# Epidemiology, Temporal Trends and Resistance Patterns of ESBL-Producing Non-Typhoidal Salmonella Isolated from Blood Cultures in Kisantu, DRC (2019–2022)

**Authors:** Jules Mbuyamba, Gaelle Nkoji-Tunda, Daniel Vita, Laurence Ngara, Edmonde Bonebe, Marie-France Phoba, Anne-Sophie Heroes, Mohamadou Siribie, Birkneh Tilahun Tadesse, Glody-Nickel Mbaa, Florian Marks, Liselotte Hardy, Jan Jacobs, Lisette Mbuyi-Kalonji, Octavie Lunguya

PMC · DOI: 10.3390/antibiotics15030271 · Antibiotics · 2026-03-06

## TL;DR

This study shows a rising trend of antibiotic-resistant Salmonella infections in children under 2 in Kisantu, DRC, from 2019 to 2022.

## Contribution

The study provides new insights into the temporal increase and resistance patterns of ESBL-producing NTS in a sub-Saharan African setting.

## Key findings

- ESBL-producing NTS prevalence peaked in children under 2 years of age.
- The likelihood of isolating ESBL-producing NTS increased from 58% in 2019 to 87% in 2022.
- High levels of extensively drug-resistant NTS were observed, but no carbapenem resistance was detected.

## Abstract

Background: Antimicrobial resistance (AMR), particularly due to extended-spectrum beta-lactamases (ESBL), is a growing threat to public health in sub-Saharan Africa. This study investigates the prevalence, epidemiological characteristics, resistance patterns and resistance dynamic over time of ESBL-producing non-typhoidal Salmonella (NTS) bacteremia in Kisantu, Democratic Republic of Congo (DRC), from 2019 to 2022. Methods: A retrospective observational study used routine bloodstream infection data from the AMR network at Saint Luc Hospital in Kisantu. Blood cultures from suspected bacteremia cases were processed using standard microbiological techniques. Bacterial identification relied on biochemical reactions. Antibiotic susceptibility testing and ESBL-producing NTS detection were performed by disk diffusion following Clinical and Laboratory Standards Institute guidelines. Associations between ESBL production and patient characteristics (age, sex) were assessed using Pearson’s Chi-square test, and annual temporal trends in ESBL-producing NTS from 2019 to 2022 were analyzed by logistic regression using 2019 as the reference year. Results: Of the 19,430 blood cultures, 1681 NTS isolates were identified, and 1568 of these were screened for ESBL. ESBL prevalence was significantly associated with age (p = 0.007), peaking in children under 2 years, but not with sex (p = 0.570). Compared with 2019, the likelihood of isolating ESBL-producing NTS increased markedly through 2022, with adjusted probabilities rising from 58% to 87%, reflecting a strong upward temporal trend. High levels of extensively drug-resistant (94.1%) were observed. No carbapenem resistance was detected. Conclusions: ESBL-producing NTS bacteremia is rising in Kisantu, DRC, mainly affecting children under 2 years. Rising resistance to key antibiotics limits treatment options and highlights the need for strengthened AMR surveillance, optimized antibiotic use, and vaccination strategies.

## Linked entities

- **Diseases:** bacteremia (MONDO:0005229)
- **Species:** Salmonella (taxon 590)

## Full-text entities

- **Genes:** ODC1 (ornithine decarboxylase 1) [NCBI Gene 4953] {aka BABS, NEDBA, NEDBIA, ODC}
- **Diseases:** meningitis (MESH:D008580), Bloodstream infections (MESH:D018805), DRC (MESH:D006479), urinary tract infections (MESH:D014552), NTS (MESH:D014435), NTS infections (MESH:D012480), Infectious (MESH:D003141), fever (MESH:D005334), diarrheal disease (MESH:D004403), Bacteremia (MESH:D016470), malaria (MESH:D008288), pneumonia (MESH:D011014), death (MESH:D003643), malnutrition (MESH:D044342), infected (MESH:D007239), injury to (MESH:D014947), Klebsiella pneumonia (MESH:D007710), XDR (MESH:D054908), AMR (MESH:D060467), ESBL (MESH:C579922), Plasmodium falciparum malaria (MESH:D016778), anemia (MESH:D000740)
- **Chemicals:** pefloxacin (MESH:D015366), penicillins (MESH:D010406), fluoroquinolones (MESH:D024841), imipenem (MESH:D015378), ciprofloxacin (MESH:D002939), cephalosporins (MESH:D002511), trimethoprim-sulfamethoxazole (MESH:D015662), clavulanic acid (MESH:D019818), ceftazidime-avibactam (MESH:C000595613), chloramphenicol (MESH:D002701), monobactams (MESH:D008997), azithromycin (MESH:D017963), citrate (MESH:D019343), Hydrogen sulfide (MESH:D006862), meropenem (MESH:D000077731), -lactamases (-), meropenem-vaborbactam (MESH:C000654127), ceftolozane-tazobactam (MESH:C000594038), ceftazidime (MESH:D002442), carbapenem (MESH:D015780), beta-lactam (MESH:D047090), agar (MESH:D000362), ampicillin (MESH:D000667), cefotaxime (MESH:D002439), cefiderocol (MESH:C000612166), ceftriaxone (MESH:D002443)
- **Species:** Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371], Klebsiella pneumoniae (species) [taxon 573], Escherichia coli (E. coli, species) [taxon 562], Enterobacterales (order) [taxon 91347], Salmonella enterica subsp. enterica serovar Typhi (no rank) [taxon 90370], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023545/full.md

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Source: https://tomesphere.com/paper/PMC13023545