Klebsiella pneumoniae: an increasing threat to public health
This review fills the paucity of information on K. pneumoniae as a nosocomial pathogen by providing pooled data on epidemiological risk factors, resistant trends and profiles and resistant and virulent genes of this organism in Asia.
Exhaustive search was conducted using PubMed, Web of Science, and Google scholar for most studies addressing the prevalence, risk factors, drug resistant-mediated genes and/or virulent factors of K. pneumoniae in Asia. Data extracted for meta-analysis were analyzed using comprehensive meta-analysis version 3. Trends data for the isolation rate and resistance rates were entered into Excel spread sheet and the results were presented in graphs.
The prevalence rate of drug resistance in K. pneumoniae were; amikacin (40.8%) [95% CI 31.9–50.4], aztreonam (73.3%) [95% CI 59.9–83.4], ceftazidime (75.7%) [95% CI 65.4–83.6], ciprofloxacin (59.8%) [95% CI 48.6–70.1], colistin (2.9%) [95% CI 1.8–4.4], cefotaxime (79.2%) [95% CI 68.0–87.2], cefepime (72.6) [95% CI 57.7–83.8] and imipenem (65.6%) [95% CI 30.8–89.0]. TEM (39.5%) [95% CI 15.4–70.1], SHV-11 (41.8%) [95% CI 16.2–72.6] and KPC-2 (14.6%) [95% CI 6.0–31.4] were some of the resistance mediated genes observed in this study. The most virulent factors utilized by K. pneumoniae are; hypermucoviscous phenotype and mucoviscosity-related genes, genes for biosynthesis of lipopolysaccharide, iron uptake and transport genes and finally, adhesive genes.
It can be concluded that, antimicrobial resistant in K. pneumoniae is a clear and present danger in Asia which needs strong surveillance to curb this menace. It is very important for public healthcare departments to monitor and report changes in antimicrobial-resistant isolates.
KeywordsKlebsiella pneumoniae Antibiotic resistance profiles Resistant genes Virulent genes Risk factors Asia
The problem of antibiotic resistance has become an albatross on the neck of clinicians, veterinarians and other infection control agents in their quest to treat and prevent infections caused by microorganisms that were once thought to have been eradicated with antimicrobials. These organisms or superbugs are returning in new forms resistant to almost all clinically important antimicrobials. Unfortunately, the pharmaceutical pipeline merely does not have enough new medicines to maintain pace with drug-resistant bacterial infections . Klebsiella pneumoniae is one of such clinically significant organisms that have acquired much public health concern. Klebsiella pneumoniae is a significant Enterobacteriaceae considered as one of the opportunistic pathogens causing broad spectra of diseases and showing increasingly frequent acquisition of resistance to antibiotics.
According to Shiri et al. , this organism accounts for about one-third of all Gram-negative infections such as urinary tract infections, cystitis, pneumonia, surgical wound infections, endocarditis and septicemia. It also causes necrotizing pneumonia, pyogenic liver abscesses and endogenous endophthalmitis . High mortality rates, extended hospitalization, coupled with high cost are often associated with infections caused by this organism . The drastic rise in the incidence of multidrug-resistant (MDR) and extremely drug-resistant (XDR) pathogens belonging to the Enterobacteriaceae group is a major economic problem as these pathogens are prevalent natural residents of human and animal microbiome. Despites its numerous clinical importance, there is still paucity of information on K. pneumoniae.
This review was therefore designed to determine the antibiotic-resistant profiles of Klebsiella pneumonia as a nosocomial pathogen and focuses on some differences between classical and non-classical subtypes, antimicrobial resistance-mediated genes, some virulent factors of this organism, and some epidemiological risk factors through a systematic review and meta-analysis. This review also looked at some trends in the isolation and resistance rates of K. pneumoniae using China as the target country.
Exhaustive search was conducted using PubMed, Web of Science, and Google scholar for most studies addressing the prevalence and/or the molecular epidemiology of drug resistant strains of K. pneumoniae in some selected countries in Asia. The search filtered articles among the years of 2005 to 2019. The applied keywords included Klebsiella pneumoniae, antibiotic resistance, resistant genes, virulent genes, epidemiological risk factors and Asia.
Inclusion and exclusion criteria
The original published articles on the prevalence of drug resistant strains of K. pneumoniae from hospital-acquired infections in some selected countries in Asia were considered. Before an article will be considered useful to this study, its antibiotic susceptibility testing should use reference standard methods and recommendations by the Clinical and Laboratory Standards Institute (CLSI) for drug susceptibility testing of K. pneumoniae against most commonly used antimicrobial agents. Due to the following reasons, some studies were excluded from this studies; articles not following CLSI recommended drug susceptibility testing methods, case reports, meta analyses or systematic reviews, letters to editor, review articles, non-English, and duplicate publication.
For the meta-analysis, information extracted from each article were authors’ name, the publication time, year of study, number of samples, antimicrobial drug resistant profiles of K. pneumoniae, resistance-mediated genes, and virulent genes.
The comprehensive Meta-analysis software version 3 was used to analyze the data. Because of the heterogeneity among studies, random effects models was used and tested with the Cochrane Q test. For trends in antimicrobial resistance and isolation rates, data were entered into excel spread sheet and graphs were plotted based on the available data.
Details of articles included in the meta-analysis
No. of K.P isolates (N)
Type of K.P strain used (n)
Liu et al.
Tian et al.
Zhao et al.
Meng et al.
Kim et al.
Xu et al.
ESBL-P KP (30)
Guo et al.
Dong et al.
Cha et al.
Alizade et al.
Lu et al.
van Dorp et al.
Shanker et al.
Huang et al.
Abrar et al.
Mitra et al.
Gautam et al.
New Delhi, Chandigarh, Vellore, Puducherry/India
ESBL-KP and Non-ESBL-KP (304)
Mansury et al.
ESBL KP (38)
Heidary et al.
Ma et al.
Overall resistance rate of Klebsiella pneumoniae to various antimicrobials
No. of events/studies
Prevalence of drug resistance, % (CI)
Overall resistant to amikacin
Overall resistant to aztreonam
Overall resistant to ceftazidime
Overall resistant to ciprpfloxacin
Overall resistant to colistin
Overall resistant to cefotaxime
Overall resistant to cefepime
Overall resistant to gentamicin
Overall resistant to imipenem
Overall resistant to levofloxacin
Overall resistant to meropenem
Overall resistant to trimethoprim_sulfamethoxazole
The prevalence of antimicrobial drug resistance among Klebsiella pneumoniae isolates according to individual studies
Liu et al. 
Tian et al. 
Zhao et al. 
Meng et al. 
Kim et al. 
Xu et al. 
Guo et al. 
Dong et al. 
Cha et al. 
Mitra et al. 
Gautam et al. 
Mansury et al. 
Heidary et al. 
Ma et al. 
The prevalence of some resistant-mediated genes among Klebsiella pneumoniae isolates
No. of events/studies
Prevalence of resistant gene
Overall prevalence of TEM genes
Overall prevalence of SHV-11 genes
Overall prevalence of CTX-M-1
Overall prevalence of CTX-M-15 genes
Overall prevalence of KPC-2 genes
Overall prevalence of NDM-1 genes
Some selected virulent factors encoded by different strains of Klebsiella pneumoniae
Hypermucoviscous phenotype and mucoviscosity-related genes
Biosynthesis of lipopolysaccharide
Iron uptake and transport
Klebsiella pneumoniae: the classical and other subtypes
Klebsiella pneumoniae can be broadly classified into two subtypes; classical Klebsiella pneumoniae (cKp) and non-classical Klebsiella pneumoniae (ncKp). The antimicrobial resistance profiles and the virulence profiles of these strains vary with the former tagged as notorious [3, 5]. Notwithstanding, several clones of these ncKp have also been implicated in causing severe and difficult to threat infections due to their continuous mutation and the acquisition of plasmids and transposons which carries resistant and virulent genes. This has led to the emergences of strains such as hypervirulent Klebsiella pneumoniae (hvKp) or hypermucoviscous Klebsiella pneumoniae (HMKP). This strain was first identified in Eastern part of Asia and has since spread worldwide . This subtype is non-resistant to most of the commonly used antimicrobials such as colistin and carbapenems. But the recent reports of carbapenem-resistant hvKp strains which belong to the sequence types 11 (ST11) , ST25 and ST65  poses a major clinical concern.
HvKp strains can cause serious infections in both immunocompetent, diseased and healthy young individuals . This hvKp is known to habour (i) sidephore; predominant of which is aerobactin which is concomitant with hypermucoviscosity, (ii) virulent factors such as; K1, K2, K20 capsular types, rmpA and rmpA2 mucoid-regulator genes . The horizontal transfer of these plasmids and transposons has led to the multidrug resistance (MDR) and the extremely drug resistance (XDR) nature of most of these subtypes. The high prevalence rate of MDR and XDR K. pneumoniae subtypes reflects a multifactorial dissemination processes that include but not limited to: the spread of high risk global multi-resistant genetic lineage ; acquisition of successful multi-resistant plasmids; and acquisition of resistant genes located on successful transposons. Klebsiella is a major source of carbapenem resistance worldwide by the dissemination of its plasmids which is facilitated by high genetic transfer (HGT) to other species. Spread of these extended-spectrum β-lactamase (ESBL) and Carbapenemase-encoding plasmids poses a major threat, as acquisition of these plasmids turn bacteria into MDR and XDR. In China, the most dominant MDR KPC-producing clone is the ST11. Once the blaKPC-2 gene is introduces into a certain location, especially in a hospital setup, under antibiotic selection pressure, further dissemination of this gene may occur which may lead to MDR and XDR strains. Hypermucoviscous K. pneumoniae (HMKP) strain types which are sporadically distributed in Asia and the Middle East are the NDM-producing isolates [12, 13]. Liu et al. , had reported the first outbreak of CR-HMKP strains which harbored blaNDM-1 gene, shared the same pulsotypes (PT) and belong to the same Sequence types (ST).
Epidemiological risk factors associated with K. pneumoniae colonization and infections
It is believed that several factors can cause the colonization of K. pneumoniae in a community as well as in a hospital setting. The cases of K. pneumoniae infections vary from country to country. In a study by Ling et al. , it was reported that, Chinese people had a colonization rate of 66.0% compared to Malay (14.3%), Indian (7.9%) and others nationals (11.8%). This is an indication that infections caused by K. pneumoniae can be locality specific although there can be some form of intercontinental similarities.
Some epidemiological risk factors associated with K. pneumoniae infections may include socio-demographic factors such as gender, age, hospitalization status, source of domestic water (river, rain, well, bottled, piped, boiled), companion animals (cats, dogs, birds), livestock (chicken, ducks, pigs, cow or water buffalo), malnutrition, co-morbidity and the use and misuse of detergents and antiseptics. In Asia, it has been reported that exposure to health care facility and history of previous overseas hospitalization (OR: 33.667; 95% CI 4.539–259.700) is one of the notifiable risk factors associated with K. pneumoniae colonization but this had been disagreed by Ling et al. , who iterated that persons with no history of overseas travel and overseas hospitalization are also at risk of K. pneumoniae colonization and infections, hence, suggesting that K. pneumoniae is a persistent organism in our community setting.
Also, admission to an ICU facility (OR: 11.899; 95% CI 4.986–28.399), antimicrobial exposure; particularly carbapenems and fluoroquinolones [14, 16], hematology patients and patients with immunodeficiency are all high risk factors for K. pneumoniae colonization and infections. Carrier levels in hospitalized patients are significantly higher, with reported rates of 77% in the stool, 19% in the pharynx, and 42% on the hands . The higher rates of colonization are primarily related to the increasing use of antibiotics [3, 17, 18]. The increase in colonization rate of K. pneumoniae as observed in these clinical samples is of epidemiological important because, Klebsiella nosocomial infection was four times higher in stool carriers compared with non-carriers . In a study in Taiwan, antibiotic use (e.g. ampicillin or amoxicillin) within the last 30 days was associated with an increased risk of liver abscess , suggesting that an increasing exposure to antimicrobials and the last period of antimicrobial administration is a major risk factor for K. pneumoniae colonization and infection.
In a study by Saleem et al. , it was reported that some risk factors associated with K. pneumoniae sepsis and mortality in a neonate intensive care units in Pakistan were; extremely low birth weight (p = 0.01, OR 6.1, 95% CI 0.8–44.4), being a male (p = 0.06, OR 9.2, 95% CI 1.3–66.9), severe thrombocytopenia (p = 0.07, OR 3.9, 95% CI 1.2–13.0), and failure to achieve microbiological clearance (p < 0.001, OR 19.6, 95% CI 4.0–98.0). The above listed factors can in combination or singly predispose individuals to K. pneumoniae colonization and infections.
Klebsiella pneumoniae is rapidly becoming known for its resistance properties to most of the last-line antibiotics that are usually used. It is especially problematic in hospitals, where it causes a range of acute infections. The increasing trends in the isolation rate of K. pneumoniae is of much concern. Economically developed areas such as China have a more advanced medical system which may increase the chance of exposure to antibiotics and this will increase the possibility of bacterial resistance. In China, the higher population density may also have increased the isolation rate among the population. In this review, although there is an increasing trend in the isolation rate, their resistance rates were not in tandem as this was evident in the decreasing trends over the years. Although, imipenem and meropenem have shown good activity against Enterobacteriaceae , the situation observed in this review reiterates the public health implications of K. pneumoniae. In Fig. 1, there is a steady increase in resistance of imipenem over the years and this can be as a result of their increasing use among the populace. Generally, the decreasing resistant rate of K. pneumoniae to most of the antimicrobials in China can be attributed to; (i) the enforcement of taking various actions for prevention of bacterial infection such as separating the pathogen carriers and enforcement of hand sanitization of medical professionals by the government through the Nosocomial Infection Control Committee, (ii) the restriction and control of the use of antibiotics by the Chinese Ministry of Hygiene, which has implemented guidelines for the rational use of antibiotics since 2006.
The global emergence and spread of genes of antimicrobial resistance such as ESBL and carbapenemase genes in K. pneumoniae isolates present a significant danger to public health. This is because carbapenems have long been deemed as the last therapeutic resort or option of antibiotics used to treat diseases and infections caused by multidrug-resistant gram-negative bacteria. The rapid global emergence of K. pneumoniae strains, resistant to almost all β-lactams, including carbapenems as seen in this study shows the organism’s ability to react quickly to selective environmental pressure modifications. The extensive use and misuse of carbapenems is one of the attributable reasons that has led to the evolution of plasmid-mediated carbapenemases, i.e. enzymes that hydrolyze all β-lactams including the last-line carbapenems . Different resistance-mediated genes mediate antimicrobial drug resistance in K. pneumoniae. The high rate of resistance to carbapenems (imipenem and meropenem) observed in this study can be partly be attributed to the presence of some carbapenemase resistant-mediated genes such as blaOXA. bla NDM and blaKPC realized in this study. In K. pneumoniae, the blaKPC genes which confers reduced susceptibility or resistance to nearly all β-lactam antibiotics by various enterobacteria are mostly carried on plasmids. The detection of carbapenemases is important from an epidemiological perspective as they are plasmid-mediated and may be transferred horizontally between different bacterial species . Dissemination of resistant determinants have been recognized as a major challenge in the treatment of bacterial infections worldwide . Also, resistance of K. pneumoniae to cephalosporin (ceftazidime, cefepime and cefotaxime) as seen in this study can also be partly be attributed to the KPC gene because the KPC enzyme hydrolyzes extended-spectrum cephalosporins. This can therefore be used to identify KPC-mediated genes that are resistant to these cephalosporins (e.g. ceftazidime, ceftriaxone, and cefotaxime).
Klebsiella pneumoniae resistance to Aminoglycosides (amikacin and gentamicin) as seen in this review may be as a result of modifications in cell permeability due to alterations in AcrAB-TolC and KpnEF efflux pump systems and due to loss of putative porin, KpnO. Also the disruptions in AcrAB-TolC may increase the susceptibility of K. pneumoniae to gentamicin . The 16S rRNA methylases which are encoded on the plasmids  confers resistance to all aminoglycosides. Mutations which confer resistance via target modification can also be a possible attributable reason for the increasing resistance of K. pneumoniae to most aminoglycosides.
The low prevalence of Polymyxin (Colistin) resistance in this review makes a lot of sense because of their restricted use in human medicine dating back between the 1980s and 2000s, due to their recognized toxicity. According to Falagas and Kasiakou , Polymyxin works by disrupting the membrane integrity through displacement of cations (Ca2+/Mg2+) in the outer membrane, by binding to the negatively charged lipopolysaccharides (LPS) which leads to cell lysis. Undoubtedly, the presence of resistance determinants will allow K. pneumoniae strains to survive the barrage of antibiotics used in treatment of hospital infections.
According to a report by Dong et al. , K. pneumoniae utilize an array of virulence factors to colonize and propagate in a host cell. These include at least (a) surface antigen, particularly capsular polysaccharide (CPS, K antigen); (b) siderophores responsible for binding ferric iron secreted by the host’s iron-binding proteins; and (c) adherence variables responsible for binding to host cell surfaces, such as fimbriae type 1 and type 3, and non-fimbrial adherence proteins.
Hypermucoviscous phenotype and mucoviscosity-related genes, genes for biosynthesis of lipopolysaccharide, iron uptake and transport genes and Adhesive genes are all virulent factors that are employed by K. pneumoniae strains in pathogenesis. Iron is a key component for K. pneumoniae’s survival. As free iron is scarce in host plasma, K. Pneumoniae acquires iron predominantly through the secretion of siderophores; molecules with a greater iron affinity than the host transport proteins . Among the siderophores secreted by K. pneumoniae, aerobactin is considers the most important virulent factor [31, 32], as it can cause severe infection by assisting in the transport of the organism from the intestinal tract to various tissues and also the multiplication of these organisms in the tissues.
The rmpA and rmpA2 are Plasmid-carried genes, which contribute to the enhancement of capsular production. Also, the MagA gene is an important gene used by K. pneumoniae strains to demonstrate an extraordinarily high resistance to human serum and phagocytosis. This gene can be used as a molecular marker for quick diagnosis and can also be useful in tracing the roots of emerging infectious diseases caused by K. pneumoniae. According to Fang et al. , the MagA protein could be a good candidate for new drug targets.
It has been shown that fimbriae contribute to diseases of the urinary tract , mediates the development of biofilms and also it is involve in the adherence of the organism to medical devices. Therefore, expression of these genes could improve K. pneumoniae’s adhesive ability to respiratory epithelial cells and also to surfaces of other medical devices such as ventilators, thereby, increasing their ability to cause ventilator-associated diseases. Fimbria, according to Huang et al.  and Stahlhut et al. , may be a major factor for biofilm-associated diseases and host entry abilities of K. pneumoniae.
Although, very positive results were obtained from this meta-analysis, it is worth noting that there were a number of limitations with this meta-analysis. This study did not utilized data from abstracts, posters and conference proceedings but only full paper publications. Because of the limited number of studies included in this meta-analysis, this study did not assess for publication bias because according to Terrin and Schmid  and Thornton and Lee , funnel plots and statistical tests for detection of publication bias are unreliable for limited number of studies.
It can be concluded that antimicrobial resistance in K. pneumoniae is a clear and present danger in Asia which needs strong surveillance to curb this menace. Although low resistance rate to colistin and imipenem were recorded in this review, more cautious efforts should be made to develop new line of antimicrobials as resistance to these drugs are surging. It is very important for public healthcare departments to monitor and report the changes in antimicrobial-resistant isolates. This will guide doctors in prescribing the proper antimicrobials in case of resistance gene evolution. It is essential to design a preparedness plan in order to tackle this public health danger. On the other side, control measures must include a multi-faceted strategy coordinated by the domestic health officials in fields.
CYE, TS, SL and YW contributed equally in the preparation and reviewing of the manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
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