Literature DB >> 29195992

Phenotypic characterization of Cronobacter spp. strains isolated from foods and clinical specimens in Brazil.

Natália Scudeller Umeda1, Ivano de Filippis2, Stephen James Forsythe3, Marcelo Luiz Lima Brandão4.   

Abstract

Several Cronobacter species are opportunistic pathogens that cause infections in humans. This study evaluated the phenotypic characteristics of 57 Cronobacter strains (C. sakazakii n=41, C. malonaticus n=10, C. dublinensis n=4, and C. muytjensii n=2) isolated from food (n=54) and clinical specimens (n=3) in Brazil. These strains included sequence types (ST): ST395-ST398, ST402, ST413 and ST433-ST439, isolated from food samples, and three C. malonaticus clinical strains previous isolated from an outbreak which were ST394 (n=1) and ST440 (n=2). Strains were tested for capsule production, biofilm formation, protease activity, hemolytic activity, cell-cell aggregation, and desiccation resistance. Capsule formation was observed with all Cronobacter strains. Forty-four (77.2%) strains showed proteolytic activity on milk agar. All strains showed β-hemolysis against erythrocytes from guinea pig, horse and rabbit. Using erythrocytes from sheep, the majority of strains (53/57; 92.9%) showed α-hemolysis and the remaining, β-hemolysis. All Cronobacter strains produced weak biofilms in microtiters polystyrene plates, which were independent of temperature (4, 25 and 37°C) and/or growth conditions. In glass tubes, formation of either a moderate or strong biofilm was observed in 15/57 (26.3%), 19/57 (33.3%) and 27/57 (47.4%), at 4, 25 and 37°C, respectively. Desiccation treatment decreased Cronobacter viability by 1.55 to >3.87Log10CFU/mL. Cell-cell aggregation was observed in 17 (29.8%) strains. This study showed that the Cronobacter species evaluated showed differing phenotypes, independent of their origin (clinical or not) and ST. Further studies are necessary to elucidate the factors affecting phenotype expression. This may identify novel bacterial targets that could be useful in the development of strategies to control Cronobacter in food chain and to prevent cases of infections.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Biofilm; Capsule; Cell-cell aggregation; Cronobacter spp.; Hemolysis; MLST; Protease

Mesh:

Substances:

Year:  2017        PMID: 29195992     DOI: 10.1016/j.foodres.2017.09.083

Source DB:  PubMed          Journal:  Food Res Int        ISSN: 0963-9969            Impact factor:   6.475


  4 in total

1.  Evaluation of commercial probiotic lactic cultures against biofilm formation by Cronobacter sakazakii.

Authors:  Anubhav Jamwal; Kavita Sharma; Rajni Chauhan; Saurabh Bansal; Gunjan Goel
Journal:  Intest Res       Date:  2018-12-03

2.  Prevalence, Distribution, and Phylogeny of Type Two Toxin-Antitoxin Genes Possessed by Cronobacter Species where C. sakazakii Homologs Follow Sequence Type Lineages.

Authors:  Samantha Finkelstein; Flavia Negrete; Hyein Jang; Jayanthi Gangiredla; Mark Mammel; Isha R Patel; Hannah R Chase; JungHa Woo; YouYoung Lee; Caroline Z Wang; Leah Weinstein; Ben D Tall; Gopal R Gopinath
Journal:  Microorganisms       Date:  2019-11-12

3.  Fatal Cronobacter sakazakii Sequence Type 494 Meningitis in a Newborn, Brazil.

Authors:  Cláudia Elizabeth Volpe Chaves; Marcelo Luiz Lima Brandão; Mara Luci Gonçalves Galiz Lacerda; Caroline Aparecida Barbosa Coelho Rocha; Sandra Maria do Valle Leone de Oliveira; Tânia Cristina Parpinelli; Luiza Vasconcellos; Stephen James Forsythe; Anamaria Mello Miranda Paniago
Journal:  Emerg Infect Dis       Date:  2018-10       Impact factor: 6.883

Review 4.  The Secretion of Toxins and Other Exoproteins of Cronobacter: Role in Virulence, Adaption, and Persistence.

Authors:  Hyein Jang; Gopal R Gopinath; Athmanya Eshwar; Shabarinath Srikumar; Scott Nguyen; Jayanthi Gangiredla; Isha R Patel; Samantha B Finkelstein; Flavia Negrete; JungHa Woo; YouYoung Lee; Séamus Fanning; Roger Stephan; Ben D Tall; Angelika Lehner
Journal:  Microorganisms       Date:  2020-02-08
  4 in total

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