2014
DOI: 10.2478/s11756-014-0392-6
|View full text |Cite
|
Sign up to set email alerts
|

Effect of temperature and arsenic on Aeromonas hydrophila growth, a modelling approach

Abstract: Aeromonas hydrophila is frequently reported from arsenic affected areas. Present study was aimed to determine the effect of arsenic and temperature on growth of A. hydrophila. The bacteria were isolated from naturally infected fish from a water body in Birbhum, West-Bengal, India, which is reported to be an arsenic-free area. Arsenic concentration in natural aquatic reservoirs (e.g., pond, lake or river) varies from 0-6 mg/L. No significant change in bacterial growth was observed within this range of arsenic e… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
3
0

Year Published

2018
2018
2023
2023

Publication Types

Select...
5
1
1

Relationship

0
7

Authors

Journals

citations
Cited by 8 publications
(3 citation statements)
references
References 43 publications
0
3
0
Order By: Relevance
“…For example, the growth of bacterial isolates from soil and water from the Hazaribagh tannery industrial area in Bangladesh decreased with increasing concentrations of As (Prosun et al 2020). Goswami et al (2014) modeled the effect of As (arsenic trioxide, As 2 O 3 ) on the growth of Aeromonas hydrophila and observed no significant change in bacterial growth within the range of 0-30.32 μM As.…”
Section: Resultsmentioning
confidence: 99%
“…For example, the growth of bacterial isolates from soil and water from the Hazaribagh tannery industrial area in Bangladesh decreased with increasing concentrations of As (Prosun et al 2020). Goswami et al (2014) modeled the effect of As (arsenic trioxide, As 2 O 3 ) on the growth of Aeromonas hydrophila and observed no significant change in bacterial growth within the range of 0-30.32 μM As.…”
Section: Resultsmentioning
confidence: 99%
“…The temperature stability of the crude Actinomycetes extracts were incubated in a water bath for 24 h at 4 °C, 25 °C, 35 °C, 45 °C, 55 °C, and 65 °C. The post-treatment extracts were tested to determine their ability to inhibit and destroy biofilms [28][29][30]66 . For biofilm inhibition test, 100 µL of crude extracts and 100 µL of bacterial cultures (OD 600 = 0.132) were transferred into 96-well microtiter plates then incubated at pathogens' respective temperatures for 24 h. Meanwhile, for biofilm destruction test, 100 µL of bacterial culture were transferred into 96-well microtiter plates then incubated at pathogens' respective temperature.…”
Section: Methodsmentioning
confidence: 99%
“…First sampling was done at 2-3 min after the primary inoculation and was carried out at every 12 h interval throughout the experimental period for optical density measurement, taken at 688 nm wavelength for visible light 17 . Measuring the optical density of a growing culture is a common method to estimate growth of the species at specific time intervals because we know that the optical density of a growing culture increases proportionately with the increased concentration of liquid culture [17][18][19] .…”
Section: Experimental Designmentioning
confidence: 99%