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Diversity of coryneforms found in infections following prosthetic joint insertion and open fractures

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Brief Report

A. yon Graevenitz, L. Frommelt, V. Ptinter-Streit, G. Funke

Diversity of Coryneforms Found in Infections following Prosthetic Joint

Insertion and Open Fractures

Summary: In a 5-year period, 73 coryneform isolates from prosthetic joint and open fracture infections in 60 patients treated in a hospital specialized in orthopedic surgery were speciated. The most frequent species were

Corynebacterium amycolatum, Coryne-

bacterium striatum, Corynebacterium diphtheriae

biotype

mitis, and Corynebacterium

jeikeium.

At least 14 isolates were deemed clinically significant as sole agents of infection.

Introduction

Infections following prosthetic joint insertion and open fractures have been reviewed in the i m m e d i a t e past by various authors [e.g., 1-5]. We have been surprised, how- ever, a b o u t the paucity of c o r y n e f o r m organisms r e p o r t e d in such infections. T h e main agents have been coagulase- negative and -positive staphylococci, followed by various streptococci and g r a m - n e g a t i v e rods [1-5]. A few reports have m e n t i o n e d " a n a e r o b i c c o r y n e b a c t e r i a " [6] or Propi-

onibacterium acnes [4], s o m e have r e p o r t e d non-speciated

" d i p h t h e r o i d s " [1, 2], and a few did not find any such bac- teria [3, 5]. In o u r pursuit of infections with c o r y n e f o r m s [7], we thought it worthwhile to speciate a collection of c o r y n e f o r m s that o n e of us (L. F.) has isolated from those infections since 1992.

Patients and Methods

All patients reviewed had been admitted to the Endo Clinic in Hamburg, Germany, either for an exchange operation necessi- tated by infection of a prosthetic joint or for correction of an infected open fracture (exogenous osteomyelitis). Generally, a preoperative aspirate was taken from the infected area, material was scraped from the area of infection intraoperatively and postoperatively; drainage fluid was obtained as well. All samples were Gram-stained, inoculated into Brain Heart Infusion (bioM6rieux, Marcy I'Etoile, France), TVLS Medium [8], the set of media devised by Lodenki~rnper [9], aerobic (5% CO2) Co- lumbia blood agar, and anaerobically incubated Brucella Agar, both with 5% sheep blood (bioMfirieux). If there was growth in the liquid media [8, 9], they were subcultured to those aerobic and anaerobic blood agar plates as well. Isolates were kept on Brain Heart Infusion (bioM~rieux) slants. They were identified as to species by a scheme elaborated by two of us [10]. Suscepti- bility testing was done by the DIN method [11].

Clinical significance of the isolates was evaluated from the pa- tients' records. All patients showed clear signs of infection as de- fined in an earlier study [6]. We judged as clearly significant those isolates that were found as monocultures in aspirates (most of these had been positive on direct Gram stains).

Questionable significance was assumed when coryneforms were isolated from scrapings or drains only. Mixed cultures were not- ed, but were not further evaluated for significance.

Results

In all, 73 isolates were recovered from 60 patients in a 5-year period (Table 1). Fourty-one c a m e from hip infec- tions, 17 f r o m k n e e infections, and 15 from variously locat- ed exogenous osteomyelitides. Fourteen isolates were d e e m e d significant, 16 were d e e m e d to be of questionable significance, and 43 were mixed with staphylococci, strep- tococci, and/or aerobically or anaerobically growing gram- negative rods.

Since o u r patients were referred from other hospitals, we were unable to d e t e r m i n e w h e t h e r prostheses previously placed contained antibiotics or not. For the s a m e reason, incubation periods could not be d e t e r m i n e d with certain- ty; they varied f r o m a few weeks to 2 years. A t the E n d o Clinic, no antibiotic prophylaxis was given for exchange o p e r a t i o n s (which involved antibiotic-impregnated acrylic c e m e n t ) [6]. Nevertheless, 22 patients had received antibi- otics for p o s t - p r i m a r y infections which we defined as those that were p r e c e d e d by earlier (primary) ones. T h e r e were 39 p r i m a r y and 34 post-primary infections.

T h e most frequent species involved was Corynebacteriurn

amycolaturn. Most isolates of this species were formerly

classified as Corynebacterium xerosis [7]. This species is frequently multiresistant [7], particularly to those anti- biotics often used in orthopedics (clindamycin, aminogly- cosides, rifampin, and sometimes also to [3-1actam antibio- tics). T h e same m a y be true for the second most frequent species, Corynebacterium striaturn [7], except that it is generally susceptible to [3:lactams. Also often multiply antibiotic-resistant is the fourth most frequent species,

Corynebacterium jeikeium [7]. It is interesting to note that

all c o r y n e f o r m s isolated from the 22 patients who received p r e o p e r a t i v e antibiotics were multi-resistant.

Received: 18 August 1997/Accepted: I7 November 1997

Prof. Dr. A. yon Graevenitz, Verena Piinter-Streit, Dr. reed. G. F, mke, In- stitut f~ir Medizinische Mikrobiologie tier Universit~t Ztirich, Gloriastr. 30, CH-8028 Ztirich, Switzerland; Dr. med. L. Frommelt, Mikrobiologi- sches Labor, Endo-Klinik D-22767 Hamburg, Germany.

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A. von Graevenitz et al.: Coryneforms in Orthopedic Infections

Table 1" Coryneform bacteria from orthopedic infections.

Species

Clinically significant a)

Hip Knee Osteo- Hip myelitis a)

pb) ppb) p pp p pp p p p

Mixed Of questionable significance

Knee Osteo- Hip Knee Osteo- Total per myelitis myelitis species P PP P PP P PP P PP P PP Corynebacterium c) amycolamm 0 2 0 1 0 0 3 4 Corynebacterium striatum 2 1 1 0 1 1 3 4 Corynebacterium diphtheriae 0 0 0 0 0 0 2 1 Corvnebacterium jeikeium 0 1 0 0 0 0 0 1 Corynebacterium Group G-1 0 0 0 0 0 0 1 0 Propionibacterium sp. 1 1 0 0 0 0 l t Corynebacteriurn sp. c) 0 0 1 0 0 0 0 0 Arthrobacter sp. 0 0 0 0 1 0 0 0 Corynebacterium sp. c) 0 0 0 0 0 0 l 0 Corynebacterium glucuronolyticum 0 0 0 0 0 0 0 0 Dermabacter hominis 0 0 0 0 0 0 i 0 Gordona sp. 0 0 0 0 0 0 0 0 Tsukarnurella sp. 0 0 0 0 0 0 0 0 Aureobacterium sp. 0 0 0 0 0 0 0 0 Corynebacwrium pseudodiphtheriticum 0 (1 0 0 0 0 0 0 t 3 1 3 0 2 0 0 1 1 22 0 l 0 2 1 2 0 0 0 0 19 2 0 1 0 0 0 1 0 0 0 7 0 0 I 2 0 0 I 0 0 0 6 1 0 0 0 2 0 1 0 0 0 5 0 0 0 0 0 1 0 0 0 0 5 ' 0 0 0 0 0 0 0 0 0 0 1 0 0 0 0 0 0 0 0 0 0 t 0 0 0 0 0 0 0 0 0 0 1 I 0 1 0 0 0 0 0 0 0 0 1 0 0 0 0 0 0 0 0 0 0 l 1 0 0 0 0 0 0 0 0 0 1 l 0 0 0 0 0 0 0 0 0 1 , 0 0 0 0 0 t 0 0 0 0 1 0 0 0 0 0 1 0 0 0 0 1

a) see text; b) p = primary, PP = post-primary; c) unable to speciate.

T h e t h i r d m o s t f r e q u e n t species was, surprisingly, C o r y n e - b a c t e r i u m diphrheriae. A l t h o u g h this will be the s u b j e c t of a s e p a r a t e r e p o r t , it s h o u l d be m e n t i o n e d here that the bi- o t y p e of all isolates except o n e (gravis) was mitis, a n d that the r i b o t y p e s a n d a n t i b i o g r a m type c o r r e s p o n d e d to those f o u n d e a r l i e r in S w i t z e r l a n d [12]. T a b l e 1 also lists f u r t h e r c o r y n e f o r r n s , each of which was r e p r e s e n t e d by o n e isolate only.

C o n c l u s i o n

T h e l i t e r a t u r e o n the s u b j e c t lists o n l y four single r e p o r t s

of c o r y n e f o r m o s t e o m y e l i t i s o n the e x t r e m i t i e s in which species were d e t e r m i n e d [13-16]. F o u r f u r t h e r r e p o r t s are e x t a n t o n cases of septic arthritis [17-20]. O u r r e p o r t shows that c o r y n e f o r m s are n o t rare in p r o s t h e t i c j o i n t in- fections a n d p o s t - f r a c t u r e o s t e o m y e l i t i d e s a n d that they m a y be c a u s a t i v e a g e n t s in such infections.

A c k n o w l e d g e m e n t

We thank Pala Das, can& reed., for submitting and keeping the strains.

R e f e r e n c e s

1. Fitzgerald, Jr., R. H., Peterson, L. F. A., Washington lI, J. A., van

Scoy, R. E., Coventry, M. B.: Bacterial colonization of wounds and sepsis in total hip arthroplasty. J. Bone Joint Surg. 55-A (1973) 1242-1250.

2. lnman, R. D., Gallegos, K. V., Brause, B. D., Redecha, P. B., Christian, C. L.: Clinical and microbial features of prosthetic joint in- fection. Am. J. Med. 77 (1984) 47-53.

3. Powers, K. A., Terpenning, M. S., Voice, R. A., Kanffman, C. A.:

Prosthetic joint infections in the elderly. Am. J. Med. 88 (1990) 9N-13N.

4. Dietz, F. R., Koontz, F. P., Found, E. M., Marsh, J. L.: The impor- tance of positive bacterial cultures of specimens obtained during clean orthopaedic operations. J. Bone Joint Surg. 73-A (1991) 1200-1207.

5. Bliss, I). G., McBride, G. G.: Infected total knee artbroplasties. Clin. Orthop. Relat. Res. 199 (1985) 207-214.

6. Buchholz, H. W., Elson, R. A., Engelbrechl, E., Lodenk~mper, H., R6ttger, J., Siegel, A.: Management of deep infection of total hip re- placement. J. Bone Joint Surg. 63-B (1981) 342-353.

7. Funke, G., yon Graevenitz, A., Clarridge HI, J. E., Bernard, K. A.:

Clinical microbiology of coryneform bacteria. Clin. Microbiol. Rev. 10 (1997) 125-1.59.

8. Caselitz, F. H., Freitag, V.: Halbfliissiges Kombinationsmedium (TVLS-Medium) zur Ztichtung anaerober Rakterien. Aerztl. I.ab. !5 (1969) 426-430.

9. Lodenkiimper, H., Stienen, G.: ZurDlerapic anaerober Infektionen. Dtsch. med. Wschr. 81 (1956) 1226-123!.

t0. yon Graevenitz, A., Funke, G.: An identification scheme for rapid[y and aerobically growing gram-positive rods Zbl. Bakt. 284 (1996) 246--254.

11. DIN Deutsches lnstitut fiir Normung e.V.: Empfindlicbkeitsprtifung yon Krankheitserregern gegen Chemotherapeutika. DIN 58940 und

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A . yon Graevenitz et al.: C o w n e f o r m s in O r t h o p e d i c I n f e c t i o n s

58944. DIN-Taschenbuch 222: Medizinische Mikrobiologie und Im- munologie. Normen und weitere Unterlagen. 2. Auflage. Beuth- Verlag GmbH, Berlin und K61n 1992, pp. 331-403.

12. Gruner, E., Opravil, M., Altwegg, M., yon Graevenitz, A.: Nontoxi-

genic Corynebacteriurn diphtheriae isolated from intravenous drug users. Clin. Infect. Dis. 18 (1994) 94-96.

13. Claeys, G. Verschraegen, G., Desmet, L., Verdonk, R., Claessens, H.: Corynebacteriurn JK (Johnson-Kaye strain) infection of a Ktintscher-nailed tibial fracture. Clin. Orthop. Relat. Res. 202 (1986) 227-229.

14. Chomarat, M., Breton, P., Dubost, J.: Osteomyelitis due to Coryne- bacterium group D2. Europ. J. Clin. Microbiol. Infect. Dis. 10 (1991) 43.

15. Weller, T. M. A., McLardy Smith, P., Crook, D. W.: Corynebacte- riurn jeikeium osteomyelitis following total hip joint replacement. J. Infect. 29 (1994) 113-114.

16. Poilane, I., Fawaz, F., Nathanson, M., Cruaud, P., Martin, T., Collignon, A., Gaudelus, J.: Corynebactermm diphtheriae osteomye- litis in an immunocompetent child: a case report. Eur. J. Pediatr. 154 (1995) 381-383.

17. Guran, Ph., Mollaret, H.-H., Chatelain, R., Gropman, M., Prigent,

F., B~al, G.: Arthrite purulente h bacille diphth6rique atoxig~ne.- Arch. franq. P6diat. 36 (1979) 926-929.

18. Valenstein, P., Klein, A., Ballow, C., Greene, W.: Corynebacterium xerosis septic arthritis. Am. J. Clin. Pathol. 89 (1988) 569-571. 19. Booth, L. V., Richards, R. H., Chandran, D. R.: Septic arthritis

caused by Corynebacteriurn xerosis following vascular surgery. Rev. Infect. Dis. 13 (1991) 548-549.

20. Damade, R., Pouchot, J., Delacroix, I., Boussougant, Y., Vinceneux, P.: Septic arthritis due to Corynebacterium diphtheriae. Clin. Infect. Dis. 16 (1993) 446-447.

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