Literature DB >> 9572021

Identification and natural antibiotic susceptibility of Morganella morganii.

I Stock1, B Wiedemann.   

Abstract

Our data should elucidate whether or not natural antibiotic susceptibility can be used as an aid for subspecies or biovar discrimination of Morganella morganii (II). Furthermore, our goal was to create a database of the natural susceptibility of M. morganii (III) and we were interested in the relative frequency of the recently described subspecific taxa (I). On the basis of trehalose fermentation (TRE), ornithine decarboxylase (ODC), and lysine decarboxylase (LDC) activities, we determined the biovar for 90 clinical isolates of M. morganii. Within these strains we examined the natural antibiotic susceptibility of 53 morganellae to 70 antibiotics by determination of the MICs with a microdilution procedure. (I): 80 strains (89%) of all morganellae belonged to M. morganii ssp. morganii (TRE-), with biovar A (LDC-, ODC+) predominating (67 strains). The remaining strains of this subspecies were identified as biovar B (LDC+, ODC+; 12 strains) and biovar C (LDC-, ODC-, one strain). Ten strains of M. morganii ssp. sibonii (TRE+) were found: four strains belonged to biovar F (LDC variable, ODC-) and six strains to biovar G (LDC-, ODC). (II): With one exception we found no significant differences in antibiotic susceptibility between different biovars. M. morganii ssp. morganii strains are more susceptible to tetracycline than strains of M. morganii ssp. sibonii, but there is no evidence that this parameter could be useful to differentiate biovars within a subspecies. It could be shown that 8 of 30 strains of biovar A and 2 of 12 strains of biovar B were tetracycline resistant. However, one M. morganii ssp. sibonii strain was clinically susceptible to tetracycline according to French and American standards. (III): The natural population of M. morganii is primarily (naturally) resistant to certain penicillins like benzylpenicillin, oxacillin, and amoxicillin, first and second generation cephalosporins (excluding cefoxitin), cefpodoxime, all antibiotics of the ML group (macrolides and lincosamides), sulfamethoxazole, glycopeptides, fosfomycin, and fusidic acid, naturally sensitive to aminoglycosides, piperacillin, mezlocillin, ticarcillin, third and fourth generation cephalosporins, carbapenems, aztreonam, quinolones, trimethoprim, cotrimoxazole, and chloramphenicol. M. morganii is naturally resistant to a wide range of antibiotics. The natural resistance pattern is useful for validation of sensitivity tests. Susceptibility to antibiotics is an unsuitable parameter for the discrimination of the described subspecific taxa of M. morganii. M. morganii strains that do not belong to biovar A are rare.

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Year:  1998        PMID: 9572021     DOI: 10.1016/s0732-8893(97)00243-5

Source DB:  PubMed          Journal:  Diagn Microbiol Infect Dis        ISSN: 0732-8893            Impact factor:   2.803


  13 in total

1.  War wound treatment complications due to transfer of an IncN plasmid harboring bla(OXA-181) from Morganella morganii to CTX-M-27-producing sequence type 131 Escherichia coli.

Authors:  Patrick McGann; Erik Snesrud; Ana C Ong; Lakshmi Appalla; Michael Koren; Yoon I Kwak; Paige E Waterman; Emil P Lesho
Journal:  Antimicrob Agents Chemother       Date:  2015-04-13       Impact factor: 5.191

2.  CAPD-related peritonitis caused by Morganella morganii.

Authors:  M T Tsai; J T Yeh; W C Yang; T H Wu
Journal:  Perit Dial Int       Date:  2013 Jan-Feb       Impact factor: 1.756

3.  Increase in antimicrobial resistance in bacteria isolated from stranded marine mammals of the Northwest Atlantic.

Authors:  Courtney C Wallace; Philip O Yund; Timothy E Ford; Keith A Matassa; Anna L Bass
Journal:  Ecohealth       Date:  2013-05-02       Impact factor: 3.184

Review 4.  Fosfomycin.

Authors:  Matthew E Falagas; Evridiki K Vouloumanou; George Samonis; Konstantinos Z Vardakas
Journal:  Clin Microbiol Rev       Date:  2016-04       Impact factor: 26.132

5.  A between-species comparison of antimicrobial resistance in enterobacteria in fecal flora.

Authors:  M Osterblad; A Hakanen; R Manninen; T Leistevuo; R Peltonen; O Meurman; P Huovinen; P Kotilainen
Journal:  Antimicrob Agents Chemother       Date:  2000-06       Impact factor: 5.191

6.  Bacteriology of Naja atra Snakebite Wound and Its Implications for Antibiotic Therapy.

Authors:  Yan-Chiao Mao; Po-Yu Liu; Dong-Zong Hung; Wei-Cheng Lai; Shih-Ting Huang; Yao-Min Hung; Chen-Chang Yang
Journal:  Am J Trop Med Hyg       Date:  2016-03-14       Impact factor: 2.345

7.  Antimicrobial susceptibility testing of carbapenems: multicenter validity testing and accuracy levels of five antimicrobial test methods for detecting resistance in Enterobacteriaceae and Pseudomonas aeruginosa isolates.

Authors:  Christine D Steward; Jasmine M Mohammed; Jana M Swenson; Sheila A Stocker; Portia P Williams; Robert P Gaynes; John E McGowan; Fred C Tenover
Journal:  J Clin Microbiol       Date:  2003-01       Impact factor: 5.948

8.  Multidrug Resistance Genes Carried by a Novel Transposon Tn7376 and a Genomic Island Named MMGI-4 in a Pathogenic Morganella morganii Isolate.

Authors:  Xing-Wei Luo; Pei-Yi Liu; Qing-Qing Miao; Rong-Jia Han; Hua Wu; Jian-Hua Liu; Dan-Dan He; Gong-Zheng Hu
Journal:  Microbiol Spectr       Date:  2022-05-05

9.  A Case of Giant Hepatic Hydatid Cyst Infected with Morganella morganii and the Literature Review.

Authors:  Ismail Necati Hakyemez; Mustafa Sit; Gulali Aktas; Tekin Tas; Fırat Zafer Mengeloglu; Abdulkadir Kucukbayrak
Journal:  Case Rep Gastrointest Med       Date:  2012-11-11

10.  Emergence of Third-Generation Cephalosporin-Resistant Morganella morganii in a Captive Breeding Dolphin in South Korea.

Authors:  Seon Young Park; Kyunglee Lee; Yuna Cho; Se Ra Lim; Hyemin Kwon; Jee Eun Han; Ji Hyung Kim
Journal:  Animals (Basel)       Date:  2020-11-06       Impact factor: 2.752

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