Pola Resistensi Antibiotik Bakteri Penyebab Infeksi Saluran Kemih di Puskesmas Ibrahim Adjie Kota Bandung
Main Article Content
Abstract
Bakteri penyebab Infeksi saluran kemih (ISK) telah mengalami resistensi terhadap berbagai antibiotik. Pola resistensi bakteri tersebut perlu diperbaharui datanya untuk memastikan pemberian antibiotik yang tepat. Tujuan penelitian mengidentifikasi dan melihat pola resistensi bakteri penyebab ISK di Puskesmas Ibrahim Adjie Kota Bandung. Koloni bakteri yang berasal dari urin 9 pasien  suspect ISK ditumbuhkan dan hanya sampel yang berasal dari 3 pasien memenuhi persyaratan terindikasi  ISK karena adanya jumlah koloni di atas  105 cfu/ml. Selanjutnya dilakukan penentuan Gram bakteri, isolasi DNA total kromosom bakteri, amplifikasi gen pengkode 16S rRNA, sekuensing (penentuan urutan nukleotida) dan uji resistensi terhadap antibiotik golongan penisilin, penisilin+inhibitor β-lactamase, sefalosporin (generasi 1,2,3,4), fluorokuinolon, aminoglikosida dan karbapenem. Hasinya didapatkan tiga isolat (P1,P2,P3) yang teridentifikasi secara genetik Escherichia coli. Isolat P1 resisten terhadap penisilin, penisilin+inhibitor β-laktamse, sefalosporin generasi 1 dan fluorokuinolon. isolat P2 resisten terhadap penisilin. Isolat P3 resisten terhadap penisilin, penisilin+inhibitor β-laktamse, sefalosporin (generasi 1,2,3,4) dan fluorokuinolon. E. coli penyebab ISK telah mengalami resistensi terhadap antibiotik penisilin, penisilin+inhibitor β-lactamase, sefalosporin (generasi 1,2,3,4) dan fluorokuinolon. Aminoglikosida dan karbapenem masih memiliki aktivitas terhadap ketiga isolat E. coli resisten.
Kata kunci: bakteri; ISK; isolasi; identifikasi; resistensi
Article Details

This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.
The authors retain the copyright and grant the journal the right of first publication simultaneously under the Creative Commons Attribution License. This license allows others to share the work with proper acknowledgment of authorship and initial publication in this journal. Authors are permitted and encouraged to deposit their articles in institutional repositories, on their personal websites, or in other online repositories after the article has been published in JSFK.
References
Kusnan A. Faktor Risiko Kejadian Infeksi Saluran Kemih pada Ibu Hamil di Laboratorium Prodia. Jurnal Ilmu Kesehatan. 2014;1(1): 2355-312.
Foxman B. Epidemiology of Urinary Tract Infections: Incidence, Mobidity, and Economic Costs. Dis Mon Journal. 2003;(49):53-70.
Flores-Mireles AL, Walker JN, Caparon M, Hultgren SJ.Urinary tract infections: epidemiology, mechanisms of infection and treatment options. Nature reviews. Microbiology.2015;13(5):269–284.
Raju CB, Tiwari SC. Urinary tract infection – A suitable approach. Lecture notes. J Ind Academy of clinical Med. 2004;2(4): 331-334.
Port,CM and Muffin G. 2009. Pathophysiology :Concepts of Altered Health States 8th Edition. Philadelphia: Lippincott Williams & Wilkins; 2009.
Farrell DJ, Morrissey I,De Rubeis D, Robbins M, Felmingham D. A UK multicentre study of the antimicrobial susceptibility of bacterial pathogens causing urinary tract infection. J Infect. 2003;46(2):94-100.
Mandal J, Acharya NS, Buddhapriya D, Parija SC. Antibiotic resistance pattern among common bacterial uropathogens with a special reference to ciprofloxacin resistant Escherichia coli. Indian J Med Res. 2012;136(5):842–849.
Rahman F, Chowdhury S, Rahman M, Ahmed D, Hossain, A. Antimicrobial Resistance Pattern of Gram-negative Bacteria Causing Urinary Tract Infection. S J Pharm Scices. 2009;2(1):44-50.
Rahardjo P, Susalit, E. Infeksi Saluran Kemih, dalam Ilmu Penyakit Dalam, Edisi IV. Jakarta: FKUI, 2006.
Harley JP, Prescott LM. Laboratory Exercises in Microbiology 5th Edition. The McGraw-Hill Companies; 2002.
(GeneJETTMGenomic DNA Purification Kit®).
https://assets.thermofisher.com/TFS-Assets/LSG/manuals/
Weisburg WG, Barns SM, Pelletier DA, Lane DJ.16S ribosomal DNA amplification for phylogenetic study. J Bacteriol. 1991;73(2):697-703.
Sambrook J, Russell D. Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory. New York: Cold Spring Harbor Laboratory Press;2001.
Clinical and Laboratory Standards Institute (CLSI). Performance standards for antimicrobial susceptibility testing; 19th informational supplement (CLSI document M100-S19). Wayne,PA: Clinical and Laboratory Standards Institute; 2009.
Bradford PA. Extended-Spectrum Betalactamases in the 21st Century: Characterization, Epidemiology and Detection of This Important Resistance Threat. Clin Microbiol Rev. 2001;(14)4:933-951.
Livermore DM. beta-Lactamases in laboratory and clinical resistance. Clin Microbiol Rev. 1995;8(4):557-84.
Carter MW, Oakton KJ, Warner M, Livermore DM. Detection of extended-spectrum β-lactamases in klebsiellae with the Oxoid combination disk method. J Clin Microbiol. 2000;38:4228–4232.
Komp Lindgren P, Karlsson A, Hughes D. (2003).Mutation rate and evolution of fluoroquinolone resistance in Escherichia coli isolates from patients with urinary tract infections. Antimicrob Agents Chemother. 2003;47(10):3222–3232.
Alós JI, Serrano MG, Gómez-Garcés JL, Perianes J. Antibiotic resistance of Escherichia coli from community-acquired urinary tract infections in relation to demographic and clinical data. Clin Microbiol Infect. 2005;11(3):199-203.
Johnson L, Sabel A, Burman WJ, Everhart RM, Rome M, MacKenzie TD, Rozwadowski J, Mehler PS, Price CS. Emergence of fluoroquinolone resistance in outpatient urinary Escherichia coli isolates. Am J Med. 2008;121(10):876-84.
Fasugba O, Gardner A, Mitchell BG, Mnatzaganian G. (2015). Ciprofloxacin resistance in community- and hospital-acquired Escherichia coli urinary tract infections: a systematic review and meta-analysis of observational studies. BMC Infect Dis. 2015:15:545.