2012
DOI: 10.7324/japs.2012.2406
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Effect of Probiotics against Marine Pathogenic Bacteria on Artemia franciscana

Abstract: Presently an effort has been made to determine the effectiveness of probiotics against marine pathogenic bacterial load ingested by Artemia franciscana nauplii. In this experiment Artemia franciscana nauplii was allowed to ingest pathogenic bacterial strains, viz. Escherichia coli, Salmonella typhi, Salmonella paratyphi, Vibrio cholerae and Shigella sp. Probiotic organism (Bioremid) was used against the pathogenic strains on Artemia franciscana nauplii. On completion of the experiment it was observed that the … Show more

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Cited by 5 publications
(2 citation statements)
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“…These nutrients are obtained from the characteristics of Artemia as a non-selective filter feeder, which means it does not select food and consumes anything that enters its mouth (Mohebbi et al, 2015). In addition to the nutrients present in A. franciscana as feed for shrimp larvae, this species can also be a vector for the spread of pathogens in shrimp larvae (Haq et al, 2012). Alternative prevention of pathogens can be done by giving disinfectants to suppress the emergence of bacteria, viruses, or other diseases, such as iodine.…”
Section: Introductionmentioning
confidence: 99%
“…These nutrients are obtained from the characteristics of Artemia as a non-selective filter feeder, which means it does not select food and consumes anything that enters its mouth (Mohebbi et al, 2015). In addition to the nutrients present in A. franciscana as feed for shrimp larvae, this species can also be a vector for the spread of pathogens in shrimp larvae (Haq et al, 2012). Alternative prevention of pathogens can be done by giving disinfectants to suppress the emergence of bacteria, viruses, or other diseases, such as iodine.…”
Section: Introductionmentioning
confidence: 99%
“…After 8 h of incubation, the Artemia nauplii were collected using sterile Miracloth, and washed with 1 mL sterile saline solution (0.85 %, NaCl), then macerated using a homogenizer (LabGEN ® 125, Cole-Parmar, USA). To estimate bacterial concentration in the tissues, the homogenate suspensions were serially diluted in sterile saline until dilution factor 10 -9 (Badhul Haq et al, 2012). A 100 µL aliquot was pipetted and spread-plated on de Man Rogosa and Sharp agar (MRS, Difco TM BD, USA), then followed by incubation at 26 ± 2 °C for 24-48 h. The experiment was performed in triplicates.…”
Section: Effect Of Encapsulation Media On Bacterial Recovery From Artmentioning
confidence: 99%