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01.12.2017 | Case report | Ausgabe 1/2017 Open Access

Journal of Medical Case Reports 1/2017

Pseudomonas oryzihabitans sepsis in a 1-year-old child with multiple skin rashes: a case report

Zeitschrift:
Journal of Medical Case Reports > Ausgabe 1/2017
Autoren:
Michael Owusu, Ellis Owusu-Dabo, Godfred Acheampong, Isaac Osei, John Amuasi, Nimako Sarpong, Augustina Annan, Hsin-Ying Chiang, Chih-Horng Kuo, Se Eun Park, Florian Marks, Yaw Adu-Sarkodie

Background

Pseudomonas oryzihabitans is the current name of a non-lactose-fermenting bacterium that used to be called Chromobacterium typhiflavum and Flavimonas oryzihabitans [1]. The species name typhiflavum was originally described by Dressel and Stickl as a variant of typhoid bacillus [2]. The bacterium is gram-negative and oxidase-negative with typical yellow-pigmented colonies visualized on agar media. It is thought to survive in moist environments, especially rice paddies, although some researchers have cultured cases from inhalational therapy equipment and hospital sinks [3, 4]. The organism has rarely been implicated as pathogenic in humans and often is not given serious attention in clinical practice.
Since the 1970s, when the first case of bacteremia in a neurosurgical patient with extradural cerebral hemorrhage secondary to P. oryzihabitans was reported, other researchers have identified the pathogen in patients with cancer, end-stage cirrhosis, sickle cell disease, and community-acquired urinary tract infections [5, 6]. P. oryzihabitans, unlike the other forms of Pseudomonas bacteria (for example, Pseudomonas aeruginosa, and Burkholderia cepacia) is susceptible to quinolones, carbapenems, β-lactamase inhibitor drugs, and trimethoprim/sulfamethoxazole [4, 7]. Treatment algorithms for managing P. oryzihabitans are not available in Ghana and many other developing countries, particularly those in sub-Saharan Africa. We report a case that is of significance because of the rare occurrence of this pathogen, the unique microbial characteristics of the bacteria, the age of the child involved, and the consequential clinical outcome.

Case presentation

A 1-year-old girl was presented to a hospital in the northeastern part of Ghana with a 1-week history of pustular rashes on her scalp and neck, which occasionally ruptured, along with discharge of yellowish purulent fluid. The child is of Mole-Dagbon ethnicity and hails from the northern part of Ghana. The patient had also experienced recurrent episodes of fever for 3 days, which had been controlled with the use of acetaminophen. The child had no known history of human immunodeficiency virus (HIV) infection, tuberculosis, or other underlying medical condition and lived with her parents, whose primary occupation was farming. The child lives in a rural area about 20 km from the hospital. On examination, the patient weighed 8 kg, was pale and febrile with a temperature of 39.7 °C, and well-hydrated. Her heart rate was 132 beats per minute, and her heart sounds were normal. Her lungs were clear, and her respiratory rate was 35 breaths per minute. A provisional diagnosis of sepsis and malaria was made.
Pending the results of laboratory tests of collected blood, urine, and stool samples, the patient was empirically treated with 270 mg of intravenous cefuroxime three times daily and 40 mg of intravenous gentamicin daily for 48 hours. Intravenous artesunate 24 mg was also administered for the first 24 hours (Table 1).
Table 1
Timeline of treatment
Parameters
Day 1
Day 2
Day 3
Day 4
Day 5
Day 6
Day 7
Total white cell count
8.8 × 109/L
Not done
8.5 × 109/L
10.8 × 109/L
Not done
Not done
9.4 × 109/L
Hemoglobin
6.6 g/dl
Not done
5.1 g/dl
12.2 g/dl
Not done
Not done
10.6 g/dl
Antibiotics
Intravenous cefuroxime 270 mg three times daily
    
Antibiotics
Intravenous gentamicin 40 mg daily
    
Antibiotics
    
Flucloxacillin suspension 5 ml four times daily
Antimalarial
Artesunate 24 mg/24 hours
      
Malaria rapid diagnostic test
Positive
      
Gram stain of broth
Positive (gram-negative rods)
    
Blood culture isolate
  
Positive
    
Hemotransfusion
  
240 ml/4 hours
    
Complete blood count investigations showed a hemoglobin concentration of 6.6 g/dl and a total white blood cell count of 8800 cells/μl (lymphocytes 52.1%, neutrophils 37.4%). The result of a malaria rapid diagnostic test was positive for malaria. The patient was given a hemotransfusion of 240 ml of whole blood over a period of 4 hours.
Results of both urine and stool cultures were negative for any bacterial growth. The blood culture sample was flagged as positive after 24 hours of incubation in an automated BD BACTEC 9050 blood culture system (BD Biosciences, San Jose, CA, USA), and a Gram stain of the culture broth revealed gram-negative rods. The broth was subcultured on blood agar, chocolate agar, and MacConkey agar (Oxoid Ltd, Basingstoke, UK) and incubated at 37 °C and 30 °C. Growth characteristics at 37 °C were poor, with grayish nonhemolytic colonies on blood agar and nonlactose fermentation on MacConkey agar. Plates incubated at 30 °C showed good pure growth on MacConkey agar and nonhemolytic colonies on blood agar. Results of biochemical investigations were negative for oxidase and urease and positive for citrate. The isolate was subjected to analytical profile index (API) 20NE and 20E (bioMérieux, Marcy-l’Étoile, France), which yielded unacceptable results.
Molecular identification was performed by extracting deoxyribonucleic acid (DNA) from a pure culture of this bacterium using SpheroLyse DNA extraction kit (Hain Lifescience GmbH, Nehren, Germany) according to the manufacturer’s instructions. The 16S ribosomal DNA (rDNA) was amplified using the primer pair 8F and 1492R [8]. The polymerase chain reaction conditions and the subsequent steps of Sanger sequencing we used were based on those described by Liu et al. [9]. The resulting 16S rDNA sequence was checked using DECIPHER (version 2.2.0; R Foundation for Statistical Computing, Vienna, Austria) to verify that it was not a chimera [10].
The procedure for molecular phylogenetic inference was based on that described by Ku et al. [11]. Briefly, the 16S rDNA sequence of the isolated strain was used as the query for sequence similarity search against the GenBank 16S rDNA sequence database. Highly similar sequences representing closely related species were selected for phylogenetic inference. All sequences were aligned using Multiple Sequence Comparison by Log-Expectation (MUSCLE) [12], and the resulting multiple sequence alignment was used to infer a maximum likelihood phylogeny using PhyML (version 3.0) [13]. The bootstrap support values were inferred based on resampling 1000 iterations.
The isolated strain reported in this study was found to be most similar to Pseudomonas oryzihabitans IAM 158 [GenBank accession NR_115005] with nucleotide sequence identity of 1455/1460 (99.7%). The molecular phylogeny also indicated that the new sequence is clustered with other P. oryzihabitans strains, which strongly supports the findings displayed in Fig. 1. The purified bacterial strain has been assigned the strain name Agogo to reflect its geographic origin and the sequence deposited in the GenBank database [accession number KX812763].
Antimicrobial susceptibility testing was done on the isolated bacteria using the Kirby-Bauer disk diffusion method following Clinical Laboratory Standards Institute guidelines [14]. The isolate was found to be susceptible to co-trimoxazole, chloramphenicol, ciprofloxacin, and gentamicin but resistant to ampicillin and cefuroxime. The rash on the patient’s scalp and skin, as well as her temperature spikes, resolved after continuous treatment with gentamicin, and her condition improved clinically. She was discharged on flucloxacillin and folic acid therapy 1 week after admission. A final diagnosis of septicemia secondary to bacterial skin infection with malaria coinfection was made.

Discussion

P. oryzihabitans is a rare bacterial isolate that has been linked to meningitis, endocarditis, diabetes mellitus, and infection with other organisms, especially in immunocompromised individuals [4, 15]. The pathogenicity of P. oryzihabitans is still a subject of debate in the scientific community, hence the need for adequate information to enable clinicians and public health practitioners to manage episodes associated with this pathogen.
Although it might be difficult to determine to what extent the severity of our patient’s illness was due to malaria or sepsis, the presence of the rare pathogen P. oryzihabitans in the blood in our patient is of importance, being the first such case reported from West Africa and only the second in sub-Saharan Africa [15]. It is possible that the pustular rashes provided an entry route for the bacteria directly from the environment, and the patient eventually progressed to sepsis. It is also possible that the child might have been exposed through skin bites or minor abrasions, either in the house or upon visiting her family’s farm. Our patient’s case is similar to one reported in South Africa, which occurred in a 4.7-year-old child who had been diagnosed with kwashiorkor, sepsis, and anemia [16]. Six cases of skin and soft tissue infections caused by P. oryzihabitans have been reported in patients with a previous histories such as surgery, immunosuppression, diabetes mellitus, trauma, bites, and lactation [17]. Although we did not perform an immunological immunodeficiency test for our patient, the result of a screening test for HIV antibody was negative, thus ruling out possible immunodeficiency disease associated with her illness.
An important feature we observed was the unique microbiological characteristics of this bacterium and the failure of the API to accurately identify the pathogen. The biochemical properties of our isolate using the Analytical Profile Index Non-Enterobacteriaceae (API NE) differed from the usual reported cases of P. oryzihabitans by being positive for gelatin hydrolysis and capric acid assimilation and negative for mannose and maltose assimilation [18]. Bosshard et al. [19] observed the low sensitivity of the API 20NE and thus recommended the use of 16S ribosomal ribonucleic acid (RNA) gene sequencing as an effective means of identification of clinically relevant nonfermenting gram-negative bacilli.

Conclusions

Our report shows that a combination of conventional and molecular technologies is the best approach to identifying Pseudomonas bacteria which may be implicated in the clinical condition of this child.

Acknowledgements

We thank the parents of the child and the staff of our hospital. The Sanger sequencing service was provided by the DNA Analysis Core Laboratory (Institute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan).

Funding

This report is on a subject recruited as part of an ongoing study conducted in partnership between the Kumasi Center for Collaborative Research based at the Kwame Nkrumah University of Science and Technology, Kumasi, Ghana, and the International Vaccine Institute, Seoul, Korea, with sponsorship from the Bill and Melinda Gates Foundation.

Availability of data and materials

All data generated or analyzed during this study are included in this published article and sequences deposited in the GenBank database.

Authors’ contributions

IO, JA, NS, and SEP reviewed the patient’s case and contributed to the writing of the manuscript. GA, AA, and MO performed conventional bacteriological analysis of the samples. HYC and CHK performed sequencing on the bacterial isolate and contributed to the writing of the manuscript. EOD, YAS, FM, and MO documented the clinical findings, verified and validated clinical data, and contributed to the writing of the manuscript. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Written informed consent was obtained from the patient’s legal guardian(s) for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Ethics approval and consent to participate

We obtained consent from the parents of the child before proceeding with publication of this report.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.

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