Colonization and infection due to carbapenemase-producing Enterobacteriaceae in liver and lung transplant recipients and donor-derived transmission: a prospective cohort study conducted in Italy.


Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 31 01 2018
revised: 05 03 2018
accepted: 01 05 2018
pubmed: 26 5 2018
medline: 11 5 2019
entrez: 26 5 2018
Statut: ppublish

Résumé

A prospective cohort study was conducted in Italy in order to describe the microbiologic aspects of colonization/infection by carbapenemase-producing Enterobacteriaceae (CPE) in donors and recipients of lung and liver transplants and the possible CPE transmission from donors to recipients. Between 15 January 2014 and 14 January 2015, all recipients of solid organ transplants (SOT) at ten lung and eight liver transplantation centres and the corresponding donors were enrolled. Screening cultures to detect CPE were performed in donors, and screening and clinical cultures in recipients with a 28-day microbiologic follow-up after receipt of SOT. Detection of carbapenemase genes by PCR, genotyping by multilocus sequence typing, and pulsed-field gel electrophoresis and whole-genome sequencing were performed. Of 588 screened donors, 3.4% were colonized with CPE. Of the liver first transplant recipients (n = 521), 2.5% were colonized before receipt of SOT and 5% acquired CPE during follow-up. CPE colonization was higher in lung first transplant recipients (n = 111, 2.7% before SOT and 14.4% after SOT). CPE infections occurred in 1.9% and 5.3% of liver or lung recipients, respectively. CPE isolates were mostly Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae belonging to CG258. Three events of donor-recipient CPE transmission, confirmed by whole-genome sequencing and/or pulsed-field gel electrophoresis, occurred in lung recipients: two involving K. pneumoniae sequence type 512 and one Verona integron-encoded metallo-β-lactamase (VIM)-producing Enterobacter aerogenes. This study showed a low risk of donor-recipient CPE transmission, indicating that donor CPE colonization does not necessarily represent a contraindication for donation unless colonization regards the organ to be transplanted. Donor and recipient screening remains essential to prevent CPE transmission and cross-infection in transplantation centres.

Identifiants

pubmed: 29800674
pii: S1198-743X(18)30409-9
doi: 10.1016/j.cmi.2018.05.003
pii:
doi:

Substances chimiques

Bacterial Proteins 0
beta-Lactamases EC 3.5.2.6
carbapenemase EC 3.5.2.6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

203-209

Investigateurs

C Farina (C)
F Vailati (F)
G Gesu (G)
C Vismara (C)
M Arghittu (M)
R Colombo (R)
E Torresani (E)
L Rossi (L)
P G Conaldi (PG)
F Gona (F)
P Cambieri (P)
P Marone (P)
C Venditti (C)
A Garcia Fernandez (AG)
C Mancini (C)
M Cusi (M)
L Henrici De Angelis (LH)
L Fossati (L)
A C Finarelli (AC)
C De Cillia (C)
G Sangiorgi (G)
A D Pinna (AD)
F Stella (F)
P Viale (P)
M Colledan (M)
M Platto (M)
M Bonizzoli (M)
A Peris (A)
R Torelli (R)
S Vesconi (S)
E Cibelli (E)
L De Carlis (L)
A De Gasperi (A)
M Ravini (M)
R Carrinola (R)
E Coluccio (E)
D Dondossola (D)
G Rossi (G)
L Santambrogio (L)
D Tosi (D)
G Feltrin (G)
C Rago (C)
U Cillo (U)
A Da Riva (A)
F Rea (F)
V Sparacino (V)
A Bertani (A)
M Canzonieri (M)
B Gridelli (B)
A Mularoni (A)
M Spada (M)
E Carrara (E)
A Maria D'Armini (AM)
P Paladini (P)
D Adorno (D)
M Valeri (M)
M Caprio (M)
P Di Ciaccio (P)
F Puoti (F)
P Berloco (P)
B D'Auria (B)
F Maldarelli (F)
G Paglialunga (G)
F Pugliese (F)
M Rossi (M)
F Venuta (F)
A Amoroso (A)
R Giacometti (R)
M Rinaldi (M)
M Salizzoni (M)

Informations de copyright

Copyright © 2018 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

Auteurs

G Errico (G)

Dipartimento di Malattie Infettive, Istituto Superiore di Sanità, Rome, Italy.

C Gagliotti (C)

Agenzia Sanitaria e Sociale Regionale Emilia-Romagna, Bologna, Italy.

M Monaco (M)

Dipartimento di Malattie Infettive, Istituto Superiore di Sanità, Rome, Italy.

L Masiero (L)

Centro Nazionale Trapianti, Istituto Superiore di Sanità, Rome, Italy.

P Gaibani (P)

Unità Operativa di Microbiologia, Policlinico Sant'Orsola Malpighi, Bologna, Italy.

S Ambretti (S)

Unità Operativa di Microbiologia, Policlinico Sant'Orsola Malpighi, Bologna, Italy.

M P Landini (MP)

Unità Operativa di Microbiologia, Policlinico Sant'Orsola Malpighi, Bologna, Italy.

S D'Arezzo (S)

Istituto Nazionale per le Malattie Infettive L. Spallanzani-IRCCS, Rome, Italy.

A Di Caro (A)

Istituto Nazionale per le Malattie Infettive L. Spallanzani-IRCCS, Rome, Italy.

S G Parisi (SG)

Dipartimento di Medicina Molecolare, Università degli Studi di Padova, Padova, Italy.

G Palù (G)

Dipartimento di Medicina Molecolare, Università degli Studi di Padova, Padova, Italy.

F Vespasiano (F)

Centro Nazionale Trapianti, Istituto Superiore di Sanità, Rome, Italy.

F Morsillo (F)

Agenzia Sanitaria e Sociale Regionale Emilia-Romagna, Bologna, Italy.

M L Moro (ML)

Agenzia Sanitaria e Sociale Regionale Emilia-Romagna, Bologna, Italy.

F Procaccio (F)

Centro Nazionale Trapianti, Istituto Superiore di Sanità, Rome, Italy.

A Ricci (A)

Centro Nazionale Trapianti, Istituto Superiore di Sanità, Rome, Italy.

P A Grossi (PA)

Clinica delle Malattie Infettive e Tropicali, Università degli Studi dell'Insubria, Varese, Italy.

A Pantosti (A)

Dipartimento di Malattie Infettive, Istituto Superiore di Sanità, Rome, Italy. Electronic address: annalisa.pantosti@iss.it.

A Nanni Costa (A)

Centro Nazionale Trapianti, Istituto Superiore di Sanità, Rome, Italy.

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Classifications MeSH