Phenotypical and Genotypical Properties of an Arcanobacterium pluranimalium Strain Isolated from a Juvenile Giraffe (Giraffa camelopardalis reticulata)
The present study was designed to characterize phenotypically and genotypically an Arcanobacterium pluranimalium strain (A. pluranimalium 4868) following necropsy from a juvenile giraffe. The species identity could be confirmed by phenotypical investigations and by MALDI-TOF MS analysis, by sequencing the 16S rDNA, pluranimaliumlysin encoding gene pla, and glyceraldehyde-3-phosphate dehydrogenase encoding gene gap with sequence similarities to A. pluranimalium reference strain DSM 13483T of 99.2%, 89.9%, and 99.1%, respectively. To our knowledge, the present study is the first phenotypic and genotypic characterization of an A. pluranimalium strain isolated from a giraffe. 1. Introduction Genus Arcanobacterium was described by Collins et al. 1982 [1] as a group of facultative anaerobic, asporogenous, and Gram-stain positive rods. According to Yassin et al. (2011) [2], this genus consists of four species, namely, Arcanobacterium haemolyticum, Arcanobacterium hippocoleae, Arcanobacterium phocae, and Arcanobacterium pluranimalium. More recently, Arcanobacterium canis and Arcanobacterium phocisimile, two species which were most closely related to A. haemolyticum, were described as novel species of this genus [3, 4]. The original species characterization of A. pluranimalium was performed with two strains isolated from a dead harbour porpoise and a dead fallow deer [5]. In the following years A. pluranimalium could also be isolated from a dog with pyoderma [6], from ovine specimens on 33 occasions, and from a milk sample of a single cow with mastitis [7]. More recently several A. pluranimalium strains recovered from various specimens were identified phenotypically and by using various molecular targets [8]. 2. Material and Methods The present study was focused on the characterization of an A. pluranimalium strain following necropsy from a juvenile giraffe by various phenotypic properties, by MALDI-TOF MS analysis, and genotypically by sequencing 16S rDNA and the A. pluranimalium-specific target genes pla and gap. The 80.5?kg female giraffe (Giraffa camelopardalis reticulata) of the present study was born in 2013. The giraffe was not accepted by its mother or wet nurse and did not accept hand rearing attempts and, because of general weakness, was euthanized three days after birth. The subsequent postmortem analysis revealed an acute hyperemia of lung and liver and a focal emphysema of the lung. The acute pneumonia was caused by a bacterial infection associated with aspirated foreign bodies. Bacteriological investigations yielded the isolation of A.
References
[1]
M. D. Collins, D. Jones, and G. M. Schofield, “Reclassification of “Corynebacterium haemolyticum” (MacLean, Liebow & Rosenberg) in the genus Arcanobacterium gen.nov. as Arcanobacterium haemolyticum nom.rev., comb.nov,” Journal of General Microbiology, vol. 128, no. 6, pp. 1279–1281, 1982.
[2]
A. F. Yassin, H. Hupfer, C. Siering, and P. Schumann, “Comparative chemotaxonomic and phylogenetic studies on the genus Arcanobacterium Collins et al. 1982 emend. Lehnen et al. 2006: proposal for Trueperella gen. nov. and emended description of the genus Arcanobacterium,” International Journal of Systematic and Evolutionary Microbiology, vol. 61, no. 6, pp. 1265–1274, 2011.
[3]
M. Hijazin, E. Prenger-Berninghoff, O. Sammra et al., “Arcanobacterium canis sp. nov., isolated from otitis externa of a dog, and emended description of the genus Arcanobacterium Collins et al. 1983 emend. Yassin et al. 2011,” International Journal of Systematic and Evolutionary Microbiology, vol. 62, pp. 2201–2205, 2012.
[4]
M. Hijazin, O. Sammra, H. ülbegi-Mohyla et al., “Arcanobacterium phocisimile sp. nov., isolated from harbour seals,” International Journal of Systematic and Evolutionary Microbiology, vol. 63, pp. 2019–2024, 2013.
[5]
P. A. Lawson, E. Falsen, G. Foster, E. Eriksson, N. Weiss, and M. D. Collins, “Arcanobacterium pluranimalium sp. nov., isolated from porpoise and deer,” International Journal of Systematic and Evolutionary Microbiology, vol. 51, no. 1, pp. 55–59, 2001.
[6]
H. ülbegi-Mohyla, A. A. Hassan, J. Alber et al., “Identification of Arcanobacterium pluranimalium isolated from a dog by phenotypic properties and by PCR mediated characterization of various molecular targets,” Veterinary Microbiology, vol. 142, no. 3-4, pp. 458–460, 2010.
[7]
G. Foster and B. Hunt, “Distribution of Arcanobacterium pluranimalium in animals examined in veterinary laboratories in the United Kingdom,” Journal of Veterinary Diagnostic Investigation, vol. 23, no. 5, pp. 962–964, 2011.
[8]
A. Balbutskaya, O. Sammra, S. Nagib et al., “Identification of Arcanobacterium pluranimalium by matrix-assisted laser desorption ionization-time of flight mass spectrometry and, as novel target, by sequencing pluranimaliumlysin encoding gene pla,” Veterinary Microbiology, vol. 168, no. 2–4, pp. 428–431, 2014.
[9]
M. Hijazin, A. A. Hassan, J. Alber et al., “Evaluation of matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) for species identification of bacteria of genera Arcanobacterium and Trueperella,” Veterinary Microbiology, vol. 157, no. 1-2, pp. 243–245, 2012.
[10]
O. Sammra, A. Balbutskaya, S. Nagib et al., “Properties of an Arcanobacterium haemolyticum strain isolated from a donkey,” Berliner und Münchener Tier?rztliche Wochenschrift, vol. 127, no. 1-2, pp. 10–14, 2014.
[11]
H. ülbegi-Mohyla, A. A. Hassan, T. Kanbar et al., “Synergistic and antagonistic hemolytic activities of bacteria of genus Arcanobacterium and CAMP-like hemolysis of Arcanobacterium phocae and Arcanobacterium haemolyticum with Psychrobacter phenylpyruvicus,” Research in Veterinary Science, vol. 87, no. 2, pp. 186–188, 2009.
[12]
P. Seng, M. Drancourt, F. Gouriet et al., “Ongoing revolution in bacteriology: routine identification of bacteria by matrix-assisted laser desorption ionization time-of-flight mass spectrometry,” Clinical Infectious Diseases, vol. 49, no. 4, pp. 543–551, 2009.
[13]
P. R. Murray, “Matrix-assisted laser desorption ionization time-of-flight mass spectrometry: usefulness for taxonomy and epidemiology,” Clinical Microbiology and Infection, vol. 16, no. 11, pp. 1626–1630, 2010.
[14]
A. Bizzini, K. Jaton, D. Romo, J. Bille, G. Prod'hom, and G. Greub, “Matrix-assisted laser desorption ionization—time of flight mass spectrometry as an alternative to 16S rRNA gene sequencing for identification of difficult-to-identify bacterial strains,” Journal of Clinical Microbiology, vol. 49, no. 2, pp. 693–696, 2011.
[15]
M. Hijazin, H. ülbegi-Mohyla, J. Alber et al., “Identification of Arcanobacterium (Trueperella) abortisuis, a novel species of veterinary importance, by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS),” Berliner und Münchener tier?rztliche Wochenschrift, vol. 125, no. 1-2, pp. 32–37, 2012.
[16]
S. J. Billington, B. H. Jost, W. A. Cuevas, K. R. Bright, and J. G. Songer, “The Arcanobacterium (Actinomyces) pyogenes hemolysin, pyolysin, is a novel member of the thiol-activated cytolysin family,” Journal of Bacteriology, vol. 179, no. 19, pp. 6100–6106, 1997.
[17]
H. B. Erta?, A. Kili?, G. ?zbey, and A. Muz, “Isolation of Arcanobacterium (Actinomyces) pyogenes from abscessed cattle kidney and identification by PCR,” Turkish Journal of Veterinary & Animal Sciences, vol. 29, no. 2, pp. 455–459, 2005.
[18]
H. ülbegi-Mohyla, M. Hijazin, J. Alber et al., “Identification of Arcanobacterium pyogenes isolated by post mortem examinations of a bearded dragon and a gecko by phenotypic and genotypic properties,” Journal of Veterinary Science, vol. 11, no. 3, pp. 265–267, 2010.
[19]
M. Hijazin, H. ülbegi-Mohyla, J. Alber et al., “Molecular identification and further characterization of Arcanobacterium pyogenes isolated from bovine mastitis and from various other origins,” Journal of Dairy Science, vol. 94, no. 4, pp. 1813–1819, 2011.
[20]
A. Moser, R. Stephan, J. Sager, S. Corti, and A. Lehner, “Arcanobacterium pluranimalium leading to a bovine mastitis: species identification by a newly developed pla gene based PCR,” Schweizer Archiv für Tierheilkunde, vol. 155, no. 6, pp. 373–375, 2013.
[21]
J. Yugueros, A. Temprano, B. Berzal et al., “Glyceraldehyde-3-phosphate dehydrogenase-encoding gene as a useful taxonomic tool for Staphylococcus spp,” Journal of Clinical Microbiology, vol. 38, no. 12, pp. 4351–4355, 2000.