Journal
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
Volume 87, Issue 16, Pages -Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/AEM.00743-21
Keywords
ExPEC; E. coli; biochemical identification; phenotypic identification; lactose negative; ST59; beta-glucuronidase negative; virulence; ONPG-MUG; phylogroup F; Escherichia coil; virulence factors
Categories
Funding
- Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [433128/2018-6, 312249/2017-9]
- Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [312249/2017-9, 2019/15578-4, 2009/00402-6, 2018/17353-7, 312066/2019-8, 304760/2015-3]
- Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) [88882.306532/2018-01, 88887.358057/2019-00, 88887.464416/2019-00, 001]
- Cristalia
- Eurofarma
- InfectoPharm
- MSD
- Pfizer
- Zambon
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Extraintestinal pathogenic Escherichia coli (ExPEC) is a major cause of infections in humans and animals globally. In a surveillance study, an E. coli strain from human blood culture was identified with unique characteristics on chromogenic agar and lacking certain biochemical traits. Genomic analysis revealed it to be of sequence type 59 (ST59), belonging to phylogroup F. Further evaluation of ST59 complex showed most strains to have a virulent genotype and unique biochemical behavior, potentially misclassifying them in epidemiological studies relying on typical phenotypes.
Extraintestinal pathogenic Escherichia coli (ExPEC) is a leading cause of human and animal infections worldwide. The utilization of selective and differential media to facilitate the isolation and identification of E coli from complex samples, such as water, food, sediment, and gut tissue, is common in epidemiological studies. During a surveillance study, we identified an E. coli strain isolated from human blood culture that displayed atypical light cream-colored colonies in chromogenic agar and was unable to produce beta-glucuronidase and beta-galactosidase in biochemical tests. Genomic analysis showed that the strain belongs to sequence type 59 (ST59) and phylogroup F. The evaluation in silico of 104 available sequenced lineages of ST59 complex showed that most of them belong to serotype O1:K1:H7, are beta-glucuronidase negative, and harbor a virulent genotype associated with the presence of important virulence markers such as pap, kpsE, chuA, fruA, and yfcV. Most of them were isolated from extraintestinal human infections in diverse countries worldwide and could be clustered/subgrouped based on papAF allele analysis. Considering that all analyzed strains harbor a virulent genotype and most do not exhibit biochemical behavior typical of E. coli, we report that they could be misclassified or underestimated, especially in epidemiological studies where the screening criteria rely only on typical biochemical phenotypes, as happens when chromogenic media are used. IMPORTANCE The use of selective and differential media guides presumptive bacterial identification based on specific metabolic traits that are specific to each bacterial species. When a bacterial specimen displays an unusual phenotype in these media, this characteristic may lead to bacterial misidentification or a significant delay in its identification, putting a patient at risk depending on the infection type. In the present work, we describe a virulent E. coli sequence type (ST59) that does not produce beta-glucuronidase (GUS negative), production of which is the metabolic trait widely used for E. coli presumptive identification in diverse differential media. The recognition of this unusual metabolic trait may help in the proper identification of ST59 isolates, the identification of their reservoir, and the evaluation of the frequency of these pathogens in places where automatic identification methods are not available.
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