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Atb new system

Manufactured by bioMérieux
Sourced in France

The ATB New system is a laboratory equipment product developed by bioMérieux. It is designed for the automated identification and antibiotic susceptibility testing of microorganisms.

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3 protocols using atb new system

1

Clinical E. coli Isolates in China

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A total of 97 non-duplicated clinical E. coli isolates were collected from 97 different patients in various departments (gastroenterology, urology, endocrinology, neurosurgery, and other wards) of the First Affiliated Hospital of Chengdu Medical College, Chengdu, Sichuan, China from 2015 to 2016. The isolates were identified using standard laboratory methods and the ATB New system (bioMérieux, Lyons, France). Patients who satisfied the following three criteria were included in the analysis: 1) age >18 years; 2) suspected of having an infection, based on their clinical symptoms (e.g. fever, abdominal pain, nausea, vomiting, dehydration and tenesmus); and 3) their bacterial culture yielded E. coli. The E. coli isolates were collected from biofluid samples including blood, urine, sputum, wound exudates and abscesses. Each isolate was further verified by PCR amplification of a 369-bp internal control region from the E. coli marker gene, alr.15 (link) All bacterial strains were stored at −80 °C and were grown on MacConkey Agar (Oxoid, Hampshire, UK).
The study protocol was approved by the Ethics Committee of Chengdu Medical College, in accordance with the Helsinki declaration. In all cases, the patients or their family members were informed and their written consents was obtained.
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2

Isolation and Identification of E. coli from Clinical Samples

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A total of 110 non-duplicated E. coli clinical isolates were collected from 110 different patients in various departments (gastroenterology, endocrinology, neurosurgery, and other wards) at the First Affiliated Hospital of Chengdu Medical College, Chengdu, Sichuan, China from 2015 to 2016. Isolates were identified using standard laboratory methods and the ATB New system (bioMérieux, Lyons, France). Each isolate was further verified by PCR amplification of a 369-bp internal control region from the E. coli marker gene alr [90 (link)]. All strains were stored at − 80 °C and bacteria were grown on MacConkey Agar (Oxoid, Hampshire, UK).
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3

Aeromonas Diversity in Aquatic Environments

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A total of 1143 isolates from fish and the aquatic environment was collected from 20 farms of six districts in four cities of Guangdong Province, P.R. China. The fish investigated included O. niloticus; C. idellus; Cirrhinus mrigala (Hamilton, 1822); Siniperca chuatsi (Basilewsky, 1855); Megalobrama amblycephala Yih, 1955; and Channa maculata (Lacepède, 1801) ♀ × C. argus (Cantor, 1842) ♂. Gills and intestines were aseptically swabbed using sterile cotton buds and inoculated into Luria-Bertani (LB) broth for preenrichment at 28 ºC ± 2 ºC for 18 h~24 h. The enriched cultures were streaked on Rimler-Shotts agar and incubated at 28 ºC ± 2 ºC for 18 h~24 h. Yellow, oxidase-positive colonies were isolated and presumptively considered as Aeromonas species. One to three Aeromonas strains were selected from each sample. The presumptive Aeromonas colonies were further investigated by biochemical typing using ATB™ New System (BioMérieux, France). The identification was confirmed by polymerase chain reaction (PCR) amplification of 16S rRNA gene and gyrB genes, which was performed as described in previous studies (Borrell et al., 1997; (link)Yáñez et al., 2003) (link). Taxonomic identification of the sequences was performed using BLAST in GenBank (http://blast.ncbi.nlm.nih.gov/).
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