Skip to main content
Download PDF

Comparative in silico characterization of Klebsiella pneumoniae hypervirulent plasmids and their antimicrobial resistance genes

Annals of Clinical Microbiology and Antimicrobials volume 21, Article number: 23 (2022) Cite this article

Abstract

Background

The hypervirulent pathotype of Klebsiella pneumoniae (hvKp) is mainly mediated by large virulent plasmids. It seems that these hypervirulent plasmids (HVPs) are accumulating antimicrobial resistance genes (ARGs) and are turning quickly into drug-resistant hypervirulent hybrids. Therefore, molecular mechanisms involved in this convergence needs to be investigated to control their global spread.

Methods

In this study, the complete sequence of 79 non-redundant hypervirulent plasmids were retrieved from GenBank and their genetic features, hypervirulence and antimicrobial resistance patterns (AMR) as well as their putative transmission capability were compared using bioinformatics tools.

Results

The majority of HVPs belonged to clonal complex (CC)23, and sequence type (ST)11. IncFIB and IncHI1B were the most prevalent plasmid replicon types. Out of 79 plasmids, 78 were positive for iutA and iucA. The iucC, iucB and iucD genes were found in 77 plasmids. Almost 26% of the HVPs were potentially conjugative of which 71% carried AGRs. ARGs against beta-lactams, carbapenems, quinolones, aminoglycosides, chloramphenicols, tetracyclines and macrolides were detected in 30% of HVPs. Class 1 integron and prophage structures harboring multiple ARGs were found in eight plasmids. Insertion sequences (IS)6, IS110 and IS1380 appeared to be important genetic elements in transmission of ARGs.

Conclusions

The high prevalence of iucA and iutA suggests their strong capability for rapid and accurate genetic markers for discrimination of hvKp in the laboratory. This study indicated the important role of mobile genetic elements (MGEs) in the emergence of drug-resistance in hypervirulent strains. The high prevalence of putative conjugative hybrids implies higher incidence of multidrug-resistant (MDR)-hvKp strains in near future.

Introduction

Unlike classical Klebsiella pneumoniae as a major nosocomial opportunistic with high level of antimicrobial resistance (AMR); hypervirulent K. pneumoniae (hvKp) is a highly virulent pathogen and sensitive to antimicrobials [1]. It has the ability to cause community-acquired infections including liver abscesses, meningitis, endophthalmitis, necrotizing fasciitis, osteomyelitis as well as pneumonia [2]. The clinical outcome of hvKp are severe and mortality rate reaches 40% in blood-stream infections [3].

The hypervirulent pathotype of K. pneumoniae is attributed to the carriage of virulence genes involved in iron acquisition, hyper capsule production and heavy metal resistance [4, 5]. This pathotype is mainly mediated by large hypervirulent plasmids (HVPs) [6, 7]. Despite multiple investigations on molecular mechanisms involved in hypervirulence of K. pneumoniae, a comprehensive study on extra-chromosomal hypervirulence reservoirs has not been conducted yet.

The importance of HVPs increases when they encode antimicrobial resistance genes (ARGs) and turn into drug-resistant hypervirulent hybrids [8]. Previously, the prevalence of drug-resistant hvKp strains was low, however; reported cases have been increased worldwide and become a new threat [9]. Several studies from Europe, South America, Australia, and North America have reported MDR-hvKp [10]. Even though various ARGs have been detected in clinical hvKp strains, our knowledge on the role of HVPs in transmission of AMR genetic determinants among hypervirulent strains is still limited. The continuous accumulation of ARGs particularly in wide-spread sequence types (ST) of hvKp is troublesome. This is even more life-threatening in case of carpabememase-producers [11]. The mortality rate of carbapenem-resistant hvKp sepsis has been reported as high as 100% [12]. In 2021, an extensively drug-resistant hvKp positive for blaNDM and blaOXA−48 was reported from a neonatal hospital [13]. Therefore, it is highly urgent to characterize AMR genetic reservoirs of HVPs to predict the future behavior of hvKp regarding antibiotic therapy.

In this analytical study, we characterized and compared the hypervirulence pattern of 79 pre-assembled HVPs of different K. pneumonia STs as well as their ARGs using bioinformatic tools. In addition, the plasmids were investigated for their replicon types, conjugation capability, plasticity and phylogenetic relationship.

Materials and methods

Preparation of initial dataset

The term “hypervirulent K. pneumoniae” was searched in the GenBank database (https://www.ncbi.nlm.nih.gov/genbank). The complete nucleotide sequence of all hypervirulent chromosomes and their plasmids were retrieved from GenBank.

Clonal relatedness of strains harboring HVPs

The distribution of HVPs among different hvKp STs were investigated. For each plasmid, the ST of its related chromosome based on seven housekeeping genes (gapA, infB, mdh, pgi, phoE, rpoB and tonB) was determined using the PubMLST database (https://pubmlst.org/) [14]. To characterize the clonal relationship of hvKp strains, the minimum spanning tree of all hvKp STs was prepared using PHYLOViZ version 2.0 [15].

Circular alignment and phylogenetic analysis of HVPs

To compare plasmids sequence plasticity, circular alignment was performed for several HVPs of major STs using the BLAST Ring Image Generator (BRIG) version 0.95 [16]. To investigate the phylogenetic relationship of the plasmids, a Neighbor Joining (NJ) tree was constructed based on genes with occurrence of > 10% in all plasmids using BacCompare (http://baccompare.imst.nsysu.edu.tw) [17]. The cladogram was visualized using iTOL (https://itol.embl.de) [18].

Genetic characterization of HVPs

The plasmids size was determined using DFAST (https://dfast.ddbj.nig.ac.jp/) [19]. The putative conjugation capability of plasmids was determined by using the MOB-suite software [20]. The presence of conjugal apparatus including oriT, relaxase, type IV coupling protein (T4CP) and type IV secretion system (T4SS) was investigated using oriTfinder (https://bioinfo-mml.sjtu.edu.cn/oriTfinder/) [21]. The incompatibility (Inc) group of plasmids was determined using MOB-suite.

Characterization of hypervirulence determinants

The encoding sequence of 14 genes involved in hypervirulent phenotype including iroB, iroC, iroD, iroN, iucA, iucB, iucC, iucD, iutA (aerobactin siderophores), peg-589 and peg-344 (metabolite transport), terB (tellurite resistance), rmpA and rmpA2 (hypermucoviscosity) [22] were retrieved from the NCBI database (https://www.ncbi.nlm.nih.gov/genbank) and blasted against all HVPs to determine their hypervirulence profile using the BLASTn software [23].

Antimicrobial resistance analysis of HVPs

All ARGs on plasmids were identified using the comprehensive antibiotic resistance database (CARD) (https://card.mcmaster.ca/analyze/rgi) [24]. To investigate the role of mobile genetic elements (MGEs) in distribution of ARGs among hvKp strains, the plasmids were submitted to PHASTER (http://phaster.ca/) to detect prophage structures [25]. The identified prophages then were submitted to ISfinder to determine the presence of insertion sequences (ISs) and transposon elements (https://isfinder.biotoul.fr/) [26]. The presence of integrons was investigated using BLASTn. The ARGs cassette arrays surrounding the integron genes were characterized using DFAST and ORFfinder (https://www.ncbi.nlm.nih.gov/orffinder/).

Results

Clonal relatedness of strains harboring HVPs

Seventy-nine non-redundant HVPs were found in GenBank. Their corresponding hvKp strains were belonged to clonal complex (CC)23 (including ST23, ST485, ST1660, ST1265, ST1946, ST268, ST36, ST65 and ST375) as well as single clonal lineages ST7, ST11, ST15, ST29, ST34, ST147, ST86, ST101, ST90, ST374, ST383, ST3685, ST83 and ST3913. See Fig. 1. Six plasmids were found in strains with undetermined ST. See Additional file 1: Table S1.

Fig. 1
figure 1

The minimum spanning tree of STs carrying the Klebsiella pneumoniae hypervirulent plasmids with similarity cut off of > 4 allelic types (green: STs carrying all 14 hypervirulent genes, purple: STs not carrying all hypervirulent genes). Clonal complex 23 (CC23) including ST23, ST1941, ST1660, ST485, ST268, ST36, ST1265, ST65, and ST375 harbored complete hypervirulence pattern. While, non-CC23 including ST11, ST3813, ST86, and ST29 lack several hypervirulence genes

Full size image

Genetic plasticity and phylogenic analysis and of HVPs

High heterogeneity was observed among different HVPs. However, they have similarity in some regions regardless of their strains STs. See Fig. 2A.

Fig. 2
figure 2

A The multiple circular alignment of 15 K. pneumoniae hypervirulent plasmids. High heterogenicity was detected among plasmids. However, they were similar in some regions. B The phylogenetic NJ dendrogram of 79 K. pneumoniae hypervirulent plasmids and distribution of drug-resistant hybrids. The subclade distribution of plasmids within the leaves was not exactly associated with their strains STs. Conjugative antimicrobial-resistant hybrids were mainly distributed in clade II and III. Besides, almost all MDR-HVPs were located in clade III. While, clade I mainly contained non-drug-resistant HVPs

Full size image

A number of 2952 of genes with > 10% occurrence rate were identified for plasmids by BacCompare. The results showed that the HVPs had 1589 unique genes. The heatmap of 79 plasmids showed that the plasmids have different allele numbers in 185 loci. See Additional file 3: Fig. S1. The phylogenetic dendrogram based on 2952 gene classified the HVPs in three main clades (I, II and III). See Fig. 2B.

Genetic characteristics of HVPs

The size of plasmids ranged from 96,085 to 479,335 bp. Twenty-one plasmids were potentially conjugative carrying all four conjugal constituents including oriT, relaxase, type IV coupling protein (T4CP) and type IV secretion system (T4SS). Three plasmids including CP034421.1, CP045692.1 and CP032834.1 were mobilizable (only lacked oriT). All plasmids were positive for T4CP and T4SS.

A number of 56 plasmids had IncFIB and IncHI1B. Thirteen plasmids had only IncFIB. A number of seven plasmids had the IncFIB and IncFII replicon types. CP025640.1 and CP029227.1 had only IncHI1B. MK181633.1, CP035384.1 and MF398271.1 had three replicon types (IncFIB, IncFIB and IncHI1B). IncFIB and IncR were detected in CP045692.1. CP040994.1 had IncFIA and IncFIB. See Additional file 1: Table S1 and Fig. 3A.

Fig. 3
figure 3

A The prevalence of different Inc groups among 79 K. pneumoniae hypervirulent plasmids. IncFIB was the most abundant (97%) replicon type among HVPs which co-existed with IncHI1B in 70% of the plasmids. B The prevalence of ARGs K. pneumoniae hypervirulent plasmids against different drug classes. The plasmids were mainly resistant to beta-lactamand aminoglycosides modifying enzymes. C The frequency of major ESBLs and carbapenemases. blaTEM, blaCTX-M and blaSHV were the most abundant ESBL genes among hypervirulent plasmids

Full size image

Hypervirulence profile

A number of 32 plasmids carried all 14 hypervirulence related genes including iroB, iroC, iroD, iroN, iucA, iucB, iucC, iucD, iutA, terB, rmpA, rmpA2, peg-589 and peg-344. Out of 79 plasmids, 78 were positive for iutA and iucA. The iucC, iucB and iucD were found in 77 plasmids. The rmpA2, peg-589 and terB genes were detected in 73, 70 and 66 HVPs, respectively. peg-344 and iroN were identified in 51 and 49 plasmids, respectively. A number of 41 plasmids were positive for iroD, iroC and iroB genes. The fewest number of hypervirulence genes was for CP040994.1 (peg-344, iroB and rmpA). The schematic comparison of plasmids hypervirulence profile has been presented in Fig. 4.

Fig. 4
figure 4

The hypervirulence profile (iroB, iroC, iroD, iroN, iucA, iucB, iucC, iucD, iutA, terB, rmpA, rmpA2, peg-589 and peg-344) of 79 K. pneumoniae hypervirulent plasmids. The iucA, iutA, iucD, iucB, iucC, rmpA2, peg-589 and terB genes were highly prevalent among plasmids

Full size image

Antimicrobial resistance associated genetic elements in HVPs

ARGs

A number of 24 plasmids carried different ARGs against extended-spectrum beta-lactams (blaTEM-1, blaDHA-1, blaCTX-M-15, blaCTX-M-24, blaSHV-11, blaSHV-64, blaSHV-5 and blaCMY-6), carbapenems (blaOXA-1, blaKPC-2 and blaNDM-1), quinolones (qnrB4, qnrB17 and qnrS1), aminoglycosides (armA, aph(3'')-Ib, aph(3')-Ia, aac(6')-Ib-cr6, aac(6′)-lb-cr5, aac(6')-Ib10, aac(6′)-lb, aac(3)-lld, aac(3)-IIe, rmtC and ant(3'')-IIa), chloramphenicol (catI, catII, cmlA1, and catB3), tetracycline (tetA, tetB, tetD, and tetR) and macrolide (mphE, msrE, and mphA). See Additional file 1: Table S1.

Quinolone resistance genes were identified in four plasmids including MK649823.1, MK191024.1, MK649829.1, and MK181633.1. Macrolide, tetracycline and chloramphenicol resistance genes were detected in 12, six, and five plasmids, respectively. A number of 25 and 23 aminoglycosidase and beta-lactamase encoding genes were found, respectively. See Fig. 3B. blaCTX-M, blaTEM and blaSHV were carried by six, five and four plasmids, respectively. CP028791.1 (blaOXA-1), MK181633.1 (blaOXA-1), MK649825.1 (blaOXA-1), MF398271.1 (blaKPC-2) and CP034201.1 (blaNDM-1) were carbapenemase producers. See Fig. 3C. Six plasmids were MDR-HVPs. See Additional file 1: Table S1.

Mobile genetic elements associated with AMR

Prophages

A number of 13 HVPs had prophage structures with Salmon_SJ46 and Escher_RCS47 being the most prevalent. The blaCTX-M and blaTEM-1 genes were major ESBLs carried by prophage structures. blaOXA-1 of CP028791.1 was detected in Escher_RCS47. Genes encoding aminoglycosides modifying enzymes in MK181633.1, CP034046.1, CP034054.1, CP040595.1 and CP028791.1 carried by different incomplete prophages (including Bacill_Shanette, Salmon_SJ46, Escher_RCS47 and Escher_Av). Some ARGs against other antimicrobial drug classes including quinolones (qnrS1), tetracycline (tetA) and chloramphenicol (catB3) were also phage-mediated. Prophages in five plasmids did not carry any ARGs. See Additional file 2: Table S2.

Integrons

Class 1 integron (intI1) was found in eight plasmids including CP034421.1, CP040595.1, CP040726.1, MK649825.1, CP030270.1, CP028791.1, CP034046.1, and MK181633.1. See Additional file 3: Fig. S2. ARGs which were found around class 1 integron were as follows: aac(3)-lld, aac(6’)-lb and aac(6’)-lb-cr5 on plasmids CP034421.1, CP040595.1 and CP028791.1, respectively; dfrA5 on CP040726.1, MK649825.1 and MK181633.1; cmlA and catB3 on CP030270.1 and CP028791.1, respectively and arr3 on CP028791.1. Class 2 integron (sat2) was detected only on CP034046.1

Insertion sequences and transposons

The IS26 (IS6-like), ISVsa5 (IS4-like), IS4321 (IS110-like), ISCfr1 (IS1182-like), ISEc9 (IS1380-like), ISKpn11(IS3-like), IS1326 (IS2-like), IS110, IS1 elements as well as TnAs3 (Tn3-like) and Tn3 family transposases were truncated by intI1 and multiple ARGs. See Additional file 3: Fig. S2. IS6, IS110 and IS1380 were frequently found on prophages surrounding beta-lactamase and other ARGs. See Additional file 3: Table S2.

Discussion

Up to now, various genetic markers have been dedicated to hvKP [27]. However, the definition of hvKP is still not fully established due to the complexity of virulence mechanisms [28]. The present study was focused on plasmid-mediated mediators of hypervirulence. We considered genes involved in iron acquisition, metabolite transport, tellurite resistance and hypermucoviscosity as markers of hypervirulence. However, hypermucoviscose has been considered a pathotype distinct from hypervirulent in some studies [29, 30]. Moreover, the chromosomal carriage of genes such as entB, mrkD, fimH, wabG, ybtS, allS and kfu has been also investigated as hypervirulence mediators in several studies [3, 8, 30].

In consistent with other studies, CC23 was the most widely distributed CC among hvKp strains [31]. However, ST11 is the most prevalent clone in China [32]. In our study, 33% of hvKp strains belonged to ST11. Almost 41% of the HVPs were positive for all 14 hypervirulence genes of which 46% were isolated from CC23 and the remaining from ST11, ST286, ST375, ST86 and ST65. See Fig. 1. The hypervirulence patterns of strains belonging to a same ST were highly similar. In this regard, Yu et al. indicated that hvKp strains belonging to ST23, ST65, ST375 and ST86 were all positive for rmpA, rmpA2, iutA, and iroN on their plasmids.

Several studies have been conducted to find a method for accurate identification of hvKp in the laboratory [33]. The string test has been considered as a phenotypic marker for hvKp. However, its results are variable and sometimes unspecific [34]. Tellurite resistance was suggested as a screening method [33, 35]. Hypervirulent populations were successfully separated based on their capsules using density-gradient centrifugation test [36]. Wu et al. distinguished hvKp based on positive string test and positive rmpA and iucA [37]. Molecular detection of rmpA and iucA was also used as hypervirulent indicator by Li et al. [3]. The peg-344, iroB, iucA, rmpA and rmpA2 genes showed > 95% diagnostic accuracy for identification of hvKp strains in 2018. The peg-344, iucA and iutA were introduced as the best markers for diagnosis of hvKp [38]. Based on the present virulence analysis, almost all HVPs harbored iucA and iutA. Therefore, molecular detection of iucA and iutA genes with accuracy of 98% can be advantageously used for precise screening of hvKp. The iucD, iucB, iucC, rmpA2, peg-589 and terB genes were also highly prevalent among HVPs (with the prevalence rate of 97%, 97%, 97%, 92%, 88% and 83%, respectively). This highlights their important role in hypervirulent pathotype of K. pneumoniae.

HvKp and classical K. pneumoniae have two distinct phenotypes with similar clonal lineages [27]. Their convergence can be mediated by the genetic integration of drug-resistant plasmids in HVPs vice versa. Another probable mechanism is the transmission of ARGs in HVPs through recombinational processes. Also, it can result from the co-existence of antibiotic-resistant plasmids along with HVPs in one individual bacterium [39, 40].

IncFIB was the most abundant (97%) replicon type among HVPs which co-existed with IncHI1B in 70% of the plasmids. The presence of specific Inc groups in majority of plasmids suggests that the formation of convergent phenotype is rarely result from plasmids integration whereas is more related to other two mentioned mechanisms. Also, it suggests that a drug-resistant plasmid with Inc groups other than IncFIB and IncHI1B has higher chance to reside in a single hvKp bacterium.

The AGRs were detected in 30% of the HVPs. MK181633.1, MK413722.1, CP025462.1, CP034046.1, CP026022.1, CP040726.1, MK649829.1 and MK649825.1 were important due to the carriage of major ESBLs. Similar to classical plasmids, blaTEM and blaCTX-M were the most prevalent beta-lactamase producers among HVPs [41]. Almost 26% of the HVPs were potentially conjugative. See Fig. 2B. Interestingly, 71% of all putative conjugative HVPs carried AGRs. MK181633.1 was a conjugative MDR-HVP carrying the highest number of beta-lactamases and aminoglycosidases-producing genes. Of four carbapenem-resistant plasmids, three (MK181633.1, MK649825.1 and CP034201.1) harboring blaOXA-1 and blaNDM-1 were potentially conjugative. See Fig. 2B. Importantly, blaKPC-2 was carried by MF398271.1, a HVP harboring all 14 hypervirulent genes. Also, all quinolone resistance genes (qnrB4, qnrB17 and qnrS1) were carried by potentially conjugative HVPs. The isolation of self-transmissible HVPs carrying major ARGs suggests the increase of resistance against most clinically used antimicrobials by a few years.

Similar to classical plasmids, class 1 integron is highly responsible for resistance to multiple drug classes in hvKp strains [42]. Importantly, our data showed that resistance to third-generation cephalosporins and aminoglycosides is mediated by prophages structures in some hypervirulent strains. The extra-chromosomal phage-mediated carriage of ESBLs in hvKp has been previously reported by Yang et al. [43]. Moreover, IS6, IS110 and IS1380 seem to be important elements for horizontal transmission of major ARGs [44].

A specific distribution of antimicrobial-resistant HVPs was observed in the NJ dendrogram. The subclade distribution of plasmids within the leaves was not exactly associated with their strains STs. Conjugative antimicrobial-resistant HVPs were mainly distributed in clade II and III. Besides, almost all MDR-HVPs were located in clade III. While, clade I mainly contains non-drug-resistant HVPs. See Fig. 2B. Importantly, the results exhibited lower presence of hypervirulent genes in clade II and III. Based on our data, majority of highly antimicrobial-resistant HVPs lacked iroN, iroD, iroC, iroB and peg344. By contrast, the full carriage of hypervirulent genes was mainly observed in plasmids belonging to clade I. This suggests that integration of antibiotic-resistant mediators in HVPs specifically occurs in plasmids with low levels of hypervirulence which are phylogenetically distinct from highly virulent plasmids to some extent.

Conclusion

We conducted a comprehensive molecular analysis on plasmids-borne mechanisms of hypervirulence. Based on the present analysis, molecular detection of the iucA and iutA genes can be advantageously utilized for accurate identification of hvKp. Moreover, we characterized the AMR genetic reservoirs of HVPs. Several ARGs against beta-lactams, carbapenems, quinolones, aminoglycosides, chloramphenicols, tetracyclines and macrolides were detected in HVPs. This study highlighted the role of MGEs in the emergence of AMR among hvKp strains. The presence of potentially conjugative MDR-HVP hybrids in this study implies higher incidence of drug-resistant hvKp strains in near future.

Availability of data and materials

The sequence of all 79 HVPs are available in the GenBank database.

Abbreviations

AMR:

Antimicrobial resistance

ARG:

Antimicrobial resistant gene

CARD:

Comprehensive antibiotic resistance database

ESBLs:

Extended-spectrum beta-lactamase

HVPs:

Hypervirulent plasmids

hvKp:

Hypervirulent Klebsiella pneumoniae

MDR:

Multidrug-resistant

MGE:

Mobile genetic element

Inc:

Incompatibility

IS:

Insertion sequence

NJ:

Neighbor joining

T4CP:

Type IV coupling protein

T4SS:

Type IV secretion system

ST:

Sequence type

References

  1. Andrade BG, de Veiga RN, Marin MF, Fonseca EL, Vicente AC. The genome of a clinical Klebsiella variicola strain reveals virulence-associated traits and a pl9-like plasmid. FEMS Microbiol Lett. 2014;360(1):13–6.

    Article  CAS  Google Scholar 

  2. Russo TA, Marr CM. Hypervirulent Klebsiella pneumoniae. Clin Microbiol Rev. 2019. https://doi.org/10.1128/CMR.00001-19.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Li J, Ren J, Wang W, Wang G, Gu G, Wu X, Wang Y, Huang M, Li J. Risk factors and clinical outcomes of hypervirulent Klebsiella pneumoniae induced bloodstream infections. Eur J Clin Microbiol Infect Dis. 2018;37(4):679–89.

    Article  Google Scholar 

  4. Paczosa MK, Mecsas J. Klebsiella pneumoniae: going on the offense with a strong defense. Microbiol Mol Biol Rev. 2016;80(3):629–61.

    Article  CAS  Google Scholar 

  5. Catalán-Nájera JC, Garza-Ramos U, Barrios-Camacho H. Hypervirulence and hypermucoviscosity: two different but complementary Klebsiella spp. phenotypes? Virulence. 2017;8(7):1111–23.

    Article  Google Scholar 

  6. Gu D, Dong N, Zheng Z, Lin D, Huang M, Wang L, Chan EW-C, Shu L, Yu J, Zhang R, et al. A fatal outbreak of ST11 carbapenem-resistant hypervirulent Klebsiella pneumoniae in a Chinese hospital: a molecular epidemiological study. Lancet Infect Dis. 2018;18(1):37–46.

    Article  Google Scholar 

  7. Choby JE, Howard-Anderson J, Weiss DS. Hypervirulent Klebsiella pneumoniae—clinical and molecular perspectives. J Intern Med. 2020;287(3):283–300.

    Article  CAS  Google Scholar 

  8. Fursova AD, Fursov MV, Astashkin EI, Novikova TS, Fedyukina GN, Kislichkina AA, Alexandrova IA, Ershova ON, Dyatlov IA, Fursova NK. Early response of antimicrobial resistance and virulence genes expression in classical, hypervirulent, and hybrid hvKp-MDR Klebsiella pneumoniae on antimicrobial stress. Antibiotics. 2022;11(1):7.

    Article  CAS  Google Scholar 

  9. Mataseje LF, Boyd DA, Mulvey MR, Longtin Y. Two hypervirulent isolates producing a KPC-2 carbapenemase from a Canadian patient. Antimicrob Agents Chemother. 2019;63(7):e00517-00519.

    Article  CAS  Google Scholar 

  10. Du P, Zhang Y, Chen C. Emergence of carbapenem-resistant hypervirulent Klebsiella pneumoniae. Lancet Infect Dis. 2018;18(1):23–4.

    Article  Google Scholar 

  11. Di Tella D, Tamburro M, Guerrizio G, Fanelli I, Sammarco ML, Ripabelli G. Molecular epidemiological insights into colistin-resistant and carbapenemases-producing clinical Klebsiella pneumoniae isolates. Infect Drug Resist. 2019;12:3783–95.

    Article  Google Scholar 

  12. Xie M, Yang X, Xu Q, Ye L, Chen K, Zheng Z, Dong N, Sun Q, Shu L, Gu D, et al. Clinical evolution of ST11 carbapenem resistant and hypervirulent Klebsiella pneumoniae. Commun Biol. 2021;4(1):650.

    Article  CAS  Google Scholar 

  13. Banerjee T, Wangkheimayum J, Sharma S, Kumar A, Bhattacharjee A. Extensively drug-resistant hypervirulent klebsiella pneumoniae from a series of neonatal sepsis in a tertiary care hospital, India. Front Med. 2021. https://doi.org/10.3389/fmed.2021.645955.

    Article  Google Scholar 

  14. Jolley KA, Bray JE, Maiden MC. Open-access bacterial population genomics: BIGSdb software, the PubMLST. org website and their applications. Wellcome Open Res. 2018;3:124.

    Article  Google Scholar 

  15. Nascimento M, Sousa A, Ramirez M, Francisco AP, Carriço JA, Vaz C. PHYLOViZ 2.0: providing scalable data integration and visualization for multiple phylogenetic inference methods. Bioinformatics. 2017;33(1):128–9.

    Article  CAS  Google Scholar 

  16. Alikhan N-F, Petty NK, Ben Zakour NL, Beatson SA. BLAST ring image generator (BRIG): simple prokaryote genome comparisons. BMC Genomics. 2011;12(1):402.

    Article  CAS  Google Scholar 

  17. Liu YY, Lin JW, Chen CC. cano-wgMLST_BacCompare: a bacterial genome analysis platform for epidemiological investigation and comparative genomic analysis. Front Microbiol. 2019;10:1687.

    Article  Google Scholar 

  18. Letunic I, Bork P. Interactive Tree Of Life (iTOL) v5: an online tool for phylogenetic tree display and annotation. Nucleic Acids Res. 2021;49(W1):W293–6.

    Article  CAS  Google Scholar 

  19. Tanizawa Y, Fujisawa T, Nakamura Y. DFAST: a flexible prokaryotic genome annotation pipeline for faster genome publication. Bioinformatics. 2018;34(6):1037–9.

    Article  CAS  Google Scholar 

  20. Robertson J, Nash JHE. MOB-suite: software tools for clustering, reconstruction and typing of plasmids from draft assemblies. Microb Genom. 2018. https://doi.org/10.1099/mgen.0.000206.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Li X, Xie Y, Liu M, Tai C, Sun J, Deng Z, Ou H-Y. oriTfinder: a web-based tool for the identification of origin of transfers in DNA sequences of bacterial mobile genetic elements. Nucleic Acids Res. 2018;46(W1):W229–34.

    Article  CAS  Google Scholar 

  22. Korf I, Yandell M, Bedell J. Blast. Sebastopol: O’ Reilly Media Inc; 2003.

    Google Scholar 

  23. Elizabeth Cha I, Rouchka EC. Comparison of current BLAST software on nucleotide sequences. Proc IPDPS (Conf). 2005;19:8–8.

    CAS  Google Scholar 

  24. Jia B, Raphenya AR, Alcock B, Waglechner N, Guo P, Tsang KK, Lago BA, Dave BM, Pereira S, Sharma AN. CARD 2017 expansion and model-centric curation of the comprehensive antibiotic resistance database. Nucleic Acids Res. 2016. https://doi.org/10.1093/nar/gkw1004.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Arndt D, Grant JR, Marcu A, Sajed T, Pon A, Liang Y, Wishart DS. PHASTER: a better, faster version of the PHAST phage search tool. Nucleic Acids Res. 2016;44(W1):W16–21.

    Article  CAS  Google Scholar 

  26. Siguier P, Perochon J, Lestrade L, Mahillon J, Chandler M. ISfinder: the reference centre for bacterial insertion sequences. Nucleic Acids Res. 2006;34(Database issue):D32-36.

    Article  CAS  Google Scholar 

  27. Rahimeh S, Mohammad M, Fereshteh S, Arezou L, Sepideh F, Amin S, Afsaneh S, Farzad B. Molecular epidemiology of hypervirulent Klebsiella pneumoniae: a systematic review and meta-analysis. Iran J Microbiol. 2021;13(3):257.

    Google Scholar 

  28. Shen P, Berglund B, Chen Y, Zhou Y, Xiao T, Xiao Y, Zhou K. Hypervirulence markers among non-ST11 strains of carbapenem- and multidrug-resistant Klebsiella pneumoniae isolated from patients with bloodstream infections. Front Microbiol. 2020. https://doi.org/10.3389/fmicb.2020.01199.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Tang M, Kong X, Hao J, Liu J. Epidemiological characteristics and formation mechanisms of multidrug-resistant hypervirulent Klebsiella pneumoniae. Front Microbiol. 2020;11: 581543.

    Article  Google Scholar 

  30. Shi Q, Lan P, Huang D, Hua X, Jiang Y, Zhou J, Yu Y. Diversity of virulence level phenotype of hypervirulent Klebsiella pneumoniae from different sequence type lineage. BMC Microbiol. 2018;18(1):94.

    Article  Google Scholar 

  31. Marr CM, Russo TA. Hypervirulent Klebsiella pneumoniae: a new public health threat. Expert Rev Anti Infect Ther. 2019;17(2):71–3.

    Article  CAS  Google Scholar 

  32. Zhou K, Xiao T, David S, Wang Q, Zhou Y, Guo L, Aanensen D, Holt KE, Thomson NR, Grundmann H. Novel subclone of carbapenem-resistant Klebsiella pneumoniae sequence type 11 with enhanced virulence and transmissibility, China. Emerg Infect Dis. 2020;26(2):289.

    Article  CAS  Google Scholar 

  33. Sanikhani R, Moeinirad M, Solgi H, Hadadi A, Shahcheraghi F, Badmasti F. The face of hypervirulent Klebsiella pneumoniae isolated from clinical samples of two Iranian teaching hospitals. Ann Clin Microbiol Antimicrob. 2021;20(1):58–58.

    Article  CAS  Google Scholar 

  34. Lan P, Jiang Y, Zhou J, Yu Y. A global perspective on the convergence of hypervirulence and carbapenem resistance in Klebsiella pneumoniae. J Glob Antimicrob Resist. 2021;25:26–34.

    Article  Google Scholar 

  35. Paterson DL, Siu K, Chang FY. Klebsiella species (K. pneumoniae, K. oxytoca, K. ozaenae and K. rhinoscleromatis). Antimicrobe. 2014;9:74–6.

    Google Scholar 

  36. Dorman MJ, Feltwell T, Goulding DA, Parkhill J, Short FL. The capsule regulatory network of Klebsiella pneumoniae defined by density-TraDISort. mBio. 2018;9(6):e01863-01818.

    Article  Google Scholar 

  37. Wu H, Li D, Zhou H, Sun Y, Shen D. Bacteremia and other body site infection caused by hypervirulent and classic Klebsiella pneumoniae. Microb Pathog. 2017;104:254–62.

    Article  Google Scholar 

  38. Russo TA, Olson R, Fang C-T, Stoesser N, Miller M, MacDonald U, Hutson A, Barker JH, La Hoz RM, Johnson JR. Identification of biomarkers for differentiation of hypervirulent Klebsiella pneumoniae from classical K. pneumoniae. J Clin Microbiol. 2018. https://doi.org/10.1128/JCM.00776-18.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Tang M, Kong X, Hao J, Liu J. Epidemiological characteristics and formation mechanisms of multidrug-resistant hypervirulent Klebsiella pneumoniae. Front Microbiol. 2020;11:581543–581543.

    Article  Google Scholar 

  40. Shen D, Ma G, Li C, Jia X, Qin C, Yang T, Wang L, Jiang X, Ding N, Zhang X, et al. Emergence of a multidrug-resistant hypervirulent Klebsiella pneumoniae sequence type 23 strain with a rare CTX-M-24-harboring virulence plasmid. Antimicrob Agents Chemother. 2019;63(3):e02273-e12218.

    Article  CAS  Google Scholar 

  41. Sahoo S, Otta S, Swain B, Kar SK. Detection and genetic characterization of extended-spectrum beta-lactamases producers in a tertiary care hospital. J Lab Phys. 2019;11(3):253–8.

    CAS  Google Scholar 

  42. Najafi M, Omidvar-Panah M, Nikkhahi F, Peymani A. Epidemiology of integrons among multidrug-resistant pathogens: an Asian update. Rev Res Med Microbiol. 2022;33(1): e33.

    Article  Google Scholar 

  43. Yang Q, Jia X, Zhou M, Zhang H, Yang W, Kudinha T, Xu Y. Emergence of ST11-K47 and ST11-K64 hypervirulent carbapenem-resistant Klebsiella pneumoniae in bacterial liver abscesses from China: a molecular, biological, and epidemiological study. Emerg Microbes Infect. 2020;9(1):320–31.

    Article  CAS  Google Scholar 

  44. Bolourchi N, Giske CG, Nematzadeh S, Mirzaie A, Abhari SS, Solgi H, Badmasti F. Comparative resistome and virulome analysis of clinical NDM-1 producing carbapenem-resistant Enterobacter cloacae complex. J Glob Antimicrob Resist. 2022. https://doi.org/10.1016/j.jgar.2022.01.021.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

The authors would like to thank the personnel at the Bacteriology Department of the Pasteur Institute of Iran for their help. This research was supported by the Pasteur Institute of Iran.

Funding

No specific funding was received for this study.

Author information

Authors and Affiliations

  1. Department of Bacteriology, Pasteur Institute of Iran, Tehran, Iran

    Negin Bolourchi, Maryam Sohrabi & Farzad Badmasti

  2. Institute of Molecular Biology and Biotechnology (IMBB), The University of Lahore (UOL), Lahore, Pakistan

    Anam Naz

  3. Microbiology Research Center (MRC), Pasteur Institute of Iran, Tehran, Iran

    Farzad Badmasti

Authors
  1. Negin Bolourchi
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Anam Naz
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Maryam Sohrabi
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Farzad Badmasti
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

FB designed the study, and critically revised the manuscript. FB, NB and MS performed all of the analyses. FB and AN revised the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Farzad Badmasti.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no known competing financial interests or personal relationships that could have influenced the work reported in this paper.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Table S1.

The genetic information, hypervirulence and antimicrobial resistance genetic patterns of 79 hypervirulent plasmids of Klebsiella pneumoniae.

Additional file 2: Table S2

. The information of prophages found in hypervirulent plasmids of Klebsiella pneumoniae.

Additional file 3. Fig. 1. 

The ARGs cassettes surrounding class 1 integron in Klebsiella pneumoniae hypervirulent plasmids. Fig. 2. The phylogenic tree and heatmap of 79 hypervirulent Klebsiella pneumoniae plasmids based on 185 loci.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Bolourchi, N., Naz, A., Sohrabi, M. et al. Comparative in silico characterization of Klebsiella pneumoniae hypervirulent plasmids and their antimicrobial resistance genes. Ann Clin Microbiol Antimicrob 21, 23 (2022). https://doi.org/10.1186/s12941-022-00514-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12941-022-00514-6

Keywords

Annals of Clinical Microbiology and Antimicrobials

ISSN: 1476-0711

Contact us