# Canine parvovirus type 2 (CPV-2) and bacterial coinfections in dogs: phenotypic and genotypic resistance profiles in northern Kazakhstan

**Authors:** Yuliya Aleshina, Aigul Zhabykpayeva, Zulkyya Abilova, Yertay Yerzhanov, Andrey Nechaev, Daniyar Madiyev, Zhanaidar Bermukhametov, Raushan Rychshanova

PMC · DOI: 10.3389/fvets.2025.1736817 · Frontiers in Veterinary Science · 2026-01-14

## TL;DR

This study examines CPV-2 infections and bacterial coinfections in dogs in Kazakhstan, finding high antimicrobial resistance linked to CPV-2.

## Contribution

The study provides new data on CPV-2 and antimicrobial resistance in northern Kazakhstan, highlighting One Health implications.

## Key findings

- CPV-2+ dogs showed higher prevalence of gram-negative bacteria and antimicrobial resistance compared to healthy dogs.
- Enterobacteriaceae showed high resistance to tetracyclines and fluoroquinolones, with sporadic carbapenem resistance.
- Resistance genes like blaTEM/OXA and aadB were more common in CPV-2+ isolates, emphasizing a link between viral infection and AMR.

## Abstract

Canine parvovirus type 2 (CPV-2) poses a serious viral threat to dogs. Despite the potential contribution of companion animals to antimicrobial resistance, data on CPV and associated bacterial coinfections remain limited. This study aimed to characterize the CPV-2 epizootic situation in Kostanay (Kazakhstan), assess bacterial coinfections and AMR profiles, including molecular markers, and evaluate their relevance to One Health.

Epizootiological monitoring revealed a CPV-2 positivity rate of 19.4% (n = 549). For microbiological and PCR studies, two groups were established: CPV-2+ (n = 198) and clinically healthy (n = 200) dogs. E. coli, Klebsiella spp., and S. aureus were identified by culture/MALDI-TOF; AMR was assessed by disc diffusion (CLSI). Resistance genes were detected by PCR: for Enterobacteriaceae, blaTEM, OXA, tetA/tetB, StrA/StrB, aadB, aphA1, qnr/qepA, and sul1/sul3; for S. aureus, blaZ, ermB/ermC, tetK/tetM, and mecA.

A total of 131 isolates were obtained (CPV-2+: 72; healthy: 59), predominantly E. coli (n = 65) and S. aureus (n = 53). CPV-2+ dogs tended to carry more gram-negative bacteria. Enterobacteriaceae were highly resistant to tetracyclines (58.4%) and fluoroquinolones (51.2%), and sporadic carbapenem resistance was detected in Klebsiella (7%). β-Lactamase determinants (blaTEM/OXA) and aminoglycoside resistance genes were more frequently detected in CPV-2+ isolates, whereas blaZ predominated in S. aureus.

CPV-2 infection is associated with a significant bacterial burden and pronounced AMR, supporting the need for improved surveillance and empirical therapy optimization. These results fill a geographical data gap in Central Asia and align with AMR trends reported in Europe and Asia, underscoring the cross-border circulation of CPV-2 and resistant bacteria and the need for a One Health approach.

## Linked entities

- **Genes:** tet(A) (tetracycline efflux MFS transporter Tet(A)) [NCBI Gene 33941499], tetB (multifunctional tetracycline-metal/H+ antiporter and Na+(K+)/H+ antiporter) [NCBI Gene 937890], STRA (serine/threonine kinase receptor associated protein) [NCBI Gene 105481604], STRB (spermatid perinuclear RNA binding protein) [NCBI Gene 105463893], aadB (aminoglycoside nucleotidyltransferase ANT(2'')-Ia) [NCBI Gene 67369350], aphA_1 (Acid phosphatase) [NCBI Gene 26239752], qepA (fluoroquinolone efflux MFS transporter QepA) [NCBI Gene 76525248], sul-1 (Putative extracellular sulfatase Sulf-1 homolog) [NCBI Gene 180619], sul-3 (Sulfatase N-terminal domain-containing protein) [NCBI Gene 183778], blaZ (penicillin-hydrolyzing class A beta-lactamase BlaZ) [NCBI Gene 48886948], erm(B) (23S rRNA (adenine(2058)-N(6))-methyltransferase Erm(B)) [NCBI Gene 8154416], erm(C) (23S rRNA (adenine(2058)-N(6))-methyltransferase Erm(C)) [NCBI Gene 74187477], tet(K) (tetracycline efflux MFS transporter Tet(K)) [NCBI Gene 39460882], tet(M) (tetracycline resistance ribosomal protection protein Tet(M)) [NCBI Gene 8154447], mecA (adaptor protein controlling oligomerization of the AAA+ protein ClpC) [NCBI Gene 936406]
- **Species:** Canis lupus familiaris (taxon 9615), Escherichia coli (taxon 562), Staphylococcus aureus (taxon 1280)

## Full-text entities

- **Diseases:** AMR (MESH:C565965), infection (MESH:D007239)
- **Chemicals:** tetracyclines (MESH:D013754), aminoglycoside (MESH:D000617), OXA (-), carbapenem (MESH:D015780), fluoroquinolones (MESH:D024841)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], Canis lupus familiaris (dog, subspecies) [taxon 9615], Klebsiella (genus) [taxon 570], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Enterobacteriaceae (enterobacteria, family) [taxon 543], Canine parvovirus 2 (no rank) [taxon 246878]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12849767/full.md

## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC12849767/full.md

---
Source: https://tomesphere.com/paper/PMC12849767