90% polymorphonuclear leukocytes.
Cultures were negative on the usual media, Chocolat Polyvitex
(BioMérieux, Marcy l'Etoile, France) in CO2,
Columbia colistin-nalidixic acid agar (BioMérieux) in
CO2, 5% horse blood Trypticase soy agar
(BioMérieux), and Schaedler broth (BioMérieux). Four days
after the second aspiration and 3 days before admission, he developed a
fever (39°C) and chills. On admission, the knee was tender, warm, and
swollen. He still had a fever. Clinical examination showed no
adenopathy or other septic localization. Abnormal laboratory findings
included a leukocyte count of 12,610/mm3 with 73%
neutrophils, a C-reactive-protein level of 221 mg/liter, and a
erythrocyte sedimentation rate of 68 mm/h. Radiographs of the knee were
normal. Arthrocentesis yielded 120 ml of purulent fluid containing 850 erythrocytes/mm3, 170,000 leukocytes/mm3, and
88% polymorphonuclear leukocytes. Direct examination was negative.
Bacterial growth was detected 17 h after inoculation of the fluid
(3 ml) in a BACTEC Peds Plus F broth (Becton Dickinson, Meylan, France)
incubated at 37°C in BACTEC 9240 (Becton Dickinson). A gram-negative
bacillus was observed and was subcultured to Chocolat Polyvitex
(BioMérieux). It was identified as a Pantoea sp. by an
ID-32E system (BioMérieux). BACTEC Peds Plus F contains a soybean-casein digest broth, resins, CO2, and a
fluorescence sensor. BACTEC 9240 (Becton Dickinson) detects increases
in CO2 produced by microorganisms. No growth was observed
on the other two culture media, 5% Columbia sheep blood
(BioMérieux) in an anaerobic jar with a gas-generating envelope
(AnaeroGen; Oxoid, Basingstoke, England) and Chocolat Polyvitex
(BioMérieux) in CO2 (CO2 Gen; Oxoid),
each inoculated with 0.05 ml of the fluid. Antimicrobial susceptibility
testing was performed with rapid ATB-E strips (BioMérieux). The
isolate was resistant to fosfomycin and mecillinam and susceptible to
other antibiotics. The patient was first treated for 48 h with 1 g of amikacin intravenously (i.v.) and 4 g of oxacilline
i.v. The latter was replaced by 6 g of cefotaxime i.v. Local
treatment included immobilization, daily aspiration, and after eight
days, joint irrigation by arthroscopy followed by 160 mg of
intra-articular gentamicin. A Pantoea sp. was isolated from
the first three daily aspirations from BACTEC Peds Plus F alone and not
from the other two media. Synovial fluid cultures were negative
thereafter. After 16 days, amikacin and cefotaxime were replaced by
oral amoxicillin (3 g/day) and minocycline (2 g/day) with a favorable outcome.
Case 2.
A 36-year-old woman with systemic lupus erythematosus
treated by hydroxychloroquine alone was hospitalized 19 days after
having injured her left thumb in a fall against a wooden fence post. She presented with septic arthritis of the interphalangeal joint. Her
leukocyte count was 6,330/mm3 with 80% neutrophils,
4.25 g of fibrinogen per liter, and a erythrocyte sedimentation
rate of 40 mm/h. A surgical excision yielded pus and a 1-cm-long wood
sliver in the thumb pulp. Pantoea agglomerans was isolated
from 5% sheep blood agar plates, both inoculated with a swab and
cultured at 37°C, one in an aerobic environment and the other in an
anaerobic environment. The septic arthritis was cured by a 3-month
treatment of oral amoxicillin-clavulanate (2 g/day) and
ciprofloxacin (2 g/day).
Discussion.
P. agglomerans, formerly named
Enterobacter agglomerans (5), is a ubiquitous
Enterobacteriaceae that is found in plants and in the feces
of humans and animals. It is less often implicated in infection than
Enterobacter aerogenes and Enterobacter cloacae and usually complicates debilitating illnesses (10). In the absence of preexisting disease, septic arthritis is rare, particularly in children or infants (6). Of the 294 patients admitted for septic arthritis to our hospital between 1979 and 1998, the two in this
report were the only cases in which P. agglomerans was isolated (2). In systemic lupus erythematosus, increased
susceptibility to infection is common during flares, in cases of severe
disease, and during steroid therapy. None of these factors were present in our second patient, and the first patient had no risk factor. It is
noteworthy that in one patient the source of contamination was a plant
thorn and in the other a sliver of wood in contact with plants and that
the incubation period before hospitalization was longer than 3 weeks.
In both of the two other documented cases infection was also due to
plant material contamination (3, 8). However, several cases
of febrile, apparently aseptic, synovitis after plant injury have been
reported (8, 11, 12). Opinion differs on the role played
by plants in the onset of long-lasting monoarthritis (4, 9).
Most authors who failed to isolate microorganisms assumed that it
results from hypersensitivity or toxic reactions (1, 8).
False negative results of bacterial culture are frequent in septic
arthritis, being estimated at 10 to 20% (7); therefore,
bacterial origin should not be ruled out (4). The use of
blood culture media for joint fluid is much debated. Several authors
have reported improved performances with blood culture media,
especially for the detection of fastidious organisms (2, 13,
14). The advantage of inoculating the fluid into blood culture
vials is diluting complement, antibodies, antibiotics, and other
factors that inhibit the growth of microorganisms (14). This
was borne out in the first patient, especially with the samples taken
on the second and third days after the beginning of the antibiotic
treatment. In the second patient, the bacteria grew on agar media. One
possible explanation is that the pus contained higher concentrations of
bacteria than did the large volume of synovial fluid aspirated from the
first patient. The sample taken was in contact with the wood sliver,
which was still embedded in the thumb.
To our knowledge, there is no previous report on the use of BACTEC Peds
Plus F broth for joint fluid culture. In the first patient, it was the
only medium that allowed bacterial growth. This result was confirmed in
three instances. If it had not been used, the diagnosis would have been
inflammatory sterile arthritis due to thorn injury. Direct bedside
inoculation of BACTEC Peds Plus by the clinician who performs
arthrocentesis could increase the sensitivity of bacterial isolation.
 |
FOOTNOTES |
*
Corresponding author. Mailing address: Faculté de
Médecine, Service de Bactériologie, 28 Place Henri Dunant,
63001 Clermont-Ferrand Cedex, France. Phone: 33 (0)4 73 60 80 18. Fax:
33 (0)4 73 27 74 94. E-mail:
christophe-dechamps{at}u-clermont1.fr.
 |
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Journal of Clinical Microbiology, January 2000, p. 460-461, Vol. 38, No. 1
0095-1137/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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