Hostname: page-component-89b8bd64d-46n74 Total loading time: 0 Render date: 2026-05-09T07:40:22.099Z Has data issue: false hasContentIssue false
  • English
  • Français

Non-O1/non-O139 Vibrio cholerae bacteraemia in mainland China from 2005 to 2019: clinical, epidemiological and genetic characteristics

Published online by Cambridge University Press:  08 July 2020

Xinyao Li ,
Yuanyuan Wu ,
Xiaojun Sun ,
Jianping Ma ,
Xiaofeng Li ,
Cuiping Liu  and
Hongxiang Xie Open the ORCID record for Hongxiang Xie [Opens in a new window]
Xinyao Li
Affiliation:
Department of Cardiology, Zhejiang Hospital, Hangzhou, China Department of Clinical Laboratory, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, China
Yuanyuan Wu
Affiliation:
Department of Shungen Conservative and Endodontic Dentistry, Jinan Stomatology Hospital, Jinan, China
Xiaojun Sun
Affiliation:
Department of Clinical Laboratory, The First Affiliated Hospital of Shandong First Medical University, Jinan, China
Jianping Ma
Affiliation:
Department of Clinical Laboratory, The First Affiliated Hospital of Shandong First Medical University, Jinan, China
Xiaofeng Li
Affiliation:
Department of Clinical Laboratory, The First Affiliated Hospital of Shandong First Medical University, Jinan, China
Cuiping Liu
Affiliation:
Department of General Medicine, The First Affiliated Hospital of Shandong First Medical University, Jinan, China
Hongxiang Xie*
Affiliation:
Department of Clinical Laboratory, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, China Department of Clinical Laboratory, The First Affiliated Hospital of Shandong First Medical University, Jinan, China
*
Author for correspondence: Hongxiang Xie, E-mail: xiehongxiang007@163.com
Rights & Permissions [Opens in a new window]

Abstract

In mainland China, the clinical, epidemiological and genetic features of non-O1/non-O139 Vibrio cholerae (NOVC) bacteraemia have been scarcely investigated. Herein, we describe a patient with NOVC bacteraemia diagnosed in our hospital and present a retrospective analysis of literature reports of 32 other cases in China, detailing the clinical epidemiology, antibiotic resistance and molecular characteristics of isolates. Most patients were male (84.8%; median age, 53 years) and had predisposing factors, such as cirrhosis, malignant tumours, blood diseases and diabetes. In addition to fever, gastroenteritis was the most frequent presenting symptom. The mortality rate during hospitalisation was 12.1%. NOVC bacteraemia cases were more common in June–August, with the majority in coastal provinces and the Yangtze River basin. Only 42.4% of cases were attributed to consumption of marine (aquatic) products. Tetracycline, third-generation cephalosporins, and fluoroquinolones were the most effective antimicrobial agents, and the highest frequencies of resistance were recorded for ampicillin/sulbactam (37.5%), amoxicillin/clavulanic acid (33.3%), ampicillin (29.2%) and sulfamethoxazole (20%). Multi-drug resistant isolates were not detected. Limited data indicate that ctxAB and tcpA genes were absent in all NOVC isolates but other putative virulence genes (hlyA, toxR, hap and rtxA) were common. Ten multilocus sequence types were identified with marked genetic heterogeneity between different isolates. As clinical manifestations of NOVC bacteraemia may vary widely, and isolates exhibit genetic diversity, clinicians and public health experts should be alerted to the possibility of infection with this pathogen because of the high prevalence of liver disease in China.

Keywords

antimicrobial resistancebacteraemiaChinacirrhosisnon-O1/non-O139 Vibrio cholerae

Information

Type
Review
Information
Epidemiology & Infection , Volume 148 , 2020 , e186
Check for updates
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2020. Published by Cambridge University Press

Introduction

Vibrio cholerae is a pathogenic Gram-negative bacillus, which is widely distributed in water environments. Vibrio cholerae can be classified into more than 200 serotypes according to the differences of its lipopolysaccharide surface O-antigen. Serotypes, O1 and O139 are associated with classic cholera outbreaks of infection worldwide [Reference Clemens1], while non-O1/non-O139 V. cholerae (NOVC) isolates do not produce the cholera-causing toxin. Although the clinical significance of these strains has been previously ignored, a number of reports have documented their role in human infections [Reference Baker-Austin2, Reference Deshayes3].

NOVC most often causes sporadic gastroenteritis and less commonly, parenteral invasive infections. The group of organisms has been estimated to cause 1–3.4% of acute diarrhoeal episodes in both developing and developed countries [Reference Deshayes3]. NOVC bacteraemia remains rare but has been reported sporadically in a few countries. Despite its large population, clinical and epidemiological data pertaining to NOVC bacteraemia cases are scarce from mainland China with little information on the distribution of virulence-associated genes and genetic relationships among isolates. Herein, we present a case of bacteraemia due to a NOVC strain in an elderly male with underlying alcoholic liver cirrhosis, and a retrospective analysis of related reports of 32 other cases in mainland China.

Case report

The patient (male, 67 years old) was admitted to the hospital because his ‘two upper limbs had been shaking spontaneously for 1 week, with aggravated salivation in the left corner of the mouth for 1 day’ on 2 July 2019. The shaking manifested at rest, disappeared during activity and sleeping, but increased during tension; excess salivation was evident on the day prior to the onset of shaking. He presented with a history of previous hypertension, alcoholic cirrhosis and diabetes mellitus, but had not been exposed to uncooked seafood or contaminated water, or a history of travel to cholera-endemic areas. On admission, his temperature was 37.0 °C; heart rate, 72/min; blood pressure, 148/77 mmHg. Physical examination revealed icteric skin sclera, mild ascites, splenomegaly, tremor in both upper limbs and positive for Romberg's Sign. Laboratory examination results were as follows: plasma ammonia 131 μmol/l, alanine aminotransferase 19 U/l, aspartate aminotransferase 25 U/l, total bilirubin 36.5 μmol/l, direct bilirubin 18.1 μmol/l, total protein 47.5 g/l, albumin 26.3 g/l, prothrombin time 16.90 s, activated partial thromboplastin time 53.00 s, D dimer 2.26 ml/l, fibrinogen 8.48 ml/l, white blood cell count 3.06 × 109/l, haemoglobin 114.0 g/l and platelet count 46 × 109/l. Ultrasonography showed intraperitoneal effusion, liver cirrhosis, splenomegaly and a hepatopathic gallbladder with multiple gallbladder stones. Chest CT showed a nodular high-density image in the right lower lung field and right pleural effusion. After admission, treatment was administered to improve blood circulation, promote brain metabolism, reduce blood ammonia and control blood sugar to alleviate symptoms. Vomiting and diarrhoea had occurred once after eating meat dumpling on the night of 2 July but was not treated as he did not notify a doctor. On the evening of 6 July, he developed a sudden high fever of 39.2 °C, and emergency laboratory tests showed a white blood cell count of 8.62 × 109/l with 85% neutrophils, and an elevated procalcitonin level of 0.145 ng/ml. A blood sample (10 ml) was taken for culture and the patient was treated empirically with cefoperazone/sulbactam for a suspected bacterial infection.

The blood culture tested positive at 8.5 h and after 24 h culture on blood agar grew β-haemolytic, oxidase-positive colonies which on subculture on TCBS agar, appeared as large yellow colonies. Vibrio cholerae was suspected and identified by the matrix-assisted laser desorption ionisation-time-of-flight analyser (MALDI-TOF, Bruker). NOVC was identified by slide agglutination tests with polyvalent O1 and O139 antisera, and later confirmed by Shandong Provincial Center for Disease Control and Prevention (CDC). Drugs tested as per CLSI 2016 guidelines showed that the isolate was susceptible to trimethoprim/sulfamethoxazole, third- and fourth-generation cephalosporins, fluoroquinolones and carbapenems. Treatment with cefoperazone/sulbactam was initiated and 2 days later, the patient's temperature returned to normal, with gradual alleviation of symptoms. The patient was finally diagnosed with hepatic encephalopathy, bacteraemia, decompensated alcoholic cirrhosis, hypertension, type 2 diabetes, right lung nodules, right pleural effusion, anaemia, thrombocytopaenia, coagulopathy and peritoneal effusion. He was transferred to the local infectious disease hospital for further treatment, and repeat blood cultures proved negative with no recurrence of fever at 1-month follow-up.

Literature review

Methods

A literature review was conducted via an electronic search on PubMed, Web of Science, Embase and Ovid by crossing the keywords ‘V. cholerae non-O1’ and ‘bacteremia’. The Boolean operator ‘AND’ was used to add the country for our area-specific search strategy after an initial screen of the literature on NOVC bacteraemia; relevant references of the searched papers were also checked. A search of Chinese-language databases (CNKI, VIP, Wanfang Data) from 1995 through 2019 was also undertaken. Two experienced clinicians reviewed the retrieved articles in full, and after elimination of duplicate studies, we retrieved 24 publications on NOVC bacteraemia from mainland China, all cases were the diagnosis of bacteraemia based on blood culture [Reference Cao4–Reference Liu27], and asked the authors for relevant medical records by E-mail. Including our case, a total of 33 cases were identified in mainland China, all of which were sporadic. Most were case reports, and the largest series comprised five patients. A database was established, and information entered included patient demographics, medical history and risk factors such as environmental exposure, clinical presentation, antimicrobial susceptibility and virulence genes of isolates, treatment, and clinical outcome. QGIS software was used for mapping NOVC isolates in Chinese provinces. Further searches were made of the PubMLST database (http://pubmlst.org/vcholerae/) for multilocus sequence typing (MLST) data to determine the degree of genetic heterogeneity among the isolates. A minimum spanning tree based on the allelic difference among seven housekeeping genes by MLST was constructed using Bionumerics (Applied Maths, Ghent, Belgium).

Results

Demographic and clinical parameters of 33 NOVC bacteraemia cases

The first NOVC bacteraemia case was described in 2005, the number of cases peaked in 2012, and 16 cases were reported since 2014 (Fig. 1). The age range was 11 days–89 years (median = 53); 28 males (84.8%) and 5 females (M/F ratio, 5.6:1). Only two cases under 18 years old were reported. The main clinical features are shown in Table 1. The most common risk factors were liver cirrhosis, followed by malignant tumour, haematologic malignancy and diabetes mellitus. Hepatitis B infection was the most common cause of liver cirrhosis (59.1%), followed by chronic alcohol consumption (18.2%). In addition to fever, abdominal pain, diarrhoea, nausea and vomiting were most common. In only 42.4% of cases, the source of infection was associated with the consumption of aquatic products or exposure to contaminated water. Four (12.1%) of the 33 patients died due to NOVC infection during hospitalisation, and two patients abandoned treatment due to serious underlying diseases, giving an estimated overall mortality rate of 18%.

Fig. 1.

Cases of NOVC bacteraemia reported annually in mainland China.

Table 1.

Demographic and clinical parameters of 32 NOVC bacteraemia in mainland China

M, male; F, female; HBC, hepatitis B-caused liver cirrhosis; –, not available or missing information

Antimicrobial resistance of isolates

Antimicrobial susceptibility testing data were not uniform due to the variation in numbers of isolates and the range of agents tested. However, resistant isolates were identified for trimethoprim/sulfamethoxazole (6 of 30 cases), ampicillin (7/24), ampicillin/sulbactam (3/8), amoxicillin/clavulanic acid (3/9), cefazolin (1/6), cefepime (1/18), ceftazidime (1/24), imipenem (3/28), nalidixic acid (1/2) and polymyxin B (3/3). Multi-drug-resistance was not detected. Isolates fully susceptible to other antimicrobials were as follows: gentamicin (26 tested), amikacin (28), levofloxacin (25), ciprofloxacin (23), piperacillin/tazobactam (18), piperacillin (20), meropenem (16), cefotaxime (16), tetracycline (16), ceftriaxone (14), cefoperazone/sulbactam (9), aztreonam (13), chloramphenicol (9), tobramycin (10), cefoxitin (6), furantoin (6), minocycline (4), cefuroxime (4), gatifloxacin (4), streptomycin (3), doxycycline (3), norfloxacin (3) and ertapenem (3).

Spatial and temporal distributions of NOVC isolates

NOVC bacteraemia cases were reported from 13 provinces, the majority being coastal provinces, and the Yangtze River basin (Fig. 2). Cases were reported from April to October, and was most common (23 cases, 70%) in June to August. Four cases were reported in September, and single cases in April, May and October; the isolation month for the remaining three cases was not reported.

Fig. 2.

The distribution of NOVC bacteraemia cases between 2005 and 2019 in mainland China according to published literature.

Distribution of virulence factors genes

Data on virulence genes were available for 15 isolates (Table 2). All were negative for cholera toxin genes. Eleven isolates were tested and positive for the rtx virulence gene (encoding repeat toxin subunit A or C, respectively), and seven were tested and positive for hap (encoding haemagglutinin protease). All, but one, of 10 isolates carried hlyA (encoding El Tor-like haemolysin), and 6/7 harboured toxR gene (encoding CT transcriptional activator). None of the tested isolates was positive for type III secretion system (T3SS) genes. Miscellaneous isolates proved positive for various other virulence genes (Table 2).

Table 2.

Details of NOVC strains reported in the literature and PubMLST database

NA, not available or missing information.

Molecular typing

MLST data were reported for 10 isolates, all of which were unique (Table 2). None of them belonged to ST80 which was the dominant ST reported from China of NOVC recovered from diarrhoeal stools [Reference Luo28]. The 10 isolates showed high diversity and were distinct from their toxigenic O1 and O139 counterparts (Fig. 3). Most STs differed from each other by three or more loci, with no evidence of clustering according to year or geographic location.

Fig. 3.

Minimum spanning tree analysis of NOVC isolates based on sequence type (ST). Ths STs are designated by the number in the circle; the size of the circle corresponds to the total number of each ST. The digits on the lines between the two circles represent the number of allelic differences.

Discussion

Following the identification of a case of NOVC bacteraemia in our hospital (Shandong province), we conducted a retrospective case series analysis of reports of 32 cases, in addition to our case, in mainland China from 2005 to 2019. Where reported, data were extracted on risk factors, epidemiology, clinical presentations and mortality as well as genetic characterisation of reported causative isolates. A review of the related literature in mainland China showed that the incidence of NOVC bacteraemia is higher in summer and autumn, and predominantly affects middle-aged males, and rarely children. Our case also occurred during this season in a 67-year-old man with mild diarrhoea and vomiting, as reported for other cases. It is not known why men are more susceptible to NOVC infection than women, but a similar trend has been noted in other Vibrio infections [Reference Baker-Austin and Oliver29]. Recently, it has been suggested that the pro-inflammatory effect of oestradiol may reduce the incidence of some bacterial infections and associated complications in women, while the susceptibility of males may be associated with testosterone-mediated immunosuppression [Reference Vazquez-Martinez30]. Additionally, behavioural and social factors such as differences in consumption levels of seafood and alcohol, and aquatic exposure may also explain this gender-related variation.

In the 350 cases of NOVC bacteraemia reviewed by Deshayes et al. [Reference Deshayes3], most cases were identified in patients with underlying diseases, especially liver disease/cirrhosis and immunosuppressed conditions. In mainland China, the most common risk factor was liver cirrhosis, followed by malignant tumour, haematologic malignancy and diabetes mellitus, which is consistent with Deshayes' report. Susceptibility to NOVC bacteraemia in patients with liver cirrhosis may be related to anatomical and physiological changes including high intestinal mucosal permeability due to inflammation and oedema, by-pass of the hepatic reticuloendothelial system by portal hypertension, complement deficiencies, impaired phagocytosis, and alterations in iron metabolism and/or inefficient chemotaxis [Reference Zmeter31]. It has also been suggested that liver disease and haematological malignancy are often accompanied by low platelet count or abnormal coagulation function, which might facilitate the passage of the bacteria into the systemic circulation, leading to bacteraemia [Reference Ma16]. Recent epidemiological data showed that the trend of liver cirrhosis between gender and age in China was similar to that observed in NOVC cases, with a disproportionate rate of liver cirrhosis in both male and elderly groups [Reference Wang32, Reference Bao33]. This feature may help to explain the observed gender differences.

The clinical manifestations of NOVC bacteraemia in our series proved to be varied. Fever, abdominal pain and diarrhoea were the most common presentations but three were blood culture-negative and had jaundice and ascites, both of which are indicative of liver cirrhosis, rather than the NOVC infection itself. Diarrhoea was usually watery with no mucus and blood. Deshayes et al. reported that a minority (12%) of NOVC bacteraemia cases had bloody (12%) or mucous stools (8%), and almost 5% had abscesses, including hepatic, prostatic, cerebral and peritoneal abscesses [Reference Deshayes3]. Additionally, pyomyositis, pneumonia, cellulitis, necrotizing fasciitis, endophthalmitis, and meningitis and other rare clinical conditions have been noted by others [Reference Maraki34–Reference Marinello38]. Our patient had an atypical clinical manifestation of NOVC bacteraemia, except for abnormal liver function tests which were shown by ultrasonography to be due to liver cirrhosis. He had only mild digestive symptoms and the diagnosis mainly depended on blood culture. Stool cultures were performed in 18 cases in the literature review series, all of which were negative for NOVC, despite them having positive blood cultures. It is possible that the stool culture was tested after the start of antimicrobial treatment, leading to the negative result. Indeed, the isolation of NOVC has been reported from various body sites including the respiratory tract, bile, uterus, urine, cerebrospinal fluid, among others [Reference De Keukeleire39].

The epidemiology of NOVC bacteraemia has yet to be clarified. Cases might be related to exposure to the aquatic environment or ingestion of aquatic products as the presence of pathogenic vibrios in aquaculture in mainland China has been documented at rates of 0.8–25.96%, with an even higher frequency in circulation and catering links [Reference Wang40–Reference Qin42]. However, the majority (57.6%) of the mainland cases reviewed here did not report a history of consumption of aquatic products or exposure to contaminated water, which suggests that other routes of infection existed. In fact, NOVC have been isolated from wild and domestic animals and in asymptomatic human carriers [Reference Baker-Austin2, Reference Kaki43]. Ma et al. [Reference Ma16] and Li et al. [Reference Li23] both reported cases of NOVC bacteraemia in patients with malignant blood diseases, and suggested that the most likely source of infection was chicken ingested prior to disease onset. Notably, reports of iatrogenic infections linked to NOVC bacteraemia in mainland China underline the importance of timely detection of the organism and isolation of patients [Reference Guo5]. Our patient had neither recently been exposed to contaminated water nor eaten raw seafood, and hence the source of contamination remains unknown. However, he had consumed a meal of meat dumplings on the day prior to the onset of fever, and in the absence of other information to the contrary, we surmised that ingestion of contaminated food was the most likely source of infection.

The exact mechanism by which NOVC invade the bloodstream remains unclear. MLST analysis showed that isolates from cases had high genotypic diversity and were distinct from the dominant NOVC clone in China (ST80), generally associated with sporadic infections [Reference Luo28]. All strains tested were negative for the virulence-encoding regions of toxigenic V. cholerae, such as ctxAB or tcpA, but possessed several genes encoding putative accessory virulence factors, including hlyA, hap, toxR, rtxA and T6SS, which might play a role in the disease process. Although OmpW gene is highly conserved in V. cholerae and can be used for the identification of this microorganism, it is worth noting that the OmpW gene might be negative in some NOVC strains. Accordingly, we speculated that these factors might contribute to bloodstream invasion in immunosuppressed conditions, due to production of haemolysin, or cytotoxin (rtxA encoded), and their ability to induce cell vacuolation [Reference Hao26]. More recently, it was suggested that naturally occurring IgG recognizing V. cholerae outer membrane protein U (OmpU) mediates a serum-killing effect in a complement C1q-dependent manner. Differences in OmpU protein level among different biotypes of V. cholerae was considered a reasonable cause for their observed differences in serum resistance, and hence the ability to cause bacteraemia [Reference Aung44]. Additionally, the presence of the cholera toxin genes ctxA and tcpA in NOVC isolates has been reported in mainland China, which might be related to horizontal transfer of these virulence genes [Reference Li45]. In our patient case, the blood culture isolate showed β-haemolytic colonies, strongly suggesting the production of haemolysin. Additionally, the patient had a poor immune function and coagulation dysfunction, making it easier for the bacteria to breach the patient's immune barrier and enter the bloodstream.

Because NOVC bacteraemia is rare, in the absence of large-scale clinical trials, there are no guidelines for the treatment of such cases. It has been suggested that third-generation cephalosporins or fluoroquinolones are the most suitable agents for these patients but the duration of treatment is also controversial (range 3–75 days; median 14 days). This duration should be adjusted according to the patient's background, clinical manifestation and disease severity (such as meningitis and abscess) [Reference Deshayes3]. The mortality rate is considered to exceed 25%, and has been significantly associated with respiratory, circulatory or neurological failure [Reference Deshayes3, Reference Chen37]. Unlike these patients, our case was an elderly male with comorbidities predisposing him to NOVC bacteraemia. However, his symptoms improved within 2 days after receiving treatment with cefoperazone/sulbactam as a single agent therapy.

Antimicrobial susceptibility testing showed our patient's isolate was susceptible to several commonly recommended antibiotics. We noted that there was significant heterogeneity in the choice, dosage and duration of antimicrobial agents in the published cases from mainland China. Existing data suggest that the administration of tetracycline, cephalosporins and fluoroquinolones remains the best choice. The resistance rates of sulfamethoxazole and ampicillin were unacceptably high, and imipenem also showed less than optimal activity. However, an important factor impeding our reviewed data from being extrapolated to clinical practice was that many authors reported only agents active in their cases, and so, wider documentation of antimicrobial resistance data is required to allow a critical assessment of resistance rates. As most NOVC infections originate from water environments, the influence of intensive use of antibiotics in agriculture and animal husbandry, and the emergence of multidrug-resistant clones, is a cause for concern. Antimicrobial susceptibility testing of naturally occurring and clinical patient isolates therefore remains critical to ensure optimal choice of agent and therapy [Reference Qiao46, Reference Baron47].

In conclusion, NOVC bacteraemia in a minority of cases can prove fatal. As sea surface temperatures continue to rise globally, there is a risk of increased proliferation of pathogenic vibrios in aquatic environments which pose a potential global threat. We should therefore maintain a high level of awareness of these infections especially in patients with a history of liver disease because of the high prevalence of hepatitis B infection in China.

Author contributions

XYL and YYW designed the study and wrote the manuscript. JPM and XFL identified the isolate as NOVC and helped to collect the data. CPL, XJS and HXX added their critical review and comments. All authors participated in preparing the manuscript and approved its publication.

Financial support

This work was supported by the National Natural Science Foundation of China (No: 81600110), Zhejiang Provincial Health Bureau (No: 2016KYA010) and Outstanding Youth Foundation of Zhejiang Provincial People's Hospital (No: ZRY2016B008) to Hong-Xiang Xie. The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.

Conflict of interest

The authors declare no conflicts of interest.

Ethical standards

This article does not contain any studies with human participants performed by any of the authors.

Data availability statement

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

Footnotes

*

These authors contributed equally to this work.

References

Clemens, JD et al. (2017) Cholera. Lancet 390, 1539–1549.CrossRefGoogle ScholarPubMed
Baker-Austin, C et al. (2018) Vibrio spp. infections. Nature Reviews Disease Primers 4, 8.CrossRefGoogle ScholarPubMed
Deshayes, S et al. (2015) Non-O1, non-O139 Vibrio cholerae bacteraemia: case report and literature review. Springerplus 4, 575.CrossRefGoogle ScholarPubMed
Cao, LJ et al. (2006) Two cases of sepsis caused by Vibrio cholera. Modern Practical Medicine 18, 282.Google Scholar
Guo, TS et al. (2007) Clinical and laboratory characteristics of septicemia in hepatic cirrhosis patients infected by non-O1 non-O139 Vibrio cholerae. Chinese Hepatology 12, 368–370.Google Scholar
Deng, X, Yin, L and Yu, H (2011) Detection of non-O1 Vibrio cholerae in blood of patients with liver cirrhosis. Practical Journal of Clinical Medicine 8, 202.Google Scholar
Wu, ZC et al. (2012) Isolation and identification of an atypical non-O1 Vibrio cholerae. Chinese Journal of Nosocomiology 22, 4422–4424.Google Scholar
Zhu, DF, Qi, CG and Huang, DW (2013) A case of sepsis caused by non-O1 non-O139 Vibrio cholerae. Chinese Journal of Clinical Laboratory Science 31, 800.Google Scholar
Wang, WQ et al. (2013) Detection of Vibrio cholerae non-O1 non-O139 from a patients with leukemia. Disease Surveillance 28, 772–774.Google Scholar
Zou, YM et al. (2013) A case report on non-O1 and non-O139 Vibrio cholerae septicaemia. Journal of Microbiology 33, 78–80.Google Scholar
Liu, AJ, Zhang, QX and Huang, XR (2014) Detection of 3 strains non-O1 non-O139 Vibrio cholerae in blood and ascites of patients with liver cirrhosis. Laboratory Medicine 29, 1076–1077.Google Scholar
Qi, CG, Zhu, DF and Huang, DW (2014) Septic shock induced by non-O1 non-O139 Vibrio cholerae in a patient with alcoholic liver cirrhosis. Chinese Journal of Clinical Infectious Diseases 2, 174–175.Google Scholar
Zou, YM et al. (2014) Identification and virulence gene detection of non-O1 and non-O139 Vibrio cholerae isolates causing septicemia. Chinese Journal of Infection and Chemotherapy 14, 186–189.Google Scholar
Xu, HB et al. (2016) Detection of Vibrio cholerae non-O1/non-O139 from the blood of patient with hepatocholangitis. Preventive Medicine Tribune 22, 485–487.Google Scholar
Zhang, Q et al. (2016) Analysis on the main virulence genes and molecular typing of non-O1/non-O139 Vibrio cholerae in bloodstream infection. Chinese Journal of Infectious Diseases 12, 732–737.Google Scholar
Ma, XB et al. (2016) A case report of non-O1 non-O139 Vibrio cholerae sepsis. International Journal of Laboratory Medicine 37, 1302–1303.Google Scholar
Ji, XT et al. (2016) An identification report of sepsis caused by non-O1 non-O139 Vibrio cholerae. World Chinese Medicine 11, 2033–2034.Google Scholar
Zhai, BC et al. (2017) Non-O1/non-O139 Vibrio cholerae septicemia in patients with liver cirrhosis and ascites. World Chinese Journal of Digestology 25, 420–425.Google Scholar
Zhu, LZ et al. (2017) A case of hepatitis B cirrhosis with non-O1 group non-O139 Vibrio cholerae sepsis. Chinese Journal of Infectious Diseases 10, 635–636.Google Scholar
Zhai, HF et al. (2018) Non-O1 and non-O139 Vibrio cholerae septicemia in patients with hepatopathy: a report of 3 cases. Chinese Journal of Clinical Infectious Diseases 3, 209–212.Google Scholar
Nie, YH and Ming, RC (2018) Analysis of a non-O1 group and non-O139 Vibrio cholerae in blood culture of a lung cancer patient. China Practical Medical 2018, 147–148.Google Scholar
Chen, YX et al. (2018) Identification of a non-O1/O139 Vibrio cholerae causing multiple organ dysfunction syndrome. Journal of Parasitic Biology 13, 831–834.Google Scholar
Li, H et al. (2019) Investigation and analysis of non-O1 non-O139 Vibrio cholerae in patients with non-Hodgkin's lymphoma. Chongqing Medicine 48, 3931–3933.Google Scholar
Shan, JH et al. (2019) Report of 1 case of non O1 group non O139 group Vibrio cholerae infected by blood. Journal of Anhui Health Vocational & Technical College 1, 138–139.Google Scholar
Lu, B et al. (2014) The first case of bacteraemia due to non-O1/non-O139 Vibrio cholerae in a type 2 diabetes mellitus patient in mainland China. International Journal of Infectious Diseases 25, 116–118.CrossRefGoogle Scholar
Hao, Y et al. (2015) A case of non-O1/non-O139 Vibrio cholerae septicemia and meningitis in a neonate. International Journal of Infectious Diseases 35, 117–119.CrossRefGoogle Scholar
Liu, Y et al. (2019) One case of nosocomial infection with non-O1 and non-O139 Vibrio cholerae sepsis. International Journal of Epidemiology and Infectious Disease 46, 258–259.Google Scholar
Luo, Y et al. (2013) Molecular analysis of non-O1/non-O139 Vibrio cholerae isolated from hospitalised patients in China. BMC Microbiology 13, 52.CrossRefGoogle ScholarPubMed
Baker-Austin, C and Oliver, JD (2018) Vibrio vulnificus: new insights into a deadly opportunistic pathogen. Environmental Microbiology 20, 423–430.CrossRefGoogle ScholarPubMed
Vazquez-Martinez, ER et al. (2018) Sexual dimorphism in bacterial infections. Biology of Sex Differences 9, 27.CrossRefGoogle ScholarPubMed
Zmeter, C et al. (2018) Non-O1, non-O139 Vibrio cholerae septicemia at a tertiary care center in Beirut, Lebanon; a case report and review. Journal of Infection and Public Health 11, 601–604.CrossRefGoogle Scholar
Wang, WJ et al. (2019) Growing burden of alcoholic liver disease in China: a review. World Journal of Gastroenterology 25, 1445–1456.CrossRefGoogle ScholarPubMed
Bao, XY et al. (2015) Changing trends of hospitalisation of liver cirrhosis in Beijing, China. BMJ Open Gastroenterology 2, e000051.CrossRefGoogle ScholarPubMed
Maraki, S et al. (2016) Non-O1, non-O139 Vibrio cholerae bacteraemic, skin and soft tissue infections. Infectious Diseases (London) 48, 171–176.CrossRefGoogle Scholar
Ma, HY, Chen, JM and Hsueh, PR (2015) Brain infarct and meningitis due to non-O1 Vibrio cholerae. Journal of Infection 70, 694–695.CrossRefGoogle Scholar
Chowdhury, G et al. (2016) Extraintestinal infections caused by non-toxigenic Vibrio cholerae non-O1/non-O139. Frontiers in Microbiology 7, 144.CrossRefGoogle ScholarPubMed
Chen, YT et al. (2015) Clinical manifestations of non-O1 Vibrio cholerae infections. PLoS ONE 10, e0116904.CrossRefGoogle ScholarPubMed
Marinello, S et al. (2017) Vibrio cholerae non-O1, non-O139 bacteraemia associated with pneumonia, Italy 2016. Infection 45, 237–240.CrossRefGoogle ScholarPubMed
De Keukeleire, S et al. (2018) Atypical manifestation of Vibrio cholerae: fear the water!. Acta Clinica Belgica 73, 462–464.CrossRefGoogle ScholarPubMed
Wang, KB et al. (2017) Pollution of pathogenic vibrio in fresh water products in Shandong Province between 2014 and 2016. Modern Preventive Medicine 44, 2924–2927.Google Scholar
Chui, HX et al. (2018) Monitoring of four common pathogenic vibrio species pollution in freshwater aquaculture of Henan in 2016. Modern Preventive Medicine 45, 732–736.Google Scholar
Qin, S et al. (2019) Contamination investigation of common pathogenic Vibrio species in freshwater aquaculture processing in Jiangsu province in 2016. Journal of Food Safety and Quality 10, 3946–3951.Google Scholar
Kaki, R et al. (2017) Non-O1/non-O139 Vibrio cholerae septicaemia in a Saudi man: a case report. JMM Case Reports 4, e005077.CrossRefGoogle Scholar
Aung, KM et al. (2016) Naturally occurring IgG antibodies provide innate protection against Vibrio cholerae bacteremia by recognition of the outer membrane protein U. Journal of Innate Immunity 8, 269–283.CrossRefGoogle ScholarPubMed
Li, F et al. (2014) Distribution of virulence-associated genes and genetic relationships in non-O1/O139 Vibrio cholerae aquatic isolates from China. Applied and Environmental Microbiology 80, 4987–4992.CrossRefGoogle ScholarPubMed
Qiao, M et al. (2018) Review of antibiotic resistance in China and its environment. Environment International 110, 160–172.CrossRefGoogle ScholarPubMed
Baron, S et al. (2016) Antimicrobial susceptibility of autochthonous aquatic Vibrio cholerae in Haiti. Frontiers in Microbiology 7, 1671.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1. Cases of NOVC bacteraemia reported annually in mainland China.

Figure 1

Table 1. Demographic and clinical parameters of 32 NOVC bacteraemia in mainland China

Figure 2

Fig. 2. The distribution of NOVC bacteraemia cases between 2005 and 2019 in mainland China according to published literature.

Figure 3

Table 2. Details of NOVC strains reported in the literature and PubMLST database

Figure 4

Fig. 3. Minimum spanning tree analysis of NOVC isolates based on sequence type (ST). Ths STs are designated by the number in the circle; the size of the circle corresponds to the total number of each ST. The digits on the lines between the two circles represent the number of allelic differences.