References
- Cieslak TJ, Robb ML, Drabick CJ, Fischer GW. Catheter-associated sepsis caused by Ochrobactrum anthropi: report of a case and review of related nonfermentative bacteria. Clin Infect Dis. 1992;14:902-907. https://doi.org/10.1093/clinids/14.4.902
- Kim GM, Jin SJ, Yoo JS, Kim CO, Choi JY, Kim JM, et al. A case of meropenem-resistant Ochrobactrum anthropi bacteremia. Infect Chemother. 2009;41:62-64. https://doi.org/10.3947/ic.2009.41.1.62
- Nasir N, Mahmood SF. Mortality in patients with respiratory and non respiratory carbapenem resistant-multidrug resistant Acinetobacter infections. J Ayub Med Coll Abbottabad. 2017;29:511-513.
- Appelbaum PC, Campbell DB. Pancreatic abscess associated with Achromobacter group Vd biovar1. J Clin Microbiol. 1980;12:282-283. https://doi.org/10.1128/JCM.12.2.282-283.1980
- Jimenez G. Antony S. Ochrobactrum anthropi - an unusual cause of line related sepsis. current knowledge of the epidemiology and clinical features of this pathogen. Br J Med Med Res. 2016;18:1-7. https://doi.org/10.9734/BJMMR/2016/29365
- Aguilera-Arreola MG, Ostria-Hernandez ML, Albarran-Fernandez E, Juarez-Enriquez SR, Majalca-Martinez C, Rico-Verdin B, et al. Correct identification of Ochrobactrum anthropi from blood culture using 16rRNA sequencing: a first case report in an immunocompromised patient in Mexico. Front Med(Lausanne). 2018;5:205. https://doi.org/10.3389/fmed.2018.00205
- Mastroiani A, Cancellieri C, Montini G. Ochrobactrum anthropi bacteremia: case report and review of the literature. Clin Microbiol Infect. 1999;5:570-573. https://doi.org/10.1111/j.1469-0691.1999.tb00437.x
- Gransden WR, Eykyn SJ. Seven cases of bacteremia due to Ochrobactrum anthropi. Clin Infect Dis. 1992;15:1068-1069. https://doi.org/10.1093/clind/15.6.1068
- Babic I, Fischer-Le Saux M, Giraud E, Boemare N. Occurrence of natural dixenic association between the symbiont Photorhabdus luminescens and bacteria related to Ochrobactrum spp. in tropical entomopathogenic Heterorhabditis spp. (Nematoda, Rhabditida). Microbiology. 2000;146:709-718. https://doi.org/10.1099/00221287-146-3-709
- Shilton CM, Brown GP, Benedict S, Shine R. Spinal arthropathy associated with Ochrobactrum anthropi in free-ranging cane toads (Chaunus [Bufo] marinus) in Australia. Vet Pathol. 2008;45:85-94. https://doi.org/10.1354/vp.45-1-85
- SitiRohani AH, TzarMN. Ochrobactrum anthropi catheter-related bloodstream infection: the first case report in Malaysia. Med J Malaysia. 2013;68:267-268.
- Menezes FG, Abreu MG, Kawagoe JY, Warth AN, Deutsch AD, Dornaus MF, et al. Ochrobactrum anthropi bacteremia in a preterm infant with cystic fibrosis. Braz J Microbiol. 2014;45:559-561. https://doi.org/10.1590/S1517-83822014005000043
- Mrozek S, Dupuy M, Hoarau L, Lourtet J, Martin-Blondel G, Geeraerts T. Brain empyema due to Ochrobactrum anthropi. Med Mal Infect. 2014;44:128-129. https://doi.org/10.1016/j.medmal.2014.01.003
- Stager CE, Davis JR. Automated systems for identification of microorganisms. Clin Microbiol Rev. 1992;5:302-327. https://doi.org/10.1128/cmr.5.3.302
- Funke G, Monnet D, deBernardis C, von Graevenitz A, Freney J. Evaluation of the VITEK 2 system for rapid identification of medically relevant gram-negative rods. J Clin Microbiol. 1998;36: 1948-1952. https://doi.org/10.1128/JCM.36.7.1948-1952.1998
- Garcia-Garrote F, Cercenado E, Bouza E. Evaluation of a newsystem, VITEK 2, for identification and antimicrobial susceptibility testing of Enterococci. J Clin Microbiol. 2000;38:2108-2111. https://doi.org/10.1128/JCM.38.6.2108-2111.2000
- Velasco J, Romero C, Lopez-Goni I, Leiva J, Diaz R, Moriyon I. Evaluation of the relatedness of Brucella spp. and Ochrobactrum anthropi and description of Ochrobactrum intermedium sp. nov., a new species with a closer relationship to Brucella spp. Int J Syst Bacteriol. 1998;48:759-768. https://doi.org/10.1099/00207713-48-3-759
- Gupta A, Chauhan K, Pandey A. Neonatal Septicaemia by Ochrobactrum anthropi: A missed pathogen. Int J Curr Microbiol App Sci. 2018;7:1651-1654. https://doi.org/10.20546/ijcmas.2018.705.195
- Berman AJ, Del Priore LV, Fischer CK. Endogenous Ochrobactrum anthropi endophthalmitis. Am J Ophthalmol. 1997;123: 560-562. https://doi.org/10.1016/s0002-9394(14)70190-4
- Haditsch M, Binder L, Tschurtschenthaler G, Watschinger R, Zauner G, Mittermayer H. Bacteremia caused by Ochrobactrum anthropi in an immunocompromised child. Infection. 1994;22:291-292. https://doi.org/10.1007/BF01739922
- Murray PR. What is new in clinical microbiology-microbial identification by MALDI-TOF mass spectrometry: a paper from the 2011 William Beaumont Hospital Symposium on molecular pathology. J Mol Diagn. 2012;14:419-423. https://doi.org/10.1016/j.jmoldx.2012.03.007
- Seng P, Drancourt M, Gouriet F, La Scola B, Fournier PE, Rolain JM, et al. Ongoing revolution in bacteriology: routine identification of bacteria by matrix-assisted laser desorption ionization time-of-flight mass spectrometry. Clin Infect Dis. 2009;49:543-551. https://doi.org/10.1086/600885
- Kim TS, Lee K, Hong YJ, Hwang SM, Park JS, Park KU, et al. MALDI-TOF MS: Its application in the clinical laboratory and a paradigm shift in clinical microbiology. Lab Med Online. 2015;5:176-187. http://doi.org/10.3343/lmo.2015.5.4.176
- Guo L, Ye L, Zhao Q, Ma Y, Yang J, Luo Y. Comparative study of MALDI-TOF MS and VITEK 2 in bacteria identification. J Thorac Dis. 2014;6:534-538. http://doi.org/10.3978/j.issn.2072-1439.2014.02.18
- Choi JU, Yu YB, Kim SH, Won S, Kim YK. Two years quaternary isolation of Gram-positive bacilli using MALDI-TOF MS in positive blood culture of a university hospital. Korean J Clin Lab Sci. 2018;50:414-421. https://doi.org/10.15324/kjcls.2018.50.4.414
- Kim M, Kwon MJ, Chung HS, Lee Y, Yong D, Jeong SH, et al. Evaluation of matrix-assisted laser desorption ionization-time of flight mass spectrometry for identification of aerobic bacteria in a clinical microbiology laboratory. Korean J Clin Microbiol. 2012;15:60-66. https://doi.org/10.5145/KJCM.2012.15.2.60
- Camoez M, Sierra JM, Dominguez MA, Ferrer-Navarro M, Vila J, Roca I. Automated categorization of methicillin-resistant Staphylococcus aureus clinical isolates into different clonal complexes by MALDI-TOF mass spectrometry. Clinl Microbiol Infect. 2016;22:161.e1-161.e7. https://doi.org/10.1016/j.cmi.2015.10.009
- Rapp E, Samuelsen o, Sundqvist M. Detection of carbapenemases with a newly developed commercial assay using matrix assisted laser desorption ionization-time of flight. J Micorobiol Methods. 2018;146:37-39. https://doi.org/10.1016/j.mimet.2018.01.008
-
Kim YA, Yong D, In YH, Park HS, Lee K. Application of matrix-assisted laser desorption ionization time-of-flight mass spectrometry to screen the extended-spectrum
$\beta$ -lactamase-producing ST131 Escherichia coli strains. Ann Clin Microbiol. 2016;19:65-69. https://doi.org/10.5145/ACM.2016.19.3.65
Cited by
- The Genus Ochrobactrum as Major Opportunistic Pathogens vol.8, pp.11, 2020, https://doi.org/10.3390/microorganisms8111797