# Correlation of OXA-1 and TEM-1 genes with antibiotic resistance to piperacillin/tazobactam in ESBL-producing Enterobacterales: insights from a multi-center analysis

**Authors:** Edwin Kamau, Brendan M. Wong, John L. MacArthur, Jamie L. Dombach

PMC · DOI: 10.3389/fcimb.2025.1694724 · Frontiers in Cellular and Infection Microbiology · 2026-01-12

## TL;DR

This study finds that the OXA-1 gene is strongly linked to resistance to piperacillin/tazobactam in ESBL-producing bacteria, with geographic variations observed.

## Contribution

The study identifies the specific role of OXA-1 in piperacillin/tazobactam resistance and highlights geographic differences in resistance patterns.

## Key findings

- OXA-1 was significantly associated with non-susceptibility to piperacillin/tazobactam (P < 0.001).
- OXA-1 and TEM-1 were linked to resistance genes for other antibiotics.
- Geographic differences in resistance patterns were observed across study sites.

## Abstract

The emergence of extended-spectrum β-lactamase (ESBL)-producing Escherichia coli and Klebsiella pneumoniae presents significant challenges in treating infections caused by these pathogens. This multi-center retrospective study investigated the prevalence of OXA-1 and TEM-1 genes in ESBL-producing E. coli and K. pneumoniae, along with their association with piperacillin/tazobactam susceptibility and additional antimicrobial resistance genes.

Clinical isolates were collected from three institutions as part of routine patient care: Tripler Army Medical Center (TAMC) in Hawaii, Madigan Army Medical Center (MAMC) in Washington, and Brooke Army Medical Center (BAMC) in Southern Texas. A total of 416 isolates were analyzed through genome sequencing and CLSI-guided susceptibility testing.

OXA-1 and TEM-1 β-lactamase enzymes were present in 20.9% (73/349) and 38.7% (135/349) of the E. coli isolates, respectively. Relative risk analysis of non-susceptibility to piperacillin/tazobactam across isolates from the three study sites revealed a highly significant association for OXA-1 (P < 0.001), whereas no significant associations were observed for TEM-1 (P = 0.424) or the combination of OXA-1 and TEM-1 (P = 0.082). When analyzed by institution, the relative risk of non-susceptibility to piperacillin/tazobactam remained highly significant for OXA-1 at TAMC and MAMC (P < 0.001 for both) but was not significant at BAMC (P = 0.21). OXA-1 and TEM-1-positive variants showed a significant association with genes conferring resistance to other antibiotics.

The OXA-1 gene plays a key role in resistance to piperacillin/tazobactam in ESBL-producing organisms, with geographic differences in non-susceptibility observed. Genetic profiling and localized data are crucial for optimizing antibiotic therapy and improving treatment outcomes.

## Linked entities

- **Genes:** OXA1L (OXA1L mitochondrial inner membrane insertase) [NCBI Gene 5018], CD248 (CD248 molecule) [NCBI Gene 57124]
- **Chemicals:** piperacillin/tazobactam (PubChem CID 461573)
- **Species:** Escherichia coli (taxon 562), Klebsiella pneumoniae (taxon 573)

## Full-text entities

- **Genes:** TEM-1 [NCBI Gene 2716540], OXA-1 [NCBI Gene 8319151], extended-spectrum beta-lactamase [NCBI Gene 13906541], beta-lactamase [NCBI Gene 7872529]
- **Diseases:** infections (MESH:D007239)
- **Chemicals:** piperacillin/tazobactam (MESH:D000077725)
- **Species:** Klebsiella pneumoniae (species) [taxon 573], Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562], Enterobacterales (order) [taxon 91347]

## Full text

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## Figures

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12832842/full.md

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Source: https://tomesphere.com/paper/PMC12832842