Literature DB >> 19095415

Spread of multidrug-resistant Proteus mirabilis isolates producing an AmpC-type beta-lactamase: epidemiology and clinical management.

Francesco Luzzaro1, Gioconda Brigante, Marco Maria D'Andrea, Beatrice Pini, Tommaso Giani, Elisabetta Mantengoli, Gian Maria Rossolini, Antonio Toniolo.   

Abstract

A remarkable increase in Proteus mirabilis strains producing acquired AmpC-type beta-lactamases (CBLs) has been observed at Ospedale di Circolo e Fondazione Macchi (Varese, Italy) over the last few years. The epidemiology and treatment outcome of infections associated with this unprecedented spread are reported. From 2004-2006, 2070 P. mirabilis isolates were investigated. Extended-spectrum beta-lactamases (ESBLs) and CBL resistance determinants were identified by gene amplification and direct sequencing. Clonal relatedness was evaluated by macrorestriction analysis. Overall, 43 CBL-positive isolates were obtained from hospitalised (n=22) and non-hospitalised (n=21) patients (median age 78.8 years). The prevalence of CBL-positive isolates increased from 0.3% in 2004 to 4.6% in 2006, whereas that of ESBL-positive isolates remained constant (ca. 10%). CBL-positive isolates were multidrug-resistant and carried the CMY-16 determinant. All but two isolates were genetically identical or closely related. Retrospective analysis of clinical records revealed that the majority of CMY-16-positive isolates were associated with urinary tract infections. Treatment with amikacin or carbapenems was consistently effective, whereas piperacillin/tazobactam produced a clinical response in seven of nine cases. This is the first report of a rapid spread of CBL-positive P. mirabilis strains endowed with remarkable antimicrobial resistance. Practical methods for CBL detection are needed for the appropriate management of related infections.

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Year:  2008        PMID: 19095415     DOI: 10.1016/j.ijantimicag.2008.09.007

Source DB:  PubMed          Journal:  Int J Antimicrob Agents        ISSN: 0924-8579            Impact factor:   5.283


  14 in total

1.  Evolution of an incompatibility group IncA/C plasmid harboring blaCMY-16 and qnrA6 genes and its transfer through three clones of Providencia stuartii during a two-year outbreak in a Tunisian burn unit.

Authors:  C Arpin; L Thabet; H Yassine; A A Messadi; J Boukadida; V Dubois; L Coulange-Mayonnove; C Andre; C Quentin
Journal:  Antimicrob Agents Chemother       Date:  2011-12-12       Impact factor: 5.191

2.  Chromosome-encoded AmpC and CTX-M extended-spectrum β-lactamases in clinical isolates of Proteus mirabilis from Korea.

Authors:  Wonkeun Song; Juwon Kim; Il Kwon Bae; Seok Hoon Jeong; Young Hee Seo; Jong Hee Shin; Sook Jin Jang; Young Uh; Jeong Hwan Shin; Mi-Kyung Lee; Kyungwon Lee
Journal:  Antimicrob Agents Chemother       Date:  2011-01-31       Impact factor: 5.191

3.  Multidrug-resistant Proteus mirabilis bloodstream infections: risk factors and outcomes.

Authors:  Mario Tumbarello; Enrico Maria Trecarichi; Barbara Fiori; Angela Raffaella Losito; Tiziana D'Inzeo; Lara Campana; Alberto Ruggeri; Eugenia Di Meco; Elvira Liberto; Giovanni Fadda; Roberto Cauda; Teresa Spanu
Journal:  Antimicrob Agents Chemother       Date:  2012-03-26       Impact factor: 5.191

Review 4.  AmpC β-lactamase-producing Enterobacterales: what a clinician should know.

Authors:  Simone Meini; Carlo Tascini; Marco Cei; Emanuela Sozio; Gian Maria Rossolini
Journal:  Infection       Date:  2019-03-06       Impact factor: 3.553

5.  Evolution and spread of a multidrug-resistant Proteus mirabilis clone with chromosomal AmpC-type cephalosporinases in Europe.

Authors:  M M D'Andrea; E Literacka; A Zioga; T Giani; A Baraniak; J Fiett; E Sadowy; P T Tassios; G M Rossolini; M Gniadkowski; V Miriagou
Journal:  Antimicrob Agents Chemother       Date:  2011-03-14       Impact factor: 5.191

6.  Enhancing resistance to cephalosporins in class C beta-lactamases: impact of Gly214Glu in CMY-2.

Authors:  Andrea Endimiani; Yohei Doi; Christopher R Bethel; Magdalena Taracila; Jennifer M Adams-Haduch; Alexandra O'Keefe; Andrea M Hujer; David L Paterson; Marion J Skalweit; Malcolm G P Page; Sarah M Drawz; Robert A Bonomo
Journal:  Biochemistry       Date:  2010-02-09       Impact factor: 3.162

7.  Emergence of multidrug-resistant Proteus mirabilis in a long-term care facility in Croatia.

Authors:  Branka Bedenić; Nataša Firis; Vesna Elveđi-Gašparović; Marija Krilanović; Krešimir Matanović; Iva Štimac; Josefa Luxner; Jasmina Vraneš; Tomislav Meštrović; Gernot Zarfel; Andrea Grisold
Journal:  Wien Klin Wochenschr       Date:  2016-05-25       Impact factor: 1.704

8.  Draft Genome Sequence of Proteus mirabilis NO-051/03, Representative of a Multidrug-Resistant Clone Spreading in Europe and Expressing the CMY-16 AmpC-Type β-Lactamase.

Authors:  Marco Maria D'Andrea; Tommaso Giani; Lucia Henrici De Angelis; Nagaia Ciacci; Marek Gniadkowski; Vivi Miriagou; Francesca Torricelli; Gian Maria Rossolini
Journal:  Genome Announc       Date:  2016-02-11

9.  Identification of emergent bla CMY-2 -carrying Proteus mirabilis lineages by whole-genome sequencing.

Authors:  M Mac Aogáin; T R Rogers; B Crowley
Journal:  New Microbes New Infect       Date:  2015-11-27

10.  Prevalence of urinary colonization by extended spectrum-beta-lactamase Enterobacteriaceae among catheterised inpatients in Italian long term care facilities.

Authors:  Luca Arnoldo; Roberta Migliavacca; Laura Regattin; Annibale Raglio; Laura Pagani; Elisabetta Nucleo; Melissa Spalla; Francesca Vailati; Antonella Agodi; Adriana Mosca; Carla Zotti; Stefano Tardivo; Ines Bianco; Adele Rulli; Paola Gualdi; Pietro Panetta; Carlo Pasini; Mino Pedroni; Silvio Brusaferro
Journal:  BMC Infect Dis       Date:  2013-03-06       Impact factor: 3.090

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