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Showing 2 results for Jebellijavan

Mahnoosh Parsaeimehr, Maryam Khazaei, Ashkan Jebellijavan , Hamid Staji,
Volume 5, Issue 1 (3-2019)
Abstract

Background: Identification of the dominant lactic acid bacteria involved in the production of traditional cheese in Semnan could be the initiative to protect national genetic resources and produce industrial cheese with desirable texture and organoleptic characteristics similar to traditional cheeses. The present study aimed to determine the biochemical, physiological, and phenotypic properties of the dominant strains of the lactic acid bacteria (LAB) isolated from the traditional cheese in Semnan, Iran using 16S rRNA gene sequence analysis.
Methods: In total, 14 cheese samples were randomly collected from the northern countryside of Semnan, Iran. The isolated gram-positive and catalase-negative colonies were analyzed in terms of morphology, culture, physiology, biochemical properties, and carbohydrate fermentation pattern. Following that, the LAB isolates were identified based on 16S rRNA gene sequence analysis, and a phylogenetic tree was drawn for the bacterial strains.
Results: In this study, 105 isolates were determined, 58 of which (55.24%) belonged to the genus Lactobacilli, and 47 isolates (44.76%) belonged to the genus Enterococci. According to the biochemical tests and 16S rDNA sequencing, the identified dominant Lactobacillus species included L. plantarum (53.6%), L. paracasei (32.7%), and L. casei (13.7%). In addition, most of the Enterococcus species were E. faecium (74.47%) and E. durans (25.53%).
Conclusion: According to the results, exploring the microbiological diversity of traditional cheese could contribute to the selection of proper bacterial strains for the manufacturing of products with consistent quality and original taste on an industrial scale.

Ashkan Jebellijavan, Seyed Hesamodin Emadi Chashmi, Hamid Staji, Hossein Akhlaghi,
Volume 6, Issue 4 (12-2020)
Abstract

Background: Helicobacter pullorum is among the most frequently reported pathogens in poultry. The present study aimed to compare the culture and polymerase chain reaction (PCR) methods to assess the prevalence of H. pullorum isolated from chicken tight samples in Semnan, Iran. The antibiotic resistance pattern of the H. pullorum isolates was also determined for the first time in Iran.
Methods: In total, 50 chicken thigh samples were collected from the local retail markets in Semnan city during January-September 2019. The samples were examined using the culture method and biochemical tests, and the final confirmation was based on PCR with the 16S rRNA gene. In addition, antibiotic resistance test was performed using the disc-diffusion method.
Results: According to the culture method and biochemical tests, 12 samples (24%) were positive for H. pullorum, eight of which (16%) showed H. pullorum in PCR as well and resistance against nalidixic acid and ciprofloxacin. On the other hand, the lowest antimicrobial resistance was observed against colistin, chloramphenicol, and fosfomycin.
Conclusion: Our promising findings indicated that PCR based on the 16S rRNA gene may be a valuable and sensitive approach to the detection of H. pullorum in chicken meat.


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