# Orthopedic infections associated with distinct Acinetobacter strains in rural area of Qingdao, China

**Authors:** Ying Wang, Dan Zhao, Yeshun Fan, Yanxiang Cui, Yingdi Wang, Xiaoxuan Guan, Linhong Yu, Shunqian Yuan, Lan Wang, Jianqiang Hu, Yisong Li, Wenbo Xia, Jie Liu

PMC · DOI: 10.3389/fcimb.2025.1601779 · 2025-07-30

## TL;DR

This study identifies different Acinetobacter species causing orthopedic infections in Qingdao, China, and highlights the need for better diagnostics to avoid unnecessary antibiotic use.

## Contribution

The study reveals the diversity of Acinetobacter species in orthopedic infections and their distinct antibiotic resistance profiles, emphasizing the limitations of current diagnostic methods.

## Key findings

- Nine Acinetobacter isolates included six A. baumannii, two A. pittii, and one A. soli with varying resistance profiles.
- Most isolates were susceptible to antibiotics, but all A. baumannii and A. pittii carried multidrug resistance genes.
- Current diagnostics led to overtreatment, suggesting a need for improved species-specific identification.

## Abstract

Acinetobacter baumannii poses a profound global health threat because of multidrug resistance and its association with nosocomial infections. However, standard clinical diagnostics often report it together with other Acinetobacter species as A. baumannii-calcoaceticus complex (ABC), which unavoidably conceals the attribution of non-A. baumannii species. This study reported orthopedic infection cases associated with different Acinetobacter species and characterized the genomes of the culture isolates to evaluate their potential impact on the clinical treatment.

Nine in-patients with A. baumannii-calcoaceticus complex identified by culture during hospitalization were enrolled by the Orthopedics Department from a local hospital in Qingdao, China. Their clinical data were reviewed. One ABC isolate from each patient was tested for drug susceptibility and subjected for whole-genome sequencing, followed by bioinformatic analyses.

Through whole-genome analysis, nine ABC isolates were identified as six A. baumannii, two A. pittii, and one A. soli with distinct antibiotic resistance profiles and phylogenetic characteristics, indicating progressing pathogen transmission across broad geographic regions in One Health perspective. All A. baumannii and A. pittii strains carried multidrug resistance genes, while A. soli bore only amvA and rsmA. Phenotypically, eight isolates were susceptible to almost all the antibiotics tested, with only one A. baumannii being multidrug resistant. Despite this, eight patients received cephalosporins following positive reports of A. baumannii-calcoaceticus complex.

Our study highlighted the limitation of current clinical diagnostic approaches for non-A. baumannii cases, which tended to be overtreated, and suggested that Acinetobacter etiology landscape should be explored further beyond A. baumannii to avoid antibiotic misuse.

## Linked entities

- **Genes:** amvA (multidrug efflux MFS transporter AmvA) [NCBI Gene 9381814], rsmA (carbon storage regulator) [NCBI Gene 878352]
- **Species:** Acinetobacter baumannii (taxon 470), Acinetobacter pittii (taxon 48296), Acinetobacter soli (taxon 487316)

## Full-text entities

- **Genes:** OXA-23 [NCBI Gene 20472025]
- **Diseases:** AMR (MESH:D060467), fractured left femur (MESH:D000092524), pneumonia (MESH:D011014), nosocomial infections (MESH:D003428), osteomyelitis (MESH:D010019), trauma (MESH:D014947), Klebsiella pneumoniae (MESH:D007710), polymicrobial infection (MESH:D060085), bloodstream infections (MESH:D018805), bleeding (MESH:D006470), A. soli infections (MESH:D007239), death (MESH:D003643), fracture (MESH:D050723), skin and soft tissue infection (MESH:D018461), inflammatory (MESH:D007249), Orthopedic infections (MESH:D009140), ABC (MESH:D048090), hip replacement (MESH:D025981), wound infections (MESH:D014946), disability (MESH:D009069), MDR (MESH:D018088)
- **Chemicals:** meropenem (MESH:D000077731), cefazolin (MESH:D002437), NA (MESH:D012964), tigecycline (MESH:D000078304), HD108 (-), ampicillin/sulbactam (MESH:C035444), ciprofloxacin (MESH:D002939), ceftriaxone (MESH:D002443), fluoroquinolone (MESH:D024841), gentamicin (MESH:D005839), cefoperazone (MESH:D002438), trimethoprim/sulfamethoxazole (MESH:D015662), minocycline (MESH:D008911), quinolone (MESH:D015363), cephalosporin (MESH:D002511), imipenem (MESH:D015378), levofloxacin (MESH:D064704), ceftazidime (MESH:D002442), tobramycin (MESH:D014031), piperacillin/tazobactam (MESH:D000077725), cefepime (MESH:D000077723), cefotaxime (MESH:D002439), amikacin (MESH:D000583), Carbapenem (MESH:D015780)
- **Species:** Acinetobacter baumannii ATCC 19606 = CIP 70.34 = JCM 6841 (strain) [taxon 575584], Apis mellifera (bee, species) [taxon 7460], Acinetobacter nosocomialis (species) [taxon 106654], Proteus mirabilis (species) [taxon 584], Helicotylenchus sp. D1-3 (species) [taxon 2012400], Acinetobacter pittii (species) [taxon 48296], Andrias davidianus (Chinese giant salamander, species) [taxon 141262], Escherichia coli (E. coli, species) [taxon 562], Acinetobacter baumannii (species) [taxon 470], Acinetobacter calcoaceticus (species) [taxon 471], Enterobacter cloacae (species) [taxon 550], Acinetobacter soli CIP 110264 (strain) [taxon 1217676], Homo sapiens (human, species) [taxon 9606], Acinetobacter pittii ATCC 19004 = CIP 70.29 (strain) [taxon 1311774], Staphylococcus aureus (species) [taxon 1280]
- **Cell lines:** HD136 — Homo sapiens (Human), Transformed cell line (CVCL_E557)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12343611/full.md

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Source: https://tomesphere.com/paper/PMC12343611