Epidemiology and molecular characterization of multidrug-resistant Gram-negative bacteria in Southeast Asia
© Suwantarat and Carroll. 2016
Received: 7 December 2015
Accepted: 20 April 2016
Published: 4 May 2016
Multidrug-resistant Gram-negative bacteria (MDRGN), including extended-spectrum β-lactamases (ESBLs) and multidrug-resistant glucose-nonfermenting Gram-negative bacilli (nonfermenters), have emerged and spread throughout Southeast Asia.
We reviewed and summarized current critical knowledge on the epidemiology and molecular characterization of MDRGN in Southeast Asia by PubMed searches for publications prior to 10 March 2016 with the term related to “MDRGN definition” combined with specific Southeast Asian country names (Thailand, Singapore, Malaysia, Vietnam, Indonesia, Philippines, Laos, Cambodia, Myanmar, Brunei).
There were a total of 175 publications from the following countries: Thailand (77), Singapore (35), Malaysia (32), Vietnam (23), Indonesia (6), Philippines (1), Laos (1), and Brunei (1). We did not find any publications on MDRGN from Myanmar and Cambodia. We did not include publications related to Shigella spp., Salmonella spp., and Vibrio spp. and non-human related studies in our review. English language articles and abstracts were included for analysis. After the abstracts were reviewed, data on MDRGN in Southeast Asia from 54 publications were further reviewed and included in this study.
MDRGNs are a major contributor of antimicrobial-resistant bacteria in Southeast Asia. The high prevalence of ESBLs has been a major problem since 2005 and is possibly related to the development of carbapenem resistant organisms in this region due to the overuse of carbapenem therapy. Carbapenem–resistant Acinetobacter baumannii is the most common pathogen associated with nosocomial infections in this region followed by carbapenem-resistant Pseudomonas aeruginosa. Although Southeast Asia is not an endemic area for carbapenem-resistant Enterobacteriaceae (CRE), recently, the rate of CRE detection has been increasing. Limited infection control measures, lack of antimicrobial control, such as the presence of active antimicrobial stewardship teams in the hospital, and outpatient antibiotic restrictions, and travel throughout this region have likely contributed to the increase in MDRGN prevalence.
KeywordsGram-negative bacteria Multidrug-resistance Southeast Asia Molecular Epidemiology
The Southeast Asian region has a history of high prevalence of multidrug-resistant Gram-negative bacteria (MDRGN) including extended-spectrum β-lactamases (ESBLs) and multidrug-resistant (MDR) glucose-nonfermenting Gram-negative bacilli (nonfermenters), especially Acinetobacter baumannii and Pseudomonas aeruginosa [1, 2]. In addition, carbapenem-resistant organisms (CRO) have recently emerged and spread to Southeast Asia . The epidemiology and molecular characteristics of MDRGN have been reported from Brunei, Indonesia, Laos, Malaysia, the Philippines, Singapore, Thailand, and Vietnam [1, 3–8]. Carbapenem–resistant Acinetobacter baumannii (CRAB) is the most common CRO associated with nosocomial infection in this region followed by carbapenem-resistant Pseudomonas aeruginosa (CRPA) [3–6]. Although Southeast Asia is not an endemic area of carbapenem-resistant Enterobacteriaceae (CRE), recently, the rate of CRE detection has been increasing [3, 4]. CREs are particularly concerning as these organisms are often disseminated by plasmids and have the potential to spread between patients causing outbreaks in several countries [1, 3–6]. We review and summarize current critical knowledge on the epidemiology and molecular characteristics of MDRGN organisms in Southeast Asia.
Literature search, definition and selection strategy
PubMed searches were performed for publications prior to 10 March 2016 with the term related to “MDRGN definition” combined with specific Southeast Asian country names (Thailand, Singapore, Malaysia, Vietnam, Indonesia, Philippines, Laos, Cambodia, Myanmar, Brunei). For epidemiologic purposes, we defined MDRGN as Gram-negative bacteria that are resistant to at least 3 classes of antimicrobial agents [1, 2]. We searched the terms Multidrug-resistant gram-negative bacteria, MDR Gram-negative bacteria, ESBL, KPC, NDM, VIM, IMP, MBL, CRE, Acinetobacter, Pseudomonas.
Results and Discussion
There were a total of 175 publications from the following countries: Thailand (77), Singapore (35), Malaysia (32), Vietnam (23), Indonesia (6), Philippines (1), Laos (1), and Brunei (1). We did not find any publications on MDRGN from Myanmar and Cambodia. We did not include publications related to Shigella spp., Salmonella spp., and Vibrio spp. and non-human related studies in our review.
English language articles and abstracts were included for analysis. After the abstracts were reviewed, data on MDRGN in Southeast Asia from 54 publications were further reviewed and included in this study.
Epidemiology and molecular characteristic of MDRGN in Southeast Asia
The OXA-type carbapenemase gene, bla OXA-23 is a predominant β-lactamase gene among A. baumannii isolates in this region and belongs to global clone 2 [11, 12]. Two global clones of A. baumannii have been reported (global clone 1 and global clone 2) worldwide . Global clone 2 corresponds to clonal complex 92 (CC92) in the multilocus sequence typing (MLST) scheme of Bartual et al. and Woodford et al. [11, 12]. Global clone 2 has emerged in Europe and spread throughout A. baumannii isolates in Asian countries, including South Korea and China and Australia . In addition, the bla OXA-40, and bla OXA-58 have been reported in a few A. baumannii isolates in this region [3, 6, 11, 12]. In P. aeruginosa, carbapenem resistance is multifactorial and involves non-carbapenamase mechanisms such as porin changes (OprD gene mutation) and a combination of efflux pump and AmpC β-lactamase hyperproduction. Metallo β-lactamase-production (MBL) has been reported in CRPA and includes IMP-type metallo-β-lactamase (bla IMP) and Verona integron-mediated MBL (bla VIM) [3, 6, 11–15]. Among CRE isolates, New Delhi MBLs (NDM) have emerged and predominate in several countries in this region [6, 16–20]. Other MBL genes such as bla IMP, bla VIM and bla OXA have been reported in some countries [6, 19, 21–23]. Klebsiella pneumoniae carbapenamase (KPC)-producing Enterobacteriaceae is less common in Southeast Asia and officially reported only from Singapore and Thailand [22, 24]. This finding is in contrast to data from North America and Europe where bla KPC is the most common β-lactamase gene reported among CRE isolates [6, 22, 24]. In addition, non-carbapenamase mechanism such as outer member protein changes (Omp gene mutation) and AmpC β-lactamase hyperproduction are common mechanisms of resistance in CRE isolates [3, 6, 25].
The majority of epidemiology and molecular studies of MDRGN in Thailand were performed on isolates from hospitalized patients [1, 5, 10, 26]. Recently, a cross sectional study from an academic tertiary care hospital in Thailand between February and May 2012 revealed a high prevalence of MDRGN (48.8 %). The percentage of MDRGN was 37.8 % for ESBL-producers, 39.3 % for CRPA, and 88.7 % for CRAB . Infections caused by MDRGN were associated with admission to medical wards, were of respiratory tract origin and hospital onset of infection. Using multivariate analysis, the only significant risk factor of MDRGN infection was previous antibiotic use within 1 year (adjusted odds ratio 6.818, 95 % CI = 1.337–34.770) . ESBLs of the bla CTX-M type are highly endemic in Thailand, especially among hospital-associated isolates [10, 26]. Kiratisin et al. , performed a molecular study on 362 isolates of ESBL-producing E. coli (n = 235) and ESBL-producing K. pneumoniae (n = 127) collected from patients with hospital-associated infection at two major university hospitals in Thailand from December 2004 to May 2005. A total of 87.3 % of isolates carried several bla genes. The prevalence of bla CTX-M was 99.6 % for ESBL-producing E. coli (CTX-M-14, -15, -27, -40, and -55) and 99.2 % for ESBL-producing K. pneumoniae (CTX-M-3, -14, -15, -27, and -55). Up to 77.0 and 71.7 % of ESBL-producing E. coli and ESBL-producing K. pneumoniae, respectively, carried bla TEM-1. ESBL-producing K. pneumoniae carried bla SHV at 87.4 % (SHV-1, -2a, -11, -12, -27, -71, and -75) but only at 3.8 % for ESBL-producing E. coli (SHV-11 and -12). The bla VEB-1 and bla OXA-10 were also found in both ESBL-producing E. coli (8.5 and 8.1 %, respectively) and ESBL-producing K. pneumoniae (10.2 and 11.8 %, respectively). None of the isolates were positive for bla PER and bla GES. Pulsed-field gel electrophoresis (PFGE) analysis demonstrated that there was no major clonal relationship among these ESBL isolates.
There are limited data on clinical and molecular epidemiology of community-onset (CO) ESBLs in Thailand. Apisarnthanarak et al. , performed a case–control study to evaluate risk factors for CO-ESBL-producing E coli infections (n = 46). Controls (n = 138) were patients without infections. Patients with prior ESBL colonization and recent antibiotic exposures, especially to third-generation cephalosporins and fluoroquinolones, were at risk for CO-ESBL-producing E coli infection. The plasmid carrying the bla CTX-M-15 gene was identified in 52 %. In addition, evidence of a high prevalence of ESBL-producing E. coli isolates recovered from healthy individuals and foods along the food production chain from farms to consumers, and in the environment has been documented in selected areas in Thailand. Among 544 healthy adult food factory workers, 906 bacterial isolates were recovered from rectal swab screening cultures and 75.5 % were positive for ESBL-producing E. coli. Moreover, 77.3 % of E. coli isolates collected from 30 healthy animal farm workers were ESBLs .
A. baumannii infections represent a key healthcare issue in Thailand. Data from the National Antimicrobial Resistance Surveillance Thailand (NARST) detected a dramatic increase in CRAB from 2.1 % in 2000 to 46.7 % in 2005 . Prevalence rates of colonization and infections of CRAB were reported to be up to 80 % in several hospitals in Thailand [30, 31]. Infection-related mortality could be as high as 63.0 % in the patients with A. baumannii bacteremia . In addition, several studies from tertiary care and academic hospitals in Thailand have reported a high rate and clonal infection from CRAB throughout the country [10, 32–35]. CRAB occurs mainly as a result of the bla OXA gene, and MBL gene acquisition [12, 36]. The bla OXA-23 is a major resistance determinant among CRAB isolates in Thailand and has been reported related to global clone 2 [12, 36–38].
The prevalence of MDR-P. aeruginosa clinical isolates was constant among 28 hospitals participating in the NARST program in Thailand from 2000 to 2005. The most common sites of isolation included sputum, pus, and urine. The prevalence of MDR-P. aeruginosa ranged from 20 % to 30 % of the isolates . Khuntayaporn et al.  performed susceptibility tests on 261 clinical isolates of MDR-P. aeruginosa (collected during 2007-2009) from eight tertiary hospitals across Thailand. Approximately 71.7 % were found to be MDR-P. aeruginosa. The results showed that the meropenem resistance rate was the highest reaching over 50 % in every hospital. Additionally, the type of hospital was a major factor affecting the resistance rate, as demonstrated by significantly higher rates of CRO among university than regional hospitals. CRPA clinical isolates in Thailand possess multifactorial resistance mechanisms [14, 40]. The decreased expression of OprD mRNA was the most common mechanism (93.7 %). This mechanism was associated with the presence of OprD mutations causing frameshift or translational stop and the reduction of antibiotic transportation in to the CRPA cell. MBL production was identified in 24 isolates (18.5 %) and weakly positive in 12 isolates (9.2 %) including bla IMP-1, bla IMP-14 and bla VIM-2. AmpC β-lactamase hyperproduction had the lowest prevalence rate (4 %) . This study indicates that the loss of OprD porin protein was the most common mechanism for imipenem resistance in P. aeruginosa clinical isolates (98 %)  which is consistent with another study .
There are few data on CRE prevalence in Thailand. However, Rimrang et al. , reported the emergence of NDM-1- and IMP-14a-producing Enterobacteriaceae in Thailand. A total of 4818 Enterobacteriaceae clinical isolates, collected between October 2010 and August 2011, were screened for the presence of carbapenemases. The study revealed 2 other isolates each of Escherichia coli, Klebsiella pneumoniae and Citrobacter freundii carried bla NDM-1 and 2 other isolates of K. pneumoniae carried bla IMP-14a. The DNA fingerprints revealed that all isolates were different strains except for clonal strains of C. freundii. All MBL producers were susceptible to colistin and tigecycline. Interestingly, 6 NDM-producing isolates were recovered from the urine of 3 patients, who had no history of travel outside Thailand. Netikul et al. , reported a novel KPC-13-producing CRE in Thailand. In addition, Kiratisin et al. , investigated the genetic characteristics of plasmid-mediated β-lactamase among non-Escherichia, non-Klebsiella Enterobacteriaceae that were non-susceptible to at least a broad-spectrum cephalosporin. From 598 isolates, 143 isolates (23.9 %) were resistant to a broad-spectrum cephalosporin, amongst which 142 (99.3 %) and 99 (69.2 %) isolates carried ESBL and AmpC β-lactamase genes, respectively. The bla KPC was not detected in isolates with reduced susceptibility to carbapenems.
The largest gram-negative resistance problem in Singapore hospitals is ESBL-producing Enterobacteriaceae particularly Klebsiella spp. and E. coli [1, 5, 6]. ESBL-producing Enterobacteriaceae were first reported in Singapore in the late 1990s and increased rapidly up to 35 % - 40 % over time. Similar to observed trends in other countries, TEM and SHV type ESBLs have spread to Singapore. These are being replaced by the newer CTX-M type ESBLs [1, 6]. CTX-M type ESBLs are currently a major resistance contributor, especially in nosocomial infections. K. pneumoniae isolates were found to be carrying genes for CTX-M-9 type and CTX-M-1 type ESBLs, and E. coli possess a CTX-M-2 type ESBL. Recently, community associated infections have also been reported and associated with CTX-M type ESBLs . Finally, some CTX-M ESBLs may also be associated with carbapenem resistance in combination with porin loss or efflux [6, 42]. Nevertheless, a recent study concluded that the worldwide spread of the gene for the bla CTX-M-15 is due to epidemic E. coli clones belonging to Achtman’s MLST 131 and ST405 .
In Singapore, carbapenem resistance is more common in Acinetobacter spp. and P. aeruginosa than in Enterobacteriaceae. However, there are several reports of new CRE genes that have recently been described in clinical isolates [6, 17, 44]. The discovery of these new genes is likely related to updated national surveillance data on CRO and more molecular characterization studies performed in Singapore compared to other countries in Southeast Asia. In addition, Singapore is a center of communication and commercial trading and travelling in this region. These factors might be also contributed to the spreading of CROs from travellers .
CRAB have emerged as important pathogens in Singapore since 1990. The prevalence of CRAB has been increasing over the time . Tan et al.  found 98 isolates of CRAB (70.5 %) from a total of 171 Acinetobacter spp. isolates (139 A. baumannii isolates) collected from 6 hospitals in Singapore during 2006-2007. The rate of carbapenem resistance in A. baumannii (70.5 %) was higher than in other Acinetobacter spp. (25.0 %) . The bla OXA-23 genes were detected in most of the CRAB isolated (91 %) in a Singapore hospital, while bla IMP-4 and bla OXA-58 genes were also detected in a few isolates [6, 45].
CRPA has emerged in Singapore during the same time as CRAB. Tan et al.  reported that 11.2 % of 188 isolates of P. aeruginosa collected during 2006–2007 were resistant to meropenem. Nevertheless, like the situation in other countries, the resistance in CRPA is related to multifactorial mechanisms. Acquired MBL genes represented 1.7 % of all P. aeruginosa isolates collected at Singapore General Hospital during 2001. The common MBLs in CRPA are bla IMP-1, bla IMP-7, and bla VIM-6 which also have been previously reported in Japan, Canada, and Malaysia .
Although mechanisms of resistance in CRE seems to be largely due to non-carbapenamase mechanisms, the emergence of CRE isolates that carry transferable carbapenamase genes have been reported from hospital and community settings in Singapore. MBLs, especially NDM-1, are a major mechanism of resistance, [6, 17, 22, 44, 46, 47]. Koh et al. , reported isolates of K. pneumoniae, E. coli, Enterobacter cloacae and Citrobacter spp. carried a variety of carbapenemase genes including bla IMP-1, bla IMP-4, bla NDM-1, bla NDM-7, bla OXA-48, bla OXA-181 and bla KPC-2. Apart from K. pneumoniae with bla OXA-181, and some K. pneumoniae with bla NDM-1, the other isolates were not clonal using PFGE analysis. Teo et al.  molecularly characterized 12 NDM-1 producing clinical Enterobacteriaceae (K. pneumoniae, E. coli, E. cloacae) isolates from 4 general hospitals in Singapore. Interestingly, none of the patients had a travel history to countries where NDM-1 has been reported. None of the isolates in the Teo study were clonally related using PFGE analysis . Enterobacteriaceae carrying bla KPC are not common in Singapore. The first KPC-producing K. pneumoniae isolate was reported from a study in 2011. This isolate carried bla KPC-2 and was identified as Pasteur’s MLST ST 11 .
The Study for Monitoring Antimicrobial Resistance Trends (SMART 2009–2011) about antimicrobial susceptibility and ESBL rates in aerobic gram-negative bacteria causing intra-abdominal infections in Vietnam, reported high ertapenem MIC90 values for A. baumannii, and P. aeruginosa (>4 μg/mL) . In addition, among the species collected, E. coli (48.1 % ESBL-positive) and K. pneumoniae (39.5 % ESBL-positive) represented the majority (46.4 %) of the isolates submitted for this study. Ertapenem MIC90 values were lowest for these 2 species at 0.12 and 0.25 μg/mL and remained unchanged for ESBL-positive isolates. Imipenem MIC90 values were also the same for all isolates and ESBL-positive strains at 0.25 and 0.5 μg/mL, respectively . Van et al.  performed antimicrobial susceptibility testing and molecular characterization on 66 A. baumannii complex clinical isolates recovered during 2009 at the National Hospital of Tropical Diseases (NHTD), a referral hospital in Hanoi, Vietnam. Most isolates were collected came from lower respiratory tract specimens from ICU patients. More than 90 % of the isolates were CRAB. Moreover, 25.4 % were resistant to all tested β-lactams, quinolones and aminoglycosides. All isolates remained susceptible to colistin. Unlike CRAB, there is limited data on CRPA prevalence in Vietnam. A novel bla IMP-51 has been reported . In Vietnam, NDM-1-producing E. coli and K. pneumoniae have emerged since 2010. Both organisms were recovered from two patients admitted to a surgical hospital. These patients had no history of travel outside Vietnam . In addition, Trung et al.  reported that A. baumannii clinical isolates carried the ESBL gene (PER-1) and genes from the bla OXA families (OXA-23, OXA-24 and OXA-58). Interestingly, one A. baumannii that carried bla NDM-1 was recovered from a suspected surgical wound infection using a novel in-house multiplex PCR assay.
In 2009, Lim et al. , performed a molecular characterization on 47 E. coli isolates from various public hospitals in Malaysia. All isolates were susceptible to imipenem whereas 36 (76.6 %) were MDR E. coli (resistant to 2 or more classes of antibiotics). The majority of ESBL-producing E. coli (87.5 %) harbored the bla TEM gene. Other ESBL-encoding genes detected were bla OXA, bla SHV, and bla CTX-M. Integron-encoded integrases were detected in 55.3 % of isolates. In addition, another study from the same leading author performed molecular characterization on 51 strains of K. pneumoniae isolated from the same hospitals in Malaysia. The majority of the strains (98 %) were susceptible to imipenem whereas 27 (52.9 %) were MDR K. pneumoniae. Forty-six of the K. pneumoniae strains harbored bla SHV, 19 harbored bla CTX-M, 5 harbored bla OXA-1 and 4 harbored bla TEM-1 .
Among a total of 54 A. baumannii isolates from the main tertiary hospital in Terengganu, Malaysia, 39 (72.2 %) were CRAB, whereas 14 (25.9 %) were categorized as extensively drug resistant (XDR) with additional resistance to polymyxin B . CRPA prevalence in Malaysia was reported as 21 % . Khosravi et al.  performed molecular characterization on 90 isolates of imipenem-resistant P. aeruginosa clinical isolates collected during 2005 to 2008 from the University of Malaysia Medical Center. A multiplex PCR assay detected 32 isolates with positive MBL genes including; bla IMP-7 (12 isolates), bla IMP-4 (2 isolates), bla VIM-2 (17 isolates), and bla VIM-11 (1 isolate). For CRE prevalence in Malaysia, a total of 321 K. pneumoniae isolates collected during April 2010-June 2012 from academic hospitals were characterized. Thirteen isolates (4.0 %) were CRKP and the majority of them were resistant to all tested antibiotics except colistin and tigecycline. Among seven different carbapenemase genes studied (bla KPC, bla IMP, bla SME, bla NDM, bla IMI, bla VIM, and bla OXA), only bla IMP4 (1.87 %) and bla NDM1 (2.18 %) were detected in this study . In addition, another study also confirmed imipenem-resistance in K. pneumoniae in Malaysia due to loss of OmpK36 (outer membrane protein) coupled with AmpC β-lactamase hyperproduction .
There are limited data on prevalence and epidemiology of MDRGN in other countries in Southeast Asia. Indonesia has rates of ESBLs greater than the overall APAC average and for most nations in Western Europe and the United States [1, 5]. In 2011, another study confirmed a high prevalence of CRO in ICU-Cipto Mangunkusumo Hospital in Indonesia. The prevalence of CRE, CRPA and CRAB are 27.6, 21.9, and 50.5 %, respectively. CRPA harboring the bla IMP-1 gene (5 %) were isolated from sputum specimens. Moreover, bla NDM-1 was detected in one K. pneumoniae isolated from sputum . In the Philippines, an E. coli isolate carrying bla IMP-26 has been reported . Antibiotic resistance has been little studied in Laos, where some antibiotics are available without restriction, but others such as carbapenems are not available. Stoesser et al.  reported 92 children (23 %) were colonized with ESBL-producing E. coli carrying bla CTX-M and K. pneumoniae carrying bla SHV or bla CTX-M, which were frequently resistant to multiple antibiotic classes. Using multivariate random-effects model, ESBL colonization was associated with prior antibiotic use within 3 months. Additional whole genome sequencing studies suggested the transmission of ESBLs in both childcare facilities and community settings. Tojo et al. , reported a case of CRAB isolates obtained from a returned traveler from Brunei. This isolate was a second case of A. baumannii harboring bla OxA-23 reported from Japan. There was no publication on MDRGN reported from Myanmar and Cambodia.
This review has some limitations. Epidemiology and prevalence of MDRGN bacteria is a dynamic issue worldwide and especially in Southeast Asia. However, a systematic review could not be performed due to limitations of available data and the difficulty in standardizing all data. The lack of international collaboration on antimicrobial surveillance studies might have an effect on the accuracy of the actual prevalence of MDRGN bacteria in this region. Molecular studies on MDRGN bacteria are not routinely performed in microbiology laboratories in several countries due to limited resources. Lastly, the formal languages in this region are diverse but we only reviewed available English literature as is commonly used for scientific publications.
In summary, MDRGNs are a major contributor of antimicrobial-resistant bacteria in Southeast Asia. The high prevalence of ESBLs has been a major problem since 2005 and is possibly related to the development of carbapenem resistant organisms in this region due to the overuse of carbapenem therapy to treat those infections. Prevalence of CROs in this region, including CRAB, CRPA and CREs, is rising. The high prevalence of MDRGNs in the hospital and community have precipitated development of CROs. Limited infection control measures, lack of antimicrobial control, such as the presence of active antimicrobial stewardship teams in the hospital, and outpatient antibiotic restrictions, and travel throughout this region have likely contributed to the increase in MDRGN prevalence. Thus, improving infection control practices and laboratory detection, along with judicious use of antimicrobial agents, and national surveillance could impact MDRGNs spread in this region.
These guidelines were prepared and approved by the Asia Pacific Society of Infection Control (APSIC) and do not necessarily reflect the opinions of Antimicrobial Resistance and Infection Control or its Editors.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Mendes RE, Mendoza M, Banga Singh KK, Castanheira M, Bell JM, Turnidge JD, Lin SS, Jones RN. Regional resistance surveillance program results for 12 Asia-Pacific nations (2011). Antimicrob Agents Chemother. 2013;57(11):5721–6.View ArticlePubMedPubMed CentralGoogle Scholar
- Rice LB. Mechanisms of resistance and clinical relevance of resistance to beta-lactams, glycopeptides, and fluoroquinolones. Mayo Clin Proc. 2012;87(2):198–208.View ArticlePubMedPubMed CentralGoogle Scholar
- Tang SS, Apisarnthanarak A, Hsu LY. Mechanisms of β-lactam antimicrobial resistance and epidemiology of major community- and healthcare-associated multidrug-resistant bacteria. Adv Drug Deliv. 2014;78:3–13.View ArticleGoogle Scholar
- Christiansen KJ, Ip M, Ker HB, Mendoza M, Hsu L, Kiratisin P, et al. In vitro activity of doripenem and other carbapenems against contemporary Gram-negative pathogens isolated from hospitalised patients in the Asia-Pacific region: results of the COMPACT Asia-Pacific Study. Int J Antimicrob Agents. 2010;36(6):501–6.Google Scholar
- Kiratisin P, Chongthaleong A, Tan TY, Lagamayo E, Roberts S, Garcia J, Davies T. Comparative in vitro activity of carbapenems against major Gram-negative pathogens: results of Asia-Pacific surveillance from the COMPACT II study. Int J Antimicrob Agents. 2012;39(4):311–6.View ArticlePubMedGoogle Scholar
- Koh TH. Gram-negative resistance in Singapore: a historical perspective. Ann Acad Med Singapore. 2008;37:847–54.PubMedGoogle Scholar
- Stoesser N, Xayaheuang S, Vongsouvath M, Phommasone K, Elliott I, Del Ojo EC, Crook DW, Newton PN, Buisson Y, Lee SJ, Dance DA. Colonization with Enterobacteriaceae producing ESBLs in children attending pre-school childcare facilities in the Lao People’s Democratic Republic. J Antimicrob Chemother. 2015;70(6):1893–7.PubMedPubMed CentralGoogle Scholar
- Tojo M, Mawatari M, Hayakawa K, Nagamatsu M, Shimada K, Mezaki K, Sugiki Y, Kuroda E, Takeshita N, Kutsuna S, Fujiya Y, Miyoshi-Akiyama T, Kirikae T, Ohmagari N. Multidrug-resistant Acinetobactor baumannii isolated from a traveler returned from Brunei. J Infect Chemother. 2015;21(3):212–4.View ArticlePubMedGoogle Scholar
- Kiratisin P, Apisarnthanarak A, Laesripa C, Saifon P. Molecular characterization and epidemiology of extended-spectrum-beta-lactamase-producing Escherichia coli and Klebsiella pneumoniae isolates causing health care-associated infection in Thailand, where the CTX-M family is endemic. Antimicrob Agents Chemother. 2008;52(8):2818–24.View ArticlePubMedPubMed CentralGoogle Scholar
- Chaisathaphol T, Chayakulkeeree M. Epidemiology of infections caused by multidrug-resistant gram-negative bacteria in adult hospitalized patients at Siriraj Hospital. J Med Assoc Thai. 2014;97 Suppl 3:S35–45.PubMedGoogle Scholar
- Kim DH, Choi JY, Kim HW, Kim SH, Chung DR, Peck KR, Thamlikitkul V, So TM, Yasin RM, Hsueh PR, Carlos CC, Hsu LY, Buntaran L, Lalitha MK, Song JH, Ko KS. Spread of carbapenem-resistant Acinetobacter baumannii global clone 2 in Asia and AbaR-type resistance islands. Antimicrob Agents Chemother. 2013;57(11):5239–46.Google Scholar
- Teo J, Lim TP, Hsu LY, Tan TY, Sasikala S, Hon PY, Kwa AL, Apisarnthanarak A. Extensively drug-resistant Acinetobacter baumannii in a Thai hospital: a molecular epidemiologic analysis and identification of bactericidal Polymyxin B-based combinations. Antimicrob Resist Infect Control. 2015;4:2.Google Scholar
- Khuntayaporn P, Montakantikul P, Mootsikapun P, Thamlikitkul V, Chomnawang MT. Prevalence and genotypic relatedness of carbapenem resistance among multidrug-resistant P. aeruginosa in tertiary hospitals across Thailand. Ann Clin Microbiol Antimicrob. 2012;13(11):25.View ArticleGoogle Scholar
- Khuntayaporn P, Montakantikul P, Santanirand P, Kiratisin P, Chomnawang MT. Molecular investigation of carbapenem resistance among multidrug-resistant Pseudomonas aeruginosa isolated clinically in Thailand. Microbiol Immunol. 2013;57(3):170–88.View ArticlePubMedGoogle Scholar
- Khosravi Y, Tee Tay S, Vadivelu J. Metallo-beta-lactamase-producing imipenem-resistant Pseudomonas aeruginosa clinical isolates in a university teaching hospital in Malaysia: detection of IMP-7 and first identification of IMP-4, VIM-2, and VIM-11. Diagn Microbiol Infect Dis. 2010;67(3):294–6.View ArticlePubMedGoogle Scholar
- Rimrang B, Chanawong A, Lulitanond A, Wilailuckana C, Charoensri N, Sribenjalux P, Phumsrikaew W, Wonglakorn L, Kerdsin A, Chetchotisakd P. Emergence of NDM-1- and IMP-14a-producing Enterobacteriaceae in Thailand. J Antimicrob Chemother. 2012;67(11):2626–30.View ArticlePubMedGoogle Scholar
- Teo J, Ngan G, Balm M, Jureen R, Krishnan P, Lin R. Molecular characterization of NDM-1 producing Enterobacteriaceae isolates in Singapore hospitals. Western Pac Surveill Response J. 2012;3(1):19–24.View ArticlePubMedPubMed CentralGoogle Scholar
- Hamzan NI, Yean CY, Rahman RA, Hasan H, Rahman ZA. Detection of bla IMP-4 and bla NDM-1 harboring Klebsiella pneumoniae isolates in a university hospital in Malaysia. Emerg Health Threats J. 2015;8:26011.PubMedGoogle Scholar
- Trung NT, Hien TT, Huyen TT, Quyen DT, Binh MT, Hoan PQ, Meyer CG, Velavan TP, Song le H. Simple multiplex PCR assays to detect common pathogens and associated genes encoding for acquired extended spectrum betalactamases (ESBL) or carbapenemases from surgical site specimens in Vietnam. Ann Clin Microbiol Antimicrob. 2015;14:23.Google Scholar
- Hoang TH, Wertheim H, Minh NB, Duong TN, Anh DD, Phuong TT, Son TH, Izumiya H, Ohnishi M, Shibayama K, Hien NT. Carbapenem-resistant Escherichia coli and Klebsiella pneumoniae strains containing New Delhi metallo-beta-lactamase isolated from two patients in Vietnam. J Clin Microbiol. 2013;51(1):373–4.View ArticlePubMedPubMed CentralGoogle Scholar
- Sheng WH, Badal RE, Hsueh PR, SMART Program. Distribution of extended-spectrum β-lactamases, AmpC β-lactamases, and carbapenemases among Enterobacteriaceae isolates causing intra-abdominal infections in the Asia-Pacific region: results of the study for Monitoring Antimicrobial Resistance Trends (SMART). Antimicrob Agents Chemother. 2013;57(7):2981–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Koh TH, Cao D, Shan QY, Bacon A, Hsu LY, Ooi EE. Acquired carbapenemases in Enterobacteriaceae in Singapore, 1996-2012. Pathology. 2013;45(6):600–3.View ArticlePubMedGoogle Scholar
- Karuniawati A, Saharman YR, Lestari DC. Detection of carbapenemase encoding genes in Enterobacteriaceae, Pseudomonas aeruginosa, and Acinetobacter baumannii isolated from patients at Intensive Care Unit Cipto Mangunkusumo Hospital in 2011. Acta Med Indones. 2013;45(2):101–6.PubMedGoogle Scholar
- Netikul T, Sidjabat H, Paterson D2, Kiratisin P. Emergence of novel bla (KPC-13) among carbapenem-resistant Enterobacteriaceae in Thailand. Int J Antimicrob Agents. 2014;44(6):568–9.View ArticlePubMedGoogle Scholar
- Palasubramaniam S, Karunakaran R, Gin GG, Muniandy S, Parasakthi N. Imipenem-resistance in Klebsiella pneumoniae in Malaysia due to loss of OmpK36 outer membrane protein coupled with AmpC hyperproduction. Int J Infect Dis. 2007;11(5):472–4.View ArticlePubMedGoogle Scholar
- Apisarnthanarak A1, Kiratisin P, Mundy LM. Clinical and molecular epidemiology of healthcare-associated infections due to extended-spectrum beta-lactamase (ESBL)-producing strains of Escherichia coli and Klebsiella pneumoniae that harbor multiple ESBL genes. Infect Control Hosp Epidemiol. 2008;29(11):1026–34.View ArticlePubMedGoogle Scholar
- Apisarnthanarak A, Kiratisin P, Saifon P, Kitphati R, Dejsirilert S, Mundy LM. Clinical and molecular epidemiology of community-onset, extended-spectrum beta-lactamase-producing Escherichia coli infections in Thailand: a case-case-control study. Am J Infect Control. 2007;35(9):606–12.View ArticlePubMedGoogle Scholar
- Boonyasiri A, Tangkoskul T, Seenama C, Saiyarin J, Tiengrim S, Thamlikitkul V. Prevalence of antibiotic resistant bacteria in healthy adults, foods, food animals, and the environment in selected areas in Thailand. Pathog Glob Health. 2014;108(5):235–45.View ArticlePubMedPubMed CentralGoogle Scholar
- Apisarnthanarak A, Buppunharun W, Tiengrim S, Sawanpanyalert P, Aswapokee N. An overview of antimicrobial susceptibility patterns for gram-negative bacteria from the National Antimicrobial Resistance Surveillance Thailand (NARST) program from 2000 to 2005. J Med Assoc Thai. 2009;92 Suppl 4:S91–4.PubMedGoogle Scholar
- Dejsirilert S, Tiengrim S, Sawanpanyalert P, Aswapokee N, Malathum K. Antimicrobial resistance of Acinetobacter baumannii: six years of National Antimicrobial Resistance Surveillance Thailand (NARST) surveillance. J Med Assoc Thai. 2009;92 Suppl 4:S34–45.PubMedGoogle Scholar
- Rattanaumpawan P, Ussavasodhi P, Kiratisin P, Aswapokee N. Epidemiology of bacteremia caused by uncommon non-fermentative gram-negative bacteria. BMC Infect Dis. 2009;13:167.View ArticleGoogle Scholar
- Inchai J, Liwsrisakun C, Theerakittikul T, Chaiwarith R, Khositsakulchai W, Pothirat C. Risk factors of multidrug-resistant, extensively drug-resistant and pandrug-resistant Acinetobacter baumannii ventilator-associated pneumonia in a Medical Intensive Care Unit of University Hospital in Thailand. J Infect Chemother. 2015;21(8):570–4.View ArticlePubMedGoogle Scholar
- Phumisantiphong U, Diraphat P, Utrarachkij F, Uaratanawong S, Siripanichgon K. Clonal spread of carbapenem-resistant Acinetobacter baumannii in the patients and their environment at BMA Medical College and Vajira Hospital. J Med Assoc Thai. 2009;92 Suppl 7:S173–80.PubMedGoogle Scholar
- Werarak P, Kiratisin P, Thamlikitkul V. Hospital-acquired pneumonia and ventilator-associated pneumonia in adults at Siriraj Hospital: etiology, clinical outcomes, and impact of antimicrobial resistance. J Med Assoc Thai. 2010;93 Suppl 1:S126–38.PubMedGoogle Scholar
- Santimaleeworagun W, Thathong A, Samret W, Preechachuawong P, Sae-lim W, Jitwasinkul T. Identification and characterization of carbapenemase genes in clinical isolates of carbapenem-resistant Acinetobacter Baumannii from general hospital in Thailand. Southeast Asian J Trop Med Public Health. 2014;45(4):874–80.Google Scholar
- Kamolvit W, Sidjabat HE, Paterson DL. Molecular epidemiology and mechanisms of carbapenem resistance of Acinetobacter spp. in Asia and Oceania. Microb Drug Resist. 2015;21(4):424–34.View ArticlePubMedGoogle Scholar
- Niumsup PR, Boonkerd N, Tansawai U, Tiloklurs M. Carbapenem-resistant Acinetobacter baumannii producing OXA-23 in Thailand. Jpn J Infect Dis. 2009;62(2):152–4.PubMedGoogle Scholar
- Thapa B, Tribuddharat C, Srifuengfung S, Dhiraputra C. High prevalence of bla (OXA)-23 in oligoclonal carbapenem-resistant Acinetobacter baumannii from Siriraj Hospital, Mahidol University, Bangkok, Thailand. Southeast Asian J Trop Med Public Health. 2010;41(3):625–35.PubMedGoogle Scholar
- Dejsirilert S, Suankratay C, Trakulsomboon S, Thongmali O, Sawanpanyalert P, Aswapokee N, Tantisiriwat W. National Antimicrobial Resistance Surveillance, Thailand (NARST) data among clinical isolates of Pseudomonas aeruginosa in Thailand from 2000 to 2005. J Med Assoc Thai. 2009;92 Suppl 4:S68–75.PubMedGoogle Scholar
- Naenna P, Noisumdaeng P, Pongpech P, Tribuddharat C. Detection of outer membrane porin protein, an imipenem influx channel, in Pseudomonas aeruginosa clinical isolates. Southeast Asian J Trop Med Public Health. 2010;41(3):614–24.PubMedGoogle Scholar
- Kiratisin P, Henprasert A. Genotypic analysis of plasmid-mediated beta-lactamases amongst Enterobacteriaceae other than Escherichia spp. and Klebsiella spp. that are non-susceptible to a broad-spectrum cephalosporin. Int J Antimicrob Agents. 2010;36(4):343–7.View ArticlePubMedGoogle Scholar
- Woodford N, Dallow JW, Hill RL, Palepou MF, Pike R, Ward ME, Warner M, Livermore DM. Ertapenem resistance among Klebsiella and Enterobacter submitted in the UK to a reference laboratory. Int J Antimicrob Agents. 2007;29(4):456–9.View ArticlePubMedGoogle Scholar
- Nicolas-Chanoine MH, Bertrand X, Madec JY. Escherichia coli ST131, an intriguing clonal group. Clin Microbiol Rev. 2014;27(3):543-74.Google Scholar
- Koh TH, Cao D, Tee NW, Teo JW. Escherichia coli with bla (IMP-8) in Singapore. Antimicrob Agents Chemother. 2014;58(1):617.View ArticlePubMedPubMed CentralGoogle Scholar
- Tan TY, Hsu LY, Koh TH, Ng LS, Tee NW, Krishnan P, et al. Antibiotic resistance in gram-negative bacilli: a Singapore perspective. Ann Acad Med Singapore. 2008;37:819–25.Google Scholar
- Koh TH, Sng LH, Wang GC, Hsu LY, Zhao Y. IMP-4 and OXA beta-lactamases in Acinetobacter baumannii from Singapore. J Antimicrob Chemother. 2007;59(4):627–32.View ArticlePubMedGoogle Scholar
- Venkatachalam I, Teo J, Balm MN, Fisher DA, Jureen R, Lin RT. Klebsiella pneumoniae Carbapenemase-producing enterobacteria in hospital, Singapore. Emerg Infect Dis. 2012;18(8):1381–3.View ArticlePubMedPubMed CentralGoogle Scholar
- Biedenbach DJ, Bouchillon SK, Hoban DJ, Hackel M, Phuong DM, Nga TT, Phuong NT, Phuong TT, Badal RE. Antimicrobial susceptibility and extended-spectrum beta-lactamase rates in aerobic gram-negative bacteria causing intra-abdominal infections in Vietnam: report from the Study for Monitoring Antimicrobial Resistance Trends (SMART 2009-2011). Diagn Microbiol Infect Dis. 2014;79(4):463–7.View ArticlePubMedGoogle Scholar
- Van TD, Dinh QD, Vu PD, Nguyen TV, Pham CV, Dao TT, Phung CD, Hoang HT, Tang NT, Do NT, Nguyen KV, Wertheim H. Antibiotic susceptibility and molecular epidemiology of Acinetobacter calcoaceticus-baumannii complex strains isolated from a referral hospital in northern Vietnam. J Glob Antimicrob Resist. 2014;2(4):318–21.View ArticlePubMedPubMed CentralGoogle Scholar
- Tada T, Nhung PH, Miyoshi-Akiyama T, Shimada K, Phuong DM, Anh NQ, Ohmagari N, Kirikae T. IMP-51, a novel IMP-type metallo-β-lactamase with increased doripenem and meropenem hydrolyzing activities, in a carbapenem-resistant Pseudomonas aeruginosa clinical isolate. Antimicrob Agents Chemother. 2015;59(11):7090–3.View ArticlePubMedPubMed CentralGoogle Scholar
- Lim KT, Yasin R, Yeo CC, Puthucheary S, Thong KL. Characterization of multidrug resistant ESBL-producing Escherichia coli isolates from hospitals in Malaysia. J Biomed Biotechnol 2009, 165637Google Scholar
- Lim KT, Yeo CC, Yasin RM, Balan G, Thong KL. Characterization of multidrug-resistant and extended-spectrum beta-lactamase-producing Klebsiella pneumoniae strains from Malaysian hospitals. J Med Microbiol. 2009;58(11):1463–9.View ArticlePubMedGoogle Scholar
- Lean SS, Suhaili Z, Ismail S, Rahman NI, Othman N, Abdullah FH, Jusoh Z, Yeo CC, Thong KL. Prevalence and Genetic Characterization of Carbapenem- and Polymyxin-Resistant Acinetobacter baumannii Isolated from a Tertiary Hospital in Terengganu, Malaysia. Microbiol 2014, 953417Google Scholar
- Lim KT, Yasin RM, Yeo CC, Puthucheary SD, Balan G, Maning N, Wahab ZA, Ismail N, Tan EA, Mustaffa A, Thong KL. Genetic fingerprinting and antimicrobial susceptibility profiles of Pseudomonas aeruginosa hospital isolates in Malaysia. J Microbiol Immunol Infect. 2009;42(3):197–209.Google Scholar