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Emergence of multidrug-resistant Shigella species harboring extended-spectrum beta-lactamase genes in pediatric patients with diarrhea from southwest of Iran
Owing to the scarce evidence about the multidrug-resistant (MDR) beta-lactamase-producing Shigella isolates in Iran, this study aimed to evaluate the occurrence of extended-spectrum beta-lactamases (ESBL) and AmpC β-lactamases in Shigella species collected in the southwest of Iran. This study was co...
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Published in: | Molecular biology reports 2020-09, Vol.47 (9), p.7097-7106 |
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description | Owing to the scarce evidence about the multidrug-resistant (MDR) beta-lactamase-producing
Shigella
isolates in Iran, this study aimed to evaluate the occurrence of extended-spectrum beta-lactamases (ESBL) and AmpC β-lactamases in
Shigella
species collected in the southwest of Iran. This study was conducted on
Shigella
species isolated from stool samples of pediatric patients aged less than 15 years suffering from diarrhea. These isolates were identified by bacteriology tests, serotyping, and polymerase chain reaction (PCR). The antibiotic resistance was determined by disc diffusion. The production of ESBLs and AmpC was investigated by phenotypic confirmatory tests and PCR. In total, 79
Shigella
isolates, including 46.8% (n = 37) of
S. flexneri
and 53.2% (n = 42) of
S. sonnei
, were isolated, respectively. The most effective antibiotic was imipenem with 93.7% of susceptibility followed by ampicillin (29.1%), and cotrimoxazole (30.4%).The resistance rates of ceftriaxone, ceftazidime, and cefotaxime were 41.8%, 34.2%, and 41.8%, respectively. Also, a total of 57 (72.2%) isolates showed MDR profiles. The phenotypic tests showed that 43.0% (34/79) of isolates can produce ESBLs, and no one was positive for ApmC. The frequency of
bla
TEM
and
bla
CTX-M
were 30.4% and 32.9%, respectively, while the
bla
PER
,
bla
SHV,
and AmpC genes were not detected. The ESBL-producing isolates had a significant (
p
-value ˂ 0.05) resistance rate against ceftriaxone, ceftazidime, cefotaxime, cefepime, erythromycin, and amikacin. The significant prevalence of MDR
Shigella
isolates harboring ESBL genes highlights the need for effective surveillance measures to prevent the more spread of drug resistance among species. |
doi_str_mv | 10.1007/s11033-020-05776-x |
format | article |
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Shigella
isolates in Iran, this study aimed to evaluate the occurrence of extended-spectrum beta-lactamases (ESBL) and AmpC β-lactamases in
Shigella
species collected in the southwest of Iran. This study was conducted on
Shigella
species isolated from stool samples of pediatric patients aged less than 15 years suffering from diarrhea. These isolates were identified by bacteriology tests, serotyping, and polymerase chain reaction (PCR). The antibiotic resistance was determined by disc diffusion. The production of ESBLs and AmpC was investigated by phenotypic confirmatory tests and PCR. In total, 79
Shigella
isolates, including 46.8% (n = 37) of
S. flexneri
and 53.2% (n = 42) of
S. sonnei
, were isolated, respectively. The most effective antibiotic was imipenem with 93.7% of susceptibility followed by ampicillin (29.1%), and cotrimoxazole (30.4%).The resistance rates of ceftriaxone, ceftazidime, and cefotaxime were 41.8%, 34.2%, and 41.8%, respectively. Also, a total of 57 (72.2%) isolates showed MDR profiles. The phenotypic tests showed that 43.0% (34/79) of isolates can produce ESBLs, and no one was positive for ApmC. The frequency of
bla
TEM
and
bla
CTX-M
were 30.4% and 32.9%, respectively, while the
bla
PER
,
bla
SHV,
and AmpC genes were not detected. The ESBL-producing isolates had a significant (
p
-value ˂ 0.05) resistance rate against ceftriaxone, ceftazidime, cefotaxime, cefepime, erythromycin, and amikacin. The significant prevalence of MDR
Shigella
isolates harboring ESBL genes highlights the need for effective surveillance measures to prevent the more spread of drug resistance among species.</description><identifier>ISSN: 0301-4851</identifier><identifier>EISSN: 1573-4978</identifier><identifier>DOI: 10.1007/s11033-020-05776-x</identifier><identifier>PMID: 32894435</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Adolescent ; Amikacin ; Ampicillin ; Animal Anatomy ; Animal Biochemistry ; Antibiotic resistance ; Antibiotics ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Bacteriology ; beta-Lactamases - genetics ; beta-Lactamases - metabolism ; Biomedical and Life Sciences ; Cefepime ; Cefotaxime ; Ceftazidime ; Ceftriaxone ; Child ; Child, Preschool ; Cotrimoxazole ; Cross-Sectional Studies ; Diarrhea ; Diarrhea - enzymology ; Diarrhea - genetics ; Diarrhea - microbiology ; Erythromycin ; Female ; Histology ; Humans ; Imipenem ; Iran ; Life Sciences ; Male ; Morphology ; Multidrug resistance ; Multidrug resistant organisms ; Original Article ; Patients ; Pediatrics ; Polymerase chain reaction ; Serotyping ; Shigella ; Shigella - enzymology ; Shigella - genetics ; Species ; β Lactamase</subject><ispartof>Molecular biology reports, 2020-09, Vol.47 (9), p.7097-7106</ispartof><rights>Springer Nature B.V. 2020</rights><rights>Springer Nature B.V. 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c290x-3aa3043787ae81b5237dfd763502a1103d0baa9a9e842d4915ac1325e6cc43e63</citedby><cites>FETCH-LOGICAL-c290x-3aa3043787ae81b5237dfd763502a1103d0baa9a9e842d4915ac1325e6cc43e63</cites><orcidid>0000-0002-6735-8192 ; 0000-0001-7419-0116</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32894435$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Farajzadeh Sheikh, Ahmad</creatorcontrib><creatorcontrib>Moradi Bandbal, Maryam</creatorcontrib><creatorcontrib>Saki, Morteza</creatorcontrib><title>Emergence of multidrug-resistant Shigella species harboring extended-spectrum beta-lactamase genes in pediatric patients with diarrhea from southwest of Iran</title><title>Molecular biology reports</title><addtitle>Mol Biol Rep</addtitle><addtitle>Mol Biol Rep</addtitle><description>Owing to the scarce evidence about the multidrug-resistant (MDR) beta-lactamase-producing
Shigella
isolates in Iran, this study aimed to evaluate the occurrence of extended-spectrum beta-lactamases (ESBL) and AmpC β-lactamases in
Shigella
species collected in the southwest of Iran. This study was conducted on
Shigella
species isolated from stool samples of pediatric patients aged less than 15 years suffering from diarrhea. These isolates were identified by bacteriology tests, serotyping, and polymerase chain reaction (PCR). The antibiotic resistance was determined by disc diffusion. The production of ESBLs and AmpC was investigated by phenotypic confirmatory tests and PCR. In total, 79
Shigella
isolates, including 46.8% (n = 37) of
S. flexneri
and 53.2% (n = 42) of
S. sonnei
, were isolated, respectively. The most effective antibiotic was imipenem with 93.7% of susceptibility followed by ampicillin (29.1%), and cotrimoxazole (30.4%).The resistance rates of ceftriaxone, ceftazidime, and cefotaxime were 41.8%, 34.2%, and 41.8%, respectively. Also, a total of 57 (72.2%) isolates showed MDR profiles. The phenotypic tests showed that 43.0% (34/79) of isolates can produce ESBLs, and no one was positive for ApmC. The frequency of
bla
TEM
and
bla
CTX-M
were 30.4% and 32.9%, respectively, while the
bla
PER
,
bla
SHV,
and AmpC genes were not detected. The ESBL-producing isolates had a significant (
p
-value ˂ 0.05) resistance rate against ceftriaxone, ceftazidime, cefotaxime, cefepime, erythromycin, and amikacin. The significant prevalence of MDR
Shigella
isolates harboring ESBL genes highlights the need for effective surveillance measures to prevent the more spread of drug resistance among species.</description><subject>Adolescent</subject><subject>Amikacin</subject><subject>Ampicillin</subject><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Antibiotic resistance</subject><subject>Antibiotics</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacteriology</subject><subject>beta-Lactamases - genetics</subject><subject>beta-Lactamases - metabolism</subject><subject>Biomedical and Life Sciences</subject><subject>Cefepime</subject><subject>Cefotaxime</subject><subject>Ceftazidime</subject><subject>Ceftriaxone</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cotrimoxazole</subject><subject>Cross-Sectional Studies</subject><subject>Diarrhea</subject><subject>Diarrhea - enzymology</subject><subject>Diarrhea - genetics</subject><subject>Diarrhea - microbiology</subject><subject>Erythromycin</subject><subject>Female</subject><subject>Histology</subject><subject>Humans</subject><subject>Imipenem</subject><subject>Iran</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Morphology</subject><subject>Multidrug resistance</subject><subject>Multidrug resistant organisms</subject><subject>Original Article</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Polymerase chain reaction</subject><subject>Serotyping</subject><subject>Shigella</subject><subject>Shigella - enzymology</subject><subject>Shigella - genetics</subject><subject>Species</subject><subject>β Lactamase</subject><issn>0301-4851</issn><issn>1573-4978</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1TAQhS1ERW8LL8ACWWLDxtR_iZMlqgqtVIlFy9qaOJMbV_nDdtTbh-FdcbgFJBasLNnnHJ-Zj5C3gn8UnJuLKARXinHJGS-MKdnhBdmJwiima1O9JDuuuGC6KsQpOYvxgXOuhSlekVMlq1prVezIj6sRwx4nh3Tu6LgOybdh3bOA0ccEU6J3vd_jMACNCzqPkfYQmjn4aU_xkHBqsWXbUwrrSBtMwAZwCUaISHNwNviJLth6SME7ukDyOKVIH33qab4NoUegXZhHGuc19Y8Y09blJsD0mpx0MER883yek2-fr-4vr9nt1y83l59umZM1PzAFoLhWpjKAlWgKqUzbtaZUBZewLanlDUANNVZatroWBTihZIGlc1phqc7Jh2PuEubvay5gRx_dNvWE8xqt1JqXpRa1yNL3_0gf5jVMuZ2VGYLRSlcmq-RR5cIcY8DOLsGPEJ6s4HaDZ4_wbIZnf8Gzh2x69xy9NiO2fyy_aWWBOgrisu0fw9-__xP7E1XxqHU</recordid><startdate>20200901</startdate><enddate>20200901</enddate><creator>Farajzadeh Sheikh, Ahmad</creator><creator>Moradi Bandbal, Maryam</creator><creator>Saki, Morteza</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6735-8192</orcidid><orcidid>https://orcid.org/0000-0001-7419-0116</orcidid></search><sort><creationdate>20200901</creationdate><title>Emergence of multidrug-resistant Shigella species harboring extended-spectrum beta-lactamase genes in pediatric patients with diarrhea from southwest of Iran</title><author>Farajzadeh Sheikh, Ahmad ; Moradi Bandbal, Maryam ; Saki, Morteza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c290x-3aa3043787ae81b5237dfd763502a1103d0baa9a9e842d4915ac1325e6cc43e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adolescent</topic><topic>Amikacin</topic><topic>Ampicillin</topic><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Antibiotic resistance</topic><topic>Antibiotics</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Bacteriology</topic><topic>beta-Lactamases - genetics</topic><topic>beta-Lactamases - metabolism</topic><topic>Biomedical and Life Sciences</topic><topic>Cefepime</topic><topic>Cefotaxime</topic><topic>Ceftazidime</topic><topic>Ceftriaxone</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cotrimoxazole</topic><topic>Cross-Sectional Studies</topic><topic>Diarrhea</topic><topic>Diarrhea - enzymology</topic><topic>Diarrhea - genetics</topic><topic>Diarrhea - microbiology</topic><topic>Erythromycin</topic><topic>Female</topic><topic>Histology</topic><topic>Humans</topic><topic>Imipenem</topic><topic>Iran</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Morphology</topic><topic>Multidrug resistance</topic><topic>Multidrug resistant organisms</topic><topic>Original Article</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Polymerase chain reaction</topic><topic>Serotyping</topic><topic>Shigella</topic><topic>Shigella - enzymology</topic><topic>Shigella - genetics</topic><topic>Species</topic><topic>β Lactamase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Farajzadeh Sheikh, Ahmad</creatorcontrib><creatorcontrib>Moradi Bandbal, Maryam</creatorcontrib><creatorcontrib>Saki, Morteza</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular biology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Farajzadeh Sheikh, Ahmad</au><au>Moradi Bandbal, Maryam</au><au>Saki, Morteza</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Emergence of multidrug-resistant Shigella species harboring extended-spectrum beta-lactamase genes in pediatric patients with diarrhea from southwest of Iran</atitle><jtitle>Molecular biology reports</jtitle><stitle>Mol Biol Rep</stitle><addtitle>Mol Biol Rep</addtitle><date>2020-09-01</date><risdate>2020</risdate><volume>47</volume><issue>9</issue><spage>7097</spage><epage>7106</epage><pages>7097-7106</pages><issn>0301-4851</issn><eissn>1573-4978</eissn><abstract>Owing to the scarce evidence about the multidrug-resistant (MDR) beta-lactamase-producing
Shigella
isolates in Iran, this study aimed to evaluate the occurrence of extended-spectrum beta-lactamases (ESBL) and AmpC β-lactamases in
Shigella
species collected in the southwest of Iran. This study was conducted on
Shigella
species isolated from stool samples of pediatric patients aged less than 15 years suffering from diarrhea. These isolates were identified by bacteriology tests, serotyping, and polymerase chain reaction (PCR). The antibiotic resistance was determined by disc diffusion. The production of ESBLs and AmpC was investigated by phenotypic confirmatory tests and PCR. In total, 79
Shigella
isolates, including 46.8% (n = 37) of
S. flexneri
and 53.2% (n = 42) of
S. sonnei
, were isolated, respectively. The most effective antibiotic was imipenem with 93.7% of susceptibility followed by ampicillin (29.1%), and cotrimoxazole (30.4%).The resistance rates of ceftriaxone, ceftazidime, and cefotaxime were 41.8%, 34.2%, and 41.8%, respectively. Also, a total of 57 (72.2%) isolates showed MDR profiles. The phenotypic tests showed that 43.0% (34/79) of isolates can produce ESBLs, and no one was positive for ApmC. The frequency of
bla
TEM
and
bla
CTX-M
were 30.4% and 32.9%, respectively, while the
bla
PER
,
bla
SHV,
and AmpC genes were not detected. The ESBL-producing isolates had a significant (
p
-value ˂ 0.05) resistance rate against ceftriaxone, ceftazidime, cefotaxime, cefepime, erythromycin, and amikacin. The significant prevalence of MDR
Shigella
isolates harboring ESBL genes highlights the need for effective surveillance measures to prevent the more spread of drug resistance among species.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>32894435</pmid><doi>10.1007/s11033-020-05776-x</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-6735-8192</orcidid><orcidid>https://orcid.org/0000-0001-7419-0116</orcidid></addata></record> |
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source | Springer Nature |
subjects | Adolescent Amikacin Ampicillin Animal Anatomy Animal Biochemistry Antibiotic resistance Antibiotics Bacterial Proteins - genetics Bacterial Proteins - metabolism Bacteriology beta-Lactamases - genetics beta-Lactamases - metabolism Biomedical and Life Sciences Cefepime Cefotaxime Ceftazidime Ceftriaxone Child Child, Preschool Cotrimoxazole Cross-Sectional Studies Diarrhea Diarrhea - enzymology Diarrhea - genetics Diarrhea - microbiology Erythromycin Female Histology Humans Imipenem Iran Life Sciences Male Morphology Multidrug resistance Multidrug resistant organisms Original Article Patients Pediatrics Polymerase chain reaction Serotyping Shigella Shigella - enzymology Shigella - genetics Species β Lactamase |
title | Emergence of multidrug-resistant Shigella species harboring extended-spectrum beta-lactamase genes in pediatric patients with diarrhea from southwest of Iran |
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