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. 2018 Jul 19;10(7):e3007. doi: 10.7759/cureus.3007

Neisseria cinerea in a Post-splenectomy Patient: A Rare Potentially Fatal Bacteremia

Ravikaran Patti 1,, Sushilkumar S Gupta 2, Sharonlin Bhardwaj 3, Prameeta Jha 1, Arindam Ghatak 4, Yizhak Kupfer 2, Chanaka Seneviratne 5
Editors: Alexander Muacevic, John R Adler
PMCID: PMC6145752  PMID: 30250769

Abstract

Neisseria cinerea is a commensal which usually resides in the human respiratory tract. Very rarely, the organism finds its way into the bloodstream causing severe bacteremia. So far, very few cases of Neisseria bacteremia have been reported. We report a case of a 78-year-old male, post-splenectomy, who presented with high fever, cough and shortness of breath. The patient was initially managed for septic shock with fluid resuscitations, vasopressors and broad-spectrum antibiotics. Later, the blood cultures grew gram-negative coccobacilli, Neisseria cinerea. The patient was successfully treated with intravenous ceftriaxone. This is the first case ever of Neisseria cinerea bacteremia in a post-splenectomy patient and ninth case overall. This case illustrates that the physicians should maintain heightened awareness for Neisseria cinerea bacteremia in post-splenectomy patients.

Keywords: neisseria cinerea, bacteremia, post splenectomy patient

Introduction

Neisseria cinerea is a non-pathogenic, gram-negative, catalase-positive and oxidase-positive diplococci [1]. It is an asaccharolytic commensal Neisseria species which usually resides in the upper respiratory tract but sometimes finds its way to bloodstream causing a life-threatening infection. Most of the patients reported with Neisseria cinerea bacteremia have some form of immunodeficiency, while a few were completely healthy. Identifying Neisseria cinerea is a challenge for microbiologists as it shares both biochemical and morphological characteristics with Neisseria gonorrhea and Branhamella catarrhalis [1]. We report first ever case of Neisseria cinerea bacteremia in a post-splenectomy patient rather than the usual encapsulated organisms.

Case presentation

A 78-year-old male presented to the emergency room with complains of high fever, and non-bloody non-bilious vomiting. This was associated with a non-productive cough and dyspnea. He had a past medical history of splenectomy following thrombotic thrombocytopenic purpura (TTP) and recurrent pneumonia. On presentation, the patient was febrile to 101.7° F, respiratory rate of 34 breaths per minute and blood pressure of 83/49 mm Hg. Complete blood count showed leukopenia with white cell count of 1.1 x 109 per liter (L), bandemia of 27% and lactic acidosis of 12.3 mmol/l on the venous blood gas. Computed tomography (CT) scan of the chest/abdomen, and pelvis with oral contrast was performed which showed consolidation in the left lower lobe of lung (Figure 1).

Figure 1. Computed tomography scan of the chest showing consolidation within medial portion of the left lower lobe (blue arrow).

Figure 1

The patient was admitted in the medical intensive care unit with the preliminary diagnosis of severe sepsis with septic shock. Sequential organ failure assessment (SOFA) score at the time of admission was 10. Sepsis bundle was initiated and intravenous (IV) crystalloid resuscitation at 30 ml/kg was immediately started, blood cultures were drawn and intravenous broad-spectrum antibiotics were initiated. Due to inadequate response to intravenous fluids, a vasopressor agent (phenylephrine) and stress dose steroid (hydrocortisone) was started. Blood cultures grew gram-negative coccobacilli, Neisseria species which was later confirmed by microbiologist as Neisseria cinerea. Antibiotics were narrowed down to IV ceftriaxone 2 gm every 12 hours based on the sensitivity.

During the course of hospitalization, the patient improved clinically and remained hemodynamically stable. Repeat blood cultures did not show any growth and the patient was discharged home after completion of two weeks of intravenous ceftriaxone.

Discussion

Neisseria cinerea was first identified in 1905 as Micrococcus cinereus by Alexander von Lingelsheim [2]. In 1962, Berger and Paepcke described it to be an asaccharolytic commensal of the human oropharynx which was later described correctly as a commensal of human oropharynx and sometimes of the urogenital tract by Knapp et al. in 1984 [2-3]. N. cinerea is an oxidase-positive and catalase-positive, gram-negative diplococci. The bacteria share many morphological and biochemical similarities with Neisseria gonorrhea and Branhamella catarrhalis. Neisseria cinerea is able to reduce glucose like N. gonorrhea but not able to utilize it for energy, making it asaccharolytic. Amino acids like cysteine, cystine, proline and arginine are required for its growth. Unlike Neisseria gonorrhea, N. cinerea can grow on mediums like Mueller-Hinton agar and trypticase soy agar, and is not resistant to colistin [4].

As described earlier, Neisseria cinerea normally colonizes human oropharynx but very rarely enters the bloodstream. All the cases of N. cinerea bacteremia reported to date are described in Table 1 [1, 4-9].

Table 1. Table listing all reported cases of Neisseria cinerea.

Patient Age (years) Comorbidities Risk of infection Additional infection  Antibiotics given Outcome Reference
1. 59 Myelodysplastic syndrome  Chemotherapy None Imipenem for 14 days Died Zhu et al. [1]
2.  58 Multiple sclerosis - Severe Trigeminal neuralgia Percutaneous glycerol rhizotomy Meningitis Ceftriaxone for seven days Survived Von Kietzell et al. [5]
3.  47  End-stage renal disease (ESRD) on hemodialysis Coughing onto arteriovenous graft site None Ciprofloxacin Survived Johnson et al. [6]
4.  46 Alcohol abuse None Acute abdomen with bacteremia  Tobramycin, clindamycin, vancomycin, piperacillin, cefoxiti, ampicillin, amikacin and cefotaxime Died Southern & Kutscher [7]
5.  2.5 Frequent upper respiratory tract infections None Otitis media and pneumonia Amoxicillin for 10 days Survived Southern & Kutscher [7]
6.  34  Intravenous drug use Intravenous drug use Tricuspid valve endocarditis Co-amoxiclav, ceftriaxone and amoxicillin Survived Benes et al. [8]
7.  17 None Facial trauma with laxation of two teeth Meningitis Cefotaxime Survived Kirchgesner et al. [9]
8. 38 Postpartum Hemolytic-uremic Syndrome (HUS) causing ESRD Eculizumab None Cefepime Survived Walsh et al. [4
9. 78  Post splenectomy and Thrombotic Thrombocytopenic purpura Post splenectomy Left lower lobe pneumonia Ceftriaxone Survived Current case

Our case is the first case of a patient who had undergone splenectomy, who developed Neisseria cinerea bacteremia reported in the literature. Usually, in such patients, encapsulated organisms such as Streptococcus pneumoniae, Haemophilus influenzae or Neisseria meningitidis are the common causes of infection. Immune deficiency was common in most of the previously described cases, and can be considered as the most vital cause leading to bacteremia. Recent reports have demonstrated that despite the use of appropriate vaccination, these immunocompromised patients are still at increased risk of infection with Neisseria bacteremia [10].

Conclusions

By reporting this case we recommend that Neisseria cinerea bacteremia should be considered in the differential diagnosis of post-splenectomy patients causing infection. A clear understanding of how Neisseria cinerea, an unusual non-encapsulated organism, causes overwhelming sepsis in a post-splenectomy patient, needs further workup. One should also be very cautious in properly isolating Neisseria cinerea due to rarity and similarities with N. gonorrhea.

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The authors have declared that no competing interests exist.

Human Ethics

Consent was obtained by all participants in this study. Not applicable issued approval Not applicable

References

  • 1.Fatal bacteremia by Neisseria cinerea in a woman with myelodysplastic syndrome: a case report. Zhu X, Li M, Cao H, Yang X. https://europepmc.org/abstract/med/26131259. Int J Clin Exp Med. 2015;8:6369–6371. [PMC free article] [PubMed] [Google Scholar]
  • 2.Studies on asaccharolytic Neisseria in the human nasopharynx (Article in German) Berger U, Paepcke E. https://www.ncbi.nlm.nih.gov/pubmed/13867688. Z Hyg Infektionskr. 1962;148:269–281. [PubMed] [Google Scholar]
  • 3.Characterization of Neisseria cinerea, a nonpathogenic species isolated on Martin-Lewis medium selective for pathogenic Neisseria spp. Knapp JS, Totten PA, Mulks MH, Minshew BH. https://www.ncbi.nlm.nih.gov/pubmed/6361062. J Clin Microbiol. 1984;19:63–67. doi: 10.1128/jcm.19.1.63-67.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Neisseria cinerea bacteremia in a patient receiving eculizumab: a case report. Walsh TL, Bean HR, Kaplan RB. Infection. 2018;46:271–274. doi: 10.1007/s15010-017-1090-4. [DOI] [PubMed] [Google Scholar]
  • 5.Meningitis and bacteremia due to Neisseria cinerea following a percutaneous rhizotomy of the trigeminal ganglion. Von Kietzell M, Richter H, Bruderer T, Goldberger D, Emonet S, Strahm C. J Clin Microbiol. 2016;54:233–235. doi: 10.1128/JCM.02041-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Neisseria cinerea bacteremia in a patient receiving hemodialysis. Johnson DH, Febre E, Schoch PE, Imbriano L, Cunha BA. Clin Infect Dis. 1994;19:990–991. doi: 10.1093/clinids/19.5.990. [DOI] [PubMed] [Google Scholar]
  • 7.Bacteremia due to Neisseria cinerea: report of two cases. Southern PM Jr, Kutscher AE. Diagn Microbiol Infect Dis. 1987;7:143–147. doi: 10.1016/0732-8893(87)90032-0. [DOI] [PubMed] [Google Scholar]
  • 8.Tricuspid valve endocarditis due to Neisseria cinerea. Benes J, Dzupova O, Krizova P, Rozsypal H. https://www.ncbi.nlm.nih.gov/pubmed/12627284. Eur J Clin Microbiol Infect Dis. 2003;22:106–107. doi: 10.1007/s10096-002-0874-2. [DOI] [PubMed] [Google Scholar]
  • 9.Meningitis and septicemia due to Neisseria cinerea. Kirchgesner V, Plesiat P, Dupont MJ, Estavoyer JM, Guibour-denche M, Riou JY, Michel-Briand Y. Clin Infect Dis. 1995;21:1351. doi: 10.1093/clinids/21.5.1351. [DOI] [PubMed] [Google Scholar]
  • 10.High risk for invasive meningococcal disease among patients receiving eculizumab (Soliris) despite receipt of meningococcal vaccine. McNamara LA, Topaz N, Wang X, Hariri S, Fox L, MacNeil JR. MMWR Morb Mortal Wkly Rep. 2017;66:734–737. doi: 10.15585/mmwr.mm6627e1. [DOI] [PMC free article] [PubMed] [Google Scholar]

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