In vitro Induction of Phenotypic Resistance to Antibiotics in some Pathogenic Bacteria
DOI:
https://doi.org/10.47430/ujmr.1722.009Keywords:
Antibiotics, Development of Resistance, Repeated ExposureAbstract
The study was carried out on the development of resistance due to repeated exposure of some bacterial isolates to antibiotics. The organisms; Salmonella typhi and Shigella dysentriae were isolated from stools using Salmonella Shigella Agar (SS Agar). Proteus mirabilis and Staphylococcus aureus were isolated from urine using Cystine Lysine Electrolite Deficient (CLED) Agar. After the isolation, standard inoculum of Salmonella typhi,Shigella dysentriae, Proteus mirabilis and Staphylococcus aureus were prepared, each and was streaked onto Mueller-Hinton Agar plates. Prepared Amoxicillin, Ciprofloxacin, and Gentamicin paper discs were placed each at the center of the plates and incubated for 24 hours, at 37oC. Zones of inhibition were formed. The zones of inhibition were measured and recorded, and then bacteria from the edges of the inhibition zones were picked up with a swab stick, and inoculated on to fresh Mueller- Hinton Agar plates. This process was repeated of 10 timesfor each. Over the course of 10 exposures to test antibiotics separately, all the test organisms developed resistance to the antibiotics gradually as seen through decrease in diameter of their zones of inhibitions. Salmonella typhi plates (from 1-10 exposure) under Ciprofloxacin, on average were reduced to 24.1mm, Gentamycin were reduced to 6.5mm and Amoxicillin were reduced to 5.8mm. Shigella dysentriae plates (from 1-10 exposure) under Ciprofloxacin, on average were reduced to 27.2mm, Gentamycin were reduced to 7.8mm and Amoxicillin were reduced to 6.0mm. Proteus mirabilis plates (from 1-10 exposure) under Ciprofloxacin, on average were reduced to 34.0mm, Gentamycin were reduced to 22.7mm and Amoxicillin were reduced to 8.5mm. Staphylococcus aureus plates (from 1-10 exposure) under Ciprofloxacin, on average were reduced to 25.9mm, Gentamycin were reduced to 15.4mm and Amoxicillin were reduced to 7.4mm. The results obtained confirmed that repeated exposure of the bacterial pathogens to antibiotics increased their resistance. Ciprofloxacin was the most active antibiotic among the test antibiotics as it has notable zone of inhibition often repeated exposure while Amoxicillin was the least active antibiotic as it showed full resistance at 4th exposure for Salmonella typhi and Shigella dysenteriae and 5th exposure for Proteus mirabilis and Staphylococcus aureus.
Downloads
References
Alekshun, M. N. and Levy, S. B. (2007). "Molecular mechanisms of antibacterial multidrug resistance". Cell 128 (6): 1037-50. doi:10.1016/j.cell.2007.03.004. PMID 17382878.
https://doi.org/10.1016/j.cell.2007.03.004
Allen, H. K., Moe, L. A. Rodbumrer, J. Gaarder, A.and HandelsmanJ.(2009). Functional metagenomics reveals diverse beta- lactamases in a remote Alaskan soil. ISME J. 3:243-251.
https://doi.org/10.1038/ismej.2008.86
Baker-Austin C, Wright M.S. Stepanauskas R, McArthur J. V. (2006). "Co-selection of antibiotic and metal resistance". Trends Microbiol.14 (4): 176-82.
https://doi.org/10.1016/j.tim.2006.02.006
Betty J. Mcgrath,T. Randall,C.Marchbanks, D. G., and Michael N. (1993). Dudley* Antimicrobial Agents and Chemotherapy, p. 1723-1725, American Society for Microbiology.In Vitro Post antibiotic Effect Following Repeated Exposure to Imipenem, Temafloxacin, and obramycin.
https://doi.org/10.1128/AAC.37.8.1723
Cassir, N. Rolain, J. M. Brouqui, P. (2014). "A new strategy to fight antimicrobial resistance: the revival of old antibiotics.". Frontiers in Microbiology5: 551.
https://doi.org/10.3389/fmicb.2014.00551
Cheesbrough, M. (2006). District laboratory practice in tropical countries, ECBS edition Cambridge University Press.
https://doi.org/10.1017/CBO9780511543470
Davies J, and Davies D, (2010). Origin and evolution of Antibiotic Resistance, Microbiology and Molecular Biology reviews. p: 417-433.
https://doi.org/10.1128/MMBR.00016-10
James C. B, (2015). Antibiotic Resistance by Repeated Exposure. Science Fair California State Project Summary 2015. Project no. j1603
Hawkey P. M. (1998).The origin and molecular basis of antibiotic resistance.BMJ; 317 (7159): 657-60.
https://doi.org/10.1136/bmj.317.7159.657
Hoffman, SJ; Outterson, K; Røttingen, JA; Cars, O; Clift, C; Rizvi, Z; Rotberg, F; Tomson, G; Zorzet, A. (2015). "An international legal framework to address antimicrobial resistance"(PDF). Bulletin of the World Health Organization 93 (2): 66.
https://doi.org/10.2471/BLT.15.152710
Leekha, Surbhi; Terrell, Christine L.; Edson, Randall S. (2011). "General Principles of Antimicrobial Therapy". Mayo Clinic Proceedings 86 (2). doi:10.4065/mcp.2010.0639. PMC 3031442. PMID 21282489.
https://doi.org/10.4065/mcp.2010.0639
Mathew, A. G; Cissell, R. and Liamthong, S. (2007). Antibiotic resistance in bacteria associated with food animal: a United States perspective of livestock production. Foodborne pathogens and Disease; 4 (2).
https://doi.org/10.1089/fpd.2006.0066
Nikaido H. (2009). "Multidrug Resistance in Bacteria". Annu. Rev. Biochem. 78: 119-46.(doi:10.1146/annurev.biochem.78.082907 .145923. PMC 2839888. PMID 19231985).
https://doi.org/10.1146/annurev.biochem.78.082907.145923
Oyeleke S. B. and Manga S.B. (2008). Essential laboratory practical in microbiology. First edition. Tobest publisher's minna nigeria p20-65s
Sule A. M, Thanni L. A, Sule Odu, A and Olusanya, O. (2002). Bacterial Pathogens associated with wound infections in Ogun state university Teaching hospital. African Journal of Chemical and Experimental Microbiology. 3(1)15.
https://doi.org/10.4314/ajcem.v3i1.7344
Velissariou, I.M. (2006). The use of fluoroquinolones in children: recent advances. Expert Rev Anti Infect Ther, 4(5): p. 853-60.
https://doi.org/10.1586/14787210.4.5.853
Witte W. (2004). "International dissemination of antibiotic resistant strains of bacterial pathogens".Infect. Genet. Evol. 4 (3): 187-91. doi:10.1016/j.meegid.2003.12.005.
https://doi.org/10.1016/j.meegid.2003.12.005
WHO, (2014). First global report on antibiotic resistance reveals serious, worldwide threat to public health" Retrieved.
Woodford N and Ellington M.J. (2007). "The emergence of antibiotic resistance by mutation". Clinical Microbiology and Infection: the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases 13 (1): 5-18.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2023 UMYU Journal of Microbiology Research (UJMR)
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.