Clinical and Microbiological Characteristics of Klebsiella pneumoniae Bloodstream Infection in a Chinese Hospital: Hypervirulent and Multiclonal.

Purpose: Hypervirulent Klebsiella pneumoniae (hvKP) is emerging globally and can cause various infections. This study aimed to investigate the clinical and microbiological characteristics of bloodstream infection (BSI) caused by hvKP. Patients and
Methods: The clinical data of hospitalized patients with K. pneumoniae BSI were retrospectively analyzed. The K. pneumoniae strains were collected and re-identified, and antimicrobial susceptibility testing was performed using the broth microdilution method. Capsular serotypes and virulence genes were detected using polymerase chain reaction, and hvKP was defined as aerobactin positive. Molecular typing was done by multilocus sequence typing. The hvKP and classic K. pneumoniae (cKP) subgroups were compared.
Results: Of the 66 nonrepetitive BSI K. pneumoniae strains included, 29 (43.9%) were hvKP. In these BSI hvKP strains, salmochelin and yersiniabactin accounted for 86.2% and 72.4%, respectively. The prevalence of rmpA, iroBCD cluster, ybtS, clbA, and allS was 89.7%, 86.2%, 72.4%, 51.7%, and 41.4%, respectively, which were all significantly different between the hvKP and cKP subgroups. Serotypes K1 and K2 were strongly associated with hypervirulence (P < 0.05). Nineteen sequence types were scattered in the 29 hvKP strains, and the most common was ST23 (24.1%). None of the hvKP strains were carbapenem resistant. Compared with cKP, hvKP was more capable of developing a liver abscess. However, the 30-day mortality rate was lower (13.8% vs 21.6%) in the hvKP subgroup than in the cKP subgroup.
Conclusion: This study demonstrated a high proportion of hvKP in BSI K. pneumoniae, most of which were RmpA and siderophore producing, and of multiclonal origin.

Introduction

Klebsiella pneumoniae is one of the major nosocomial pathogens, which can cause various severe infections, including bloodstream infection (BSI). BSI is a systemic infection and usually results in relatively high mortality due to the virulence factors of K. pneumoniae.

Recently, hypervirulent K. pneumoniae (hvKP), as a variant of K. pneumoniae, has emerged as a major threat to individuals. hvKP has several unique characteristics compared with the classic K. pneumoniae (cKP). Hypermucoviscosity is regarded as an important feature of hvKP, which is mainly mediated by rmpA and/or rmpA2 with overproduction of capsular polysaccharide. Previously, hypermucoviscosity has been used to define hvKP.1,2

Siderophore production is another distinguishing trait of hvKP. Siderophores are dominantly responsible for iron acquisition, contributing to bacterial virulence. Four kinds of siderophores have been reported in K. pneumoniae: aerobactin, salmochelin, yersiniabactin, and enterobactin. Of these, the siderophore aerobactin is dominantly produced (>90%) and has been established as an essential virulence factor in hvKP.3,4 In addition, hvKP infections are more common in healthy individuals from the community, with invasive and metastatic lesions.

The definition of hvKP has not reached a consensus. The hypermucoviscous phenotype has been used to define hvKP in earlier publications.1,2 However, this designation of hvKP by the mucoid phenotype alone is imperfect because not all hvKP strains are hypermucoviscous,5 and some cKP can be hypermucoviscous.6

A few recent studies have defined hvKP based on the genetic background.7–11 Still, many knowledge gaps exist regarding hvKP, and hence the awareness about hvKP needs to be increased urgently. Furthermore, the characteristics of hvKP strains and their differences from cKP are less well-known. Actually, data on hvKP in BSI are extremely limited.2,7 This retrospective study mainly aimed to investigate the clinical and molecular characteristics of patients with K. pneumoniae BSI, especially to delineate the virulence-associated factors. The hvKP and cKP subgroups were compared.

Patients and Methods

Patients

Patients hospitalized at the First Hospital of Quanzhou, a teaching hospital located in Eastern China, from January 2019 to March 2020, with a positive blood culture of K. pneumoniae were enrolled. Clinical data were extracted from the electronic medical records system, including demographic characteristics, site of infections, underlying diseases, intensive care unit (ICU) stay, length of hospital stay, organ failure, prior hospitalization, and clinical outcomes. The 30-day mortality was used to evaluate the clinical outcomes of K. pneumoniae BSI. A community-acquired BSI was defined as a positive blood culture within 48 h after admission, and a hospital‐acquired BSI was designated as a positive culture beyond 48 h after admission.2,10,12 The clinical and microbiological data were compared between patients with cKP BSI and those with hvKP BSI. The present study complied with the Declaration of Helsinki and was approved by the Research Ethics Board at the First Hospital of Quanzhou (212–2018) with a waiver of informed consent for the following reasons: (1) the retrospective nature of the study, (2) the patient data was anonymous, and (3) the strains used in this study were part of the routine hospital laboratory procedure.

Strains

During the study period, all K. pneumoniae strains isolated from blood cultures were collected, and only the first isolation of K. pneumoniae from the same patient was included for further assessment. The strains were re-identified using matrix-assisted laser desorption ionization–time-of-flight mass spectrometry (bioMérieux, Marcy-l’Étoile, France) and stored at −80℃ for further use. Strains with aerobactin positive were defined as hvKP.3,8,9

Antimicrobial Susceptibility Testing

Antimicrobial susceptibility testing was carried out using the broth microdilution method, and 15 antimicrobial agents were tested, including cefotaxime, ceftazidime, cefepime, aztreonam, ampicillin-sulbactam, amoxicillin-clavulanic acid, piperacillin-tazobactam, imipenem, meropenem, amikacin, gentamicin, ciprofloxacin, levofloxacin, chloramphenicol, and colistin. The results were interpreted according to the Clinical and Laboratory Standards Institute.13 Escherichia coli ATCC25922 was used as a quality control strain for determining antimicrobial susceptibility.

Identification of the Hypermucoviscous Phenotype

The string test was used to detect the hypermucoviscous phenotype of K. pneumoniae strains as described in previous studies.1,14 It was considered positive when the viscous string was more than 5 mm in length.

Detection of Capsular Serotypes and Virulence Genes

Six capsular serotypes (K1, K2, K5, K20, K54, and K57) and 14 virulence genes (including rmpA/rmpA2 for mucoviscosity, iroBCD cluster for siderophore salmochelin, iucABCD cluster for siderophore aerobactin, ybtS for siderophore yersiniabactin, clbA/clbB/clbN/clbQ for colibactin, wabG for the biosynthesis of the outer core lipopolysaccharide (LPS), uge for biosynthesis of the capsule and smooth LPS, fimH for type 1 fimbrial adhesin, mrkD for type 3 fimbrial adhesin, and alls for allantoin metabolism) were amplified by polymerase chain reaction (PCR) as described in previous studies.1,10,15–21 The primers used in this study are summarized in . The PCR products were visualized and analyzed by agarose gel electrophoresis and sequencing.

Multilocus Sequence Typing

Multilocus sequence typing (MLST) was performed as described in a previous study.8 New alleles and sequence types (STs), which did not completely match with those of STs in the MLST database, were temporarily designated as a new ST (nST) in this study.

Statistical Analysis

Categorical variables were recorded as frequency rates and percentages, and continuous variables were expressed as median and interquartile range (IQR) values. SPSS (version 19.0, IBM SPSS Statistics for Windows, IBM Corp., Armonk, New York, United States) was used for analyzing the data. The chi-square test or Fisher’s exact test was used for categorical variables. The Student t-test or Mann–Whitney U-test was used for continuous variables. A P value <0.05 indicated a statistically significant difference.

Results

Distribution and Prevalence of Virulence Genes in BSI K. pneumoniae Strains

During this study period, 66 patients with a positive blood culture of K. pneumoniae were included, and 66 nonrepetitive K. pneumoniae strains were collected. Among these strains, 29 (43.9%) were positive for siderophore aerobactin and consequently designated as hvKP strains. The remaining 37 (56.1%) K. pneumoniae were considered as cKP. Another two siderophores, salmochelin and yersiniabactin, accounted for 53.0% (n = 35) and 54.5% (n = 36), respectively, in all these BSI K. pneumoniae strains (Table 1). Forty-three (65.2%) strains were positive for rmpA and/or rmpA2 (both rmpA and rmpA2, n = 32; rmpA only, n = 2; and rmpA2 only, n = 9). Of note, 26 of the 32 (81.3%) strains co-carrying rmpA and rmpA2 were hvKP strains, while 11 strains with rmpA or rmpA2 only were all cKP strains. Two genes (clbA and clbB) of the pks colibactin gene cluster together with another two genes (clbN and clbQ) were simultaneously detected in 18 (27.3%) strains. A relatively low prevalence of alls (22.7%, n = 15) was noted. On the contrary, a high prevalence of uge (98.5%, n = 65) and wabG (84.8%, n = 56) was found. Interestingly, 65 (98.5%) strains had an mrkD gene, whereas 26 (39.4%) harbored a fimH gene.

Table 1

Microbiological Characteristics of K. pneumoniae Causing Bloodstream Infection

	No. (%) of Strains
	Total (n=66)	hvKP (n=29)	cKP (n=37)	P valuea
Age, median (IQR), y	63 (50–74)	58 (50–73)	64 (47–77)	0.936
Virulence genes
iucABCD cluster	29 (43.9)	29 (100)	0 (0)	<0.001
iroBCD cluster	35 (53.0)	25 (86.2)	10 (27.0)	<0.001
ybtS	36 (54.5)	21 (72.4)	15 (40.5)	<0.001
rmpA	34 (51.5)	26 (89.7)	8 (21.6)	<0.001
clbA	18 (27.3)	15 (51.7)	3 (8.1)	<0.001
allS	15 (22.7)	12 (41.4)	3 (8.1)	0.001
uge	65 (98.5)	28 (96.6)	37 (100)	0.439
wabG	56 (84.8)	25 (86.2)	31 (83.8)	>0.999
fimH	26 (39.4)	12 (41.4)	14 (37.8)	0.770
mrkD	65 (98.5)	28 (96.6)	37 (100)	0.439
String test
Positive	29 (43.9)	22 (75.9)	7 (18.9)	<0.001
Negative	37 (56.1)	7 (24.1)	30 (81.1)	<0.001
Serotypes
K1	14 (21.2)	12 (41.4)	2 (5.4)	<0.001
K2	12 (18.2)	9 (31.0)	3 (8.1)	0.017
K5	3 (4.5)	0 (0)	3 (8.1)	0.250
K20	1 (1.5)	1 (3.4)	0 (0)	0.439
K54	1 (1.5)	0 (0)	1 (2.7)	>0.999
K57	2 (3.0)	2 (6.9)	0 (0)	0.189
K-nontypable	33 (50.0)	5 (17.2)	28 (75.7)	<0.001

Notes: aP values indicate differences between hvKP and cKP. P < 0.05 was considered statistically significant.

Abbreviations: hvKP, hypervirulent K. pneumoniae; cKP, classic K. pneumoniae; IQR, interquartile range.

As shown in Table 1, the iroBCD gene cluster (86.2% vs 27.0%), ybtS (72.4% vs 40.5%), rmpA (89.7% vs 21.6%), clbA (51.7% vs 8.1%), and allS (41.4% vs 8.1%) were significantly more prevalent in hvKP than in cKP (P ≤ 0.001). Nonetheless, the prevalence of uge (96.6% vs 100%), wabG (86.2% vs 83.8%), fimH (41.4% vs 37.8%), and mrkD (96.6% vs 100%) genes was similar in both the hvKP and cKP groups.

Antimicrobial Susceptibility of BSI K. pneumoniae

The tested antibiotics had good antibacterial activity against the BSI K. pneumoniae strains in vitro (Table 2). The susceptibility of hvKP to seven β-lactam agents was significantly higher than that of cKP (P < 0.05). Notably, no hvKP strain was found resistant to imipenem and meropenem.

Table 2

Antimicrobial Susceptibility of Hypervirulent and Classic K. pneumoniae Causing BSI

	No. (%) of Susceptible Strains
	Total (n=66)	hvKP (n=29)	cKP (n=37)	P valuea
Cefotaxime	54 (81.8)	29 (100)	25 (67.6)	0.001
Ceftazidime	55 (83.3)	29 (100)	26 (70.3)	0.002
Cefepime	57 (86.4)	29 (100)	28 (75.7)	0.004
Aztreonam	58 (87.9)	29 (100)	29 (78.4)	0.007
Ampicillin-sulbactam	17 (77.3)	13 (96.6)	4 (62.2)	0.002
Amoxicillin-clavulanic acid	54 (81.8)	29 (100)	25 (67.6)	0.001
Piperacillin-tazobactam	58 (87.9)	29 (100)	29 (78.4)	0.007
Imipenem	63 (95.5)	29 (100)	34 (91.9)	0.25
Meropenem	63 (95.5)	29 (100)	34 (91.9)	0.25
Amikacin	64 (97.0)	29 (100)	35 (94.6)	0.50
Gentamicin	62 (93.9)	29 (100)	33 (89.2)	0.125
Ciprofloxacin	54 (81.8)	27 (93.1)	27 (73.0)	0.035
Levofloxacin	59 (89.4)	28 (96.6)	31 (83.8)	0.124
Chloramphenicol	55 (83.3)	25 (86.2)	30 (81.1)	0.743
Colistin	66 (100)	29 (100)	37 (100)	NA

Notes: aP values indicate differences between hvKP and cKP. P < 0.05 was considered statistically significant.

Abbreviations: BSI, bloodstream infection; hvKP, hypervirulent K. pneumoniae; cKP, classic K. pneumoniae; NA, not available.

String Test

A total of 29 (43.9%) BSI K. pneumoniae strains were string test positive in the present study. The positive rate was 75.9% (n = 22) in hvKP strains and 18.9% (n = 7) in cKP strains (P < 0.001, Table 1), suggesting that defining hvKP by string test only was not suitable.

Serotype Identification

Of the 66 BSI K. pneumoniae strains, 14 (21.2%) K1, 12 (18.2%) K2, 3 (4.5%) K5, 1 (1.5%) K20, 1 (1.5%) K54, and 2 (3.0%) K57 capsular serotypes were identified. In hvKP strains, K1, K2, K5, K20, K54, and K57 capsular serotypes accounted for 41.4% (n = 12), 31.0% (n = 9), 0 (n = 0), 3.4% (n = 1), 0 (n = 0), and 6.9% (n = 2), respectively, and only 5 (17.2%) strains were K-nontypable (Table 1). Nevertheless, the prevalence of these six serotypes was quite low (5.4%, 8.1%, 8.1%, 0, 2.7%, and 0) in cKP BSI K. pneumoniae strains (Table 1). Taken together, these results suggested a good correlation between hypervirulence and K1/K2 capsular serotypes.

MLST

Among the 66 BSI K. pneumoniae strains, 43 had known STs (involving 30 STs), and the remaining 23 strains each had an nST (), indicating high diversity of these BSI strains. The most common ST was ST23 (n = 7, 10.6%) belonging to clonal complex (CC) 23, followed by ST86 (n = 3). Four strains (6.1%) were categorized as CC65, containing two ST65, one ST25, and one ST375. CC23 and CC65 were the most common CCs in this study.

Nineteen STs were scattered in the 29 hvKP strains, including ST23 (n = 7), ST65 (n = 2), ST86 (n = 2), ST380 (n = 2), ST412 (n = 2), and other 14 distinct STs (), while 39 different STs were distributed in the 39 cKP strains ().

Interestingly, of the 14 K. pneumoniae strains with K1 serotype (hvKP, n = 12), 7 (50%) belonged to ST23, which were all hvKP strains (), indicating a strong correlation between ST23 and K1 serotype in hvKP strains. Differently, among the 12 K2 serotype strains (9 hvKP and 3 cKP), ST86 (n = 3, 25%) was the most common ST, followed by ST380 (n = 2) and ST65 (n = 2). In a word, the present study indicated an association between certain STs and K serotypes (eg, ST23-K1 and ST86-K2).

Clinical Characteristics of BSI Caused by K. pneumoniae Strains

The demographic and clinical data of the 66 enrolled patients with K. pneumoniae BSI are summarized in Table 3. These patients were divided into hvKP and cKP subgroups based on their corresponding isolated K. pneumoniae strains. Of the 66 patients, the median age was 63 years (ranging from 0 to 90 years; IQR, 50–74), and 39 patients (59.1%) were male. Forty-eight (72.7%) patients had a community-acquired BSI, of which 24 were in the hvKP subgroup. Although the percentage of the community-acquired BSI in the hvKP subgroup was higher than that in the cKP subgroup (82.8% vs 64.9%, respectively), no significant difference existed between the two subgroups (P > 0.05; Table 3).

Table 3

Clinical Characteristics of Patients with K. pneumoniae Bloodstream Infection

	No. (%) of Patients
	Total (n=66)	With hvKP (n =29)	With cKP (n =37)	P valuea
Age, median (IQR), y	63 (50–74)	58 (50–73)	64 (47–77)	0.936
Sex
Male	39 (59.1)	15 (51.7)	24 (64.9)	0.281
Female	27 (40.1)	14 (48.3)	13 (35.1)	0.281
Community-acquired	48 (72.7)	24 (82.8)	24 (64.9)	0.105
Hospital-acquired	18 (27.3)	5 (17.2)	13 (35.1)	0.105
Abscess	17 (25.8)	13 (44.8)	4 (10.8)	0.002
Liver abscess	14 (21.2)	12 (41.4)	2 (5.4)	<0.001
Skin abscess	1 (1.5)	1 (3.4)	0 (0)	0.439
Peripancreatic abscess	1 (1.5)	0 (0)	1 (2.7)	>0.999
Abdominal wall abscess	1 (1.5)	0 (0)	1 (2.7)	>0.999
Other types of infections
Pneumonia	26 (39.4)	10 (34.5)	16 (43.2)	0.470
Urinary tract infection	15 (22.7)	5 (17.2)	10 (27.0)	0.346
Abdominal infection	10 (15.2)	1 (3.4)	9 (24.3)	0.045
Skin and soft tissue infection	3 (4.5)	2 (6.9)	1 (2.7)	0.578
≥2 sites of infection	52 (78.8)	23 (79.3)	29 (78.4)	0.901
≥3 sites of infection	19 (28.8)	9 (31.0)	10 (27.0)	0.721
Underlying diseases
Diabetes	38 (57.6)	19 (65.5)	19 (51.4)	0.248
Hypertension	11 (16.7)	3 (10.3)	8 (21.6)	0.375
Coronary heart disease	7 (10.6)	4 (13.8)	3 (8.1)	0.690
Chronic kidney disease	6 (9.1)	3 (10.3)	3 (8.1)	>0.999
Cancer	15 (22.7)	5 (17.2)	10 (27.0)	0.346
Hospitalization in recent 90 days	19 (28.8)	3 (10.3)	16 (43.2)	0.003
ICU stay	20 (30.3)	9 (31.0)	11 (29.7)	0.909
Septic shock	18 (27.3)	7 (24.1)	11 (29.7)	0.613
Organ failure	14 (21.2)	5 (17.2)	9 (24.3)	0.485
Median duration of hospital stay (IQR)	22.3 (9–24.5)	15.5 (9–22)	27.8 (9.5–29.8)	0.138
Outcome
Discharged	54 (81.8)	25 (86.2)	29 (78.4)	0.413
Died	12 (18.2)	4 (13.8)	8 (21.6)	0.413
Readmitted in the following 90 days	13 (24.1)	6 (24.0)	7 (24.1)	0.858

Notes: aP values indicate differences between hvKP and cKP. P < 0.05 was considered statistically significant.

Abbreviations: hvKP, hypervirulent K. pneumoniae; cKP, classic K. pneumoniae; IQR, interquartile range; NT, not tested.

Seventeen (25.8%) patients developed abscesses, including liver abscess (n = 14), skin abscess (n = 1), peripancreatic abscess (n = 1), and abdominal wall abscess (n = 1). The percentage of patients with a liver abscess was significantly higher in the hvKP subgroup than in the cKP subgroup (P < 0.001), indicating the ability of hvKP to develop a liver abscess. Besides abscesses, pneumonia (n = 26), urinary tract infection (n = 15), abdominal infection (n = 10), and skin and soft tissue infection (n = 3) afflicted 39 patients (Table 3), which were all more common in the cKP subgroup, although no statistical difference except for abdominal infection was found between the two groups. Actually, most (n = 52, 78.8%) of the 66 patients had ≥2 sites of infections.

Underlying diseases were noted in all 66 patients (Table 3), including diabetes (n = 38, 57.6%), hypertension (n = 11, 16.7%), coronary heart disease (n = 7, 10.6%), chronic kidney disease (n = 6, 9.1%), and cancer (n = 15, 22.7%). Among these underlying diseases, diabetes, coronary heart disease, and chronic kidney disease were more prevalent in the hvKP subgroup, while hypertension and cancer were more prevalent in the cKP subgroup (Table 3). However, no significant statistical differences existed between the hvKP and cKP subgroups in these diseases (P > 0.05). Interestingly, of the 38 patients with diabetes, 12 (31.6%) developed a liver abscess. Among the remaining 28 patients without diabetes, only 2 (7.1%) developed a liver abscess (P = 0.016), demonstrating a strong association between diabetes and liver abscess.

Additionally, 19 (28.8%) patients had a history of hospitalization within 90 days prior to admission. A significant difference in hospitalization within recent 90 days was found between the hvKP subgroup and the cKP subgroup, with 10.3% and 43.2%, respectively (P = 0.003; Table 3).

Although no statistical significance was noted, the cKP subgroup seemed to have a higher percentage of ICU stay, septic shock, and organ failure (30.3%, 27.3%, and 21.2%, respectively) and longer median hospital stay in this study (Table 3), suggesting that patients with cKP were prone to develop a severe disease and have a longer hospital stay.

The 30-day mortality rate of K. pneumoniae BSI was 18.2% in this study, and it was higher (21.6%) in the cKP subgroup (Table 3). After discharge from the hospital, 13 (24.1%) patients were readmitted to the hospital in the following 90 days, with 6 in the hvKP subgroup and 7 in the cKP subgroup (Table 3). Of them, four patients (4/13, 30.8%) were due to bacterial infection, including three (3/6, 50%) in the hvKP subgroup and one (1/7, 14.3%) in the cKP subgroup.

Discussion

The present retrospective study provided insights into the clinical and microbiological characteristics of patients with K. pneumoniae BSI, especially revealing the distribution of virulence genes in hvKP. A relatively high percentage (43.9%) of hvKP in BSI K. pneumoniae strains was found to carry multiple virulence genes in this study, and these pathogens were of multiclonal origin.

The hypermucoviscosity and the iron acquisition systems (siderophores) are common in hvKP strains, which are considered as the main features of hvKP. In the present study, strains with iucA gene (for siderophore aerobactin) were defined as hvKP, and a relatively higher proportion of BSI hvKP was found compared with previous studies (21.6–31.4%).2,7,10 The prevalence of hvKP in BSI was relatively high in China, but varied in different regions, which might partially result from the geographical difference and the inconsistent definition of hvKP. Recently, Harada et al revealed that 25.5% (n = 26) of BSI K. pneumoniae strains at hospitals across Japan were hvKP (defining hvKP as positive for any of rmpA, rmpA2, iroBCDN, iucABCD, and iutA).22

Previous studies showed that various virulence factors could concurrently be present in hvKP.3 This study revealed that BSI hvKP strongly related to rmpA, iroBCD cluster, ybtS, clbA, and allS. The siderophore aerobactin is a dominant and critical siderophore for hvKP, which plays an important role in systemic infection.3 In this study, 43.9% of BSI hvKP strains carried the iucABCD cluster, which was consistent with a recent study from South Korea (41.5% of BSI K. pneumoniae carried iucA gene).23 Lan et al from China reported that a lower percentage of BSI K. pneumoniae was iucA positive (28.9%).10 In this study, more than half of the BSI K. pneumoniae were also found to possess genes for other two siderophores (salmochelin and yersiniabactin). The exact role of these siderophores in BSI hvKP needs to be further investigated.

Colibactin, which is encoded by the pks gene cluster and exerts as genotoxins, was first found in E. coli and was associated with BSI.24 The presence of the pks gene cluster has been related to early mortality in patients with BSI caused by K. pneumoniae.23 The real role of colibactin in the pathogenesis of hvKP remains to be explored. Colibactin was detected in 27.3% of BSI K. pneumoniae strains in the present study, consistent with the studies by Lan et al and Kim et al (26.8% and 27.3%, respectively).10,23 Putze et al reported a much lower rate (3.5%) of clinical K. pneumoniae being colibactin positive in Europe.25 Additionally, the colibactin-positive rate was 16.7% in K. pneumoniae isolated from various clinical samples in Taiwan.26

Interestingly, in this study, all colibactin-producing hvKP strains except one co-carried ybtA. Kim et al reported that 27.3% (n = 158) of BSI K. pneumoniae strains co-harbored the pks gene cluster and ybtA.23 Additionally, although allantoin metabolism genes do not seem to be important for systemic infection,6 this study demonstrated 22.7% of BSI K. pneumoniae strains with allS, suggesting a potential role of allS in BSI. Taken together, more studies are needed to clarify the real role of these virulence factors in BSI.

The present study suggested the association between hypervirulence and K1/K2/K20/K57 capsular serotypes, consistent with other studies from China.2,8,9 Additionally, this study revealed that 72.4% of hvKP strains were K1 and K2 capsular serotypes, while only 13.5% of cKP belonged to these two serotypes. These findings indicated that K1 and K2 capsular serotypes played key roles in hvKP BSI. K5 and K54 capsular serotypes were not detected in BSI hvKP strains in the present study, consistent with previous studies.2,7

In this study, the BSI-causing K. pneumoniae strains were of multiclonal origin, despite the most common ST (ST23) accounting for 10.6%. Similarly, Liu et al reported that 42 STs were identified in the 70 BSI K. pneumoniae strains.2 Wu et al demonstrated that more than 36 STs were established in 79 BSI K. pneumoniae strains.27

This study revealed that hvKP strains were more susceptible to tested antibiotics than cKP, consistent with previous studies.1,8,10 The confluence of hypervirulence and multidrug resistance, especially carbapenem resistance, is extremely alarming. Although carbapenem-resistant hvKP has been described in previous studies,7,9,28–30 it was not found in the present study. This might be partially attributed to the regional difference.

Although various infections had developed in patients with BSI in the present study, a liver abscess was more likely to be associated with hvKP, suggesting the capability of hvKP to develop a liver abscess, which was in agreement with previous studies.1,8,11 The results of this study also indicated a strong association between diabetes and liver abscess (mainly by hvKP, 85.7%), in accordance with an earlier study.16 Thus, it is reasonable to conclude that patients with diabetes may be prone to suffer from hvKP liver abscess and develop hvKP BSI afterward. This was in line with a theory that diabetes is a risk factor for an hvKP infection, and the confluence of diabetes and liver abscess is likely to develop secondary infections.31 Although diabetes was identified as an independent risk factor for hvKP BSI in a previous study,7 more studies are needed to clarify this.

Although no significant difference in the 30-day mortality rate was noted between cKP and hvKP subgroups, the percentage of mortality was higher in the cKP BSI subgroup than in the hvKP BSI subgroup in the present study, consistent with earlier studies in patients with BSI.2,7 Recently, a study reported that the hypermucoviscosity (as a marker for defining hvKP in several studies) displayed an inverse association with 30-day mortality in BSI K. pneumoniae strains.23 Similarly, Hwang et al recently reported that the 30-day mortality in patients with cKP pneumonia (26.9%) was higher than that in patients with hvKP pneumonia (17.9%).32 This might be attributed to patients in the cKP subgroup usually having more and much severe underlying diseases, as well as greater age. Additionally, a higher percentage (43.2% in cKP vs 10.3% in hvKP) of a history of hospitalization in recent 90 days may be partially contributed to the higher mortality in the cKP subgroup. Finally, in the present study cKP BSI strains were more resistant to the common empiric antibiotics and then likely caused treatment failure, which might also be contributed to the higher mortality in those patients.33 More prospective studies are needed to confirm the real role of hvKP in the mortality of patients with BSI.

This study had several limitations. First, the presence of the aerobactin gene was detected, and hvKP was defined on the basis of aerobactin positivity. However, the aerobactin production was not assessed. Further studies defining hvKP by assessing the quantitative production of aerobactin would be warranted, and studies in vitro and in vivo may be needed to confirm the real virulence of K. pneumoniae. Second, this was a single-center experience with a relatively small study sample. Multicenter studies with a larger population are required.

Conclusions

This study demonstrated a high proportion of hvKP in BSI K. pneumoniae. These hvKP strains had a strong correlation with various virulence factors and were of multiclonal origin. It provided insights into the clinical and microbiological features of BSI caused by K. pneumoniae strains, highlighting the significance of clinical awareness, and might be helpful in the clinical management of hvKP BSI.