Skip to main content
Log in

Rapid identification of canine uropathogens by matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry and the clinical factors that correlated bacterial species and antimicrobial resistance

  • Research
  • Published:
Veterinary Research Communications Aims and scope Submit manuscript

Abstract

Using the matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI-TOF MS) method for bacterial diagnosis, rapid urine sample preparation can reduce time relapsing of diagnosis and improve discriminatory power in coinfection cases. We aimed to evaluate rapid urine preparation procedures before MALDI-TOF MS application using dog clinical urine samples in comparison with standard microbiological diagnostic methods by agreement analysis. We determined the frequency and distribution of bacteria and bacterial resistance and their correlations to clinical history. Three experimental procedures comprising direct centrifugation, 10% sodium dodecyl sulfate digestion, and ultrasonic preparation were performed for method validation and sensitivity. Sterile urine containing Escherichia coli and/or Staphylococcus aureus were used as simulated samples. By ultrasonic preparation, the microorganisms could be detected 1.46–1.51 × 105 CFU, which was considered the most suitable technique. This preparation was significantly consistent with the routine method based on data from Hospital Information Systems for 50 urine samples from canine cystitis. By standard protocol, Enterobacteriaceae and Staphylococcus pseudintermedius were found in most of the 155 urine samples with cystitis. Extended-spectrum beta-lactamase-producing Enterobacteriaceae was found in 25–30% of the samples. Imipenem resistance was found in 70% of Acinetobacter baumannii cases; almost all were resistant to second-generation fluoroquinolones and tetracyclines. The most efficient antibiotic for treating bacterial urinary tract infection was amoxicillin plus clavulanic acid. A. baumannii and Pseudomonas aeruginosa were susceptible to pradofloxacin. Prolonged urine catheterization was linked to lower urinary tract infections by Enterobacter spp., which also correlated with chronic kidney disease.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Code Availability

Not applicable.

Data Availability

Not applicable.

References

  • Alibi S, Ferjani A, Gaillot O, Marzouk M, Courcol R, Boukadida J (2015) Identification of clinically relevant Corynebacterium strains by Api Coryne. MALDI-TOF-mass spectrometry and molecular approaches. Pathol Biol 63:153–157. https://doi.org/10.1016/j.patbio.2015.07.007

    Article  CAS  PubMed  Google Scholar 

  • Barsanti JA, Blue J, Edmunds J (1985) Urinary tract infection due to indwelling bladder catheters in dogs and cats. J Am Vet Med Assoc 187:384–388

    CAS  PubMed  Google Scholar 

  • Bartges JW (2012) Chronic kidney disease in dogs and cats. Vet Clin North Am Small Anim Pract 42:692

    Article  Google Scholar 

  • Bubenik LJ, Hosgood GL, Waldron DR, Snow LA (2007) Frequency of urinary tract infection in catheterized dogs and comparison of bacterial culture and susceptibility testing results for catheterized and noncatheterized dogs with urinary tract infections. J Am Vet Med Assoc 231:893–899. https://doi.org/10.2460/javma.231.6.893

    Article  PubMed  Google Scholar 

  • Chew DJ, Daniels JB (2011) Diagnosis and treatment of routine and difficult urinary infections in dogs 83rd Annual Western Veterinary Conference. Las Vegas; United States

  • Clinical and Laboratory Standards Institute (2022) Performance standards for antimicrobial susceptibility testing. 32nd informational supplement. M100-S24. National Committee for Clinical Laboratory Standards, Wayne, PA

    Google Scholar 

  • Delanghe J, Speeckaert M (2014) Preanalytical requirements of urinalysis. Biochem Med 24:89–104

    Article  CAS  Google Scholar 

  • Fernandes AM, Sousa A, Conceição L, Gomes da Silva F, Cayuela M, Mendonca A, Almeida A, Dutra V, Sousa V (2019) Urinary infection in dogs with chronic kidney disease: aetiology and resistance. Semina: Ciências Agrárias 40:3741

    CAS  Google Scholar 

  • Ferreira L, Sanchez-Juanes F, Gonzalez-Avila M, Cembrero-Fucinos D, Herrero-Hernandez A, Gonzalez-Buitrago JM, Munoz-Bellido JL (2010) Direct identification of urinary tract pathogens from urine samples by matrix-assisted laser desorption ionization-time of flight mass spectrometry. J Clin Microbiol 48:2110–2115

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Fonseca JD, Mavrides DE, Graham PA, McHugh TD (2021) Results of urinary bacterial cultures and antibiotic susceptibility testing of dogs and cats in the UK. J Small Anim Pract 62(12):1085–1091

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Garcês A, Lopes R, Silva A, Sampaio F, Duque D, Brilhante-Simões P (2022) Bacterial isolates from urinary tract infection in dogs and cats in Portugal, and their antibiotic susceptibility pattern: a retrospective study of 5 years (2017–2021). Antibiot (Basel) 11(11):1520. https://doi.org/10.3390/antibiotics11111520

    Article  CAS  Google Scholar 

  • Garcia V, Abat C, Rolain JM (2016) Report of the first Vagococcus lutrae human infection. Marseille France New Microbes New Infect 9:56–57

    Article  CAS  PubMed  Google Scholar 

  • Gentilini F, Turba ME, Pasquali F, Mion D, Romagnoli N, Zambon E, Terni D, Peirano G, Pitout JDD, Parisi A, Sambri V, Zanoni RG (2018) Hospitalized pets as a source of carbapenem-resistance. Front Microbiol 9:2872

    Article  PubMed  PubMed Central  Google Scholar 

  • Grauer GF (2005) Early detection of renal damage and disease in dogs and cats. Vet Clin North Am Small Anim Pract 35:581–596. https://doi.org/10.1016/j.cvsm.2004.12.013

    Article  PubMed  Google Scholar 

  • Huber H, Zweifel C, Wittenbrink MM, Stephan R (2013) ESBL-producing uropathogenic Escherichia coli isolated from dogs and cats in Switzerland. Vet Microbiol 162:992–996. https://doi.org/10.1016/j.vetmic.2012.10.029

    Article  CAS  PubMed  Google Scholar 

  • Hutchins RG, Vaden SL, Jacob ME, Harris TL, Bowles KD, Wood MW, Bailey CS (2014) Vaginal microbiota of spayed dogs with or without recurrent urinary tract infections. J Vet Intern Med 28:300–304. https://doi.org/10.1111/jvim.12299

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kitagawa KSK, Shigemura K, Onuma KI, Nishida M, Fujiwara M, Kobayashi S, Yamasaki M, Nakamura T, Yamamichi F, Shirakawa T, Tokimatsu I (2017) Improved bacterial identification directly from urine samples with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. J Clin Lab Anal 32:e22301

    Article  PubMed  PubMed Central  Google Scholar 

  • Kruger JM, Osborne CA, Ulrich LK (1996) Cystocentesis. Diagnostic and therapeutic considerations. Vet Clin North Am: Small Anim Pract 26:353–361. https://doi.org/10.1016/S0195-5616(96)50215-9

    Article  CAS  PubMed  Google Scholar 

  • Li W, Sun E, Wang Y, Pan H, Zhang Y, Li Y, Zhang X, Li C, Du L, Wang C (2019) Rapid identification and antimicrobial susceptibility testing for urinary tract pathogens by direct analysis of urine samples using a MALDI-TOF MS-based combined protocol. Front Microbiol 10:1182. https://doi.org/10.3389/fmicb.2019.01182

    Article  PubMed  PubMed Central  Google Scholar 

  • Maeda H, Hayashi K, Ishige T, Sunagawa T, Tanigawa S, Mishina M, Watanabe T, Sogawa K (2018) Use of the MALDI BioTyper system and rapid BACpro with MALDI-TOF MS for rapid identification of microorganisms causing bacterial urinary tract infection in feline urine samples. J Vet Med Sci 80:1490–1494. https://doi.org/10.1292/jvms.18-0145

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • March Rosselló GA, Gutiérrez Rodríguez MP, de Lejarazu Leonardo RO, Orduña Domingo A, Bratos Pérez MA (2013) Procedure for microbial identification based on matrix-assisted laser desorption/ionization-time of flight mass spectrometry from screening-positive urine samples. APMIS 122:790–795. https://doi.org/10.1111/apm.12208

    Article  CAS  PubMed  Google Scholar 

  • Marques C, Gama LT, Belas A, Bergström K, Beurlet S, Briend-Marchal A, Broens EM, Costa M, Criel D, Damborg P, van Dijk MA, van Dongen AM, Dorsch R, Espada CM, Gerber B, Kritsepi-Konstantinou M, Loncaric I, Mion D, Misic D, Movilla R, Overesch G, Perreten V, Roura X, Steenbergen J, Timofte D, Wolf G, Zanoni RG, Schmitt S, Guardabassi L, Pomba C (2016) European multicenter study on antimicrobial resistance in bacteria isolated from companion animal urinary tract infections. BMC Vet Res 12:213. https://doi.org/10.1186/s12917-016-0840-3

    Article  PubMed  PubMed Central  Google Scholar 

  • McHugh ML (2012) Interrater reliability: the kappa statistic. Biochem Med 22:276–282. https://doi.org/10.11613/BM.2012.031

    Article  Google Scholar 

  • Norris CR, Williams BJ, Ling GV, Franti CE, Johnson Ruby AL (2000) Recurrent and persistent urinary tract infections in dogs: 383 cases (1969–1995). J Am Anim Hosp Assoc 36:484–492. https://doi.org/10.11613/BM.2012.031

    Article  CAS  PubMed  Google Scholar 

  • Oviaño M, Bou G (2018) Matrix-assisted laser desorption ionization-time of flight mass spectrometry for the rapid detection of antimicrobial resistance mechanisms and beyond. Clin Microb Rev 28(1):e00037–e00018. https://doi.org/10.1128/CMR.00037-18

    Article  Google Scholar 

  • Penna B, Varges R, Martins R, Martins G, Lilenbaum W (2010) In vitro antimicrobial resistance of Staphylococci isolated from canine urinary tract infection. Can Vet J 51:738–742

    PubMed  PubMed Central  Google Scholar 

  • Polzin DJ (2011) Chronic kidney disease in small animals. Vet Clin North Am Small Anim Pract 41:15–30. https://doi.org/10.1016/j.cvsm.2010.09.004

    Article  PubMed  Google Scholar 

  • Punia M, Kumar A, Charaya G, Kumar T (2018) Pathogens isolated from clinical cases of urinary tract infection in dogs and their antibiogram. Vet World 11:1037–1042. https://doi.org/10.14202/vetworld.2018.1037-1042

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Qekwana DN, Phophi L, Naidoo V, Oguttu JW, Odoi A (2018) Antimicrobial resistance among Escherichia coli isolates from dogs presented with urinary tract infections at a veterinary teaching hospital in South Africa. BMC Vet Res 14:228. https://doi.org/10.1186/s12917-018-1552-7

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Rampacci E, Bottinelli M, Stefanetti V, Hyatt DR, Sgariglia E, Coletti M, Passamonti F (2018) Antimicrobial susceptibility survey on bacterial agents of canine and feline urinary tract infections: weight of the empirical treatment. J Glob Antimicrob Resist 13:192–196. https://doi.org/10.1016/j.jgar.2018.01.011

    Article  PubMed  Google Scholar 

  • Seguin MA, Vaden SL, Altier C, Stone E, Levine JF (2003) Persistent urinary tract infections and reinfections in 100 dogs (1989–1999). J Vet Intern Med 17:622–631

    PubMed  Google Scholar 

  • Sorensen TM, Jensen AB, Damborg P, Bjornvad CR, Guardabassi L, Jessen LR (2016) Evaluation of different sampling methods and criteria for diagnosing canine urinary tract infection by quantitative bacterial culture. Vet J 216:168–173. https://doi.org/10.1016/j.tvjl.2016.08.007

    Article  CAS  PubMed  Google Scholar 

  • Weese JS, Blondeau J, Boothe D, Guardabassi LG, Gumley N, Papich M, Jessen LR, Lappin M, Rankin S, Westropp JL, Sykes J (2019) International Society for Companion Animal Infectious Diseases (ISCAID) guidelines for the diagnosis and management of bacterial urinary tract infections in dogs and cats. Vet J 247:8–25. https://doi.org/10.1016/j.tvjl.2019.02.008

    Article  PubMed  Google Scholar 

  • Weese JS, van Duijkeren E (2010) Methicillin-resistant Staphylococcus aureus and Staphylococcus pseudintermedius in veterinary medicine. Vet Microbiol 140:418–429

    Article  CAS  PubMed  Google Scholar 

  • Windahl U, Holst BS, Nyman A, Grönlund U, Bengtsson B (2014) Characterisation of bacterial growth and antimicrobial susceptibility patterns in canine urinary tract infections. BMC Vet Res 10:217

    Article  PubMed  PubMed Central  Google Scholar 

  • Yudhanto S, Hung CC, Maddox CW, Varga C (2022) Antimicrobial resistance in bacteria isolated from canine urine samples submitted to a veterinary diagnostic laboratory, Illinois, United States. Front Vet Sci 4:9:867784. https://doi.org/10.3389/fvets.2022.867784

    Article  Google Scholar 

  • Zogg AL, Zurfluh K, Schmitt S, Nüesch-Inderbinen M, Stephan R (2018) Antimicrobial resistance, multilocus sequence types and virulence profiles of ESBL producing and non-ESBL producing uropathogenic Escherichia coli isolated from cats and dogs in Switzerland. Vet Microbiol 216:79–84. https://doi.org/10.1016/j.vetmic.2018.02.011

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

This research was funded by the Academic Affair, Faculty of Veterinary Science, Chulalongkorn University. The team from World Tech Enterprise Ltd., Thailand, provided instruction on sample preparation for MALDI-TOF analysis. We are appreciative to the veterinarians and the Chulalongkorn University Faculty of Veterinary Science’s Veterinary Diagnostic Laboratory for their assistance in gathering the necessary data.

Funding

This research project was supported by Faculty of Veterinary Science, Chulalongkorn University.

Author information

Authors and Affiliations

Authors

Contributions

Conceptualization: Nuvee Prapasarakul; Methodology: Nutthee Am-in, Sawang kesdangsakonwut, Sirilak Surachetpong; Formal analysis and investigation: Artitaya Pinthanon, Chayanan Nithitarnwat, Chadaporn Pintapin, Chonradee Siripanee, Jitrapa Yindee; Writing - original draft preparation: Artitaya Pinthanon, Chayanan Nithitarnwat, Chadaporn Pintapin, Chonradee Siripanee, Nutthee Am-in; Writing - review and editing: Nuvee Prapasarakul; Funding acquisition: Nuvee Prapasarakul.

Corresponding author

Correspondence to Nuvee Prapasarakul.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Ethics approval

This experiment was approved by the Faculty of Veterinary Science Institutional Biosafety Committee (agreement no. IBC2031056).

Consent to participate

All authors participated voluntarily in the research.

Consent for publication

All authors give consent for publication.

Statement of Animal Ethics.

No ethical approval was required as this study used clinical samples from a diagnostic laboratory.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary Material 1

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Pinthanon, A., Nithitarnwat, C., Pintapin, C. et al. Rapid identification of canine uropathogens by matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry and the clinical factors that correlated bacterial species and antimicrobial resistance. Vet Res Commun 47, 1457–1469 (2023). https://doi.org/10.1007/s11259-023-10096-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11259-023-10096-z

Keywords

Navigation