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  1. Article ; Online: Salmonella enterica serovar Typhi and S. Paratyphi A: need to expand the QRDR region?

    Walther-Rasmussen, Jan / Høiby, Niels

    Epidemiology and infection

    2011  Volume 139, Issue 8, Page(s) 1281–3; author reply 1283

    MeSH term(s) Amino Acid Substitution ; Anti-Bacterial Agents/pharmacology ; DNA Gyrase/genetics ; Drug Resistance, Bacterial ; Genes, Bacterial ; Mutation, Missense ; Quinolones/pharmacology ; Salmonella paratyphi A/drug effects ; Salmonella paratyphi A/genetics ; Salmonella typhi/drug effects ; Salmonella typhi/genetics
    Chemical Substances Anti-Bacterial Agents ; Quinolones ; DNA Gyrase (EC 5.99.1.3)
    Language English
    Publishing date 2011-08
    Publishing country England
    Document type Comment ; Letter
    ZDB-ID 632982-2
    ISSN 1469-4409 ; 0950-2688
    ISSN (online) 1469-4409
    ISSN 0950-2688
    DOI 10.1017/S0950268810002487
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Class A carbapenemases.

    Walther-Rasmussen, Jan / Høiby, Niels

    The Journal of antimicrobial chemotherapy

    2007  Volume 60, Issue 3, Page(s) 470–482

    Abstract: Carbapenems, such as imipenem and meropenem, are most often used to treat infections caused by enterobacteria that produce extended-spectrum beta-lactamases, and the emergence of enzymes capable of inactivating carbapenems would therefore limit the ... ...

    Abstract Carbapenems, such as imipenem and meropenem, are most often used to treat infections caused by enterobacteria that produce extended-spectrum beta-lactamases, and the emergence of enzymes capable of inactivating carbapenems would therefore limit the options for treatment. Carbapenem resistance in Enterobacteriaceae is rare, but class A beta-lactamases with activity against the carbapenems are becoming more prevalent within this bacterial family. The class A carbapenemases can phylogenetically be segregated into six different groups of which four groups are formed by members of the GES, KPC, SME, IMI/NMC-A enzymes, while SHV-38 and SFC-1 each separately constitute a group. The genes encoding the class A carbapenemases are either plasmid-borne or located on the chromosome of the host. The bla(GES) genes reside as gene cassettes on mainly class I integrons, whereas the bla(KPC) genes and a single bla(IMI-2) gene are flanked by transposable elements on plasmids. Class A carbapenemases hydrolyse penicillins, classical cephalosporins, monobactam, and imipenem and meropenem, and the enzymes are divided into four phenotypically different groups, namely group 2br, 2be, 2e and 2f, according to the Bush-Jacoby-Medeiros classification system. Class A carbapenemases are inhibited by clavulanate and tazobactam like other class A beta-lactamases.
    MeSH term(s) Animals ; Anti-Bacterial Agents/pharmacology ; Anti-Bacterial Agents/therapeutic use ; Bacterial Proteins/antagonists & inhibitors ; Bacterial Proteins/genetics ; Bacterial Proteins/metabolism ; Carbapenems/pharmacology ; Carbapenems/therapeutic use ; Drug Resistance, Bacterial ; Humans ; Klebsiella pneumoniae/enzymology ; Klebsiella pneumoniae/genetics ; Serratia marcescens/enzymology ; Serratia marcescens/genetics ; Structure-Activity Relationship ; beta-Lactamase Inhibitors ; beta-Lactamases/genetics ; beta-Lactamases/metabolism
    Chemical Substances Anti-Bacterial Agents ; Bacterial Proteins ; Carbapenems ; beta-Lactamase Inhibitors ; beta-Lactamases (EC 3.5.2.6) ; carbapenemase (EC 3.5.2.6)
    Language English
    Publishing date 2007-09
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 191709-2
    ISSN 1460-2091 ; 0305-7453
    ISSN (online) 1460-2091
    ISSN 0305-7453
    DOI 10.1093/jac/dkm226
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: OXA-type carbapenemases.

    Walther-Rasmussen, Jan / Høiby, Niels

    The Journal of antimicrobial chemotherapy

    2006  Volume 57, Issue 3, Page(s) 373–383

    Abstract: In recent years, the number of class D beta-lactamases with carbapenem-hydrolysing properties has increased substantially. Based on amino acid sequence identities, these class D or OXA-type carbapenemases are divided into eight distantly related groups, ... ...

    Abstract In recent years, the number of class D beta-lactamases with carbapenem-hydrolysing properties has increased substantially. Based on amino acid sequence identities, these class D or OXA-type carbapenemases are divided into eight distantly related groups, and they are only remotely related to other class D beta-lactamases. A putative ancestor to one of the plasmid-encoded OXA-type carbapenemases has been found. OXA-type carbapenemases are not integrated into integrons as gene cassettes like many class D oxacillinases, but most of the OXA-type carbapenemases are instead encoded by chromosomal genes. Some of these OXA-type carbapenemases are widely dispersed in Pseudomonas aeruginosa and especially in Acinetobacter baumannii. Although most of the OXA-type carbapenemases show only weak carbapenemase activity, carbapenem resistance may result from a combined action an OXA-type carbapenemase and a secondary resistance mechanism such as porin deficiencies or overexpressed efflux pumps. This article reviews the phylogeny and the genetic environments of the encoding genes and kinetic properties of the OXA-type carbapenemases.
    MeSH term(s) Acinetobacter baumannii/enzymology ; Anti-Bacterial Agents/metabolism ; Anti-Bacterial Agents/pharmacology ; Bacterial Proteins/classification ; Bacterial Proteins/metabolism ; Drug Resistance, Bacterial ; beta-Lactamases/classification ; beta-Lactamases/metabolism
    Chemical Substances Anti-Bacterial Agents ; Bacterial Proteins ; beta-Lactamases (EC 3.5.2.6) ; carbapenemase (EC 3.5.2.6)
    Language English
    Publishing date 2006-03
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 191709-2
    ISSN 1460-2091 ; 0305-7453
    ISSN (online) 1460-2091
    ISSN 0305-7453
    DOI 10.1093/jac/dki482
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Cefotaximases (CTX-M-ases), an expanding family of extended-spectrum beta-lactamases.

    Walther-Rasmussen, Jan / Høiby, Niels

    Canadian journal of microbiology

    2004  Volume 50, Issue 3, Page(s) 137–165

    Abstract: Among the extended-spectrum beta-lactamases, the cefotaximases (CTX-M-ases) constitute a rapidly growing cluster of enzymes that have disseminated geographically. The CTX-M-ases, which hydrolyze cefotaxime efficiently, are mostly encoded by transferable ... ...

    Abstract Among the extended-spectrum beta-lactamases, the cefotaximases (CTX-M-ases) constitute a rapidly growing cluster of enzymes that have disseminated geographically. The CTX-M-ases, which hydrolyze cefotaxime efficiently, are mostly encoded by transferable plasmids, and the enzymes have been found predominantly in Enterobacteriaceae, most prevalently in Escherichia coli, Salmonella typhimurium, Klebsiella pneumoniae, and Proteus mirabilis. Isolates of Vibrio cholerae, Acinetobacter baumannii, and Aeromonas hydrophila encoding CTX-M-ases have also been reported. The CTX-M-ases belong to the molecular class A beta-lactamases, and the enzymes are functionally characterized as extended-spectrum beta-lactamases. This group of beta-lactamases confers resistance to penicillins, extended-spectrum cephalosporins, and monobactams, and the enzymes are inhibited by clavulanate, sulbactam, and tazobactam. Typically, the CTX-M-ases hydrolyze cefotaxime more efficiently than ceftazidime, which is reflected in substantially higher MICs to cefotaxime than to ceftazidime. Phylogenetically, the CTX-M-ases are divided into four subfamilies that seem to have descended from chromosomal beta-lactamases of Kluyvera spp. Insertion sequences, especially ISEcp1, have been found adjacent to genes encoding enzymes of all four subfamilies. The class I integron-associated orf513 also seems to be involved in the mobilization of blaCTX-M genes. This review discusses the phylogeny and the hydrolytic properties of the CTX-M-ases, as well as their geographic occurrence and mode of spread.
    MeSH term(s) Cefotaxime/metabolism ; Cephalosporins/metabolism ; Clavulanic Acid/pharmacology ; Drug Resistance, Bacterial/genetics ; Enterobacteriaceae/drug effects ; Enterobacteriaceae/enzymology ; Enterobacteriaceae/genetics ; Enzyme Inhibitors/pharmacology ; Gene Transfer, Horizontal ; Monobactams/metabolism ; Penicillanic Acid/analogs & derivatives ; Penicillanic Acid/pharmacology ; Penicillins/metabolism ; Phylogeny ; Sulbactam/pharmacology ; beta-Lactamases/genetics ; beta-Lactamases/metabolism
    Chemical Substances Cephalosporins ; Enzyme Inhibitors ; Monobactams ; Penicillins ; Clavulanic Acid (23521W1S24) ; Penicillanic Acid (87-53-6) ; beta-lactamase CTX-2 (EC 3.5.2.-) ; beta-Lactamases (EC 3.5.2.6) ; Cefotaxime (N2GI8B1GK7) ; Sulbactam (S4TF6I2330) ; tazobactam (SE10G96M8W)
    Language English
    Publishing date 2004-03
    Publishing country Canada
    Document type Journal Article ; Review
    ZDB-ID 280534-0
    ISSN 1480-3275 ; 0008-4166
    ISSN (online) 1480-3275
    ISSN 0008-4166
    DOI 10.1139/w03-111
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Plasmid-borne AmpC beta-lactamases.

    Walther-Rasmussen, Jan / Høiby, Niels

    Canadian journal of microbiology

    2002  Volume 48, Issue 6, Page(s) 479–493

    Abstract: Historically, it was thought that ampC genes encoding class C beta-lactamases were located solely on the chromosome but, within the last 12 years, an increasing number of ampC genes have been found on plasmids. These have mostly been acquired by ampC- ... ...

    Abstract Historically, it was thought that ampC genes encoding class C beta-lactamases were located solely on the chromosome but, within the last 12 years, an increasing number of ampC genes have been found on plasmids. These have mostly been acquired by ampC-deficient pathogenic bacteria, which consequently are supplied with new and additional resistance phenotypes. This review discusses the phylogenetic origin of the plasmid-encoded AmpC beta-lactamases, their occurrence, and mode of spread, as well as their hydrolytic properties.
    MeSH term(s) Bacterial Proteins ; Gram-Negative Bacteria/enzymology ; Gram-Negative Bacteria/genetics ; Molecular Sequence Data ; Phylogeny ; Plasmids/genetics ; Structure-Activity Relationship ; beta-Lactam Resistance/genetics ; beta-Lactamases/genetics ; beta-Lactamases/metabolism
    Chemical Substances Bacterial Proteins ; AmpC beta-lactamases (EC 3.5.2.6) ; beta-Lactamases (EC 3.5.2.6)
    Language English
    Publishing date 2002-06
    Publishing country Canada
    Document type Journal Article ; Review
    ZDB-ID 280534-0
    ISSN 1480-3275 ; 0008-4166
    ISSN (online) 1480-3275
    ISSN 0008-4166
    DOI 10.1139/w02-039
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Emergence of extended-spectrum beta-lactamases in clinical isolates of Salmonella enterica in Tehran, Iran.

    Hamidian, Mohammad / Tajbakhsh, Mercedeh / Walther-Rasmussen, Jan / Zali, Mohammad-Reza

    Japanese journal of infectious diseases

    2009  Volume 62, Issue 5, Page(s) 368–371

    Abstract: The purpose of the current study was to investigate the presence and molecular type(s) of extended-spectrum beta-lactamases (ESBLs) in Salmonella spp. isolates obtained from patients with diarrhea in hospitals of Tehran, Iran. Over a period of 17 months, ...

    Abstract The purpose of the current study was to investigate the presence and molecular type(s) of extended-spectrum beta-lactamases (ESBLs) in Salmonella spp. isolates obtained from patients with diarrhea in hospitals of Tehran, Iran. Over a period of 17 months, 129 Salmonella spp. were isolated from fecal samples and tested for susceptibility using the Kirby-Bauer disk diffusion method; then, screening for ESBL-producing isolates and determination of their minimum inhibitory concentrations were carried out using the combined disk method and standard agar dilution method, respectively. The presence and type of ESBL-encoding genes were determined by PCR and sequence analysis. The isolates were all identified as Salmonella enterica of different serovars. The highest resistance in the collected Salmonella isolates was to nalidixic acid (45.7%), followed by tetracycline (43.4%), trimethoprim-sulfamethoxazole (36.4%), ampicillin (15.5%), and chloramphenicol (14.7%). All the isolates were susceptible to ciprofloxacin, gentamicin, and cefoxitin. Three S. enterica isolates were resistant to ampicillin, piperacillin, ceftazidime, cefotaxime, ceftriaxone, cefpodoxime, cephalothin, and aztreonam. PCR and DNA sequencing revealed that two of the three isolates harbored both a bla(CTX-M-15) and a bla(TEM) gene while the third one carried only a bla(CTX-M-15) gene. This is the first study providing structural data for a CTX-M-type beta-lactamase produced by Salmonella isolates recovered in Iran.
    MeSH term(s) Anti-Bacterial Agents/pharmacology ; DNA, Bacterial/chemistry ; DNA, Bacterial/genetics ; Diarrhea/microbiology ; Feces/microbiology ; Humans ; Iran ; Microbial Sensitivity Tests ; Molecular Sequence Data ; Polymerase Chain Reaction ; Salmonella Infections/microbiology ; Salmonella enterica/drug effects ; Salmonella enterica/isolation & purification ; Sequence Analysis, DNA ; beta-Lactam Resistance ; beta-Lactamases/biosynthesis ; beta-Lactamases/genetics
    Chemical Substances Anti-Bacterial Agents ; DNA, Bacterial ; beta-Lactamases (EC 3.5.2.6)
    Language English
    Publishing date 2009-09
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 1478383-6
    ISSN 1884-2836 ; 1344-6304
    ISSN (online) 1884-2836
    ISSN 1344-6304
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Extended-spectrum beta-lactamases in Taiwan: epidemiology, detection, treatment and infection control.

    Yu, Wen-Liang / Chuang, Yin-Ching / Walther-Rasmussen, Jan

    Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi

    2006  Volume 39, Issue 4, Page(s) 264–277

    Abstract: Extended-spectrum beta-lactamases (ESBLs) efficiently hydrolyze extended-spectrum beta-lactams such as cefotaxime, ceftriaxone, ceftazidime, and aztreonam. ESBLs are most often plasmid-mediated. In Taiwan, the prevalence of ESBLs in bacteria has risen, ... ...

    Abstract Extended-spectrum beta-lactamases (ESBLs) efficiently hydrolyze extended-spectrum beta-lactams such as cefotaxime, ceftriaxone, ceftazidime, and aztreonam. ESBLs are most often plasmid-mediated. In Taiwan, the prevalence of ESBLs in bacteria has risen, ranging from 8.5 to 29.8% in Klebsiella pneumoniae and 1.5 to 16.7% in Escherichia coli isolates. The most prevalent types of ESBLs are SHV-5, SHV-12, CTX-M-3, and CTX-M-14 in isolates of K. pneumoniae and E. coli, with differences between institutions. SHV-12 and CTX-M-3 have been reported as the most common ESBLs in isolates of Enterobacter cloacae and Serratia marcescens, respectively. Molecular epidemiology studies suggest that the ESBL-encoding genes have been disseminated either by proliferation of epidemic strains or by transfer of plasmids carrying the resistance traits. The current ESBL screen guidelines of the Clinical and Laboratory Standards Institute (formerly National Committee for Clinical Laboratory Standards) are issued for E. coli, Klebsiella spp., and Proteus mirabilis. Owing to the lack of standard methods, it remains difficult to assure the presence of ESBL in an isolate co-harboring an AmpC beta-lactamase, particularly in cases where the latter is produced in larger amounts than the former. Empirical therapy with piperacillin-tazobactam to replace third-generation cephalosporins may help to reduce the occurrence of ESBLs in an institution with a high prevalence of ESBL producers. Carbapenems remain the drugs of choice for serious infections caused by ESBL-producing organisms. To retard the selection for carbapenem-resistant bacteria, 7-alpha-methoxy beta-lactams or fourth-generation cephalosporins can be therapeutic alternatives for mild-to-moderate infections provided that the pharmacokinetic and pharmacodynamic target can be easily achieved.
    MeSH term(s) Carbapenems/therapeutic use ; Enterobacteriaceae/enzymology ; Enterobacteriaceae/genetics ; Enterobacteriaceae/isolation & purification ; Enterobacteriaceae Infections/drug therapy ; Enterobacteriaceae Infections/epidemiology ; Enterobacteriaceae Infections/microbiology ; Enterobacteriaceae Infections/prevention & control ; Humans ; Molecular Epidemiology ; Taiwan/epidemiology ; beta-Lactamases/biosynthesis ; beta-Lactamases/genetics ; beta-Lactams/therapeutic use
    Chemical Substances Carbapenems ; beta-Lactams ; beta-Lactamases (EC 3.5.2.6)
    Language English
    Publishing date 2006-08
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1497590-7
    ISSN 1684-1182 ; 0253-2662
    ISSN 1684-1182 ; 0253-2662
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Detection of novel gyrA mutations in nalidixic acid-resistant isolates of Salmonella enterica from patients with diarrhoea.

    Hamidian, Mohammad / Tajbakhsh, Mercedeh / Tohidpour, Abolghasem / Rahbar, Mohammad / Zali, Mohammad Reza / Walther-Rasmussen, Jan

    International journal of antimicrobial agents

    2011  Volume 37, Issue 4, Page(s) 360–364

    Abstract: The aim of the current study was to detect mutations in the gyrA gene of quinolone-resistant Salmonella spp. isolates recovered in Tehran, Iran. Between April 2008 and September 2009, 174 Salmonella spp. were collected and assayed for quinolone ... ...

    Abstract The aim of the current study was to detect mutations in the gyrA gene of quinolone-resistant Salmonella spp. isolates recovered in Tehran, Iran. Between April 2008 and September 2009, 174 Salmonella spp. were collected and assayed for quinolone resistance and detection of gyrA mutations. Isolates identified as Salmonella enterica were tested for susceptibility by the disk diffusion method. Polymerase chain reaction (PCR) amplification and sequencing of the gyrA gene segment encoding the quinolone resistance-determining region (QRDR) were performed for the nalidixic acid-resistant isolates. Amongst the 174 recovered Salmonella spp. isolates, 89 were resistant to nalidixic acid, of which 9 were resistant to enrofloxacin; 10 isolates had reduced susceptibility to nalidixic acid. None of the isolates were resistant to ciprofloxacin, but a single isolate showed reduced susceptibility. Twelve types of amino acid replacement were found in the QRDR region of GyrA, namely the previously described substitutions in positions 83 and 87 as well as five new substitutions Leu41-Pro, Arg47-Ser, Ser111-Thr, Ala118-Thr and Asp147-Gly. Double substitutions in both positions 83 and 87 were not identified. A Gly133-Glu substitution was identified in a single S. enterica serotype Typhi isolate.
    MeSH term(s) DNA Gyrase/genetics ; Diarrhea/microbiology ; Drug Resistance, Microbial/genetics ; Humans ; Microbial Sensitivity Tests ; Mutation ; Nalidixic Acid/pharmacology ; Polymerase Chain Reaction ; Salmonella enterica/drug effects ; Salmonella enterica/genetics
    Chemical Substances Nalidixic Acid (3B91HWA56M) ; DNA Gyrase (EC 5.99.1.3)
    Language English
    Publishing date 2011-04
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 1093977-5
    ISSN 1872-7913 ; 0924-8579
    ISSN (online) 1872-7913
    ISSN 0924-8579
    DOI 10.1016/j.ijantimicag.2010.12.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Prevalence of putative virulence markers in Campylobacter jejuni and Campylobacter coli isolated from hospitalized children, raw chicken, and raw beef in Tehran, Iran.

    Hamidian, Mohammad / Sanaei, Maryam / Bolfion, Mehdi / Dabiri, Hossein / Zali, Mohammad-Reza / Walther-Rasmussen, Jan

    Canadian journal of microbiology

    2011  Volume 57, Issue 2, Page(s) 143–148

    Abstract: The incidence of the virulence-associated genes cdtA, cdtB, cdtC, cadF, dnaJ, racR, and pldA has been investigated in Campylobacter jejuni and Campylobacter coli collected from raw chicken and beef from retailers in Tehran, Iran, and from hospitalized ... ...

    Abstract The incidence of the virulence-associated genes cdtA, cdtB, cdtC, cadF, dnaJ, racR, and pldA has been investigated in Campylobacter jejuni and Campylobacter coli collected from raw chicken and beef from retailers in Tehran, Iran, and from hospitalized children (age, ≤14 years) suffering from diarrhea. Campylobacter spp. were collectively identified by morphological and biochemical methods. Campylobacter jejuni and C. coli were discriminated from other Campylobacter spp. by amplification of a specific conserved fragment of the 16S rRNA gene. The distinction between C. jejuni and C. coli was subsequently made by molecular determination of the presence of the hipO gene in C. jejuni or the ask gene in C. coli. Fragments of the studied virulence-associated genes, cdtA, cdtB, cdtC, cadF, racR, dnaJ, and pldA, were amplified by PCR and subjected to horizontal gel electrophoresis. A total of 71 isolates of C. jejuni and 24 isolates of C. coli from meat were analyzed, while the numbers of isolates from the hospitalized children were 28 and 9, respectively. The unequal distribution of C. jejuni and C. coli in the samples has also been reported in other studies. Statistical analyses by the use of the two-tailed Fisher's exact test of the occurrence of the virulence genes in the isolates of different origins showed that the occurrence of the dnaJ gene was consistently significantly higher in all C. jejuni isolates than in C. coli. The occurrence of the other virulence markers did not differ significantly between species in the majority of the isolates. The PCR results also showed that the occurrence of the virulence markers in the analyzed isolates was much lower than in other studies, which may be caused by a divergent genomic pool of our isolates in comparison with others.
    MeSH term(s) Adolescent ; Animals ; Campylobacter coli/classification ; Campylobacter coli/genetics ; Campylobacter coli/isolation & purification ; Campylobacter jejuni/classification ; Campylobacter jejuni/genetics ; Campylobacter jejuni/isolation & purification ; Chickens/microbiology ; Child ; Child, Preschool ; DNA, Bacterial/genetics ; Diarrhea/microbiology ; Feces/microbiology ; Food Microbiology ; Genes, Bacterial ; Humans ; Infant ; Iran ; Meat/microbiology ; Polymerase Chain Reaction/methods ; Prevalence ; RNA, Ribosomal, 16S/genetics ; Virulence Factors/genetics
    Chemical Substances DNA, Bacterial ; RNA, Ribosomal, 16S ; Virulence Factors
    Language English
    Publishing date 2011-02
    Publishing country Canada
    Document type Journal Article
    ZDB-ID 280534-0
    ISSN 1480-3275 ; 0008-4166
    ISSN (online) 1480-3275
    ISSN 0008-4166
    DOI 10.1139/w10-089
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Detection of novel gyrA mutations in nalidixic acid-resistant isolates of Salmonella enterica from patients with diarrhoea

    Hamidian, Mohammad / Tajbakhsh, Mercedeh / Tohidpour, Abolghasem / Rahbar, Mohammad / Zali, Mohammad Reza / Walther-Rasmussen, Jan

    International journal of antimicrobial agents. 2011 Apr., v. 37, no. 4

    2011  

    Abstract: The aim of the current study was to detect mutations in the gyrA gene of quinolone-resistant Salmonella spp. isolates recovered in Tehran, Iran. Between April 2008 and September 2009, 174 Salmonella spp. were collected and assayed for quinolone ... ...

    Abstract The aim of the current study was to detect mutations in the gyrA gene of quinolone-resistant Salmonella spp. isolates recovered in Tehran, Iran. Between April 2008 and September 2009, 174 Salmonella spp. were collected and assayed for quinolone resistance and detection of gyrA mutations. Isolates identified as Salmonella enterica were tested for susceptibility by the disk diffusion method. Polymerase chain reaction (PCR) amplification and sequencing of the gyrA gene segment encoding the quinolone resistance-determining region (QRDR) were performed for the nalidixic acid-resistant isolates. Amongst the 174 recovered Salmonella spp. isolates, 89 were resistant to nalidixic acid, of which 9 were resistant to enrofloxacin; 10 isolates had reduced susceptibility to nalidixic acid. None of the isolates were resistant to ciprofloxacin, but a single isolate showed reduced susceptibility. Twelve types of amino acid replacement were found in the QRDR region of GyrA, namely the previously described substitutions in positions 83 and 87 as well as five new substitutions Leu41-Pro, Arg47-Ser, Ser111-Thr, Ala118-Thr and Asp147-Gly. Double substitutions in both positions 83 and 87 were not identified. A Gly133-Glu substitution was identified in a single S. enterica serotype Typhi isolate.
    Keywords Salmonella enterica ; acid tolerance ; amino acids ; ciprofloxacin ; diarrhea ; enrofloxacin ; genes ; mutation ; nalidixic acid ; patients ; polymerase chain reaction ; serotypes ; Iran
    Language English
    Dates of publication 2011-04
    Size p. 360-364.
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 1093977-5
    ISSN 0924-8579
    ISSN 0924-8579
    DOI 10.1016/j.ijantimicag.2010.12.013
    Database NAL-Catalogue (AGRICOLA)

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