Corrado Girmenia, Alessandra Serrao and Martina Canichella
Dipartimento di Ematologia, Oncologia, Anatomia
Patologica e Medicina Rigenerativa, Azienda Policlinico Umberto I,
Sapienza University of Rome, Rome, Italy
Published: July 1, 2016
Received: May 18, 2016
Accepted: May 25, 2016
Mediterr J Hematol Infect Dis 2016, 8(1): e2016032, DOI
10.4084/MJHID.2016.032
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Abstract
Infections by Carbapenem-Resistant Enterobacteriaceae (CRE), in particular, carbapenem-resistant Klebsiella pneumoniae
(CRKp), are a significant public health challenge worldwide. Resistance
to carbapenems in enterobacteriaceae is linked to different mechanisms,
including the production of the various types of enzymes like KPC, VIM,
IMP, NDM, and OXA-48. Despite several attempts to control the spread of
these infections at the local and national level, the epidemiological
situation for CRKp had worsened in the last years in the Mediterranean
area. The rate and types of CRKp isolates greatly differ in the various
Mediterranean countries. KPC-producing K. pneumoniae
is diffused particularly in the European countries bordering the
Mediterranean Sea and is endemic in Greece and Italy. On the contrary,
OXA-48-producing K. pneumoniae is endemic in Turkey and Malta and diffused at inter-regional level particularly in some North
African and Middle East countries. The spread of these multiresistant
pathogens in the world and the Mediterranean countries has been related
to various epidemiological factors including the international transfer
of patients coming from endemic areas.
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Introduction
Infections by Carbapenem-Resistant Enterobacteriaceae (CRE), in particular carbapenem-resistant Klebsiella pneumoniae
(CRKp), are a significant public health challenge worldwide.[1-4] These
pathogens are characterized by multiantibiotic resistance which
involves penicillins, all cephalosporins, monobactams, carbapenems, and
even β-lactamase inhibitors. They are generally only susceptible to a
few antibiotics, and there is high mortality among patients with
bloodstream infections caused by these organisms. Many CRKp isolates
remain susceptible to colistin, tigecycline, and one or more
aminoglycoside, but some are resistant even to these drugs.[5,6]
Moreover, only a few drugs are in development against CRE.[7] The
prognosis of infections by CRKp is particularly poor in high risk
immunocompromised populations as intensive care unit (ICU), solid
organ transplant (SOT), hematological malignancies (HEM)
and stem cell transplant (SCT) patients.[8-15]
Resistance
to carbapenems in enterobacteriaceae is linked to different mechanisms,
in particular the production of strong carbapenemases, but also of
beta-lactamases that possess weak carbapenemase activity when combined
with decreased permeability due to porin loss or alteration. Strong
carbapenemases that are responsible for nonsusceptibility to
carbapenems, without additional permeability defects, belong to Ambler
molecular class A, B, or D. These enzymes are carried either on
chromosome or acquired via plasmids.[16,17]
K. pneumoniae
carbapenemase (KPC) enzymes are currently the most clinically
significant enzymes among the class A carbapenemases. KPC producing K. pneumoniae
had the widest dissemination in the last few years being diffused with
important regional, interregional and endemic spread in several
countries. To date, more than 20 different KPC variants have been
described, even though KPC-2 and -3 remain the most commonly identified
variants.[18] The class B beta-lactamases or metallo-beta-lactamases
(MBLs) have also been identified in various enterobacterial species,
including K. pneumoniae.[19]
They are mainly New Delhi metallo-beta-lactamase (NDM-1), Verona
integron-encoded metallo-beta-lactamase (VIM), and Imipenemase (IMP)
type enzymes, with the first group being the most commonly identified
worldwide. Carbapenem-hydrolysing oxacillinase-48 (OXA-48) is the most
frequently reported class D beta-lactamase and microorganisms producing
this enzyme have almost reached the same spread of KPC-producing K.
pneumoniae.[17,19,20]
In 2012, the European Centre for Disease
Prevention and Control (ECDC) launched the ‘European survey of
carbapenemase-producing Enterobacteriaceae (EuSCAPE)’ project to gain
insights into the occurrence and epidemiology of CRE and to increase
the awareness of the spread of CRE, in Europe.[21] The epidemiological
situation for CRKp had worsened since 2010 and CRKp continued to spread
in European hospitals, particularly in the Mediterranean area.
The
aim of this review is to describe the recent epidemiological data on
the diffusion of CRKp infections in Mediterranean countries.
Epidemiology of CRKp in Mediterranean countries
The epidemiology of the various types of CRKp is characterized by a
distribution which does not necessarily overlap in the different
countries (Figure 1). It is
well defined in Europe and Israel where several national and
multinational epidemiological surveys have been performed in the last
years, on the contrary, the data from North African and Middle East
regions, other than Israel, are less accurate.[22]
|
Figure
1. Current epidemiological stages of carbapenem-resistant Klebsiella
pneumoniae by type of carbapenemase in the Mediterranean countries |
Class A KPC type producing K. pneumoniae: KPC was initially reported from K. pneumoniae strains isolated in the United States in the late 1990s. KPC producing K. pneumoniae has since spread across the United States and the overall prevalence of carbapenem resistance among Klebsiella spp.
isolates causing hospital-acquired infections in U.S. hospitals was
approximately 12% between 2009 and 2010.[23-29] KPC-producing K. pneumoniae
has since spread worldwide. The first country besides the United States
that experienced a nationwide outbreak was Israel in late 2005 where
the pathogen rapidly became endemic.[30,31] It was the first outbreak
of KPC-producing K. pneumoniae in the Mediterranean area, presumably
coming from U.S. Hospital-level interventions were implemented but
were unable to contain its spread, therefore in 2007 the Israeli
Ministry of Health launched a nationwide intervention, which in few
months was able to contain the outbreak nationally, with a 79% relative
reduction in the incidence compared with its peak the previous year. In
Israel KPC-positive K. pneumoniae
was declared as an endemic phenomenon until 2010, while, thanks to the
nationwide infection-control intervention, since 2011 the
epidemiological scale downgraded to inter-regional spread.[32]
Since the Israeli epidemic, several sporadic cases and outbreaks of KPC type K. pneumoniae isolates have been reported in many European countries. In 2007 two cases of KPC-2 positive K. pneumoniae
infection were diagnosed in France and Sweden, respectively, but both
cases were documented in patients transferred from Greece.[33,34] In
the same year an outbreak of KPC-2-positive K. pneumoniae was
reported from a tertiary hospital in Crete and within 2 years of these
reports, the multiresistant pathogen disseminated into all Greek
tertiary-care hospitals, not only in Intensive Care Units, but also in
medical and surgical wards.[35-41] According to the data of the
European Antimicrobial Resistance Surveillance Network (EARS-Net) of
the European Centre for Disease Prevention and Control (ECDC) the
epidemiology of KPC-positive K. pneumoniae in
Greece was considered at an endemic stage since 2010, and since
2011 the rate of resistance to carbapenems (mainly due to KPC
production) was constantly over 60% in invasive K. pneumoniae isolates.[42]
In Italy, the first KPC-positive K. pneumoniae
strains were isolated in 2008 from an inpatient with a complicated
intra-abdominal infection in Florence and in 2009 from two patients
admitted to a teaching hospital in Rome.[43,44] Since then several
cases and outbreaks by KPC-2 and KPC-3 K. pneumoniae
strains were reported as a consequence of a rapid dissemination in
almost all hospitals in the north, middle and south regions of the
country.[8,9,13,14,45-51] KPC-positive K. pneumoniae
have spread rapidly and extensively in Italy, with a sharp increase
reported by the EARS-Net surveillance system for bacteraemia isolates,
from 1–2% carbapenem resistance in 2006–09 to 26.7% in 2011 and 32.9%
in 2014. Since 2013, in Italy the epidemiology of KPC-positive K. pneumoniae was declared at an endemic stage.[42]
The first two KPC positive K. pneumoniae
clinical isolates (one KPC-2 and one KPC-3) in France were found
in 2005.[52,53] They were recovered from two patients with a recent
hospital admission in New York City (USA). A further case was described
two years later from a patient transferred from a Greek hospital (see
above).[33] Subsequently, other nosocomial clusters have been reported,
generally related to patients transferred from other European endemic
areas.[54,55]
In 2012, a national reference centre was established
to examine all carbapenem-resistant Enterobacteriaceae in France.
Throughout 7 months, out of 160 carbapenemase-positive
Enterobacteriaceae identified, 19 (11.9%) KPC-producing K. pneumoniae
cases were documented.[1] Five of these 19 cases were linked to recent
stays in Israel, Italy, Kuwait, and China, none was community acquired.
According to the EARS-Net data, in 2014 less than 1% of the invasive K. pneumoniae
isolates in France were resistant to carbapenems and sporadic hospital
outbreaks with no autochthonous inter-institutional transmission have
been reported.[42,56]
The first eight cases of KPC-3-positive K. pneumoniae
colonizations reported in Spain have been documented in 2009.[57] These
patients were in five different wards in a hospital in Madrid, and none
had recently travelled to KPC-endemic countries. Since then, sporadic
KPC-positive isolates have been identified in the same hospital and in
other hospitals in Valencia. A slight increase of KPC-positive K. pneumoniae
invasive isolates was observed in the following years in Spain as
documented by the EARS-Net surveillance (from 0.3% in 2011 to 2,3% in
2014). In a multicentre prospective epidemiological study carried out
in 83 Spanish hospitals from February to May 2013, out of 374 K. pneumoniae
isolates 282 (74.4%) were carbapenemase producers but in only 3 (0.1%)
cases the carbapenem resistance was related to KPC production.[58,59]
In the period 2014-2015, KPC-positive K. pneumoniae was reported at regional stage almost exclusively in the territory of Madrid and Valencia.[56]
To date, only sporadic epidemiological data on KPC-positive K. pneumoniae isolates have been reported in other European countries bordering the Mediterraneum. Forty-eight KPC-2 producing K. pneumoniae
isolates, collected during a period from February 2011 to August 2013,
were recorded in 9 of 40 centers in Croatia, limited to the northwest
region of the country.[60,61] According to the EARS-Net data, in 2014
0.9% of the invasive K. pneumoniae isolates in Croatia and Slovenia were resistant to carbapenems.[42]
A KPC-3 positive K. pneumoniae strain
was isolated in Albania in 2014 in an ICU patient with no history of
recent travel to endemic areas.[62] According to the EuSCAPE data no
case of KPC-positive K. pneumoniae has been reported in 2014-2015 from Montenegro, Malta and Turkey.
With
regard to North African and the Middle East regions (excluding Israel),
in most of the countries, there is no description or only single cases
of KPC producers K. pneumoniae isolates.[22] A case of KPC-3-producing K. pneumoniae
meningitis in a 6-month-old child has been reported in Algeria.[63]
Three studies from tertiary care hospitals in Egypt showed a high
prevalence of KPC related carbapenem non-susceptible K. pneumoniae (70% in one study) isolates suggesting an underestimated epidemiological phenomenon in that country.[64-66]
Class B MBLs type producing K. pneumoniae:
Class B MBLs are mostly of the VIM and IMP types and, more recently, of
NDM-1 type.[67] IMP-type beta-lactamases were the first acquired MBLs
to be identified. They have been detected in a series of clinically
relevant Gram-negative bacilli including K. pneumoniae but with a much lower frequency compared all other carbapenemases. IMP producing K. pneumoniae,
which is dominant in the Asian continent and Australia, has been only
sporadically detected in Europe and the Mediterranean area.[22]
The
VIM type MBL is the most commonly found class B carbapenemase which has
been identified in all continents.[19,68] Italy was the first
Mediterranean country to report acquired MBLs, with sporadic isolates
of VIM-4-producing K. pneumoniae.[69]
Since then, single or sporadic hospital outbreaks caused by VIM-1 like
enzymes were described from various regions in this country.[70,71] VIM
producing K. pneumoniae
have not undergone wide dissemination in the other Mediterranean
countries, with the exception of Greece where several cases and
outbreaks have been reported in the last years.[67,72] Finally, single
reports and local outbreaks of VIM- type producers have been reported
in other countries of the Mediterranean area, such as France,[73]
Spain,[58] Morocco,[74] Egypt,[75] Algeria,[76] and Tunisia.[77]
The NDM-1 enzyme is a more recently reported class B carbapenemase identified mostly in E.coli and K. pneumoniae
and to a lesser extent in other enterobacteriaceae. NDM-1 producers
have been reported in the environment and in the community. It arose
from India in 2008 and spread rapidly over Indian subcontinent in the
following few years and international travel has a significant impact
on its rapid worldwide spread.[19,78,79] The European epidemiology for
CRE changed between 2013 and 2015 for NDM-producing Enterobacteriaceae
with several countries reporting regional or inter-regional spread but
with no endemic situation. Single or sporadic hospital outbreaks caused
by NDM-1 producing K. pneumoniae
strains were reported from many countries in the Mediterranean area:
France,[80] Italy,[81] Spain,[82,83] Morocco,[84] Tunisia in a patient
transferred from Libya,[85] and Egypt.[86] In these countries the
dissemination of NDM-producing CRE, including K. pneumoniae,
was still limited and cases were mostly acquired abroad. Finally, an
emergence of autochthonous and imported NDM-1 producing K. pneumoniae
was reported in Turkey, especially in hospitals from cities close to
the Syrian border, and in Greece.[87-90] Sporadic cases or single
hospital outbreaks by NDM-1 positive K. pneumoniae have been observed in Lebanon (imported from Iraq), Israel and other Middle East Mediterranean countries.[91-93]
Class D OXA-48 type producing K. pneumoniae:
Class D beta-lactamases, also named OXAs for oxacillinases, have more
than 440 known variants with 232 of them showing carbapenemase
activity. OXA-48 represents the main enzyme isolated around the
world.[17] It was initially identified in K. pneumoniae in a strain from Istanbul, Turkey in 2001.[94] The OXA-48-positive K. pneumoniae
strains rapidly diffused in Turkey with hospital outbreaks in the main
cities of the country.[95] The epidemic was under controlled and in
2015 OXA-48 K. pneumoniae was considered endemic in Turkey.[56]
Identification
of this novel and powerful resistance determinant outside of Turkey
indicated that spread was larger than expected. OXA-48 producing
isolates disseminated to the Middle East, North Africa and Europe and
several nosocomial outbreaks were reported from many Mediterranean
countries including France, Spain, Lebanon, Israel, Tunisia and
Morocco.[97-108] Several cases of OXA-48 K. pneumoniae
infections in Libyan refugees transferred to hospitals of European
countries have been reported, suggesting that the epidemiology of such
multiresistant microorganisms in Libya, and probably in other north
African countries, is underestimated.[109-113] Dramatic epidemiological
findings occurred in Malta where dissemination of OXA-48-producing
Enterobacteriaceae had changed the country’s epidemiological level from
rare sporadic occurrence before 2010 to an endemic situation by
2013.[42,56] Presumably, the influx of injured Libyan war victims to
the country’s only tertiary care hospital in 2011 contributed to the
first outbreak and spread of OXA-48-producing Enterobacteriaceae in the
country. Despite initial control of the outbreak, the situation rapidly
became endemic in this hospital and OXA-48-producing K. pneumoniae
and other enterobacteria spread to other health and residential care
entities on the Maltese islands. EARS-Net data for Malta showed an
increase in the percentage of invasive OXA-48–producing K. pneumoniae in Malta, from 3.8% in 2011, to 5.8% in 2013 and 9.9% in 2014.[42]
In summary, in 2014-2015 the epidemiological stage for the spread of OXA-48 producing K. pneumoniae
in the Mediterranean area was: endemic level in Turkey and Malta,
inter-regional diffusion in France, Spain, Lebanon, Tunisia, Morocco
and Libya, regional diffusion in Italy and Croatia, single or sporadic
hospital outbreaks in Israel, Slovenia, Albania, single cases or never
reported in Greece, Albania, Montenegro, Syria, Egypt and Algeria.
Conclusions
Despite several attempts to control the spread of CRKp at the local
and national level, the epidemiological situation for these
multiresistant pathogens had worsened in the last years in the
Mediterranean area. The rate and types of CRKp isolates greatly differ
in the various countries being the diffusion of these multiresistant
pathogens related to various geographic and epidemiological factors
including the international transfer of patients coming from endemic
areas.
The political and economic relationship and the
increasing phenomenon of migration in the Mediterranean basin should
lead to a continuous epidemiological survey of multiresistant bacteria
in order to define and plan appropriate infection-control intervention
at national and international level.
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