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Case Report Posttraumatic Skin and Soft-Tissue Infection due to Pseudomonas fulva Fernando Cobo, Gemma Jiménez, Javier Rodríguez-Granger, and Antonio Sampedro Department of Microbiology, Complejo Hospitalario Universitario de Granada, Granada, Spain Correspondence should be addressed to Fernando Cobo; [email protected] Received 18 July 2016; Accepted 14 September 2016 Academic Editor: Peter Olumese Copyright © 2016 Fernando Cobo et al. is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. We report a case of posttraumatic skin and soſt-tissue infection in a patient with a leſt thigh wound aſter a traffic accident. Pseudomonas fulva was isolated from a wound aspirate and was identified to the species level by Maldi-tof. e patient responded to drainage, debridement of wound, and two weeks of intravenous antibiotic therapy. Follow-up aſter 3 weeks was satisfactory with healthy cover of the injured area. 1. Introduction Pseudomonas fulva was first described in 1963 and belongs to fluorescent group of Pseudomonas [1]. is microorgan- ism is mainly recovered from rice seed samples, rice, and petroleum fields and oil brine and from the gills of some mollusks [2]. ese bacilli are an uncommon pseudomonal opportunistic pathogen causing very rare infection in human population. Until now, only two infections have been docu- mented in humans: an isolate causing meningitis in a 2-year- old girl aſter placement of a cerebral shunt system [3] and an isolate causing bacteremia in a 56-year-old man who suffered a trauma [4]. In our knowledge, we are describing the third case of infection by P. fulva in a patient with a trauma due to a traffic accident. 2. Case Report A 73-year-old man presented to the emergency department of our hospital due to a right hip fracture because of a traffic accident. e patient had also a lacerated wound on the leſt thigh with underlying bone injury at this level. Aſter initial assessment and management, a stabilizing surgery fol- lowed by cleaning and suturing of the wound was per- formed. Aſter 48 h of admission, a serohematic exudate together with swelling and erythematous changes was ob- served in the wound. A new cleaning and debridement was carried out, taking at this moment an aspirate from the exudate for microbiologic study. Empirical treatment with teicoplanin (6 mg/kg/i.v daily) plus cefepime (1 gr/i.v/12 h) was then started. Aſter centrifugation, the sample was inoculated in aerobic and anaerobic blood agar (BD Columbia Agar 5% Sheep- blood, Becton Dickinson), chocolate agar (BD Choco Agar, Becton Dickinson), and thioglycollate broth (BD Fluid ioglycollate Medium), all incubated at 37 C. Approxi- mately, 1 mL of the sample was inoculated into an aerobic blood culture bottle (BACTEC, 9240 BD, Becton Dickinson, Franklin Lakes, NJ, USA). A Gram stain of the sample re- vealed no microorganisms. Aſter 18 hours of incubation, both thioglycollate broth and blood culture bottle were positives, and subcultures in the same plates were carried out. A Gram stain of both fluids revealed Gram-negative bacilli. Aſter 18 hours of incubation, pathogen growth was observed on all plates. e strain was small, straightedged, and slightly yellowish. e oxidase was clearly positive. e Gram-negative rod was identified by mass spectrometry (Bruker Biotyper, Billerica, MA, USA) as P. fulva (score 2.295), and susceptibility to this strain was then tested by a microdilution method (MicroScan, Beckman-Coulter Inc.). According the CLSI recommendations [5], the isolate was susceptible to aminoglycosides, ciprofloxacin, piperacillin- tazobactam, imipenem, and ceſtazidime, whereas it was intermediate to meropenem and cefepime. e antibiotic Hindawi Publishing Corporation Case Reports in Infectious Diseases Volume 2016, Article ID 8716068, 2 pages http://dx.doi.org/10.1155/2016/8716068
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Page 1: Case Report Posttraumatic Skin and Soft-Tissue Infection ...downloads.hindawi.com/journals/criid/2016/8716068.pdf · carbapanemase production and the patient was treated with piperacillin-tazobactam,

Case ReportPosttraumatic Skin and Soft-Tissue Infection due toPseudomonas fulva

Fernando Cobo, Gemma Jiménez, Javier Rodríguez-Granger, and Antonio Sampedro

Department of Microbiology, Complejo Hospitalario Universitario de Granada, Granada, Spain

Correspondence should be addressed to Fernando Cobo; [email protected]

Received 18 July 2016; Accepted 14 September 2016

Academic Editor: Peter Olumese

Copyright © 2016 Fernando Cobo et al.This is an open access article distributed under the Creative CommonsAttribution License,which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

We report a case of posttraumatic skin and soft-tissue infection in a patient with a left thigh wound after a traffic accident.Pseudomonas fulva was isolated from a wound aspirate and was identified to the species level by Maldi-tof. The patient respondedto drainage, debridement of wound, and two weeks of intravenous antibiotic therapy. Follow-up after 3 weeks was satisfactory withhealthy cover of the injured area.

1. Introduction

Pseudomonas fulva was first described in 1963 and belongsto fluorescent group of Pseudomonas [1]. This microorgan-ism is mainly recovered from rice seed samples, rice, andpetroleum fields and oil brine and from the gills of somemollusks [2]. These bacilli are an uncommon pseudomonalopportunistic pathogen causing very rare infection in humanpopulation. Until now, only two infections have been docu-mented in humans: an isolate causing meningitis in a 2-year-old girl after placement of a cerebral shunt system [3] and anisolate causing bacteremia in a 56-year-old man who suffereda trauma [4]. In our knowledge, we are describing the thirdcase of infection by P. fulva in a patient with a trauma due toa traffic accident.

2. Case Report

A 73-year-old man presented to the emergency departmentof our hospital due to a right hip fracture because of a trafficaccident. The patient had also a lacerated wound on theleft thigh with underlying bone injury at this level. Afterinitial assessment and management, a stabilizing surgery fol-lowed by cleaning and suturing of the wound was per-formed. After 48 h of admission, a serohematic exudatetogether with swelling and erythematous changes was ob-served in the wound. A new cleaning and debridement was

carried out, taking at this moment an aspirate from theexudate for microbiologic study. Empirical treatment withteicoplanin (6mg/kg/i.v daily) plus cefepime (1 gr/i.v/12 h)was then started.

After centrifugation, the samplewas inoculated in aerobicand anaerobic blood agar (BD Columbia Agar 5% Sheep-blood�, Becton Dickinson), chocolate agar (BD Choco Agar,Becton Dickinson), and thioglycollate broth (BD� FluidThioglycollate Medium), all incubated at 37∘C. Approxi-mately, 1mL of the sample was inoculated into an aerobicblood culture bottle (BACTEC, 9240 BD, Becton Dickinson,Franklin Lakes, NJ, USA). A Gram stain of the sample re-vealed no microorganisms. After 18 hours of incubation,both thioglycollate broth and blood culture bottle werepositives, and subcultures in the same plates were carriedout. A Gram stain of both fluids revealed Gram-negativebacilli. After 18 hours of incubation, pathogen growth wasobserved on all plates. The strain was small, straightedged,and slightly yellowish. The oxidase was clearly positive. TheGram-negative rod was identified by mass spectrometry(Bruker Biotyper, Billerica, MA, USA) as P. fulva (score2.295), and susceptibility to this strain was then tested by amicrodilution method (MicroScan, Beckman-Coulter Inc.).According the CLSI recommendations [5], the isolate wassusceptible to aminoglycosides, ciprofloxacin, piperacillin-tazobactam, imipenem, and ceftazidime, whereas it wasintermediate to meropenem and cefepime. The antibiotic

Hindawi Publishing CorporationCase Reports in Infectious DiseasesVolume 2016, Article ID 8716068, 2 pageshttp://dx.doi.org/10.1155/2016/8716068

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2 Case Reports in Infectious Diseases

therapy was changed to intravenous ceftazidime (2 gr/8 h) for2 weeks, and follow-up after 3 weeks was satisfactory withhealthy cover of the injured area.

3. Discussion

P. fulva is a Gram-negative rod which belongs to genusPseudomonas and shares genotypic characteristics with thefluorescent Pseudomonas group, above all with P. putida.This species was first described in 1963 [1], but recentlyseven of these strains were recharacterized [6]. These bacilliproduce a yellowbut nofluorescent pigment and also producearginine hydrolysis and catalase [6]. Oxidase activity isvariable, being positive in three cases described by Uchinoet al. [6], in one case described by Seok et al. [4], and inour case. In only an isolate described by Almuzara et al.,oxidase test was negative [3]. The variable oxidase reactionmay be a phenotypic characteristic of this species and, likein Aeromonas, may be negative if performed on strains fromdifferential media such as MacConkey agar but positive ifperformed on strains from nondifferential media [7]. Inblood agar, these strains are small, round, and yellowish.

P. fulva is mainly isolated from environmental sources,above all rice paddies, and rarely affects humans. Until now,only three cases of P. fulva have been reported in the medicalliterature. One case was isolated from sputum in a patientwith cystic fibrosis [8], but the clinical significance of thisreport was not definitively clarifying.However, the remainingtwo cases had clinical significance. In 2010, Almuzara etal. [3] reported the first case of human infection due toP. fulva in a 2-year-old female with acute meningitis afterplacement of shunt system. The isolate shows a VIM-2carbapanemase production and the patient was treated withpiperacillin-tazobactam, colistin, and ciprofloxacin. At thesame year, Seok et al. [4] reported a case of bacteremia dueto this bacterium in a patient hospitalized due to a trauma.This patient was treated with piperacillin-tazobactam andclindamycin with satisfactory outcome. Due to its rarity,treatment of choice to P. fulva has not been established, sosusceptibility testing to the isolates should be performed inorder to give the correct therapy. Moreover, care should betaken because this species may acquire resistance genes suchas carbapenemases [3].

Little is known about the transmission of this infection tohumans, but the existence of traumatisms and/or placementofmedical devicesmay help to develop the infection from theenvironmental sources.

In summary, P. fulva is a very rare infection in humansand only three cases have been described until now. Al-though this bacterium is usually an environmental microor-ganism, physicians and microbiologists should be awareof this infection above all in patients with posttraumaticinfections.

Competing Interests

Authors declare no competing interests.

References

[1] H. Lizuka and K. Komagata, “New species of Pseudomonasbelonging to fluorescent group. (Studies on themicroorganismsof cereal grains. Part V),”NipponNogeikagakuKaishi, vol. 37, pp.137–141, 1963.

[2] G.-L. Xie, L. A. Soad, J. Swings, and T. W. Mew, “Diversity ofGram negative bacteria antagonistic against major pathogensof rice from rice seed in the tropic environment,” Journal ofZhejiang University: Science, vol. 4, no. 4, pp. 463–468, 2003.

[3] M. N. Almuzara, M. Vazquez, N. Tanaka et al., “First case ofhuman infection due to Pseudomonas fulva, an environmentalbacterium isolated from cerebrospinal fluid,” Journal of ClinicalMicrobiology, vol. 48, no. 2, pp. 660–664, 2010.

[4] Y. Seok, H. Shin, Y. Lee et al., “First report of bloodstreaminfection caused by Pseudomonas fulva,” Journal of ClinicalMicrobiology, vol. 48, no. 7, pp. 2656–2657, 2010.

[5] Clinical and Laboratory Standards Institute, “Performancestandards for antimicrobial susceptibility testing,” Tech. Rep.M100-s18, Clinical and Laboratory Standards Institute, Wayne,Pa, USA, 2015.

[6] M. Uchino, O. Shida, T. Uchimura, and K. Komagata, “Rechar-acterization of Pseudomonas fulva Iizuka and Komagata 1963,and proposals of Pseudomonas parafulva sp. nov. and Pseu-domonas cremoricolorata sp. nov.,” Journal of General andApplied Microbiology, vol. 47, no. 5, pp. 247–261, 2001.

[7] L. K. Hunt, T. L. Overman, and R. B. Otero, “Role of pH inoxidase variability of Aeromonas hydrophila,” Journal of ClinicalMicrobiology, vol. 13, no. 6, pp. 1054–1059, 1981.

[8] S.Warwick, B. Duke, S. Soleimanian, and D.Wareham, “A diag-nostic algorithm for accurate identification of non-fermentativeGram-negative rods and epidemic strains of Pseudomonasaeruginosa from cystic fibrosis patients,” in Proceedings of the18th European Congress of Clinical Microbiology and InfectiousDiseases, Abstract P-1971, Barcelona, Spain, April 2008.

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