Case Reports in Transplantation
Volume 2015 (2015), Article ID 863131, 3 pages
http://dx.doi.org/10.1155/2015/863131

Case Report

Hafnia alvei Urosepsis in a Kidney Transplant Patient

Mario Stanic,¹ Edgar Meusburger,¹ Gabriele Hartmann,² and Karl Lhotta¹

¹Department of Nephrology and Dialysis, Academic Teaching Hospital Feldkirch, 6800 Feldkirch, Austria
²Institute for Pathology, Academic Teaching Hospital Feldkirch, 6800 Feldkirch, Austria

Received 10 February 2015; Accepted 1 April 2015

Academic Editor: Sandeep Mukherjee

Copyright © 2015 Mario Stanic et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Hafnia alvei, a gram-negative facultative anaerobic, rod-shaped bacterium, is a rare cause of infection in humans. We report on a renal transplant patient who developed H. alvei pyelonephritis and urosepsis. The source of infection remains enigmatic but is most likely the intestinal tract. Appropriate antibiotic therapy with cefepime followed by oral ciprofloxacin brought about rapid resolution of symptoms and complete recovery. H. alvei may cause severe infection in transplant patients without predisposing factors such as hospitalization, invasive procedures, or antibiotic treatment.

1. Introduction

Hafnia alvei is a facultative anaerobic gram-negative bacterium belonging to the Enterobacteriaceae family. Although this genus was first described in 1954, very little is known about its role in human infectious diseases. H. alvei can be recovered from soil, water, and many animal species, especially mammals, where it colonises primarily the gastrointestinal tract [1]. In humans, H. alvei seems to be a member of the normal gut microbiome as a nonpathogenic inhabitant, although some studies conclude that these bacteria cause significant clinical gastroenteritis [1, 2], especially in children [3], but also in adult patients suffering from chronic disease or after previous antibiotic therapy [4]. It would appear that H. alvei is a microorganism with limited pathogenicity in humans that may cause clinically significant infections only in immunocompromised individuals, for example, those with malignancy or after organ transplantation [5, 6]. We here describe a renal transplant recipient who suffered from H. alvei urosepsis.

2. Case Report

The 56-year-old woman developed end-stage renal disease due to IgA nephropathy. In August 2012 she underwent preemptive kidney transplantation, receiving a kidney allograft from her husband. Her posttransplant course was stable with a serum creatinine of 0.90 mg/dL (eGFR 75 mL/min), and medical therapy consisted of tacrolimus (blood levels between 5 and 7 ng/mL), azathioprine, simvastatin, and pantoprazole.

Two days before admission in November 2014 she experienced headache, shivering, nausea, repeated vomiting, and diarrhea. At admission she had fever of 38°C. Blood tests showed a mild leukocytosis of 10.5 G/L (neutrophils 84%) and CRP of 20 mg/dL and her serum creatinine had increased to 1.30 mg/dL. An ultrasound of the transplant was unremarkable. The urinary sediment contained multiple leukocytes and bacteria. A diagnosis of transplant pyelonephritis was made and cefepime 2 g b.i.d. was commenced. Cultures taken from urine and blood samples taken on admission grew H. alvei identified by matrix-assisted laser desorption ionisation time-of-flight mass spectrometry (MALDI TOF) (MALDI Biotyper©Microflex LT, Bruker Daltonics, Bremen, Germany). No coinfection with other bacteria could be identified. The results of antimicrobial susceptibility testing using the VITEK 2 system (bioMerieux) are shown in Table 1.

Table 1: Susceptibility testing of H. alvei recovered from the blood culture.

Sensitive
Resistant

Cefotaxime/ceftazidime
Ampicillin

Cefepime
Amoxicillin/clavulanic acid

Ertapenem/meropenem
Piperacillin/tazobactam

Gentamicin
Fosfomycin

Ciprofloxacin

Trimethoprim/sulfamethoxazole

Under antibiotic therapy the patient’s symptoms and fever subsided and serum creatinine decreased to 0.90 mg/dL within two days. After five days antibiotic therapy was switched to ciprofloxacin 500 mg b.i.d. and the patient was discharged. At an outpatient control one week later she was in excellent clinical condition, laboratory parameters had normalised, and antibiotic therapy could be discontinued.

3. Discussion

Although relatively little is known about the role of H. alvei in human clinical infection, some common themes do emerge. First of all, H. alvei is rarely found in human specimens, mostly from the respiratory and gastrointestinal tract, urine, blood, wounds, and abscesses [9, 10]. In the majority of these cases, however, the bacterium does not seem to be related to the clinical infection. For example, whether H. alvei can cause acute gastroenteritis is still a matter of debate [1, 2]. Günthard and Pennekamp found H. alvei in 80 specimens but considered it to be pathogenetic in only three patients (two with septicemia and one with peritonitis). Secondly, most patients seem to have underlying conditions which predispose them to infection. For example, in the series studied by Günthard and Pennekamp, 93% of the patients had an underlying disease, mainly malignancy. Thirdly, in most cases infection with H. alvei is nosocomial. Rodríguez-Guardado in a collective of 36 patients with extraintestinal infection due to H. alvei over an eleven-year period found that 25 were nosocomial and eleven community-acquired [10]. In addition to underlying comorbidities, 76% of patients had other predisposing risk factors such as surgery, intravenous catheter insertion, or antibiotic therapy [9–11]. And lastly, in most specimens a coinfection with other, more pathogenic bacteria such as Staphylococcus aureus was seen [10].

At our institution 40 H. alvei isolates have been detected over the last ten years. Most positive specimens were obtained from respiratory tract secretions in intubated patients or from infections after abdominal surgery. Only three positive blood cultures were found and two of these patients had an underlying malignancy.

Several cases of H. alvei infection have been described in stem cell and particularly solid organ transplant recipients. Intestinal colonization and possible infection with H. alvei have been reported in a 9-year-old girl after hematopoietic stem cell transplantation for Fanconi’s anemia. Two patients, one 61-year-old woman and a 2-year-old boy, developed hepatic abscess after liver transplantation. The first patient had coinfection with Enterococcus faecalis and Candida albicans and the second with Enterococcus faecalis. Immunosuppressive and antimicrobial treatment are specified in Table 2. Günthard and Pennekamp reported a positive specimen in a lung transplant patient, but without further details.

Table 2: H. alvei infections in transplant recipients.

Author
Age
Sex
Underlying disease
Type of transplant
Immunosuppression
Risk factors
Antibiotic treatment
Outcome

Savini et al. [5]
9
F
Fanconi’s anaemia
Allogeneic stem cells
Cyclosporine steroids
antilymphocyte antibody
Graft versus host disease
Ceftazidime, amikacin, and teicoplanin
Cured

Barry et al. [6]
61
F
Primary biliary cirrhosis
Liver
Unknown
Recurrent rejection, additional infection
Piperacillin/
tazobactam, gentamicin, and amphotericin B
Died

Barry et al. [6]
2
M
Autoimmune hepatitis
Liver
Unknown
Previous high dose steroids and OKT3 therapy
Trimethoprim/
sulfamethoxazole, gentamicin, and ampicillin
Cured

Cardile et al. [7]
45
F
Diabetic nephropathy
Kidney
Tacrolimus
MMF
prednisone
Diabetes
ureteral stent
Cefixime
Cured

Benito et al. [8]
69
F
Autosomal dominant polycystic kidney disease
Kidney
Cyclosporine azathioprine steroids
Hepatitis C
Imipenem and clarithromycin
Cured

This study
56
F
IgA nephropathy
Kidney
Tacrolimus azathioprine
None
Cefepime and ciprofloxacin
Cured

Clinically significant H. alvei infection has also been reported in two renal transplant recipients.

The first patient was a 69-year-old female who developed sepsis and pneumonia nine years after renal transplantation. Basal immunosuppression consisted of cyclosporine, azathioprine, and steroids. The patient also suffered from hepatitis C infection. She developed hypotension, oliguria, and coagulopathy and recovered after hemodynamic support and antibiotic therapy with imipenem and clarithromycin.

The second case was a 45-year-old female suffering from ESRD due to diabetic nephropathy. Her course after transplantation was complicated by acute humoral rejection and chronic rejection. H. alvei pyelonephritis developed after ureteral stent implantation for hydroureteronephrosis. The patient recovered after treatment with ceftriaxone, cefixime, and removal of the stent.

Our case is similar to these two reports. We also were unable to identify the source of the infection. Certain foods, especially meat and fish, may harbour H. alvei in large amounts [12]. As H. alvei is part of the normal gut microbiota, we believe that the gastrointestinal tract, as common in urinary tract infections, was the most likely source of infection. None of these kidney transplant patients had a coinfection with other more aggressive bacteria. The two other patients, however, had additional comorbidities, namely, diabetes in one and hepatitis C infection in the other patient. In one patient H. alvei infection developed after an invasive procedure. The other two patients had triple immunosuppressive therapy including prednisolone, whereas our patient only had double therapy without steroids. All three patients ultimately recovered after appropriate antibiotic therapy.

In conclusion, H. alvei can cause severe infection such as urosepsis, pyelonephritis, and pneumonia in renal allograft recipients. Antimicrobial therapy with carbapenems, quinolones, or fourth-generation cephalosporins is necessary to cure the infection.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

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