- About this Journal
- Abstracting and Indexing
- Aims and Scope
- Article Processing Charges
- Articles in Press
- Author Guidelines
- Bibliographic Information
- Citations to this Journal
- Contact Information
- Editorial Board
- Editorial Workflow
- Free eTOC Alerts
- Publication Ethics
- Submit a Manuscript
- Subscription Information
- Table of Contents
Case Reports in Critical Care
Volume 2013 (2013), Article ID 920729, 3 pages
Shigella Bacteremia in a Patient with Visceral Leishmaniasis
1School of Biomedical and Laboratory Sciences, University of Gondar, P.O. Box 196, Gondar, Ethiopia
2Leishmanaisis Research and Treatment Center, University of Gondar, P.O. Box 196, Gondar, Ethiopia
3Department of Internal Medicine, University of Gondar, P.O. Box 196, Gondar, Ethiopia
4Institute of Tropical Medicine, Antwerp, Belgium
Received 30 June 2013; Accepted 24 July 2013
Academic Editors: C. Lazzeri, K. Lenz, and G. Pichler
Copyright © 2013 Mengistu Endris 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.
Bacteremia due to Shigella is rare. A 26-year-old HIV-negative male presented with a persistent high-grade fever of two months duration to the Leishmaniasis Research and Treatment Center of University of Gondar Hospital. He was anorexic and had lost significant weight (from 76 to 57 kg in 4 months, BMI = 17.2 kg/m2). He also complained of headache, chills, and rigor. In the last one year, he was experiencing a few episodes of acute bloody diarrhea, the last episode being two months ago. Microscopy from splenic aspiration showed Leishman-Donovan bodies with parasite load of +3. The blood culture showed Shigella species, but the stool was culture negative. The isolate was sensitive to most tested antibiotic discs, sulfamethoxazole, ceftriaxone, gentamicin, tetracycline, and norfloxacilin, except ampicillin. Therefore, requesting blood culture for identifying unexpected type of organisms causing infections in patients with underlying diseases like visceral leishmaniasis should be encouraged.
Bacteremia due to Shigella is rare. Shigella is a gram-negative, nonmotile facultative anaerobe that causes infection typically confined to the gastrointestinal tract . The disease is mediated by enterotoxin and manifests with acute bloody diarrhea and fever often occurring in an outbreak due to contamination of water . There are few reports of Shigella causing meningitis, osteomyelitis, and sepsis mostly in neonates, malnourished children, and immuno compromised hosts [3–8]. It is highly likely that such kind of infection be missed and associated with high risk of death.
Shigella rarely invades the bloodstream and results in septic shock. Macrophages not only fail to kill Shigella bacteria that they phagocytize, but also are killed by them . Due to overlapping manifestations of sepsis, blood culture is not a routine examination in visceral leishmaniasis (VL) patients. To the best of our knowledge, Shigella bacteremia was not reported in patients with VL in Ethiopia. Here we report a case of Shigella bacteriemia in a patient with VL.
2. Case Description
2.1. Clinical Presentation
A 26-year-old male presented with a persistent high-grade fever of two months duration to the Leishmaniasis Research and Treatment Center of University of Gondar Hospital. He was anorexic and had lost significant weight (from 76 to 57 kg in 4 months). He also complained of headache, chills, and rigor.
In the last one year, he was experiencing some acute episodes of bloody diarrhea, the last episode being two months ago. He was treated with unspecified medications at a health center and then improved.
He lived in malaria and VL endemic areas and had suffered from repeated malaria attacks. Since the last eight years he had noticed left upper quadrant swelling. He has tinnitus, vertigo, and blurring of vision. He has no history of epistaxis or easy bleeding. He has no self or family history of diabetes mellitus. He has no cough or other respiratory symptoms.
On presentation he was acutely sick looking and febrile (39.2°C), tachycardic (112/minute), and tachypneic (28/minute). His blood pressure was 90/60 mmHg. His body mass index was 17.2 kg/m2. He had splenomegaly of 9 cm below the coastal margin. He had some palmer pallor but no edema.
His peripheral blood count showed pancytopenic pattern: total white blood cell count of 800 cells/μL, hemoglobin of 8 gm/dL, and platelet of 51,000/μL. His absolute neutrophil count was 432/μL. Rk 39 rapid deep-stick serology test for leishmaniasis was positive. Microscopy from splenic aspiration showed Leishman-Donovan bodies of grade +3 parasite loads. His human immunodeficiency virus (HIV) serology test was negative. Urinalysis, liver enzymes, and bilirubin were all normal. There was no hemoparasite detected on blood-film examination. The stool had no intestinal helminthes using saline wet mount.
The patient was treated with intravenous ceftriaxone for 7 days and sodium stibogluconate (SSG) for 30 days. His vital signs stabilized after 7 days. The blood count started to improve starting from the first week of treatment and normalized at the end of the month.
Taking blood culture for VL patients was not routine. Blood culture was taken based on clinical indications for septic patients. As one of the common causes of mortality among VL patients was sepsis, blood culture was taken for this patient taking into account his presentation with systemic inflammatory response syndrome and severe neutropenia.
Ten mL of blood was drawn from the patient and inoculated on 45 mL brain heart infusion (BHI) following the standard procedure . The culture was incubated at 37°C; after 4 days of incubation it showed positive sign. Then the sample was inoculated on blood agar plate and MacConkey agar plates. Gram-negative rod-shaped bacteria were seen under the microscope using Gram stain. It was then further tested by biochemical tests such as indole test, triple sugar iron agar, nitrate and simmon citrate, and lysine decarboxylase. The bacteria isolated was gram-negative, rod, nonmotile, and negative for citrate, indole, and urea. Neither lactose nor glucose was fermented by the bacteria. The laboratory result showed Shigella species.
The antimicrobial susceptibility of the isolate was done using the disc diffusion technique, and the result was interpreted according to Clinical and Laboratory Standards Institute . The isolate was sensitive to all the tested antibiotic discs, sulfamethoxazole, ceftriaxone, gentamicin, tetracycline, and norfloxacilin, except ampicillin.
The stool sample was also collected from the patient and processed to find Shigella using Salmonella Shigella (SS) agar. There was no Shigella grown on the stool culture.
Bacteremia due to shigellosis is clinically unexpected. As this patient was having VL that manifests typically with chronic fever, weight loss, pancytopenia, and its complications like other bacterial superinfections and bleeding, it is very difficult to know whether the Shigella bacteremia had unique clinical manifestations or not.
Majority of the Shigella bacteremia cases occurred in children and adults with an underlying disease, such as diabetes, leukemia, sickle cell disease, malignancy, cirrhosis, immunosuppressive therapy, and HIV infection [3–8].
This patient used to have recurrent diarrhea despite repeated treatments done for him. Though the appropriateness of the treatments given cannot be proven, frequent relapse of the disease potentiates the failure of his immunity to clear the infection. Shigella infection represents an interesting paradigm of imbalance of the host immune mechanism to regulate infection and of bacterial strategies developed to escape killing by host immune cells that are equipped with a large repertoire of antimicrobial weapons to control microbial infection .
Leishmaniasis is associated with many immunological disorders including depression of cell-mediated immunity to Leishmania or other non related antigens . In patient with VL the skin, respiratory tract, and middle ear were the most common sites of infections, and Pseudomonas aeroginosa and Staphylococcus aureus were the most common etiologic agents .
The underlying disease in our case described here was VL. The patient was having severe leucopenia and malnutrition. Immune suppressive and debilitating conditions like VL may allow Shigella to easily pass the intestinal epithelia and get into the blood stream.
The clinical significance of Shigella bacteremia is not clear . Higher case fatality rate among bacteremic Shigella infection was reported than the nonbacteremic ones. However, this may be difficult to conclude as the high mortality could be from the severe underlying disease than the Shigella bacteremia. In the review of records of 2018 patients with shigellosis in a hospital in Bangladish between 1976 and 1983, it was found that severe complications occurred more frequently after Shigella bacteremia than in controls . Luckily our patient was not having any of the complications even if he has an underlying VL. The review also showed similar median duration of illness between the Shigella bacteremia patients and the controls (five and four days), but in our patient since the patient was having VL which is characterized by chronic symptoms it is difficult to know the exact duration of symptoms of Shigella bacteremia. Mostly patients reported with Shigella bacteremia had positive result on stool culture as well; however, that was not true in our case.
The presence of Shigella bacteremia in a VL patient indicates that VL is one of the immune suppressive conditions that can predispose for bacteremia due to atypical pathogens. Therefore, requesting blood culture to identify unexpected type of organisms causing infections in patients with underlying diseases like VL should be encouraged. Obviously, this type of evidence-based management will improve the treatment outcome of patients.
Conflict of Interests
The authors have declared that no conflict of interests exists.
The authors would like to thank the Gondar Leishmaniasis Treatment and Research Center team members for their kind cooperation in the management of our case.
- G. J. Tortora, B. R. Funke, and C. L. Case, “Microbial diseases of the digestive system,” in Microbiology an Introduction, L. Berriman, Ed., pp. 712–713, Pearson Benjamin Cummings, San Francisco, Calif, USA, 10th edition, 2010.
- B. G. Marcia, “Microbiology,” in Epidemiology, Microbiology, and Pathogenesis of Shigella Infection, B. C. Stephen and S. E. Morven, Eds., pp. 12–13, 2012.
- R. M. Kligler and P. D. Hoeprich, “Shigellemia,” Western Journal of Medicine, vol. 141, no. 3, pp. 375–378, 1984.
- M. J. Struelens, G. Mondal, M. Roberts, and P. H. Williams, “Role of bacterial and host factors in the pathogenesis of Shigella septicemia,” European Journal of Clinical Microbiology and Infectious Diseases, vol. 9, no. 5, pp. 337–344, 1990.
- S. A. Erqou, E. Teferra, A. Mulu, and A. Kassu, “A case of shigellosis with intractable septic shock and convulsions,” Japanese Journal of Infectious Diseases, vol. 60, no. 5, pp. 314–316, 2007.
- J. Huebner, W. Czerwenka, E. Gruner, and A. von Graevenitz, “Shigellemia in AIDS patients: case report and review of the literature,” Infection, vol. 21, no. 2, pp. 122–124, 1993.
- D. H. Baskin, J. D. Lax, and D. Barenberg, “Shigella bacteremia in patients with the acquired immune deficiency syndrome,” American Journal of Gastroenterology, vol. 82, no. 4, pp. 338–341, 1987.
- G. Bekele, D. Fekade, and M. Gedebou, “Shigellaemia in adults: case reports and literature review,” Ethiopian Medical Journal, vol. 24, no. 1, pp. 25–29, 1986.
- J. Vandepitte, J. Verhaegen, K. Engbaek, et al., Eds., Basic Laboratory Procedures in Clinical Bacteriology, WHO, Geneva, Switzerland, 2nd edition, 2003.
- Clinical and Laboratory Standards Institute, Performance Standards for Antimicrobial Susceptibility Testing, Clinical and Laboratory Standards Institute, Wayne, Pa, USA, 2009.
- A. Phalipon and P. J. Sansonetti, “Shigella's ways of manipulating the host intestinal innate and adaptive immune system: a tool box for survival?” Immunology and Cell Biology, vol. 85, no. 2, pp. 119–129, 2007.
- E. M. Carvalho, R. S. Teixeira, and W. D. Johnson Jr., “Cell-mediated immunity in American visceral leishmaniasis: reversible immunosuppression during acute infection,” Infection and Immunity, vol. 33, no. 2, pp. 498–502, 1981.
- T. M. Andrade, E. M. Carvalho, and H. Rocha, “Bacterial infections in patients with visceral leishmaniasis,” Journal of Infectious Diseases, vol. 162, no. 6, pp. 1354–1359, 1990.
- A. J. Trevett, B. O. Ogunbanjo, S. Naraqi, and J. D. Igo, “Shigella bacteraemia in adults,” Postgraduate Medical Journal, vol. 69, no. 812, pp. 466–468, 1993.
- M. J. Struelens, D. Patte, I. Kabir, A. Salam, S. K. Nath, and T. Butler, “Shigella septicemia: prevalence, presentation, risk factors, and outcome,” Journal of Infectious Diseases, vol. 152, no. 4, pp. 784–790, 1985.