Emerging Infections Due to Shewanella spp.: A Case Series of 128 Cases Over 10 Years

Introduction

Shewanella species are Gram-negative bacilli that are motile and non-fermenting. It was first discovered 90 years ago by Derby and Hammer in 1931, during an investigation for the cause of surface taint on properly pasteurized butter. Contamination of dairy products with this organism led to despicable flavor and odor despite appropriate storage. The organism was initially given the name Achromobacter putrefaciens. Later in 1941, Long and Hammer proposed that it should be renamed as Pseudomonas putrefaciens under the genus of Pseudomonas. They also further isolated the organism from other dairy products like milk and cream, and other sources like soil, water samples, creamery floors, equipment and sewers. In subsequent decades, this species was implicated in spoilage of fish and fishery products by James Shewan and other authors (1). In 1985, this organism was reclassified to the family of Vibrionaceae as a result of phylogenetic studies. A new genus, Shewanella, was given to this organism in honor of James Shewan for his dedication to marine microbiology. Since its discovery 90 years ago, numerous case reports and case series have been published regarding this species. However, infections by Shewanella species were rare, and knowledge regarding Shewanella-associated infections remained limited.

Materials and Methods

We conducted a retrospective analysis of patients with Shewanella infection over 10 years, from April 1, 2010 to December 31, 2020 in Pamela Youde Nethersole Eastern Hospital (PYNEH), a 1700-bed regional hospital in Hong Kong. Patients who had insufficient data for analysis were excluded. Data from the Clinical Management System, the Clinical Information System (IntelliVue Clinical Information Portfolio, Philips Medical, Amsterdam, Netherlands) and the medical records were reviewed retrospectively. Background medical comorbidities, demographics, clinical and microbiologic characteristics of Shewanella infection were retrieved and evaluated.

Definitions

Clinical significance of Shewanella infections was classified into “definite,” “probable,” and “colonization” as described previously (2). “Definite” Shewanella infection was defined as isolation of Shewanella from a normally sterile site or pure growth from other infected sites as a single organism. “Probable” Shewanella infection was defined as isolation of Shewanella from infected sites, which is polymicrobial. “Colonization” by Shewanella was defined by the isolation of Shewanella from sites without clinical signs or symptoms of infection. Sites of isolation were classified into intra-abdominal specimens (including bile and peritoneal swabs), skin and soft tissue specimens, blood, respiratory tract, and other specimens.

Empirical antibiotics were defined as the antibiotics administered within 24 h of collection of specimens with Shewanella being isolated. Subsequent antibiotics were defined as the antibiotics administered beyond 24 h of specimen collection.

Clinical outcomes being evaluated included hospital length of stay, need for Intensive Care Unit (ICU) admission and hospital mortality. The Acute Physiology and Chronic Health Evaluation (APACHE) IV score was used in those admitted to the ICU to quantify disease severity and predict the risk of mortality in the index admission. It comprises 129 variables derived from the worst values in the initial 24 h of admission. Required variables for calculating the APACHE IV score include the patient's demographic and chronic health variables, physiological and laboratory parameters, and disease-specific subgroups.

Microbiology

Clinical samples were submitted to the microbiology laboratory in PYNEH for incubation and processing. Shewanella species was identified by Matrix-Assisted Laser Desorption Ionization–Time-Of-Flight (MALDI-TOF) Mass Spectrometry (MS). Susceptibility testing was performed on the isolates to classify them into Resistant (R), Intermediate resistant (I) or Susceptible (S) strains to the tested antibiotics, based on the Clinical and Laboratory Standards Institute (CLSI) criteria. Before June 2018, the disc diffusion method was employed and the CLSI minimal inhibitory concentration (MIC) breakpoint for Pseudomonas aeruginosa was adopted. Since June 2018, the broth micro-dilution method was performed for susceptibility testing and the CLSI MIC breakpoint for Other Non-Enterobacteriaceae (ONE) was used.

Ethics

This study was approved by the Hong Kong East Cluster Ethics Committee of the Hospital Authority (HKECREC-2020-072).

Results

Demographics and Medical Comorbidities

A total of 128 patients with Shewanella infection were identified during the 10-year study period (Table 1). 79 (61.7%) were men, and 49 (38.3%) were women. The median age was 78 (interquartile range, IQR 65–87). 81 patients (63.3%) had an underlying hepatobiliary disease, 34 (26.6%) had an underlying malignancy, 33 (25.8%) had chronic kidney disease or end-stage renal failure, and 29 (22.7%) had diabetes mellitus. Among the 34 patients with an underlying malignancy, 58.8% (n = 20) had cancer of the hepatobiliary tract.

TABLE 1

Table 1. Clinical characteristics of Shewanella-associated sepsis.

Microbiology

Among 128 patients, 154 specimens were available for further analysis. Twenty-five episodes were considered “definite” infections, 75 episodes were considered “probable” infections, and 54 episodes were considered “colonization.” Co-isolates were very common (88.3%). The 3 most common organisms involved in co-infection with Shewanella were Enterococcus (49.4%), Escherichia Coli (48.1%) and Klebsiella species (27.3%). Table 2 listed all co-isolates involved in co-infection with Shewanella.

TABLE 2

Table 2. Common organisms involved in co-infection with Shewanella (specimen n = 154).

Shewanella was isolated from intra-abdominal specimens (58.4%), skin and soft tissue specimens (20.1%), blood (8.4%), sputum (8.4%) and other specimens (4.7%). The most common clinical manifestation was hepatobiliary infections (n = 93, 60.4%), followed by skin and soft tissue (n = 36, 23.4%), respiratory (n = 13, 8.4%) and gastrointestinal (n = 7, 4.5%) infections. For those with hepatobiliary infections, 91.4% was related to gallstone or bile duct stone. For those with skin and soft tissue infection, 36.1% had chronic wounds due to either diabetes mellitus or chronic venous insufficiency. Seawater exposure was noted in 6 patients (4.7%), which were all classified as probable infections due to polymicrobial growth from infected sites.

Among 128 recruited patients, 118 patients (92.2%) were infected with Shewanella algae, while 10 patients (7.8%) were infected with Shewanella putrefaciens. The antibiotic susceptibility of Shewanella is shown in Table 3. The identified organisms were usually susceptible to ceftazidime (98.7%), gentamicin (97.4%), cefoperazone-sulbactam (93.5%), ciprofloxacin (90.3%), and piperacillin (88.3%). Only 76.6% of isolates were susceptible to imipenem-cilastatin. One isolate showed resistance to multiple antibiotics, including ceftazidime, cefoperazone-sulbactam, ciprofloxacin, piperacillin and imipenem-cilastatin, and remained susceptible only to gentamicin and ticarcillin-clavulanate.

TABLE 3

Table 3. Antibiotic susceptibility of Shewanella (specimen n =154).

Amoxicillin-clavulanate was prescribed as an empirical antibiotic in 40.3% of the cases. The carbapenem group (ertapenem or meropenem) was chosen in 23.3% of the cases. Cefuroxime (8.4%), piperacillin-tazobactam (8.4%), aminoglycosides (gentamicin or amikacin, 8.4%), levofloxacin (7.1%) and ampicillin (3.2%) were less commonly used as empirical options. For subsequent antibiotics given after susceptibility results were available, carbapenem group (ertapenem, meropenem or imipenem-cilastatin, 28.6%) and piperacillin or piperacillin-tazobactam (23.3%) were commonly used. Amoxicillin-clavulanate (19.5%) became less prevalent than it was as an empirical choice.

Carbapenem group was the second most commonly prescribed empirical antibiotic class. Thirty out of 128 patients in our cohort received carbapenem empirically. Imipenem-resistant strains were detected in 5 of them with 1 hospital death, making up mortality rate of 20% (1 out of 5) among patients receiving carbapenems inappropriately. Out of the other 25 patients who received initial carbapenems appropriately, there was 1 hospital death resulting in mortality rate of 4% (1 out of 25). The two-tailed P value by Fisher's exact test was 0.3103, indicating that the association between presence of carbapenem resistance and mortality was not statistically significant.

Clinical Outcomes

The median hospital length of stay was 5 days (IQR 2–12). The overall hospital mortality was 8.6%. Eleven patients (8.6%) required admission to the Intensive Care Unit (ICU). The median ICU length of stay was 4 days (IQR 2–8). The APACHE IV predicted risk of death was 0.34 (IQR 0.15–0.77). Among the patients admitted to the ICU, 1 patient (9.1%) died during the ICU stay, and 2 patients (18.2%) died during the hospitalization.

Discussion

Since its discovery 90 years ago, there has been increasing understanding of the emerging Shewanella species. Nevertheless, knowledge regarding the clinical manifestations of Shewanella species is still primarily derived from isolated case reports or small case series. Here, we report the largest case series of Shewanella-associated infections in 128 patients over 10 years.

Risk Factors

Male predominance was frequently described in literature (2–4). Consistent with the previous studies (2, 4, 5), the male to female ratio in our study was 1.6:1. It was postulated that male predominance could be a genetic predisposition or a result of greater occupational or recreational marine exposure (4, 5). However, marine exposure was only identified in 6 patients (4.7%) in our case series and cannot solely account for the male predominance.

Important underlying conditions associated with Shewanella-associated infections found in our study were hepatobiliary diseases (63.3%), malignancy (26.6%), chronic kidney disease (25.8%), and diabetes mellitus (22.7%). Hepatobiliary disease is well known to be associated with Shewanella infections in several case reports and case series (2, 3, 6–9). Chen et al. (3) reported a case series of 16 Shewanella putrefaciens-associated skin and soft tissue infections, in which hepatobiliary disorder has been identified in 75% of the cases. To et al. (2) reported half of the patients with Shewanella bacteremia had an underlying hepatobiliary disease, while Liu et al. (9) reported 28 out of 59 (47.4%) bacteremic patients having an underlying hepatobiliary disease. In our series, 81 out of 128 patients (63.3%) had an underlying hepatobiliary disease, which included choledocholithiasis, cholecystitis, cholangitis, liver abscess and malignant biliary obstruction. Eleven of our patients had Shewanella bacteremia, of which 6 (54.5% of bacteremic patients) had a hepatobiliary disease. One proposed mechanism is the lipophilic property and bile affinity of Shewanella species, as demonstrated by frequent isolation of the species from oil emulsions and fatty foods (3, 10). Another proposed mechanism was hepatic dysfunction resulting in iron overload, which suppresses neutrophilic activity and causes impaired phagocytosis, facilitating bacterial invasion and bacteremia (9, 11). This was speculated to be associated with Shewanella infections in expert opinion (2, 9).

Previous studies have also shown important associations between an underlying malignancy and Shewanella infections (2, 12, 13). Malignancy was present in 26.6% of patients in our study, and more than half (20 out of 34, 58.8%) were malignancies involving the hepatobiliary tract. Previous case reports postulated that cancer patients were predisposed to Shewanella infections due to immunosuppression (13), neutropenia (14, 15), and aggressive chemotherapeutic regimens being used (15).

Patients with chronic kidney disease (CKD) made up 25.8% of our study cohort. Significant correlation between CKD and Shewanella infection was not demonstrated in the existing literature. Isolated case reports have described peritonitis caused by Shewanella species in uremic patients on peritoneal dialysis (16–20). Shewanella infection (21) and septicemia (22) was also reported as rare case reports in patients receiving hemodialysis. These infections in hemodialysis patients reported in the literature were complications of the vascular access, either as catheter-related bloodstream infections or as an infected arterio-venous graft. In contrast to previous studies, none of our uremic patients suffered from Shewanella peritonitis due to underlying peritoneal dialysis. There were 3 cases of bacteremia in our subgroup of patients with CKD. None of these bacteremic patients had underlying vascular access. Two of them suffered from cholangitis, and 1 of them had necrotizing fasciitis. Our study was the first to demonstrate an association between Shewanella-associated infections and CKD per se and not as a complication of the dialysis modality employed. One possible explanation was the dysregulated iron homeostasis contributing to anemia in CKD, recently demonstrated to be related to raised hepcidin levels in uraemia (23). An overall positive iron balance may result (23). Iron then binds in high affinity to siderophores being produced by Shewanella species (24, 25).

A substantial portion of our cohort had underlying diabetes mellitus, accounting for approximately one-fifth (22.7%) of the cases. The association between diabetes and Shewanella infections has already been depicted in previous case reports and case series (2, 18, 20). Diabetic patients also frequently develop lower extremity ulcers. Patients with chronic wounds and ulcers are prone to skin and soft tissue infections by Shewanella species (26–33). These infections may or may not be preceded by contaminated water exposure to the wounds or ulcers. These infected skin lesions can potentially cause bacteremia, as described in one case series of 6 patients with an underlying burn wound or ulcerative skin lesion who developed Shewanella putrefaciens bacteremia (14). In our study, 13 patients had chronic wound conditions, including diabetics ulcers, chronic venous insufficiencies, and malignant melanoma with fungating wounds, making up 36.1% (13 out of 36) of all skin and soft tissue infections. Consistent with other studies (27), the majority of our patients with chronic wounds did not have preceding seawater exposure. The only case documented to have contaminated water exposure was a patient with chronic venous insufficiency who did dressing to his ulcer at home with non-sterile tap water (Case 6, Table 4).

TABLE 4

Table 4. Cases with marine exposure.

Shewanella species is a renowned marine organism, making seawater contact is a well-recognized risk factor for Shewanella-associated infections. Marine-related occupations or recreational activities such as diving (34), swimming (18), fishing (2, 18, 21) and crabbing (2) were identified to be important predisposing events to Shewanella infections. However, the importance of marine exposure in Shewanella infections varies in the literature. Holt et al. (34) reported a striking identification of seawater contact history in 85% (47 out of 55) cases of Shewanella algae ear infections. On the contrary, To et al. (2) identified only 2 out of 29 cases with a marine association, suggesting that an alternative vehicle or route of Shewanella infection may be present. In our series, only 6 out of 128 patients had documented seawater contact. All these cases had co-isolates present in the cultured specimens and were classified as “probable” infections. Most of them (5 out of 6) had skin and soft tissue infection after marine exposure, while 1 had respiratory tract infection after non-fatal drowning. Table 4 displayed details of the 6 cases. Our study echoes with the findings of To et al. (2), which was also carried out in Hong Kong, that the majority of Shewanella-associated infections did not have documented seawater contact. The warm climate in Hong Kong is favorable for Shewanella species (2, 35). Residing near seas and seacoasts was also identified as a potential risk factor for Shewanella infections (16). Hong Kong is located in close proximity to the seacoast, with high seafood demand and consumption. A possible route of transmission would be contaminated seafood in the waters of Hong Kong, which is ingested raw or undercooked (2, 9). These may explain the relatively large number of local cases recorded in Hong Kong.

Clinical Presentations

Shewanella-associated infections are categorized into hepatobiliary infections, skin and soft tissue infections, bacteremia, and miscellaneous infections (5). Otitis media is a separate category of Shewanella-associated infection primarily described in the pediatric population and runs a relatively benign clinical course (34). Rarer involvement includes endophthalmitis (36), infective endocarditis (37), pericarditis (13), cerebellar abscess (38) and splenic abscess (39) described only in isolated case reports.

Hepatobiliary infections were predominant (60.4%, 93 out of 154 specimens) in our case series. This was consistent with the study by To et al., which was also carried out in Hong Kong (2), where intra-abdominal foci were the most typical site from which Shewanella species were isolated. In contrast, most other studies rarely isolated Shewanella species from the hepatobiliary system or intra-abdominally. Our findings may be attributed to the fact that a heavy proportion of our cohort had pre-existing hepatobiliary disorder (63.3%), which predisposed them to hepatobiliary tract infections. 51.6% (48 out of 93 specimens) of these hepatobiliary infections were classified as asymptomatic “colonization” while 40.9% (38 out of 93 specimens) were classified as “probable” infections. All isolates classified as “probable” infections and “colonization” had heavy co-isolates of enteric organisms like Escherichia coli, Klebsiella species and Enterococcus species. Similar polymicrobial and asymptomatic colonization of the PTBD was also observed in the study by To et al. (2). In To's study, none of the bile specimens was classified as “definite” infections (2). In our series, 7.5% (7 out of 93) of bile specimens were classified as “definite” infections, all of them being bacteremia. Our study showed that in patients with an underlying hepatobiliary disorder, asymptomatic colonization of the biliary tract and existing drains by Shewanella and other enteric organisms was prevalent. These colonizing organisms may evolve into genuine and severe infections like bacteremia in appropriate clinical settings, such as acute biliary obstruction.

The overall 30-day mortality in our series was 8.6%. When only “definite” infections were considered, the mortality rate was significantly increased to 28.6%. In the Hong Kong study by To et al. (2), the overall 30-day mortality was 20.6%, much higher than our series. Among those with “definite” infections, they reported a mortality rate of 28%, and it was very similar to ours. Interestingly, one South African case series of 16 cases of Shewanella bacteremia reported only 7% overall mortality (14), suggesting a relatively benign clinical course even in cases of bacteremia. In a Denmark study by Holt et al., which focused on Shewanella-associated ear infections, the overall mortality was 0% due to the benign nature of ear infections (34). Overall, the reported mortality rate of Shewanella-associated infections in existing literature varied from 0 to 16% (2, 3, 5, 14, 34).

Antibiotic Susceptibility

Our study showed that the majority (>97%) of Shewanella species were susceptible to ceftazidime and gentamicin. This was consistent with a prior study in Hong Kong carried out 10 years ago. Shewanella was found to be uniformly susceptible (100%) toward ceftazidime and aminoglycosides (gentamicin, amikacin, and tobramycin) (2). Susceptibility to cefoperazone-sulbactam, ciprofloxacin and piperacillin in our cohort also remained similar to that reported in the prior Hong Kong study (2). Alarmingly, resistance toward carbapenems has risen significantly over the past 10 years. Imipenem-resistant strains were detected in 3.7% of isolates in that study (2), hence 96.3% of Shewanella species were still imipenem-susceptible. Our study detected imipenem-resistant strains in 23.4% of isolates, with only 76.6% of isolates remaining imipenem-susceptible. In addition, resistance toward carbapenem may develop during therapy in initially susceptible strains (40). Kim et al. described a case of Shewanella algae bacteremia showing initial susceptibility to imipenem (40). Despite treatment with imipenem, the patient developed an epidural abscess requiring surgical drainage. The isolate from the epidural abscess was resistant to imipenem, and cefepime was used instead for subsequent treatment. It was postulated that a carbapenem-hydrolyzing class D beta-lactamase might play a role in the emergence of carbapenem resistance in the course of treatment for Shewanella algae (40, 41). Whole genome sequencing of Shewanella algae isolates showed expression of a higher level of blaOXA-55-like transcription and beta-lactamase activity in carbapenem-resistant strains, as compared to carbapenem-susceptible isolates (42). Shewanella xiamenensis was reported to harbor blaOXA-48-like class D carbapenemase genes (43). Shewanella oneidensis was shown to carry blaOXA-54 genes that encoded the class D beta-lactamase OXA-54 and led to significant hydrolysis of imipenem (44). Presence of these blaOXA genes for carbapenem-hydrolyzing class D beta-lactamase in Shewanella species could explain for reduced carbapenem activity toward Shewanella species.

Of note, carbapenem was a popular choice as an empirical antibiotic (23.3%, 30 out of 128 patients) in the treatment of Shewanella-associated infection in our study. 16.6% (5 out of 30) of patients received carbapenem as an inappropriate empirical choice, as carbapenem-resistant strains were eventually detected in these patients. Hospital mortality differed between those who received carbapenems appropriately and inappropriately at 4 and 20% respectively, although the difference failed to reach a statistical significance (p = 0.3103). However, a major confounder to interpret this association is our limited sample size. Overall, carbapenem susceptibility appeared to be variable and inconsistent. The use of carbapenems in Shewanella infections may need to be mindfully re-evaluated in the future in light of increasing resistance toward carbapenems and propensity to develop resistance toward carbapenems during treatment.

Limitations

Our study was a retrospective study, and information on exposure history was subject to recall bias. For instance, the number of cases with seawater exposure prior to Shewanella infection may be under-estimated as marine contact history could be easily missed by the inattentive and unaware patient.

Secondly, different versions of CLSI MIC breakpoints were being used in our study period because of a change in the method employed for susceptibility testing in the 10-year period. This may have an impact on interpretation of the increasing carbapenem resistance as previously discussed. However, we must also acknowledge that the susceptibility pattern to other classes of antibiotics did not differ significantly despite a change in the CLSI criteria being used. Although we did not apply a consistent system of CLSI interpretation throughout the study period, the significantly increasing trend of carbapenem resistance should not be undermined or ignored.

Thirdly, identification of Shewanella species was based on MALDI-TOF Mass Spectrometry in our study. This may be unreliable as only few representative species are present in the current database. Increasing number of novel species have been identified in the Shewanella genus. For instance, Shewanella chilikensis and Shewanella carassii are phylogenetically related to Shewanella algae and are also implicated in human infections (42, 45, 46). Identification of these species requires dedicated techniques such as whole genome sequencing (42). It is possible that some samples of Shewanella algae in our study were in fact these novel Shewanella species, which were being “mis-identified” as Shewanella algae.

Fourthly, phylogenetic analysis or molecular characterization of antimicrobial resistance mechanisms were not carried out in our study.

Conclusions

To our knowledge, this is the largest case series of Shewanella infections. Underlying hepatobiliary diseases and malignancies were consistent predisposing factors to Shewanella infections across the literature. In our cohort, hepatobiliary infections were predominant, and the majority were related to gallstone or bile duct stone disease. Patients with chronic skin ulcers, with or without marine exposure, were prone to Shewanella-associated skin and soft tissue infections. Most Shewanella species remained susceptible to third and fourth generation cephalosporins, as well as aminoglycosides. A trend of increasing carbapenem resistance was observed. The emergence of carbapenem resistance may also occur during treatment for an initially susceptible strain. Options other than carbapenems may need to be considered in treating Shewanella-associated infections.

Data Availability Statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.

Ethics Statement

The studies involving human participants were reviewed and approved by Hong Kong East Cluster Ethics Committee of the Hospital Authority (HKECREC-2020-072). Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.

Author Contributions

WN helped with manuscript conception, data collection, data interpretation, writing of the manuscript, and critical review of the manuscript. H-PS helped with data collection, data interpretation, and critical review of the manuscript. KT and SS helped with critical review of the manuscript. All authors contributed to the article and approved the submitted version.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Acknowledgments

The authors wish to thank Dr. Jimmy Lam for his assistance.

References

1. Shewan JM Hobbs G, Hodgkiss W. A determinative scheme for the identification of certain genera of. Gram-negative bacteria, with special reference to the pseudomonadaceae. J Appl Bacteriol. (1960) 23:379–90. doi: 10.1111/j.1365-2672.1960.tb00211.x

CrossRef Full Text | Google Scholar

2. To KKW, Wong SSY, Cheng VCC, Tang BSF, Li IWS, Chan JFW, et al. Epidemiology and clinical features of Shewanella infection over an eight-year period. Scand J Infect Dis. (2010) 42:757–62. doi: 10.3109/00365548.2010.490562

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Chen YS, Liu YC, Yen MY, Wang JH, Wang JH, Wann SR, et al. Skin and soft-tissue manifestations of Shewanella putrefaciens infection. Clin Infect Dis. (1997) 25:225–9. doi: 10.1086/514537

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Martín-Rodríguez AJ, Martín-Pujol O, Artiles-Campelo F, Bolaños-Rivero M, Römling U. Shewanella spp. infections in Gran Canaria, Spain: retrospective analysis of 31 cases and a literature review. JMM Case Rep. (2017) 4:e005131. doi: 10.1099/jmmcr.0.005131

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Janda JM, Abbott SL. The genus Shewanella: from the briny depths below to human pathogen. Crit Rev Microbiol. (2014) 40:293–312. doi: 10.3109/1040841X.2012.726209

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Otsuka T, Noda AT. Noguchi Nakamura H, Ibaraki K, Yamaoka K. Shewanella infection in decompensated liver disease: a septic case. J Gastroenterol. (2007) 42:87–90. doi: 10.1007/s00535-006-1957-0

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Tsai MS, You HL, Tang YF, Liu JW. Shewanella soft tissue infection: case report and literature review. Int J Infect Dis. (2008) 12:e119–24. doi: 10.1016/j.ijid.2008.03.020

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Myung DS, Jung YS, Kang SJ, Song YA, Park KH, Jung SI, et al. Primary shewanella algae bacteremia mimicking vibrio septicemia. J Korean Med Sci. (2009) 24:1192. doi: 10.3346/jkms.2009.24.6.1192

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Liu PY, Lin CF, Tung KC, Shyu CL, Wu MJ, Liu JW, et al. Clinical and microbiological features of shewanella bacteremia in patients with hepatobiliary disease. Intern Med. (2013) 52:431–8. doi: 10.2169/internalmedicine.52.8152

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Pivnick H. Pseudomonas rubescens. A new species from soluble oil emulsions. J Bacteriol. (1955) 70:1. doi: 10.1128/jb.70.1.1-6.1955

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Tajiri T, Tate G, Masunaga A, Miura K, Masuda S, Kunimura T, et al. Autopsy cases of fulminant bacterial infection in adults: Clinical onset depends on the virulence of bacteria and patient immune status. J Infect Chemother. (2012) 18:637–45. doi: 10.1007/s10156-012-0384-9

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Saidel-Odes L, Borer A, Riesenberg K, Schlaeffer F. Shewanella spp. infection following treatment for upper gastrointestinal bleeding. Scand J Infect Dis. (2009) 39:360–1. doi: 10.1080/00365540600978948

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Tan CK, Lai CC, Kuar WK, Hsueh PR. Purulent pericarditis with greenish pericardial effusion caused by Shewanella algae. J Clin Microbiol. (2008) 46:2817–9. doi: 10.1128/JCM.01018-08

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Brink AJ, Van Straten A, Van Rensburg A. Shewanella (Pseudomonas) putrefaciens bacteremia. Clin Infect Dis. (1995) 20:1327–32. doi: 10.1093/clinids/20.5.1327

CrossRef Full Text | Google Scholar

15. Krsnik I, Arribalzaga K, Romanyk J. Shewanella alga bacteremia and associated cellulitis in a patient with multiple myeloma. Haematologia (Budap). (2002) 32:79–80. doi: 10.1163/156855902760262808

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Yim SY, Kang YS, Cha DR, Park DW, Youn YK, Jo YM, et al. Fatal PD peritonitis, necrotizing fasciitis, and bacteremia due to Shewanella putrefaciens. Perit Dial Int. (2010) 30:667–9. doi: 10.3747/pdi.2010.00084

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Takata T, Chikumi H, Morishita S, Hamada S, Hoi S, Iyama T, et al. Shewanella algae bacteremia in an end-stage renal disease patient: a case report and review of the literature. Intern Med. (2017) 56:729. doi: 10.2169/internalmedicine.56.7616

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Bhandari S, Pan TLT, Horvarth J, Tiller D. CAPD swimming in shewanella. Nephrol Dial Transplant. (2000) 15:1484–5. doi: 10.1093/ndt/15.9.1484

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Shanmuganathan M, Goh BL, Lim C, Norfadhlina Z, Fairol I. Shewanella algae peritonitis in patients on peritoneal dialysis. Perit Dial Int. (2016) 36:574–5. doi: 10.3747/pdi.2015.00287

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Dan M, Gutman R, Biro A. Peritonitis caused by Pseudomonas putrefaciens in patients undergoing continuous ambulatory peritoneal dialysis. Clin Infect Dis. (1992) 14:359–60. doi: 10.1093/clinids/14.1.359

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Jammula P, Gupta R, Agraharkar M. Vascular steal syndrome and shewanella alga infection requiring amputation in a hemodialysis patient. Saudi J Kidney Dis Transpl. (2003) 14:511–515.

PubMed Abstract | Google Scholar

22. Iwata M, Tateda K, Matsumoto T, Furuya N, Mizuiri S, Yamaguchi K. Primary Shewanella alga septicemia in a patient on hemodialysis. J Clin Microbiol. (1999) 37:2104–5. doi: 10.1128/JCM.37.6.2104-2105.1999

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Wish JB, Aronoff GR, Bacon BR, Brugnara C, Eckardt KU, Ganz T, et al. Positive Iron balance in chronic kidney disease: how much is too much and how to tell? Am J Nephrol. (2018) 47:72–83. doi: 10.1159/000486968

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Gram L. Siderophore-mediated iron sequestering by shewanella putrefaciens. Appl Environ Microbiol. (1994) 60:2132-6. doi: 10.1128/aem.60.6.2132-2136.1994

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Rutschlin S, Gunesch S, Böttcher T. One Enzyme, three metabolites: shewanella algae controls siderophore production via the cellular substrate pool. Cell Chem Biol. (2017) 24:598.e10-604. doi: 10.1016/j.chembiol.2017.03.017

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Kim JH, Cooper RA, Welty-Wolf KE, Harrell LJ, Zwadyk P, Klotman ME. Pseudomonas putrejaciens bacteremia. Rev Infect Dis. (1989) 11:97–104. doi: 10.1093/clinids/11.1.97

CrossRef Full Text | Google Scholar

27. Appelbaum PC, Bowen AJ. Opportunistic infection of chronic skin ulcers with Pseudomonas putrefaciens. Br J Dermatol. (1978) 98:229–31. doi: 10.1111/j.1365-2133.1978.tb01628.x

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Vandepitte J, Debois J. Pseudomonas putrefaciens as a cause of bacteremia in humans. J Clin Microbiol. (1978) 7:70–2. doi: 10.1128/jcm.7.1.70-72.1978

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Eschete ML, Williams F, West BC. Pseudomonas putrefaciens and group a β-Hemolytic Streptococcus Septicemia. Arch Intern Med. (1980) 140:1533–4. doi: 10.1001/archinte.1980.00330220081030

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Levy PY, Tessier JL. Arthritis due to Shewanella putrefaciens. Clin Infect Dis. (1998) 26:536. doi: 10.1086/517088

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Paccalin M, Grollier G, Le Moal G, Rayeh F, Camiade C. Rupture of a primary aortic aneurysm infected with Shewanella Alga. Scand J Infect Dis. (2009) 33:774–5. doi: 10.1080/003655401317074626

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Finkelstein R, Oren I. Soft tissue infections caused by marine bacterial pathogens: epidemiology, diagnosis, and management. Curr Infect Dis Rep. (2011) 13:470–77. doi: 10.1007/s11908-011-0199-3

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Chen SCA, Lawrence RH, Packham DR, Sorrell TC. Cellulitis due to Pseudomonas putrefaciens: possible production of exotoxins. Rev Infect Dis. (1991) 13:642–3. doi: 10.1093/clinids/13.4.642

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Holt HM, Søgaard P, Gahrn-Hansen B. Ear infections with Shewanella alga: a bacteriologic, clinical and epidemiologic study of 67 cases. Clin Microbiol Infect. (1997) 3:329–33. doi: 10.1111/j.1469-0691.1997.tb00622.x

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Holt HM, Gahrn-Hansen B, Bruun B. Shewanella algae and shewanella putrefaciens: clinical and microbiological characteristics. Clin Microbiol Infect. (2005) 11:347–52. doi: 10.1111/j.1469-0691.2005.01108.x

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Hou YC, Hu FR. Shewannela putrefaciens endophthalmitis after penetrating keratoplasty. Am J Ophthalmol. (1997) 124:114–5. doi: 10.1016/S0002-9394(14)71657-5

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Dhawan B, Chaudhry R, Mishra BM, Agarwal R. Isolation of Shewanella putrefaciens from a rheumatic heart disease patient with infective endocarditis. J Clin Microbiol. (1998) 36:2394. doi: 10.1128/JCM.36.8.2394-2394.1998

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Yilmaz G, Aydin K, Bektas D, Caylan R, Caylan R, Koksal I. Cerebellar abscess and meningitis, caused by Shewanella putrefaciens and Klebsiella pneumoniae, associated with chronic otitis media. J Med Microbiol. (2007) 56:1558–60. doi: 10.1099/jmm.0.47044-0

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Basir N, Yong AML, Chong VH. Shewanella putrefaciens, a rare cause of splenic abscess. J Microbiol Immunol Infect. (2012) 45:151–3. doi: 10.1016/j.jmii.2011.09.007

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Kim DM, Kang CI, Lee CS, Kim H-B, Kim EC, Kim NJ, et al. Treatment failure due to emergence of resistance to carbapenem during therapy for shewanella algae bacteremia. J Clin Microbiol. (2006) 44:1172–4. doi: 10.1128/JCM.44.3.1172-1174.2006

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Héritier C, Poirel L, Nordmann P. Genetic and biochemical characterization of a chromosome-encoded carbapenem-hydrolyzing ambler class D β-lactamase from shewanella algae. Antimicrob Agents Chemother. (2004) 48:1670. doi: 10.1128/AAC.48.5.1670-1675.2004

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Ohama Y, Aoki K, Harada S, Nagasawa T, Sawabe T, Nonaka L, et al. Genetic environment surrounding bla OXA-55-like in clinical isolates of shewanella algae clade and enhanced expression of bla OXA-55-like in a carbapenem-resistant isolate. mSphere. (2021) 6:e0059321. doi: 10.1128/mSphere.00593-21

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Antonelli A, Di Palo DM, Galano A, Becciani S, Montagnani C, Pecile P, et al. Intestinal carriage of Shewanella xiamenensis simulating carriage of OXA-48-producing Enterobacteriaceae. Diagn Microbiol Infect Dis. (2015) 82:1–3. doi: 10.1016/j.diagmicrobio.2015.02.008

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Poirel L, Héritier C, Nordmann P. Chromosome-encoded ambler class d-lactamase of shewanella oneidensis as a progenitor of carbapenem-hydrolyzing oxacillinase. Antimicrob Agents Chemother. (2004) 48:348–51. doi: 10.1128/AAC.48.1.348-351.2004

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Martín-Rodríguez AJ, Suárez-Mesa A, Artiles-Campelo F, Römling U, Hernández M. Multilocus sequence typing of Shewanella algae isolates identifies disease-causing Shewanella chilikensis strain 6I4. FEMS Microbiol Ecol. (2019) 95:1–10. doi: 10.1093/femsec/fiy210

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Sucharita K, Sasikala C, Park SC, Baik KS, Seong CN, Ramana CV. Shewanella chilikensis sp. nov, a moderately alkaliphilic gammaproteobacterium isolated from a lagoon. Int J Syst Evol Microbiol. (2009) 59:3111–5. doi: 10.1099/ijs.0.010918-0

PubMed Abstract | CrossRef Full Text | Google Scholar