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Inicio Enfermedades Infecciosas y Microbiología Clínica Ulcerative keratitis due to Kocuria palustris: An emerging pathogen
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Vol. 37. Núm. 6.
Páginas 422-423 (junio - julio 2019)
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Vol. 37. Núm. 6.
Páginas 422-423 (junio - julio 2019)
Scientific letter
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Ulcerative keratitis due to Kocuria palustris: An emerging pathogen
Queratitis ulcerativa por Kocuria palustris: un patógeno emergente
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5715
Maria Almagro-Molto
Autor para correspondencia
malmagrom@gmail.com

Corresponding author.
, Sebastian Suerbaum, Sören Schubert
Max von Pettenkofer-Institut für Hygiene und Medizinische Mikrobiologie, Faculty of Medicine, Ludwig Maximilian University, Munich, Germany
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Species from the genus Kocuria, earlier belonging to the genus Micrococcus, have been described as the causative agents of bacteremia, endocarditis, peritonitis, cholecystitis, urinary tract infection, brain abscesses and keratitis.1 The increased clinical cases reported recently demonstrate the expanding spectrum of human infections caused by these microorganisms. Kocuria palustris was first described in 19992 and reported together with Rothia mucilaginosa as the etiologic agent of an ulcerative keratitis case in 2014.3 We describe the first case of a K. palustris infection in pure culture.

A 68 year old woman was admitted to our hospital with suspicion of corneal ulcer in the left eye. She had been operated from cataract 10 years ago and had suffered from several swelling episodes. The patient underwent trabeculoctomy six months before the day of the admission. She had been using her monthly soft contact lenses until 2 days before the admission, when the first symptoms were present. She referred inflammation and swelling in the left eye. She showed epiphora and visual loss. Her left eye presented an erythematous conjunctiva, chemosis and opacification together with a central fluorescein-positive ulcer of approximately 1.4mm–2.6mm depth. In the fundus ultrasound of the left eye, vitreous opacities were observed. Suspicion of sub-scleral fissure was then suggested. However, no other signs of endophthalmitis or systemic infection symptoms were observed. Her right eye was unsuspicious. The final diagnosis was an ulcerative keratitis in the left eye possibly associated to the incorrect use of contact lens.

A corneal scraping and a corneal ulcer smear of the left eye were performed in order to identify the etiologic infectious agent. The patient started therapy with topical levofloxacin (5mg/ml) and gentamicin (5mg/ml) eye drops every hour, plus dexamethasone (1mg/ml) eye drops twice daily. The corneal ulcer scraping sample was cultured in a thioglycolate broth at 37°C. The 16s ribosomal RNA PCR performed from the smear sample was positive. The gene sequence analysis revealed K. palustris. After 4 days of incubation, the thioglycolate demonstrated microbial growth. A creamy colony grew on the blood agar plate subculture after 24h of incubation at 37°C. K. palustris identification was confirmed using MALDI-TOF. Susceptibility testing was performed following the European Committee on Antimicrobial Susceptibility Testing (EUCAST) standardized methodology. The MIC for different antimicrobial agents using the Etest method were as follows: penicillin G 0.125μg/ml; clindamycin 0.125μg/ml; vancomycin 0.38μg/ml; gentamicin 0.19μg/ml; moxifloxacin 0.5μg/ml; rifampicin 0.016μg/ml and linezolid 0.75μg/ml. On the day 5, the patient was discharged with a significant clinical improvement and the treatment was adjusted to topical levofloxacin (5mg/ml) eye drops four times daily for the three following days. On the follow-up visit, one month later, the patient showed no signs of infection.

Isolates belonging to the former genus Micrococcus are usually regarded as normal flora from skin and mucous membranes. Kocuria species have been isolated from the environment and clinical samples forming complex biofilms together with a variety of other microorganisms.4,5 The clinical significance of Kocuria species overall is frequently ignored, as clinical microbiology laboratories consider it a contaminant due to its ubiquitous presence in the human microbiota.6 However, the reports of Kocuria spp. clinical cases in the last years have highlighted its significance as a potential and invasive pathogen especially in neonates and immunocompromised patients.1,7

Ocular infections due to Kocuria spp. have been also described, including cases of keratitis,3,8 keratoconjunctivitis9 and canaliculitis.10 This rare infection showed an unpredictable clinical course with frequent serious complications. As in the case described here, there is usually a previous history of an eye disorder. The infection management could require evisceration, keratoplasty and amniotic membrane graft treatment in complicated cases; and involved treatment with antimicrobials in all of the cases. Due to its susceptibility pattern, Kocuria spp. is generally covered in the empiric or initial directed antibiotic treatment with broad spectrum antibiotics. However, resistances to ampicillin, tetracycline and quinolones have been described.1,8

The present report implies that Kocuria spp. should be taken in consideration when isolated from corneal ulcer samples, especially in patients with a previous history of eye disorders.

References
[1]
S. Purty, R. Saranathan, K. Prashanth, K. Narayanan, J. Asir, C. Sheela Devi, et al.
The expanding spectrum of human infections caused by Kocuria species: a case report and literature review.
Emerg Microbes Infect, 2 (2013), pp. e71
[2]
G. Kovacs, J. Burghardt, S. Pradella, P. Schumann, E. Stackebrandt, Marialigeti K:.
Kocuria palustris sp. nov., and Kocuria rhizophila sp. nov., isolated from the rhizoplane of the narrow-leaved cattail (Typha angustifolia).
Int J Syst Bacteriol, 49 (1999), pp. 167-173
[3]
R.M. Mattern, J. Ding.
Keratitis with Kocuria palustris and Rothia mucilaginosa in Vitamin A deficiency.
Case Rep Ophthalmol, 5 (2014), pp. 72-77
[4]
V. Kandi, P. Palange, R. Vaish, A.B. Bhatti, V. Kale, M.R. Kandi, et al.
Emerging bacterial infection: identification and clinical significance of Kocuria species.
Cureus, 8 (2016), pp. e731
[5]
J. Dotis, N. Printza, S. Stabouli, F. Papachristou.
Kocuria species peritonitis: although rare, we have to care.
Perit Dial Int, 35 (2015), pp. 26-30
[6]
K. Becker, F. Rutsch, A. Uekötter, F. Kipp, J. König, T. Marquardt, et al.
Kocuria rhizophila adds to the emerging spectrum of micrococcal species involved in human infections.
J Clin Microbiol, 46 (2008), pp. 3537-3539
[7]
M.K. Lee, S.H. Choi, D.W. Ryu.
Descending necrotizing mediastinitis caused by Kocuria rosea: a case report.
BMC Infect Dis, 13 (2013), pp. 475
[8]
L. Pedro-Aguilar, A. Ramirez-Miranda, V.M. Bautista-de Lucio, A. Navas, M. Ortiz-Casas, E.O. Graue-Hernandez.
Epidemiology and outcomes of Kocuria keratitis.
Eye Contact Lens, 42 (2016), pp. e20-e24
[9]
N. Inada, J. Shoji, S. Yamagami.
Atopic keratoconjunctivitis complicated by Kocuria koreensis keratitis: the first case.
Allergy Asthma Clin Immunol, 13 (2017), pp. 6
[10]
M.J. Ali, A. Pujari, S. Motukupally, M.N. Naik.
Kocuria rosea canaliculitis: a clinicomicrobiological correlation.
Ophthalmic Plast Reconstr Surg, 30 (2014), pp. e139-e140
Copyright © 2018. Elsevier España, S.L.U. and Sociedad Española de Enfermedades Infecciosas y Microbiología Clínica
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