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http://dx.doi.org/10.4142/jvs.21040

Risk factors for canine magnesium ammonium phosphate urolithiasis associated with bacterial infection  

Uttamamul, Nahathai (Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University)
Jitpean, Supranee (Division of Surgery, Faculty of Veterinary Medicine, Khon Kaen University)
Lulitanond, Aroonlug (Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University)
Wonglakorn, Lumyai (Clinical Microbiology Unit, Srinagarind Hospital, Khon Kaen University)
Sae-ung, Nattaya (Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University)
Boonsiri, Patcharee (Department of Biochemistry, Faculty of Medicine, Khon Kaen University)
Daduang, Jureerut (Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University)
Tavichakorntrakool, Ratree (Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University)
Publication Information
Journal of Veterinary Science / v.23, no.1, 2022 , pp. 6.1-6.8 More about this Journal
Abstract
Background: With limited information available, the association among urinary tract infections, urease-producing bacteria and the presence of magnesium ammonium phosphate (MAP) urolithiasis in canines in Thailand requires more study. Objectives: This study aimed to investigate the association between demographic characteristics of canines and the presence of MAP urolithiasis in canines, and to evaluate antimicrobial susceptibility patterns of bacteria isolated from canine uroliths. Methods: A total of 56 canines admitted for treatment with surgical removal of uroliths were recruited. Demographic characteristics and clinical chemistry data were recorded. Bacteria isolated from the removed uroliths were identified. Chemical compositions of the uroliths were analyzed by Fourier transform infrared spectrometer. Potential risk factors were determined with univariable and multivariable logistic regression analyses. Results: Of 56 canine urolithiasis, bacteria were isolated from uroliths of 38 canines (27 MAP and 11 non-MAP) but not from uroliths of 18 canines (5 MAP and 13 non-MAP). The most common bacteria found in nidus of MAP uroliths was Staphylococcus pseudintermedius (approximately 51%). An antimicrobial resistance was frequently found in Staphylococci isolates (42.86%). Multivariate logistic regression analysis showed that the predictors of MAP urolith in canine urolithiasis were being female (p = 0.044; adjusted odds ratio [OR], 10.22; 95% confidence interval [CI], 1.06-98.24) and the positive urolith culture (p = 0.012; adjusted OR, 8.60; 95% CI, 1.60-46.30). Conclusions: Our results indicate that S. pseudintermedius (a urease-producing bacterium) is the major causative bacteria of MAP uroliths. A positive urolith culture and being female are risk factors of MAP urolithiasis in canines.
Keywords
Risk factors; dog; magnesium ammonium phosphate; urolithiasis; bacterial infection;
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1 Detkalaya O, Vichukit K, Kornkasem S, Thanaperm P, Lekcharoensuk C. Association between urinary tract infection, gender, age and the occurrence of magnesium ammonium phosphate compared with calcium oxalate uroliths in dogs. J Mahanakorn Vet Med. 2020;15(1):13-23.
2 Seguin MA, Vaden SL, Altier C, Stone E, Levine JF. Persistent urinary tract infections and reinfections in 100 dogs (1989-1999). J Vet Intern Med. 2003;17(5):622-631.   DOI
3 Zechner V, Sofka D, Paulsen P, Hilbert F. Antimicrobial resistance in Escherichia coli and resistance genes in coliphages from a small animal clinic and in a patient dog with chronic urinary tract infection. Antibiotics (Basel). 2020;9(10):652.   DOI
4 Palma D, Langston C, Gisselman K, McCue J. Canine struvite urolithiasis. Compend Contin Educ Vet. 2013;35(8):E1.
5 Poole K. Multidrug resistance in Gram-negative bacteria. Curr Opin Microbiol. 2001;4(5):500-508.   DOI
6 Detkalaya O, Detkalaya SN, Lekcharoensuk C. Epidemiology of canine urolithiasis in Thailand during 2006-2013. J Kasetsart Vet. 2017;(27):39-53.
7 Borghi L, Nouvenne A, Meschi T. Nephrolithiasis and urinary tract infections: 'the chicken or the egg' dilemma? Nephrol Dial Transplant. 2012;27(11):3982-3984.   DOI
8 Broomfield RJ, Morgan SD, Khan A, Stickler DJ. Crystalline bacterial biofilm formation on urinary catheters by urease-producing urinary tract pathogens: a simple method of control. J Med Microbiol. 2009;58(Pt 10):1367-1375.   DOI
9 Wong C, Epstein SE, Westropp JL. Antimicrobial susceptibility patterns in urinary tract infections in dogs (2010-2013). J Vet Intern Med. 2015;29(4):1045-1052.   DOI
10 Lulich JP, Berent AC, Adams LG, Westropp JL, Bartges JW, Osborne CA. ACVIM Small animal consensus recommendations on the treatment and prevention of uroliths in dogs and cats. J Vet Intern Med. 2016;30(5):1564-1574.   DOI
11 Vaara M. Agents that increase the permeability of the outer membrane. Microbiol Rev. 1992;56(3):395-411.   DOI
12 Perry LA, Kass PH, Johnson DL, Ruby AL, Shiraki R, Westropp JL. Evaluation of culture techniques and bacterial cultures from uroliths. J Vet Diagn Invest. 2013;25(2):199-202.   DOI
13 Seaman R, Bartges JW. Canine struvite urolithiasis. Compend Contin Educ Vet. 2001;13(5):407-420.
14 Sosnar M, Bulkova T, Ruzicka M. Epidemiology of canine urolithiasis in the Czech Republic from 1997 to 2002. J Small Anim Pract. 2005;46(4):177-184.   DOI
15 von Wintersdorff CJ, Penders J, van Niekerk JM, Mills ND, Majumder S, van Alphen LB, et al. Dissemination of antimicrobial resistance in microbial ecosystems through horizontal gene transfer. Front Microbiol. 2016;7:173.   DOI
16 Calabro S, Tudisco R, Bianchi S, Grossi M, De Bonis A, Isabella Cutrignelli M. Management of struvite uroliths in dogs. Br J Nutr. 2011;106 Suppl 1:S191-S193.   DOI
17 Wallerstrom BI, Wagberg TI. Canine urolithiasis in Sweden and Norway: Retrospective survey of prevalence and epidemiology. J Small Anim Pract. 1992;33(11):534-539.   DOI
18 Tavichakorntrakool R, Prasongwattana V, Sungkeeree S, Saisud P, Sribenjalux P, Pimratana C, et al. Extensive characterizations of bacteria isolated from catheterized urine and stone matrices in patients with nephrolithiasis. Nephrol Dial Transplant. 2012;27(11):4125-4130.   DOI
19 Osborne CA, Lulich JP, Polzin DJ, Allen TA, Kruger JM, Bartges JW, et al. Medical dissolution and prevention of canine struvite urolithiasis. Twenty years of experience. Vet Clin North Am Small Anim Pract. 1999;29(1):73-111.   DOI
20 Bergey DH, Holt JG. Bergey's Manual of Determinative Bacteriology. 9th ed. Philadelphia: Lippincott Williams & Wilkins; 2000.
21 CLSI. Performance Standards for Antimicrobial Susceptibility Testing. CLSI Supplement M100. 27th ed. Wayne: Clinical and Laboratory Standards Institute; 2017.
22 Tion M, Dvorska J, Saganuwan S. A review on urolithiasis in dogs and cats. Bulg J Vet Med. 2015;18(1):1-18.   DOI
23 Hunprasit V, Osborne CA, Schreiner PJ, Bender JB, Lulich JP. Epidemiologic evaluation of canine urolithiasis in Thailand from 2009 to 2015. Res Vet Sci. 2017;115:366-370.   DOI
24 Smanthong N, Tavichakorntrakool R, Saisud P, Prasongwatana V, Sribenjalux P, Lulitanond A, et al. Biofilm formation in trimethoprim/sulfamethoxazole-susceptible and trimethoprim/sulfamethoxazoleresistant uropathogenic Escherichia coli. Asian Pac J Trop Biomed. 2015;5(6):485-487.   DOI