Evidence map›Paper›PMID 41410726›Full record

ArticleAntonie van Leeuwenhoek2025

Unveiling the genomic and phenotypic landscape of Acinetobacter species from different environmental sources in Brazil.

Amanda Yaeko Yamada, Anna Luiza Bauer Canellas, Matheus Nunes Diniz, Pedro Smith Pereira Ferraro, Daniel de Sena Miranda, Ana Beatriz Nascimento Costa, Marlon Benedito Nascimento Santos, Karoline Rodrigues Campos, Claudio Tavares Sacchi, Beatriz Balthazar Abdon and 5 more

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Article in Antonie van Leeuwenhoek, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Amanda Yaeko YamadaCentro de Bacteriologia, Instituto Adolfo Lutz, Avenida Dr. Arnaldo 351, São Paulo, SP, 01246-902, Brazil.
Anna Luiza Bauer CanellasInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Av. Carlos Chagas Filho, 373, Cidade Universitária, Rio de Janeiro, RJ, 21941-902, Brazil.
Matheus Nunes DinizInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Av. Carlos Chagas Filho, 373, Cidade Universitária, Rio de Janeiro, RJ, 21941-902, Brazil.
Pedro Smith Pereira FerraroCentro de Bacteriologia, Instituto Adolfo Lutz, Avenida Dr. Arnaldo 351, São Paulo, SP, 01246-902, Brazil.
Daniel de Sena MirandaCentro de Bacteriologia, Instituto Adolfo Lutz, Avenida Dr. Arnaldo 351, São Paulo, SP, 01246-902, Brazil.
Ana Beatriz Nascimento CostaCentro de Bacteriologia, Instituto Adolfo Lutz, Avenida Dr. Arnaldo 351, São Paulo, SP, 01246-902, Brazil.
Marlon Benedito Nascimento SantosLaboratório Estratégico, Instituto Adolfo Lutz, Avenida Dr. Arnaldo 351, São Paulo, SP, 01246-902, Brazil.
Karoline Rodrigues CamposLaboratório Estratégico, Instituto Adolfo Lutz, Avenida Dr. Arnaldo 351, São Paulo, SP, 01246-902, Brazil.
Claudio Tavares SacchiLaboratório Estratégico, Instituto Adolfo Lutz, Avenida Dr. Arnaldo 351, São Paulo, SP, 01246-902, Brazil.
Beatriz Balthazar AbdonInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Av. Carlos Chagas Filho, 373, Cidade Universitária, Rio de Janeiro, RJ, 21941-902, Brazil.
Gabrielle da Silva Oliveira AlvesInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Av. Carlos Chagas Filho, 373, Cidade Universitária, Rio de Janeiro, RJ, 21941-902, Brazil.
Matheus de Oliveira Nithack MarquesInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Av. Carlos Chagas Filho, 373, Cidade Universitária, Rio de Janeiro, RJ, 21941-902, Brazil.
Guilherme MuricyMuseu Nacional, Universidade Federal do Rio de Janeiro, Quinta da Boa Vista, s/no., Rio de Janeiro, RJ, CEP 20940-040, Brazil.
Marinella Silva LaportInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Av. Carlos Chagas Filho, 373, Cidade Universitária, Rio de Janeiro, RJ, 21941-902, Brazil.
Carlos Henrique CamargoCentro de Bacteriologia, Instituto Adolfo Lutz, Avenida Dr. Arnaldo 351, São Paulo, SP, 01246-902, Brazil. carlos.camargo@ial.sp.gov.br.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico CNPq, 443302/2019-7, 309158/2023-0, 405020/2023-6Conselho Nacional de Desenvolvimento Científico e Tecnológico CNPq/MS, 175464/2023-5, 444395/2023-7Coordenação de Aperfeiçoamento de Pessoal de Nível Superior CAPES, 88887.820714/2023-00Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro FAPERJ E-26/211.284/2021, E-26/204.045/2024Fundação de Amparo à Pesquisa do Estado de São Paulo FAPESP 2017/50333-7, 2018/21192-9, 2018/21193-5, 2022/11794-7, 2024/22464-3; 2025/10643-3
6 · The paper itself

Abstract

This study aimed to investigate the diversity of Acinetobacter spp. isolated from aquatic environments along the Brazilian coast, with a focus on environmental reservoirs of clinically relevant resistance genes. Twenty-three Acinetobacter isolates were recovered from marine animals, floating plastic, and surface water samples collected in two contrasting Brazilian regions: the heavily polluted Guanabara Bay (Rio de Janeiro) and the pristine Fernando de Noronha Archipelago (Pernambuco). Seven species were identified, with A. venetianus (n = 13) and A. johnsonii (n = 4) being the most frequent. Two A. johnsonii isolates carried the metallo-β-lactamase gene blaNDM-1, along with resistance to fluoroquinolones and carbapenems. Resistance to polymyxins and aminoglycosides was also observed in A. haemolyticus, A. baumannii, and A. modestus. ApaI-PFGE dendrogram and phylogenetic analyses based on single nucleotide position (SNPs) revealed high genetic diversity, and global comparisons placed the environmental isolates in lineages distinct from those commonly associated with healthcare-associated infections. This study highlights the diversity of Acinetobacter spp. in aquatic environments and their potential role as reservoirs of clinically important resistance genes, including blaNDM-1. By uncovering resistance mechanisms in environmental Acinetobacter strains, this work reinforces the relevance of environmental surveillance for One Health initiatives, particularly in regions with significant anthropogenic impact.

Indexed as

AcinetobacterAnimalsAnti-Bacterial Agentsbeta-LactamasesBrazilDrug Resistance, BacterialGenetic VariationGenome, BacterialGenomicsMicrobial Sensitivity TestsPhenotypePhylogenyAnti-Bacterial Agentsbeta-LactamasesAcinetobacterAntimicrobial resistanceblaNDM-1Marine environmentWhole-genome sequencing

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.