Polymerase chain reaction detection of genes responsible for multiple antibiotic resistance Staphylococcus aureus isolated from food of animal origin in Egypt
The aim of our study was polymerase chain reaction (PCR) detection of the genes responsible for the multiple antibiotic resistance isolated from food of animal origin in Egypt. A total of 125 samples were randomly collected from milk, meat, and their products from Giza and Beni-Suef Governorates mar...
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Published in: | Veterinary World Vol. 10; no. 10; pp. 1205 - 1211 |
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Abstract | The aim of our study was polymerase chain reaction (PCR) detection of the genes responsible for the multiple antibiotic resistance
isolated from food of animal origin in Egypt.
A total of 125 samples were randomly collected from milk, meat, and their products from Giza and Beni-Suef Governorates markets. The
isolates were subjected to antimicrobial sensitivity tests using four antibacterial disks (Oxoid), and then the polymerase chain reaction (PCR) was performed for detection of antibiotic resistance genes.
Out of 125 samples, 19
isolates were detected. All detected isolates were multiple drug resistance (MDR). The penicillin-, erythromycin-, kanamycin-, and tetracycline-resistant isolates were examined by PCR for resistance genes
, (
, and
,
, and
. The isolates harbored these resistance genes with percentage of 100% (100%, 0%, and 100%), 62.5%, and 100%, respectively.
Contaminated foods of animal origin may represent a source of MDR
that can be a major threat to public health. |
---|---|
AbstractList | AIMThe aim of our study was polymerase chain reaction (PCR) detection of the genes responsible for the multiple antibiotic resistance S. aureus isolated from food of animal origin in Egypt. MATERIALS AND METHODSA total of 125 samples were randomly collected from milk, meat, and their products from Giza and Beni-Suef Governorates markets. The S. aureus isolates were subjected to antimicrobial sensitivity tests using four antibacterial disks (Oxoid), and then the polymerase chain reaction (PCR) was performed for detection of antibiotic resistance genes. RESULTSOut of 125 samples, 19 S. aureus isolates were detected. All detected isolates were multiple drug resistance (MDR). The penicillin-, erythromycin-, kanamycin-, and tetracycline-resistant isolates were examined by PCR for resistance genes blaZ, (msrA, ermB, and ermC), aac(6')aph (2"), and tetK. The isolates harbored these resistance genes with percentage of 100% (100%, 0%, and 100%), 62.5%, and 100%, respectively. CONCLUSIONContaminated foods of animal origin may represent a source of MDR S. aureus that can be a major threat to public health. Aim: The aim of our study was polymerase chain reaction (PCR) detection of the genes responsible for the multiple antibiotic resistance S. aureus isolated from food of animal origin in Egypt. Materials and Methods: A total of 125 samples were randomly collected from milk, meat, and their products from Giza and Beni-Suef Governorates markets. The S. aureus isolates were subjected to antimicrobial sensitivity tests using four antibacterial disks (Oxoid), and then the polymerase chain reaction (PCR) was performed for detection of antibiotic resistance genes. Results: Out of 125 samples, 19 S. aureus isolates were detected. All detected isolates were multiple drug resistance (MDR). The penicillin-, erythromycin-, kanamycin-, and tetracycline-resistant isolates were examined by PCR for resistance genes blaZ, (msrA, ermB, and ermC), aac(6')aph (2"), and tetK. The isolates harbored these resistance genes with percentage of 100% (100%, 0%, and 100%), 62.5%, and 100%, respectively. Conclusion: Contaminated foods of animal origin may represent a source of MDR S. aureus that can be a major threat to public health. Keywords: food of animal origin, multiple antibiotic resistance, polymerase chain reaction, resistance genes, Staphylococcus aureus. The aim of our study was polymerase chain reaction (PCR) detection of the genes responsible for the multiple antibiotic resistance isolated from food of animal origin in Egypt. A total of 125 samples were randomly collected from milk, meat, and their products from Giza and Beni-Suef Governorates markets. The isolates were subjected to antimicrobial sensitivity tests using four antibacterial disks (Oxoid), and then the polymerase chain reaction (PCR) was performed for detection of antibiotic resistance genes. Out of 125 samples, 19 isolates were detected. All detected isolates were multiple drug resistance (MDR). The penicillin-, erythromycin-, kanamycin-, and tetracycline-resistant isolates were examined by PCR for resistance genes , ( , and , , and . The isolates harbored these resistance genes with percentage of 100% (100%, 0%, and 100%), 62.5%, and 100%, respectively. Contaminated foods of animal origin may represent a source of MDR that can be a major threat to public health. Aim: The aim of our study was polymerase chain reaction (PCR) detection of the genes responsible for the multiple antibiotic resistance S. aureus isolated from food of animal origin in Egypt. Materials and Methods: A total of 125 samples were randomly collected from milk, meat, and their products from Giza and Beni-Suef Governorates markets. The S. aureus isolates were subjected to antimicrobial sensitivity tests using four antibacterial disks (Oxoid), and then the polymerase chain reaction (PCR) was performed for detection of antibiotic resistance genes. Results: Out of 125 samples, 19 S. aureus isolates were detected. All detected isolates were multiple drug resistance (MDR). The penicillin-, erythromycin-, kanamycin-, and tetracycline-resistant isolates were examined by PCR for resistance genes blaZ, (msrA, ermB, and ermC), aac(6')aph (2''), and tetK. The isolates harbored these resistance genes with percentage of 100% (100%, 0%, and 100%), 62.5%, and 100%, respectively. Conclusion: Contaminated foods of animal origin may represent a source of MDR S. aureus that can be a major threat to public health. |
Audience | Professional |
Author | Khairy, Eman A Samy, A A Salam, Hala S H Koraney, Aya A Seedy, Fawzy R El |
AuthorAffiliation | 1 Department of Bacteriology, Mycology and Immunology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef, Egypt 2 Department of Microbiology and Immunology, National Research Center, Cairo, Egypt |
AuthorAffiliation_xml | – name: 2 Department of Microbiology and Immunology, National Research Center, Cairo, Egypt – name: 1 Department of Bacteriology, Mycology and Immunology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef, Egypt |
Author_xml | – sequence: 1 givenname: Fawzy R El surname: Seedy fullname: Seedy, Fawzy R El organization: Department of Bacteriology, Mycology and Immunology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef, Egypt – sequence: 2 givenname: A A surname: Samy fullname: Samy, A A organization: Department of Microbiology and Immunology, National Research Center, Cairo, Egypt – sequence: 3 givenname: Hala S H surname: Salam fullname: Salam, Hala S H organization: Department of Bacteriology, Mycology and Immunology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef, Egypt – sequence: 4 givenname: Eman A surname: Khairy fullname: Khairy, Eman A organization: Department of Microbiology and Immunology, National Research Center, Cairo, Egypt – sequence: 5 givenname: Aya A surname: Koraney fullname: Koraney, Aya A organization: Department of Microbiology and Immunology, National Research Center, Cairo, Egypt |
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Cites_doi | 10.1016/j.tvjl.2011.08.030 10.1016/j.foodcont.2005.09.013 10.1016/j.foodcont.2005.01.006 10.1128/AEM.07487-11 10.1111/lam.12709 10.3855/jidc.599 10.1016/j.foodcont.2014.04.008 10.1016/j.micres.2006.01.015 10.1089/vbz.2010.0072 10.1016/j.ijfoodmicro.2014.11.020 10.1056/NEJMoa010315 10.17221/1856-VETMED 10.1016/j.jiph.2011.06.001 10.1016/j.foodcont.2015.02.013 10.1016/j.foodcont.2016.01.024 10.1016/j.micpath.2016.06.005 10.1586/14787210.6.5.733 10.1016/S0168-1605(00)00351-2 10.1016/j.ijmm.2009.08.015 10.1080/10408399609527721 10.1128/JCM.05214-11 10.1128/AAC.44.2.231-238.2000 10.1016/j.vetmic.2007.10.006 10.1056/NEJMoa012261 10.1128/AAC.00155-06 10.1016/S1369-5274(00)00241-1 10.1016/j.fm.2016.10.029 10.1371/journal.pone.0148789 10.1016/j.ijfoodmicro.2014.12.002 10.1089/mdr.2004.10.321 10.1007/s00284-009-9553-1 10.1371/journal.pone.0030092 10.1093/cid/cir181 10.1007/s11250-017-1251-6 10.1016/j.ijantimicag.2007.06.020 10.1093/jac/dkp256 |
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Keywords | resistance genes multiple antibiotic resistance food of animal origin Staphylococcus aureus polymerase chain reaction |
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Snippet | The aim of our study was polymerase chain reaction (PCR) detection of the genes responsible for the multiple antibiotic resistance
isolated from food of animal... Aim: The aim of our study was polymerase chain reaction (PCR) detection of the genes responsible for the multiple antibiotic resistance S. aureus isolated from... AIMThe aim of our study was polymerase chain reaction (PCR) detection of the genes responsible for the multiple antibiotic resistance S. aureus isolated from... |
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SubjectTerms | Antibiotic resistance Antibiotics Contamination Drug resistance Erythromycin Food contamination food of animal origin Genetic aspects Health aspects Health risks Kanamycin Meat Microbial drug resistance Multidrug resistance multiple antibiotic resistance Penicillin Polymerase chain reaction Public health resistance genes Staphylococcus aureus |
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Title | Polymerase chain reaction detection of genes responsible for multiple antibiotic resistance Staphylococcus aureus isolated from food of animal origin in Egypt |
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