Literature DB >> 23317867

Antibiotic resistance and growth of the emergent pathogen Escherichia albertii on raw ground beef stored under refrigeration, abuse, and physiological temperature.

Keila L Perez1, M Jahangir Alam, Alejandro Castillo, T Matthew Taylor.   

Abstract

Escherichia albertii is an emerging gram-negative facultative rod that has been implicated in multiple cases of human diarrheal disease, particularly in young children. When biochemical and other typing methods have been used, this organism has often been misidentified due to similarities with other members of the family Enterobacteriaceae. Isolates have been reported to be capable of producing attachment and effacement lesions via the synthesis of intimin, cytolethal distending toxin, and a variant form of Shiga toxin. The purposes of this study were to characterize the antibiotic resistance characteristics and the growth of individual strains of E. albertii on raw ground beef at different storage temperatures. Nalidixic acid-resistant strains of E. albertii were inoculated onto raw ground beef to a target of 4.0 log CFU/g, and samples were then aerobically incubated at 5, 22, or 35°C for various time periods prior to microbiological enumeration of the pathogen on lactose-free MacConkey agar containing 50 mg of nalidixic acid per liter and 0.5% L-rhamnose. Antibiotic resistance was determined using a broth microdilution assay. E. albertii did not grow at 5°C, with populations declining slowly over 14 days of refrigerated storage. Strains of the organism grew well under abusive storage, increasing by 2.5 to 3.1 log CFU/g and 4.1 to 4.3 log CFU/g after 24 h at 22 and 35°C, respectively. All strains were resistant to tetracycline but were sensitive to tested cephalosporins and chloramphenicol. Resistance to penicillin was observed, but susceptibility to other members of the b -lactam group, including ampicillin, amoxicillin, and clavulanic acid, was recorded. E. albertii represents an emerging pathogen with a probable foodborne transmission route. Future research should focus on verifying food process measures able to inactivate the pathogen.

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Year:  2013        PMID: 23317867     DOI: 10.4315/0362-028X.JFP-12-277

Source DB:  PubMed          Journal:  J Food Prot        ISSN: 0362-028X            Impact factor:   2.077


  4 in total

1.  Evaluating the occurrence of Escherichia albertii in chicken carcass rinses by PCR, Vitek analysis, and sequencing of the rpoB gene.

Authors:  Rebecca L Lindsey; Paula J Fedorka-Cray; Melanie Abley; Jennifer B Turpin; Richard J Meinersmann
Journal:  Appl Environ Microbiol       Date:  2014-12-29       Impact factor: 4.792

2.  Detection of Escherichia albertii from chicken meat and giblets.

Authors:  Eriko Maeda; Koichi Murakami; Nobuyuki Sera; Kenitiro Ito; Shuji Fujimoto
Journal:  J Vet Med Sci       Date:  2015-03-08       Impact factor: 1.267

3.  Multidrug-Resistant Escherichia albertii: Co-occurrence of β-Lactamase and MCR-1 Encoding Genes.

Authors:  Qun Li; Hong Wang; Yanmei Xu; Xiangning Bai; Jianping Wang; Zhengdong Zhang; Xiang Liu; Yimao Miao; Ling Zhang; Xinqiong Li; Nianli Zou; Guodong Yan; Xi Chen; Jie Zhang; Shanshan Fu; Ruyue Fan; Jianguo Xu; Juan Li; Yanwen Xiong
Journal:  Front Microbiol       Date:  2018-02-16       Impact factor: 5.640

4.  Pan-Genome Reverse Vaccinology Approach for the Design of Multi-Epitope Vaccine Construct against Escherichia albertii.

Authors:  Khurshid Jalal; Kanwal Khan; Diyar Ahmad; Ajmal Hayat; Zarrin Basharat; Muhammad Naseer Abbas; Saad Alghamdi; Mazen Almehmadi; Muhammad Umar Khayam Sahibzada
Journal:  Int J Mol Sci       Date:  2021-11-26       Impact factor: 5.923

  4 in total

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