key: cord-0999005-k507ichh
authors: Taggar, Gurleen; Attiq Rheman, Muhammad; Boerlin, Patrick; Diarra, Moussa Sory
title: Molecular Epidemiology of Carbapenemases in Enterobacteriales from Humans, Animals, Food and the Environment
date: 2020-10-13
journal: Antibiotics (Basel)
DOI: 10.3390/antibiotics9100693
sha: 6929c71bfcf4f12d378ab147706734a51f9e5978
doc_id: 999005
cord_uid: k507ichh

The Enterobacteriales order consists of seven families including Enterobacteriaceae, Erwiniaceae, Pectobacteriaceae, Yersiniaceae, Hafniaceae, Morganellaceae, and Budviciaceae and 60 genera encompassing over 250 species. The Enterobacteriaceae is currently considered as the most taxonomically diverse among all seven recognized families. The emergence of carbapenem resistance (CR) in Enterobacteriaceae caused by hydrolytic enzymes called carbapenemases has become a major concern worldwide. Carbapenem-resistant Enterobacteriaceae (CRE) isolates have been reported not only in nosocomial and community-acquired pathogens but also in food-producing animals, companion animals, and the environment. The reported carbapenemases in Enterobacteriaceae from different sources belong to the Ambler class A (bla(KPC)), class B (bla(IMP), bla(VIM), bla(NDM)), and class D (bla(OXA-48)) β-lactamases. The carbapenem encoding genes are often located on plasmids or associated with various mobile genetic elements (MGEs) like transposons and integrons, which contribute significantly to their spread. These genes are most of the time associated with other antimicrobial resistance genes such as other β-lactamases, as well as aminoglycosides and fluoroquinolones resistance genes leading to multidrug resistance phenotypes. Control strategies to prevent infections due to CRE and their dissemination in human, animal and food have become necessary. Several factors involved in the emergence of CRE have been described. This review mainly focuses on the molecular epidemiology of carbapenemases in members of Enterobacteriaceae family from humans, animals, food and the environment.

The actual pandemic outbreak of the COVID-19 killing several thousands of people along with its serious negative global economic impacts worldwide is a clear indication that a lot of efforts need to be deployed to fight against infectious diseases and the increased global issue of antimicrobial resistance. The World Health Organization (WHO) published a global priority list of antimicrobial resistant pathogenic bacteria including some Enterobacteriales for which new antibiotics are urgently needed [1] . The genera within the order Enterobacteriales are composed of Gram-negative bacteria of class Gammaproteobacteria, which encompasses many harmless symbiotic and pathogenic strains, including members of the genera Dickeya, Pectobacterium, Brenneria, Erwinia and Pantoea [2] . The pathogenic strains mainly Klebsiella pneumoniae, Yersinia pestis, Escherichia spp., Salmonella enterica serovars and Enterobacter spp. cause a broad range of intestinal and extra intestinal diseases in humans and animals [3] . The expended spectrum cephalosporins (ESC) and cephamycins are frequently used against infectious humans and animals [3] . The expended spectrum cephalosporins (ESC) and cephamycins are frequently used against infectious diseases caused by Enterobacteriaceae. Due to the emergence of multidrug resistance, carbapenems in addition to tigecycline and colistin are among the last line of defense against Enterobacteriaceae, because co-resistance to both colistin and tigecycline among the carbapenem-resistant Enterobacteriaceae (CRE) has been rarely reported [4, 5] . Carbapenems are a powerful group of broad-spectrum antibiotics which, in many cases, are the last line of defense against multi-resistant bacterial infections. Carbapenems are classified under β-lactams antibiotics, slightly different from the penicillin by substitution of a carbon atom for a sulfur atom and addition of a double bond to the five-membered ring of the penicillin nucleus ( Figure 1 ). Carbapenems bind tightly to the bacterial penicillin-binding proteins (PBPs), which are vital for elongation and cross-linkage of the cell wall peptidoglycan, leading to bacterial lysis [6] (Figure 2 ).

Currently four of carbapenems (imipenem, meropenem, ertapenem and doripenem) are approved for clinical use in the United States of America [7] and additional three of them (biapenem, faropenem, panipenem) in Canada. During the last decade, several monitoring studies have reported the emergence of carbapenem resistant Enterobacteriaceae (CRE) [8] . The three major mechanisms of carbapenem resistance in these bacteria include: (i) the presence of β-lactamase enzymes called carbapenemases, and (ii) the combined effect of other β-lactamases with bacterial cell membrane permeability due to alteration or mutations in the porins and/or (iii) increased efflux pump-action ( Figure 3 ). The modification of penicillin binding proteins (PBPs) has been reported as the forth mechanism of resistance to carbapenems in Gram-negative bacteria [9] . Carbapenems bind tightly to the bacterial penicillin-binding proteins (PBPs), which are vital for elongation and cross-linkage of the cell wall peptidoglycan, leading to bacterial lysis [6] (Figure 2 ).

Currently four of carbapenems (imipenem, meropenem, ertapenem and doripenem) are approved for clinical use in the United States of America [7] and additional three of them (biapenem, faropenem, panipenem) in Canada. During the last decade, several monitoring studies have reported the emergence of carbapenem resistant Enterobacteriaceae (CRE) [8] . The three major mechanisms of carbapenem resistance in these bacteria include: (i) the presence of β-lactamase enzymes called carbapenemases, and (ii) the combined effect of other β-lactamases with bacterial cell membrane permeability due to alteration or mutations in the porins and/or (iii) increased efflux pump-action ( Figure 3 ). The modification of penicillin binding proteins (PBPs) has been reported as the forth mechanism of resistance to carbapenems in Gram-negative bacteria [9] . Carbapenemases induce resistance essentially by hydrolysis of carbapenem using active catalytic substrates either serine or zinc [10] as indicated in Table 1 . The non-metallo-carbapenemase-A (Nmc-A) was first described to cause carbapenem resistance in Enterobacteriaceae in 1993 [11] . According to the Ambler's molecular classification, class B metallo β-carbapenemases (MBL types), class A (Klebsiella pneumoniae carbapenemases (KPC) types), and class D oxacillinases (OXA types) are epidemiologically important in Enterobacteriaceae [12] [13] [14] . The genes encoding these carbapenemases can be located either on the chromosome or on mobile genetic elements (MGEs) like plasmids, integrons, and transposons [15, 16] . The carbapenemases KPC and NDM (New Delhi metallo β-carbapenemases) producing bacteria have shown resistance against most of the β-lactams, fluoroquinolones, and aminoglycosides [17] . However, OXA type in particular OXA-48-like carbapenemases are less active against carbapenems and can induce a high resistance level only when associated with extended-spectrum β-lactamases (ESBLs) [18, 19] . The dissemination of carbapenemases genes by MGEs among clinical isolates is a source of serious public health and food safety concerns. Enterobacteriaceae with acquired carbapenem resistance genes have been isolated from humans, animals, food, and the environment. The aim of this review is to discuss the molecular epidemiology of carbapenemases in Enterobacteriaceae. 

The β-lactams antibiotics such as penicillins and cephalosporins have been wildly used against pathogenic Enterobacteriaceae because of their broad-spectrum activity [20] . However, this practice contributed to the emergence and spread of several types of β-lactamases including ESBLs. To overcome the resistance against extended spectrum cephalosporins (ESC) and cephamycins in Enterobacteriaceae, carbapenems have been introduced in human medicines. According to the recent 2020 Canadian Antimicrobial Resistance Surveillance System (CARSS) annual report, the carbapenems use in human medicine has been increased from 3.0 to 6.8 defined daily doses (DDDs) per 1000 inhabitants between 2014 and 2018 in Canada. Consequently, a concomitant nine-fold increase in the number of patients colonized by carbapenemases-producing organisms (CROs) without signs of infection has been reported in Canada [20] . Globally, the population of CRE is increasing dramatically [21, 22] . There could be several factors leading to the spread of carbapenemase-producing pathogens in humans. These factors include continuous exposure to antibiotics, usage of different concentrations of antibiotics, and contamination of surgical equipment used [12, 23, 24] .

The prevalence of carbapenem-producing Enterobacteriaceae (CPE) is high in humans with advanced age, primarily, due to their frequent visits to hospitals, long-term stay in health care facilities, tertiary care hospitals, and teaching hospitals [25] [26] [27] [28] [29] [30] . Hospital stay represents a particularly high risk to be colonize or in developing an infection with a CRE. Recent studies found 

The β-lactams antibiotics such as penicillins and cephalosporins have been wildly used against pathogenic Enterobacteriaceae because of their broad-spectrum activity [20] . However, this practice contributed to the emergence and spread of several types of β-lactamases including ESBLs. To overcome the resistance against extended spectrum cephalosporins (ESC) and cephamycins in Enterobacteriaceae, carbapenems have been introduced in human medicines. According to the recent 2020 Canadian Antimicrobial Resistance Surveillance System (CARSS) annual report, the carbapenems use in human medicine has been increased from 3.0 to 6.8 defined daily doses (DDDs) per 1000 inhabitants between 2014 and 2018 in Canada. Consequently, a concomitant nine-fold increase in the number of patients colonized by carbapenemases-producing organisms (CROs) without signs of infection has been reported in Canada [20] . Globally, the population of CRE is increasing dramatically [21, 22] . There could be several factors leading to the spread of carbapenemase-producing pathogens in humans. These factors include continuous exposure to antibiotics, usage of different concentrations of antibiotics, and contamination of surgical equipment used [12, 23, 24] .

The prevalence of carbapenem-producing Enterobacteriaceae (CPE) is high in humans with advanced age, primarily, due to their frequent visits to hospitals, long-term stay in health care facilities, tertiary care hospitals, and teaching hospitals [25] [26] [27] [28] [29] [30] . Hospital stay represents a particularly high risk to be colonize or in developing an infection with a CRE. Recent studies found that CRE colonization among ICU patients showing new emerging mechanisms of resistance continue to rise in the United States of America [31, 32] . There seems to have no different in other developed countries. For instance, Canada's Nosocomial Infection Surveillance Program data suggested that incidences of bla NDM , bla KPC , bla OXA-48 , and bla VIM producing K. pneumoniae and Enterobacter spp. increased significantly in Canadian health care facilities since 2007 [33] . These health care facilities could be a reservoir for patient spreading CPE to multiple regions. For instance, bla KPC -producing K. pneumonia have been reported in hospital outbreaks in many European countries such as Greece, Italy, Spain, France and Germany [3, [34] [35] [36] [37] [38] [39] [40] . A recent study reported cases of bla NDM-1 and bla KPC-2 -producing K. pneumonia among transplanted patients in Brazil [41] . Although, little is known about the spread and clinical relevance of CRE in Africa, two studies reported their prevalence in hospital and community settings among several African countries [42, 43] . Issues about carbapenemases include their potential link with multidrug-resistance genes on the same MGEs. For instance, the bla KPC gene encoding KPC enzyme to hydrolyze all β-lactams was found on plasmids carrying multiple other antimicrobial resistance determinants [44, 45] . Outbreaks caused by multidrug resistant and bla KPC -positive K. pneumoniae opportunistic pathogenic strains have been reported in North America, Europe, Asia and South America [3, [46] [47] [48] . A recent study from China reported a Morganella morganii isolate, an opportunistic pathogen, harboring bla NDM-5 gene on a self-transmissible IncX3 plasmid from a stool sample of a cancer patient [49] .

Another important factor responsible for worldwide dissemination of CRE is the international travelling and medical tourism. There are several reports demonstrating the role of travelling to affected developed countries in the epidemiology of CRE. Pathogenic strains of K. pneumoniae and Enterobacter cloacae containing bla KPCs have been isolated from patients from France and Greece hospitalized in New York [50, 51] . Overcrowding coupled with poor sanitation conditions including inappropriate waste management system and misuse of antibiotics could play roles in the spread of antimicrobial resistance genes in general and those for carbapenemases in particular. Furthermore, urbanization and globalization are greatly involved in spreading antimicrobial resistance pathogens all over the world. Accordingly, class B MBL, bla NDM-1-producing K. pneumoniae, Escherichia coli, E. cloacae, Citrobacter spp., Proteus spp., and Klebsiella oxytoca strains were originally isolated in India. These same bla NDM-1 producing K. pneumoniae and E. coli strains were subsequently isolated from Sweden and UK patients who had travelled to India recently. The patients in Sweden and UK may either have been hospitalized or underwent any medical intervention in India which could led to their infection or colonization by these pathogenic strains producing bla NDM-1 [52] [53] [54] . A similar scenario has been reported in Canada and the United States where bla NDM-1 -producing Enterobacteriaceae were isolated from patients who visited and received medical cares in the Indian subcontinent [55, 56] . Furthermore, a recent study reported two hyper-virulent K. pneumoniae clones of ST86 harboring plasmid mediated bla KPC-2, isolated from a Canadian patient who visited Greece [57] . Likewise, a novel bla KPC-3 variant (bla was recently identified in multi-drug resistant K. pneumoniae clinical isolate conferring resistance to ceftazidime-avibactam in Switzerland that was most likely acquired in Greece [58] . Several studies have demonstrated that medical tourism is another way to introduce CREs from an endemic country to a non-endemic country [59] [60] [61] . For instance, a case has been reported in an Israelis hospital where four non-Israelis patients, were positive for bla OXA-48 -producing Enterobacteriaceae [61] . The OXA-48 positive bacteria were absent from this hospital before these patients' admission in the Israel, two and one of them were respectively hospitalized in Jordan and Georgia where bla OXA-48 producing Enterobacteriaceae were prevalent, demonstrating thus the role of medical tourism in the epidemiology of CRE [60] .

Carbapenems are not licensed for the treatment of infectious diseases in companion animals in most of countries. As a result, pathogenic strains of Enterobacteriaceae causing infections in companion animals are not usually screened for carbapenemase resistance genes in veterinary laboratories. The possible way companion animals may get infected with CRE is through direct contact with colonized hosts and contaminated environment. Eventually, companion animal may become a reservoir for CPE [62] [63] [64] [65] . For instance, a bla OXA-48 carbapenemase-producing K. pneumoniae has been transmitted from human to companion animals (dogs) through contaminated hands [66] . In 2015, the transmission of an IncX3 plasmid bearing bla NDM-5 in E. coli ST167 was detected in dogs and humans in Finland [67] . A recent study found IncX3 plasmid mediated bla NDM-5 in E. coli ST410 in four Korean dogs implying the HGT an important mechanism of their spread among companion animals. Carbapenemase-producing E. coli ST131 has also been reported repeatedly in both household members and their companion animals [68] [69] [70] . An Australian study also reported the IncHI2 type plasmid bearing bla IMP-4 in Salmonella Typhimurium isolates from infected cats [71] . Importantly this variant showed sequence similarity to two bla IMP-8 carrying IncHI2 plasmids from Enterobacter spp. from humans with an indication of nosocomial spread and broader risk to humans, animals and the environment. Enterobacteriaceae producing carbapenemase (bla NDM-1 and bla OXA-48 ) have been isolated from companion animals like dogs, cats, and horses in the USA, Germany, Greece and UK [66, [72] [73] [74] [75] . Another recent study in Switzerland reported the isolation of various carbapenemase-producing Enterobacteriales in companion animal clinics mainly associated with poor clinical practices [76] . The isolation of CRE in companion animals brings the attention to reconsider the use of any off-label use of carbapenems in the veterinary medicines. Even carbapenems are not registered to use in companion animals, these antibiotic are used as off-label for the treatment of urinary tract infections in dogs and horses and to treat after surgical procedure infections caused by multidrug resistance E. coli in the UK and some other European union countries [77] . Identification of CPE in companion animals could become significant for public health due to not only host-to-host transmission but also possible gene transfers between commensals and pathogens. Due to selection pressure, treated animals (pets) may become colonized with CPE that could be transmitted to human through fecal -oral contaminations.

Carbapenemases-producing Enterobacteriaceae is not only a threat to humans; but animals may also get colonized and/or affected by CPE. The CPE could be isolated from food producing animals such as chicken, swine and cattle. A geographical distribution of CPE isolates from animal clinical samples has been recently reported [9] .

Various studies reported the presence of CPE in livestock which could constitute a food safety issue. Based on these studies, bla VIM-1 and bla NDM-1 were the most prevalent carbapenemase enzymes among Enterobacteriaceae in food producing animals [78] [79] [80] [81] [82] . In Germany, bla VIM-1 producing S. enterica and E. coli have been isolated from swine and chicken farms. In both cases, bla VIM-1 gene was located on an IncHI2 type plasmid. These isolates showed multidrug resistance due to the presence of other resistance genes including bla ACC-1 , bla ADD-1 and strA/B in addition to the bla VIM-1 on same IncHI2 type plasmids [80, 81] . Apart from bla VIM-1 , three E. coli isolates were found to carry the bla NDM-5 gene on a IncX3 transferrable plasmid, including one co-harboring the colistin resistance mcr-1 gene on IncHI2 plasmid of ST446 and the other two belonged to ST2, isolated from three dairy cows in China [83] . Moreover, a novel IncX3-type plasmid harboring a bla NDM variant (bla NDM-20 ,) due to three point mutations compared to bla NDM-1 , was recovered recently in an E. coli ST1114 from swine in China thus, suggesting that food-animal could be a source of new carbapenemase genes [84] .

CREs from food-producing animals could find their way into the food chain, leading to an alarming food safety issue. For public health concerns with respect to risk of transfer to humans via the food source, several resistance surveillance systems for retail meat are in place which include carbapenem susceptibility monitoring in many countries. Interestingly, CRO could be isolated from the food that escape resistance surveillance programs such as seafood [85] . Besides live animals, several reports demonstrating the spread of CPE in retail meat in Egypt, China and Pakistan [86] [87] [88] .

As reported in 2016 in China, the increasing spread of carbapenem and colistin-resistant E. coli clone ST167 from chicken meat harboring bla NDM-9 and mcr-1 co-located on a plasmids has raised concerns worldwide because of potential transfer of this resistance plasmids to other Gram-negative pathogens and to other countries [88] . Moreover, VIM-1 producing S. enterica serovar Infantis have been isolated from minced pork meats in Germany [89] and NDM-1 producing S. enterica serovar Indiana have been isolated from chicken carcasses in China [90] . Additionally, a recent study reported the contamination of retail meat samples from pork, chicken and beef with E. coli and K. pneumonia containing bla NDM genes located on IncX3 plasmid [91] . Between 2016 to 2018, a substantial increase of such CRE from 9.4% to 22. 2% in the retail meat samples was reported.

As stated above CRE could be found in seafood as reported as VIM-1 producing E. coli from retail squid, sea squirt, clams and seafood medley in Germany, China and Korea [92] . Trading of seafood from endemic countries to non-endemic countries could result in the spread of carbapenem resistance genes. For instance, the Canadian Integrated Program for Antimicrobial Resistance Surveillance (CIPARS) reported carbapenem-resistant Enterobacter spp. in fresh and frozen raw shrimp collected imported from Southeast Asia to Canada [93] . A recent study from Netherlands reported the isolation of E. cloacae ST813 bearing plasmid with bla IMI-2 and a novel Ambler class A carbapenemases bla FLC-1 from a frozen vannamei white shrimp (Litopenaeus vannamei) originating in India. This new bla FLC-1 carbapenemases was found to be related to previously known French imipenemase (FRI), with 82% amino acid identity to bla FRI-1 and 87% to bla FRI-5 [94] . Although rare but raw milk containing OXA-48-producing K. pneumoniae ST530, an epidemic clone, was reported in Lebanon [95] .

A role for fresh produces in spreading antimicrobial-resistant has been suggested by several studies. In China, fresh lettuce was found to be contaminated with E. coli ST877 co-producing NDM-1 and KPC-2, while also carrying fosA3 and floR genes on a transferrable IncA/C2 type plasmid [96] . Various species of CRE were recovered from leek, radish, basil, spinach, lettuce, traditional and commercial salads in Iran and OXA-48 producing K. pneumonia were detected in fresh vegetables from Algeria [97] . It has also been suggested that international trade of fresh vegetables and spices could be the possible route for the spread of CRE. Coriander imported from Asia to Switzerland and many other countries was positive to bla OXA-181 -producing Klebsiella variicola [98, 99] . Consequently, there is a need for resistance surveillance programs for both carbapenemase-producing pathogenic and non-pathogenic organisms in the food chain to find the potential reservoirs of carbapenemase genes and to prevent their spread from food to humans.

As discussed above, several studies demonstrate the spread of CPE all around the world among humans and animals. However, there are very few reports on the role of environmental contamination in the spread of CPE. The environment, surrounded by the CPE carriers, may be contaminated with these bacteria and further act as a vector for their dissemination. Dissemination of environmental CPE (eCPE) can negatively impact human health [100] . The prevalence rate of eCPE is high especially around intensive care units, acute and long-term health care facilities. Exposure of health care personnel to infected patients and cleaning methods used in the health facilities could potentially be responsible for dissemination of eCPE [101] . A study reported the presence of eCPE on the bed surface, personal table and infusion pump used by one CPE-infected patient [101] . The potential presence of eCPE on health care personnel brings attention toward the importance of adopting cleaning methods used in hospitals to disinfect the surfaces and material used by CPE carriers [102] . In hospitals, carbapenems are frequently used to treat infectious diseases caused by extended spectrum cephalosporinase (ESC) producing bacteria. Carbapenems are not entirely metabolized in the body and some residues present in human excreta can get into hospital sewage. Due to selection pressure, there is a chance that pathogens present in hospital effluent may become resistant against carbapenems. It has been reported that hospital sewage may act as a reservoir for resistance genes and a point where organisms likely acquire resistance through horizontal gene transfer events [103] . For instance, NDM-4 producing E. coli with downstream bleomycin resistance gene, ble MBL on a plasmid type associated with complete IS Aba125 were isolated from hospital sewage in India, suggesting hospital wastes as major reservoir of resistance genes [104] . Likewise, antibiotic residues released into the municipal wastewater along with human excreta could contribute to selection of CPE the ground and surface water sources. A VIM-1-producing resistant K. pneumoniae strain has been isolated from rivers in Spain, Switzerland and Sweden [105] [106] [107] . The presence of CRE in wastewater is a potential concern because this environment may serve as major reservoir leading to HGT events and an increased risk of carbapenem resistance spreading into the environment. The data collected from a recent US survey of seven wastewater treatment plants reported the detection of 20% carbapenem-resistant E. coli isolates of sequence types associated with extra-intestinal infections in humans harboring predominantly bla VIM and bla KPC genes [108] . Similarly, a study from the United States documented the presence of CRE including E. coli and P. mirabilis isolates harboring bla IMP-27 gene on IncQ1 plasmids in both environmental and fecal samples of swine production system [109] . The presence of bla KPC-2 gene has been reported in the United States in the metagenome from the feces of beef cattle regardless of antibiotic use in the farm [110] . Moreover, two most recent studies reported the presence and survival of carbapenem-resistant organisms harboring a plasmid-borne bla OXA-23 gene from swine manure environment from a Croatian pig farm and NDM-5 producing E. coli ST156 from a poultry farm in China. These suggest the possible dissemination of CRE in the food chain through animal manure fertilization [111, 112] . On the other hand, irrigation water and various water matrices are also considered as major source of fresh produce contamination with resistant bacteria including CRE that can potentially be transferred to the consumer especially when consumed raw [113] . Likewise, a recent study reported carbapenem resistant K. pneumoniae isolates from Austrian rivers showing genetic similarities to clinical isolates from hospitals raises concerns regarding the role of surface water in the of dissemination of CRE [114] . Surprisingly, tap water could serve as reservoir of community exposure to CRE in high income countries. A recent multi-state study form United States screened drinking water samples from both public and private water systems in six states and detected 6.4% CRE harboring bla OXA-48 -type carbapenemase gene [115] . Another Recent study from Egypt, investigated the occurrence of β-lactamase and CRE in the integrated agriculture-aquaculture environment and isolated several Enterobacteriaceae strains resistant carrying predominantly the carbapenemase resistant gene bla KPC either alone or with the β-lactamase genes (bla CTX-M-15 , bla SHV , bla TEM , and bla PER-1 ). This study suggests transmission of the resistance genes among Enterobacteriaceae strains in integrated agriculture-aquaculture system with serious public health implication [116] .

Spread of CRE: The most frequently identified carbapenem genes are the ambler class A including bla KPC followed by class B metallo-beta lactamases (MLBs) such as bla NDM , and the class D OXA-type gene like bla OXA-48 (Table 1) . Since its identification in the North Carolina, USA in 1996, in K. pneumonia patient, the epidemiology of bla KPC producing isolates has expanded mostly globally in Africa, America, Asia, Australia, and Europe especially the clonal group (CG) 258, which includes the lineages ST258 and ST11). Since 2015, several outbreaks related to ST258 have been documented in hospital of Israel closely related to strain found in New York [117] . Likewise, the class B metallo-beta lactamases genes, including bla NDM , bla SME , bla GES , bla VIM , and bla IMP , have also been disseminated worldwide, bla NDM-1 being the most prevalent worldwide [118] . The gene bla NDM-1 was first detected in a K. pneumonia isolate from a Swedish patient of Indian origin in 2008 in a multidrug-resistant K. pneumoniae, suffering from urinary tract infection acquired in India [119] . Subsequently, the bla NDM-1 was also found in K. pneumonia isolate from Croatia, from a patient arrived from Bosnia and Herzegovina. The second geographical origin of bla NDM-1 considered to be eastern Balkans. In May 2010, a case of infection with bla NDM-1 producing E. coli was reported in Coventry in the United Kingdom. Moreover, the bla NDM-1 gene was also reported in Australia, Austria, Belgium, China, Canada, France, Germany, Hong Kong, Japan, Netherland, Norway, and Sweden. Likewise, the bla SME were reported in England with sporadic reports of such gene in USA. Since 2004 and it has also been reported in Argentina, Australia, Brazil, Canada and Switzerland but the increasing number of this gene have been reported in America and UK [120] . The bla VIM gene was originally described in Italian Pseudomonas aeruginosa in the mid-1990s and afterwards CRE carrying bla VIM were predominantly reported in Europe and large number of cases were also reported in other countries including Africa, Taiwan, Mexico, Saudi Arabia and the United States. However, the bla VIM gene was found in Greece with more than 48 variants of this gene showing global dissemination [121] . Furthermore, the bla IMP gene was first originated in south pacific Asia predominantly among isolates of E. coli and Enterobacter on class 1 integrons and genomic evidences are now emerging of its dissemination globally [122] . Finally, among the various variants known of Class D today, the bla OXA-48 gene was first identified in Turkey in 2001. Although endemic during that time mostly in Turkey and Malta but since 2015, it has been spread to multiple countries including Singapore, Algeria, Korea, south Africa and have recently emerged in Canada and other western countries.

CRE carriage: Several studies particularly in China and also around the globe have recently attempted to investigate the carriage of CRE in animals and humans that possibly contributes to its dissemination in societies and healthcare facilities [123, 124] . For instance, a recent case study in Singapore determined the duration of CRE carriage among various hospital workers by investigating 21 CRE carriers for more than 1 year. The authors of this study reported a mean carriage duration of 86 days among hospital workers and further suggested that the prolonged carriage could be associated with use of antimicrobial drugs and the probability of decolonization in a year was 98.5% [124] . Despite reports in healthcare facilities, a recent study by Zhai, et al. [125] monitored the carriage of CRE in a Chinese poultry farm for over a year (January 2017 to April 2018). During this period these authors collected 350 cloacal samples from four broiler farms in additional to 582 environmental samples and found that CRE negative 1-day-old broilers acquired bla NDM within 24 h of transfer. Furthermore, the same study also analyzed the persistence and transmission of bla NDM -producing bacteria in a Chinese poultry farm and found that the IncX3 plasmid accounts for 71% of bla NDM carriage that persisted in farm over 16 months and about 20% also carried either the colistin resistance mcr-1 or mcr-8 gene. This study further suggests that the contaminated in-house environment contributes to the persistence and transmission of bla NDM producing bacteria in Chinese poultry farms.

Food chain transmission: The rise of CRE in food-producing animals and food supply is of growing concern globally and, given the risks of CRE to human health, there have been a zero-tolerance policy and an international ban on the sale of food items contaminated with CRE in several countries [126] . Therefore, prevention of CRE occurrence and spread in food-producing, wildlife and companion animals is a major public health priority to protect both persons with direct exposure and consumers. Authorities in European countries have already reacted by establishing active carbapenem resistance surveillance programs targeting food-producing animals mainly poultry, pork, cattle, and retail meat products [127] . There is concern that without these programs the presence of carbapenem genes in bacteria has the potential to enter the food supply undetected and subsequently transmission to humans [19] . For example, in 2014 a study by Morrison and Rubin [85] , reported a 3.94% prevalence of CPOs in seafood imported in Canada that could pose a potential risk for transfer to clinically relevant bacteria and eventually to humans which is certainly of concerns. Strong evidences exist that the transmission of resistance might have taken place from animals to humans. Although many of these evidences were not direct and were based on the similarities between the carbapenem resistance genes of bacteria isolated from food-producing animals including poultry, pigs, cattle and from humans having close contact with these animals such as farm workers, animal caretakers and their family members [128] . To support risk assessment for zoonotic CRE, a comprehensive systematic review on CRE that carried bla VIM , bla KPC , bla NDM , blaIMP and bla OXA , from wildlife, food-producing, and companion animals was conducted recently by Köck, el al [72] . This study was primarily focused on the dissemination of CRE in livestock, food items including seafood, companion animals and their potential of transmission to exposed humans. The most prevalent carbapenem genes were bla VIM , bla KPC , bla NDM , bla OXA , and blaIMP in E. coli and K. pneumoniae isolates. Interestingly, only two independent studies reported that 33-67% of exposed humans on poultry farms carried CRE closely related to isolates from the poultry farm environment suggesting fecal-oral transmission or transmission via the food sources has the higher potential to spread CREs to healthier population. Wang, et al. tested six fecal specimens from farmers and workers from a Chinese commercial chicken farm, of which three (50%) were positive for plasmid-borne bla NDM-5 producing E. coli and demonstrated that two of the farmers isolates shared sequence types (ST10, ST746) with isolates from local dogs, flies, and chickens and clustered closely together, suggesting exposure and transmission to human on the farm environment. In their follow up study, Wang et al. [129] demonstrated clonal commonality between bla NDM -positive E. coli isolates from chicken farms, slaughterhouses, supermarkets, and humans, belonging to sequence types ST10 and ST156. Recently, another study in Egypt by Elshafiee et al. [130] provided strong evidences of direct transmission of CRE to humans from farm animals. Another study by Li et al. [124] , investigated the prevalence, risk factors, and drivers of CRE transmission between humans and their backyard animals in rural China that provided direct evidence of inter-host transmission of bla NDM producing E. coli between humans and backyard animals. Moreover, the incidence of carbapenem resistant genes in food-producing animals has also been reported from several other countries with chickens and pig being the most investigated species, in which carbapenem resistant genes has been most frequently detected [128] .

Detection of CRE: In the recent past, several molecular genotyping methods such as microarrays, single and multiplex polymerase chain reaction (PCR) assays have been used to detect the common carbapenemases, including bla KPC , bla NDM , bla IMP , bla VIM and bla OXA-48 , in bacterial isolates or directly from clinical specimens [131] . However, these molecular methods can accurately detect specific carbapenemase genes but cannot detect novel carbapenemase genes. On the other hand, whole genome sequencing (WGS) is a powerful new method with vastly improved resolution over current gold-standard techniques that not only identifying CRE but also providing detailed insights into their evolution and dissemination [132] . WGS potentially represent the ultimate molecular detection by probing the complete genomic content, chromosomal and extrachromosomal, of bacteria for the detection of carbapenem resistant genes. Moreover, WGS provide an opportunity to extrapolate additional information, including strain relatedness, molecular epidemiology, plasmids of replicon types harboring the carbapenemase, prediction of factors influencing carbapenem resistance for example point mutation and presence of other resistance factors and data can be analyzed in real-time or stored for future analysis. There is no doubt that WGS enhances our ability to characterize and resolve outbreaks of carbapenem resistant bacterial populations, understand and predict epidemiological trends, and create new machine learning tools for rapid detection of novel variants. As new algorithms are developing for tracking of transmission of carbapenem resistant bacteria in various fields including health care facilities and agricultural products (poultry, beef, and pork), likely to become increasing efficient and interpreting with the level of precision necessary to guide the modification of infection control procedures and food safety measures to limit the spread of CPO, allowing WGS to gain broader acceptance [133] .

Role of insertion sequences, transposons and integrons: Dissemination of CPE among humans and animals has been enhanced by the horizontal transfer of CR genes on MGEs such as insertion sequences, transposons and integrons and their associated plasmids. [16, 50, [134] [135] [136] [137] . The genetic analysis of bla IMP and bla IVIM from endemic areas in Southern Europe and Southeast Asia showed an association between both genes with class 1 integrons [138] . Molecular typing method such as PCR based replicon typing and plasmid multi-locus sequence typing (pMLST) methods have been used to identify a range of plasmid incompatibility groups responsible for the epidemiology of CR genes [139] [140] [141] . Most of the CR genes associated with the Ambler class A, class B, and Class D β-lactamases are located on plasmids, except Ambler class A CR genes (bla SME-1 to 3 , bla IMI and bla NMC-A ), which are usually located on the chromosome (Table 1) . Some bla KPC , bla VIM , bla IMP , and bla OXA type carbapenemases genes have been located within transposons on plasmids which are responsible for the spread of such CR genes among Enterobacteriaceae. In addition, clonal expansion also acts as a way to spread the CR genes as described for bla KPC in K. pneumoniae ST258 [142] and bla NDM-5 in E. coli on the IncX3 type plasmid [143] . The insertion sequences and transposons play a role in the genetic variability. Accordingly, ISAba1/3 and ISAba125 have been reported to induce expression of several carbapenem resistance genes such as bla OXA-23-51-66 -like and bla NDM-1 in A. baumannii and K. pneumoniae [144] [145] [146] [147] [148] . Similarly, a novel Tn4401 transposon variant (Tn4401h, a188-bp deletion) on conjugative plasmids has been associated with enhanced bla KPC expression and the degree of phenotypic resistance to carbapenemases in K. pneumoniae [149] .

Plasmid: Plasmids belonging to different incompatibility groups play an important role in the epidemiology of CR genes. Plasmid-mediated spread of bla NDM-1 gene in Enterobacteriaceae has attracted attention, primarily, due to its predominant presence in nosocomial isolates (K. pneumoniae), as well as in community-acquired isolates (E. coli). Another characteristic is the propensity of conjugative plasmids to transfer resistant genes among other Enterobacteriaceae [150, 151] . The bla NDM-1 gene was first detected in New Delhi, and in the Indian subcontinents [52] . Since then it has been isolated in UK, Pakistan, Bangladesh, Central and South America, the US and Canada [151] . In this case, urbanization and international travelling were described to contribute in the propagation of the bacterial clones and plasmids with bla NDM-1 gene from Indian subcontinent to other countries and continents [151] . Genetic studies demonstrated that the bla NDM-1 gene was associated with different bacterial clones and has spread among Enterobacteriaceae and non-Enterobacteriaceae species. This bla NDM-1 gene is carried by a broad range of multidrug plasmids belonging to the IncA/C, IncL/M, IncN and IncF incompatibility groups [45] . These plasmids with bla NDM-1 gene, also harbor other genes conferring resistance to aminoglycosides, quinolones, trimethoprim, sulphonamides, tetracyclines, colistin and heavy metal [3, 44, 152, 153] . Moreover, bla NDM-1 has been identified in E. coli ST90, ST131 and E. cloacae ST231 whereas bla NDM-5 gene in ST101, ST167, and ST405 clones bearing diverse transmitting vectors were responsible for community acquired infections [154, 155] . Thus, infections caused by NDM pathogens could be difficult to be treated [52, 156, 157] .

Some CR genes including bla OXA-48 are associated with a single type of plasmid incompatibility group in Enterobacteriaceae [39, 158] . The dissemination of bla OXA-48 gene among K. pneumoniae, E. coli and E. cloacae is due to the presence of this gene on mono-drug resistance plasmids belonging to the IncL/M incompatibility group sharing common characteristics such as self-transferability, no additional antibiotic resistance genes and size of plasmid range between 60-70 kbp [45] . In companion animals, the bla OXA-48 gene was found to be located on a multidrug-resistance plasmids belong to same IncL/M incompatibility group also carrying and extended spectrum β-lactamases and Amp C β-lactamases [45, 66, 159] .

The bla KPC genes have usually been located on self-transferable and multidrug-resistant large size plasmids, which are varying in size as well as phage-like plasmids [160, 161] . The transferability of the bla KPC plasmids has been reported between C. freundii and K. oxytoca belonging to two different bacterial genera [162, 163] . These plasmids also carry additional antibiotic resistance genes for aminoglycosides, ESBLs and fluoroquinolones [164] . Different K. pneumoniae clones and different strains may carry KPC β-lactamase. In all reported cases, the bla KPC gene has been associated with the Tn3 type transposon named Tn4401. This transposon may be a major source for transmission of bla KPC gene [160] .

The driving factor for the continuous increase in antibiotic resistance is antimicrobial usage in human and veterinary medicine as well as in agriculture. The European Surveillance of Antibiotic Consumption Network data in 2017 reported that in 10 out of 25 countries, consumption of carbapenems among humans increased since 2012, while only one country (Portugal) showed a decreasing trend during the same period (https://ecdc.europa.eu/en/publications-data/summary-latest-data-antibioticconsumption-eu-2017). The carbapenems resistance in addition to ESC and cephamycins resistance in Enterobacteriaceae represent an important threat for public health. Out of the three classes, the class A carbapenemases KPC has spread globally and become more prevalent in the USA and Greece. The class B carbapenemase VIM and IMP has also been reported worldwide, but seem more endemic in Taiwan, Japan, and some European countries. The carbapenemase KPC, IMP, VIM, NDM, and OXA types have been mainly reported in nosocomial K. pneumonia strains. Pathogenic E. coli strains carrying bla NDM-1 and bla OXA-48 genes also have been found in community acquired infections. Therefore, proper identification and surveillance programs of carbapenem resistance pathogens and non-pathogenic strains have become necessary to support the control of CRE infections in both animals and humans. Source attribution studies along with developing alternative infection control strategies are warranted. 

The authors declared no conflict of interest.

Gloval Priority List of Antiviotic-Resistand Bacteria to Guide Research, Discovery, and Development of New Antibiotics

Genome-based phylogeny and taxonomy of the 'Enterobacteriales': Proposal for Enterobacterales ord. nov. divided into the families Enterobacteriaceae, Erwiniaceae fam

Global spread of Carbapenemase-producing Enterobacteriaceae

Colistin and tigecycline resistance in Carbapenem-resistant Enterobacteriaceae: Checkmate to our last line of defense

Infections caused by Carbapenem-resistant Enterobacteriaceae: An update on therapeutic options

Carbapenems: Past, present, and future

Pharmacology of specific drug groups

Epidemiology of Carbapenemase-producing Enterobacteriaceae and Acinetobacter baumannii in Mediterranean countries

Carbapenemase-producing Enterobacteriaceae in animals and methodologies for their detection

Evolution of New Delhi metallo-β-lactamase (NDM) in the clinic: Effects of NDM mutations on stability, zinc affinity, and mono-zinc activity

Analysis of a Carbapenem-hydrolyzing class A beta-lactamase from Enterobacter cloacae and of its LysR-type regulatory protein

The versatile β-Lactamases

Updated functional classification of β-Lactamases

Metallo-β-lactamases: Structure, function, epidemiology, treatment options, and the development pipeline

Chromosomal integration of the Klebsiella pneumoniae Carbapenemase gene, blaKPC, in Klebsiella species is elusive but not rare

Carbapenemases on the move: It's good to be on ICEs

Emergence of extensively drug-resistant and pandrug-resistant Gram-negative bacilli in Europe

Carbapenem resistance: A review

Beta-lactamases in Enterobacteriaceae infections in children

Novel Carbapenem-hydrolyzing β-Lactamase, KPC-1, from a Carbapenem-resistant strain of Klebsiella pneumoniae

Emergence of Carbapenem-resistant Enterobacteriaceae in a UK paediatric hospital

The β-lactamase threat in Enterobacteriaceae, Pseudomonas and Acinetobacter

Risk Assessment on the Spread of Carbapenemase-Producing Enterobacteriaceae (CPE) through Patient Transfer between Healthcare Facilities, with Special Emphasis on Cross-Border Transfer

Detection of OXA-48-like Carbapenemase-producing Klebsiella pneumoniae in a tertiary care center in Turkey: Molecular characterization and epidemiology

Hospital-acquired infections due to gram-negative bacteria

In vitro antibacterial activity of Doripenem against gram-negative blood isolates in a Korean tertiary care center

Metallo-β-lactamases among Enterobacteriaceae from routine samples in an Italian tertiary care hospital and long-term care facilities during

Microbiological features of KPC-producing Enterobacter isolates identified in a U.S. hospital system

Epidemiology of Carbapenem-resistant Enterobacteriaceae at a long-term acute care hospital

The likelihood of developing a Carbapenem-resistant infection during the hospital stay

Diversity of resistance mechanisms in Carbapenem-resistant Enterobacteriaceae at a health care system in Northern California

Emergence of Carbapenemase-producing Enterobacteriaceae

An outbreak of infection due to β-Lactamase Klebsiella pneumoniae Carbapenemase 2-producing K. pneumoniae in a Greek University Hospital: Molecular characterization, epidemiology, and outcomes

An update of the evolving epidemic of blaKPC-2-carrying Klebsiella pneumoniae in Greece (2009-10)

Carbapenem-non-susceptible Enterobacteriaceae in Europe: Conclusions from a meeting of national experts

Control of a multi-hospital outbreak of KPC-producing Klebsiella pneumoniae type 2 in France

Carbapenemase-producing Enterobacteriaceae in Spain in 2012

The real threat of Klebsiella pneumoniae Carbapenemase-producing bacteria

Large hospital outbreak of KPC-2-producing Klebsiella pneumoniae: Investigating mortality and the impact of screening for KPC-2 with polymerase chain reaction

Carbapenemase-producing Klebsiella pneumoniae from transplanted patients in Brazil: Phylogeny, resistome, virulome and mobile genetic elements harboring blaKPC-2 or blaNDM-1

The spread of Carbapenemase-producing bacteria in Africa: A systematic review

Antimicrobial susceptibility testing in predicting the presence of carbapenemase genes in Enterobacteriaceae in South Africa

Genetic features of the widespread plasmid coding for the Carbapenemase OXA-48

Global dissemination of Carbapenemaseproducing Klebsiella pneumoniae: Epidemiology, genetic context, treatment options, and detection methods

Control of Carbapenemase-producing Enterobacteriaceae outbreaks in acute settings: An evidence review

Diverse mechanisms of resistance in Carbapenem-resistant Enterobacteriaceae at a health care system in Silicon Valley

Detection and genomic characterization of a Morganella morganii isolate from China that produces NDM-5

Plasmid-mediated Carbapenem-hydrolyzing β-Lactamase KPC-2 in Klebsiella pneumoniae isolate from Greece

Plasmid-mediated Carbapenem-hydrolyzing β-Lactamase KPC in a Klebsiella pneumoniae isolate from France

Emergence of a new antibiotic resistance mechanism in India, Pakistan, and the UK: A molecular, biological, and epidemiological study

Prevalence of metallo-β-lactamase NDM-1-producing multi-drug resistant bacteria at two Pakistani hospitals and implications for public health

The role of international travel in the worldwide spread of multiresistant Enterobacteriaceae

New Delhi Metallo-β-Lactamase

Endometritis and bacteremia with a New Delhi Metallo-Beta-Lactamase 1 (NDM-1)-containing organism in a remote traveler

Report on two hypervirulent Klebsiella pneumoniae producing a blaKPC-2 Carbapenemase from a Canadian patient

KPC-50 confers resistance to Ceftazidime-Avibactam associated with reduced Carbapenemase activity

Intercontinental spread from Israel to Colombia of a KPC-3-producing klebsiella pneumoniae strain

Introduction of OXA-48-producing Enterobacteriaceae to Israeli hospitals by medical tourism

Centre for Disease Prevention and Control. Outbreak of VIM-Producing Carbapenem Resistant Pseudomonas aeruginosa Linked to medical Tourism to Mexico

Control of Carbapenemase-producing Enterobacteriaceae: Beyond the hospital

Hospitalized pets as a source of Carbapenem-resistance

First detection of New Delhi Metallo-β-Lactamase-5-producing Escherichia coli from companion animals in Korea

Antimicrobial-resistant Enterobacteriaceae recovered from companion animal and livestock environments

Emergence of OXA-48 Carbapenemase-producing Escherichia coli and Klebsiella pneumoniae in dogs

Sharing more than friendship-transmission of NDM-5 ST167 and CTX-M-9 ST69 Escherichia coli between dogs and humans in a family

Fluoroquinolone-resistant extraintestinal pathogenic Escherichia coli, including O25b-ST131, isolated from faeces of hospitalized dogs in an Australian veterinary referral centre

Multiple-host sharing, long-term persistence, and virulence of Escherichia coli clones from human and animal household members

Escherichia coli ST131, an intriguing clonal group

Isolation and plasmid characterization of Carbapenemase (IMP-4) producing Salmonella enterica Typhimurium from cats

Carbapenem-resistant Enterobacteriaceae in wildlife, food-producing, and companion animals: A systematic review

IMP-45-producing multidrug-resistant Pseudomonas aeruginosa of canine origin

Extended-spectrum β-lactamase, Carbapenemase and AmpC producing Enterobacteriaceae in companion animals

Occurrence and characterization of Escherichia coli ST410 co-harbouring blaNDM-5, blaCMY-42 and blaTEM-190 in a dog from the UK

Poor infection prevention and control standards are associated with environmental contamination with Carbapenemase-producing Enterobacterales and other multidrug-resistant bacteria in Swiss companion animal clinics

Multidrug-resistant E. coli and Enterobacter extraintestinal infection in 37 dogs

Escherichia coli producing VIM-1 Carbapenemase isolated on a pig farm

Carbapenemase-producing Acinetobacter spp. in Cattle

Salmonella enterica subsp. enterica producing VIM-1 Carbapenemase isolated from livestock farms

Spread and persistence of VIM-1 Carbapenemase-producing Enterobacteriaceae in three German swine farms in

Identification of New Delhi Metallo-β-lactamase 1 in Acinetobacter lwoffii of food animal origin

Characterization of NDM-5-positive extensively resistant Escherichia coli isolates from dairy cows

Novel variant of New Delhi Metallo-β-lactamase, NDM-20, in Escherichia coli

Carbapenemase producing bacteria in the food supply escaping detection

Extended-spectrum β-Lactamases and/or Carbapenemases-producing Enterobacteriaceae isolated from retail chicken meat in Zagazig

Carbapenemases and extended-spectrum β-Lactamase-producing multidrug-resistant Escherichia coli isolated from retail chicken in Peshawar: First report from Pakistan

Carbapenem-resistant and colistin-resistant Escherichia coli co-producing NDM-9 and MCR-1

VIM-1-producing Salmonella infantis isolated from swine and minced pork meat in Germany

Genomic characterization of a large plasmid containing a bla NDM-1 gene carried on Salmonella enterica serovar Indiana C629 isolate from China

Rapid increase in Carbapenemase-producing Enterobacteriaceae in retail meat driven by the spread of the blaNDM-5-carrying IncX3 plasmid in China from

Carbapenemase-producing Escherichia coli isolated from retail seafood

Carbapenem-resistant Enterobacter spp. in retail seafood imported from Southeast Asia to Canada

Novel Carbapenemases FLC-1 and IMI-2 encoded by an Enterobacter cloacae complex isolated from food products

OXA-48 and CTX-M-15 extended-spectrum beta-lactamases in raw milk in Lebanon: Epidemic spread of dominant Klebsiella pneumoniae clones

Emergence of Escherichia coli co-producing NDM-1 and KPC-2 Carbapenemases from a retail vegetable

First detection of Klebsiella pneumoniae producing OXA-48 in fresh vegetables from Béjaïa city

First detection of Klebsiella variicola producing OXA-181 Carbapenemase in fresh vegetable imported from Asia to Switzerland

Carbapenem-resistant Acinetobacter baumannii and Enterobacteriaceae in South and Southeast Asia

Dissemination of NDM-1 positive bacteria in the New Delhi environment and its implications for human health: An environmental point prevalence study

Environmental contamination by Carbapenem-resistant Enterobacteriaceae

Increased mortality among Carbapenemase-producing Carbapenem-resistant Enterobacteriaceae carriers who developed clinical isolates of another genotype

Genomic analysis of hospital plumbing reveals diverse reservoir of bacterial plasmids conferring Carbapenem resistance

Detection of bla NDM-4 in Escherichia coli from hospital sewage

Characteristics of extended-spectrum β-Lactamase-and Carbapenemase-producing Enterobacteriaceae isolates from rivers and lakes in Switzerland

Related Carbapenemase-producing Klebsiella isolates detected in both a hospital and associated aquatic environment in Sweden

Carbapenemase-producing Enterobacteriaceae recovered from a Spanish river ecosystem

Survey of US wastewater for Carbapenem-resistant Enterobacteriaceae

Carbapenemase-Producing Enterobacteriaceae Recovered from the Environment of a Swine Farrow-to-finish operation in the United States

Functional blaKPC-2 sequences are present in U.S. beef cattle feces regardless of antibiotic use

Kisic, I. Carbapenem-resistant Acinetobacter baumannii recovered from swine manure

Characterization of an NDM-5 Carbapenemase-producing Escherichia coli ST156 isolate from a poultry farm in Zhejiang

Critical threat associated with carbapenem-resistant gram-negative bacteria: Prioritizing water matrices in addressing total antibiotic resistance

Whole genome sequencing reveals resemblance between ESBL-producing and carbapenem resistant Klebsiella pneumoniae isolates from Austrian rivers and clinical isolates from hospitals

Multi-state study of Enterobacteriaceae harboring extended-spectrum beta-lactamase and Carbapenemase genes in U

Emergence of β-lactamase-and Carbapenemase-producing Enterobacteriaceae at integrated fish farms

Carbapenemase-producing organisms: A global scourge

Carbapenem resistance in Enterobacteriaceae: Here is the storm! Trends Mol

Characterization of a new Metallo-β-Lactamase gene, blaNDM-1, and a novel erythromycin esterase gene carried on a unique genetic structure in Klebsiella pneumoniae sequence type 14 from India

Epidemiology of β-Lactamase-producing pathogens

Novel variant (blaVIM-4) of the Metallo-β-Lactamase gene blaVIM-1 in a clinical strain of Pseudomonas aeruginosa

Global molecular epidemiology of IMP-producing Enterobacteriaceae

Emerging carriage of NDM-5 and MCR-1 in Escherichia coli from healthy people in multiple regions in China: A cross sectional observational study

Inter-host transmission of Carbapenemase-producing Escherichia coli among humans and backyard animals

Contaminated in-house environment contributes to the persistence and transmission of NDM-producing bacteria in a Chinese poultry farm

Centre for Disease Prevention and Control. Carbapenem-Resistant Enterobacteriaceae, second Update

Review of antimicrobial resistance surveillance programmes in livestock and meat in EU with focus on humans

Carbapenemase-producing bacteria in food-producing animals, wildlife and environment: A challenge for human health

Comprehensive resistome analysis reveals the prevalence of NDM and MCR-1 in Chinese poultry production

Carbapenem-resistant Pseudomonas aeruginosa originating from farm animals and people in Egypt

Carbapenemases in Enterobacteriaceae: Detection and antimicrobial therapy

From theory to practice: Translating whole-genome sequencing (WGS) into the clinic

A Primer on infectious disease bacterial genomics

Analysis of antibiotic resistance regions in Gram-negative bacteria

Gene flow, mobile genetic elements and the recruitment of antibiotic resistance genes into Gram-negative pathogens

Combinatorial events of insertion sequences and ICE in Gram-negative bacteria

Horizontal transfer of Carbapenemase-encoding plasmids and comparison with hospital epidemiology data

Identification of diverse integron and plasmid structures carrying a novel Carbapenemase among Pseudomonas species

Genetic characterization of blaNDM-harboring plasmids in carbapenem-resistant Escherichia coli from Myanmar

Replicon typing of plasmids encoding resistance to newer β-Lactams

Resistance plasmid families in Enterobacteriaceae

Worldwide diversity of Klebsiella pneumoniae that produce β-Lactamase blaKPC-2gene1

New Delhi Metallo-β-Lactamase 5-producing Klebsiella pneumoniae sequence type 258

Role of ISAba1 and ISAba125 in governing the expression of bla ADC in clinically relevant Acinetobacter baumannii strains resistant to cephalosporins

In vivo selection of reduced susceptibility to Carbapenems in Acinetobacter baumannii related to ISAba1-mediated overexpression of the natural blaOXA-66

Oxacillinase gene

Transposition of Tn125encoding the NDM-1 Carbapenemase in Acinetobacter baumannii

Molecular characterization of NDM-1-producing Klebsiella pneumoniae ST29, ST347, ST1224, and ST2558 causing sepsis in neonates in a tertiary care hospital of North-East India

Class D β-Lactamases: Are they all Carbapenemases?

Enhanced Klebsiella pneumoniae Carbapenemase expression from a novel Tn4401 deletion

NDM-1-A cause for worldwide concern

Does broad-spectrum beta-lactam resistance due to NDM-1 herald the end of the antibiotic era for treatment of infections caused by Gram-negative bacteria?

Detection and characterization of a clinical Escherichia coli ST3204 strain coproducing NDM-16 and MCR-1

Heavy metal resistance genes are associated with blaNDM-1-and blaCTX-M-15-carrying Enterobacteriaceae

Escherichia coli ST131-H22 as a foodborne uropathogen

Diverse vectors and mechanisms spread New Delhi Metallo-β-Lactamases among Carbapenem-resistant Enterobacteriaceae in the Greater Boston area

New Delhi metallo-β-lactamase: A cautionary tale

NDM Metallo-β-Lactamases and their bacterial producers in health care settings

Spread of OXA-48-encoding plasmid in Turkey and beyond

Coexistence of blaOXA-48 and truncated blaNDM-1 on different plasmids in a Klebsiella pneumoniae isolate in China

Genetic structures at the origin of acquisition of the β-Lactamase blaKPC gene

A phage-like plasmid carrying blaKPC-2 gene in Carbapenem-resistant Pseudomonas aeruginosa

Detection of the Klebsiella pneumoniae Carbapenemase type 2 Carbapenem-hydrolyzing enzyme in clinical isolates of Citrobacter freundii and K. oxytoca carrying a common plasmid

Plasmid-mediated transmission of KPC-2 Carbapenemase in Enterobacteriaceae in critically ill patients

Emergence of Serratia marcescens, Klebsiella pneumoniae, and Escherichia coli isolates possessing the plasmid-mediated Carbapenem-hydrolyzing β-Lactamase KPC-2 in intensive care units of a Chinese hospital