Abstract
Paenochrobactrum pullorum is a gram-negative bacterium and is not usually considered a human pathogen. This is the first case report of P. pullorum, highlighting the importance of understanding its clinical significance. The author reports a case of P. pullorum bacteremia from bilateral lower extremity wound infection.
Keywords: ciprofloxacin, gram-negative bacteremia, maldi-tof ms, brucellaceae, paenochrobactrum pullorum
Introduction
Paenochrobactrum pullorum is a gram-negative bacterium known for its nitrogen-fixing capabilities and has been isolated from various environmental sources, including the poultry environment [1]. It is not usually considered a human pathogen, and this is the first case report of P. pullorum bacteremia, emphasizing the importance of understanding its clinical impact. A 46-year-old homeless male with multiple comorbidities presented with bilateral lower extremity wound infections. He was found to have P. pullorum bacteremia.
Case presentation
A 46-year-old homeless male with multiple comorbidities, including emphysema, bipolar disorder, schizophrenia, and a history of a motor vehicle accident in 2000 with traumatic brain injury, presented with bilateral lower extremity wound infections. He reported smoking half a pack of cigarettes per day and using marijuana but denied using alcohol or recreational drugs intravenously. He denied recent travel and exposure to animals or birds. On physical exam, his phalanges from bilateral feet came off with the socks when the staff removed his shoes (Figure 1).
Figure 1. Bilateral exposed metatarsal bones due to auto amputation-necrotic stump area with a very foul-smelling purulent scanty discharge.
A: dorsal view; B: plantar view
He essentially had auto amputations of the trans metatarsal of both lower extremities with gangrene. There was an exposed metatarsal bone on the right lower extremity. The patient was showered, and the wounds were cleaned. In the emergency department, the patient was febrile to 102.4°F and tachycardic at 139 beats per minute. Labs revealed leukocytosis, acute kidney injury, sedimentation rate of 108 mm/hour, hemoglobin A1C of 6.1%, and lactic acid of 4.9 mmol/L (Table 1).
Table 1. Complete blood count and comprehensive metabolic panel results on admission.
| Parameter | Results | Reference range | Units | ||
| White blood cell count | 18.81 | 4.40-11.00 | 10x3/mm3 (cubic millimeter) | ||
| Red blood cell count | 3.11 | 4.50-5.90 | 10x6/mm3 | ||
| Hemoglobin (Hb) | 9.1 | 13.2-16.5 | g/dL (grams per deciliter) | ||
| Hematocrit | 29 | 39-49 | % | ||
| Mean corpuscular volume (MCV) | 94 | 80-94 | fL or fl (femtoliter) | ||
| Mean corpuscular hemoglobin (MCH) | 29 | 27-31 | pg (picograms per cell) | ||
| Mean corpuscular hemoglobin concentration (MCHC) | 31 | 33-37 | g/dL | ||
| Red cell distribution width (RDW) | 14.5 | 11.5-16.1 | % | ||
| Platelets | 708 | 130-440 | 10x3/mm3 | ||
| Mean platelet volume | 8.6 | 7.2-11.1 | fL | ||
| Sodium | 137 | 135-145 | mmol/L (millimoles per liter) | ||
| Potassium | 4.5 | 3.5-5.0 | mmol/L | ||
| Chloride | 101 | 96-110 | mmol/L | ||
| Bicarbonate | 18 | 21-31 | mmol/L | ||
| Glucose | 135 | 80-100 | mg/dL (milligrams per deciliter) | ||
| Blood urea nitrogen | 33.1 | 6.0-21.0 | mg/dL | ||
| Creatinine | 1.5 | 0.6-1.4 | mg/dL | ||
| Calcium | 8.8 | 8.8-11.1 | mg/dL | ||
| Total protein | 6.6 | 5.9-8.4 | g/dL | ||
| Albumin | 2.8 | 3.2-5.2 | g/dL | ||
| Bilirubin total | 1.35 | 0.00-1.20 | mg/dL | ||
| Alkaline phosphatase | 145 | 40-129 | U/L (units per liter) | ||
| Aspartate aminotransferase | 36 | 10-50 | U/L | ||
| Alanine aminotransferase | 34 | 10-50 | U/L | ||
| Glomerular filtration rate (GFR) | 59 | 60-180 | mL/min/1.73 m2 | ||
Blood cultures were obtained, and empiric broad-spectrum antibiotics with IV vancomycin and piperacillin/tazobactam were started. After 48 hours of incubation, two out of two blood culture bottles were positive for gram-negative rods, which were identified as P. pullorum (beta-lactamase negative) using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) [2]. Wound cultures grew polymicrobial growth including P. pullorum. He underwent simultaneous bilateral below-knee amputations (Figure 2).
Figure 2. Bilateral below knee amputation (BKA).
A: right BKA; B: left BKA
Histopathology of the below-the-knee amputation revealed acute osteomyelitis, active ulcers, large vessels with calcification within the wall, and viable skin, soft tissue, and bone at the margin. The sensitivity report of P. pullorum was not available and the patient was treated with oral ciprofloxacin 500 mg twice daily for two weeks. He was discharged in a stable condition (Table 2).
Table 2. Complete blood count and comprehensive metabolic panel results upon discharge.
| Parameter | Results | Reference range | Units |
| White blood cell count | 7.36 | 4.40-11.00 | 10x3/mm3 |
| Red blood cell count | 3.61 | 4.50-5.90 | 10x6/mm3 |
| Hemoglobin (Hgb) | 10.5 | 13.2-16.5 | g/dL |
| Hematocrit (Hct) | 34 | 39-49 | % |
| Mean corpuscular volume (MCV) | 95 | 80-94 | fL |
| Mean corpuscular hemoglobin (MCH) | 29 | 27-31 | pg |
| Mean corpuscular hemoglobin concentration (MCHC) | 31 | 33-37 | g/dL |
| Red cell distribution width (RDW) | 15.6 | 11.5-16.1 | % |
| Platelets | 603 | 130-440 | 10x3/mm3 |
| Mean platelet volume (MPV) | 8.6 | 7.2-11.1 | fL |
| Neut% | 62 | 40-74 | % |
| Lymph% | 22 | 19-48 | % |
| Mono% | 7.5 | 3.4-10.0 | % |
| Eos% | 3.8 | 0.0-7.0 | % |
| Baso% | 1.4 | 0.0-1.5 | % |
| Neut# | 4.6 | 1.9-8.0 | 10x3 |
| Lymph# | 1.6 | 1.0-4.9 | 10x3 |
| Mono# | 0.6 | 0.2-1.0 | 10x3 |
| Eos# | 0.3 | 0.0-0.7 | 10x3 |
| Baso# | 0.1 | 0.0-0.2 | 10x3 |
| Sodium | 135 | 135-145 | mmol/L |
| Potassium | 4.9 | 3.5-5.0 | mmol/L |
| Chloride | 103 | 96-110 | mmol/L |
| Bicarbonate | 24 | 21-31 | mmol/L |
| Glucose | 94 | 80-100 | mg/dL |
| Blood urea nitrogen | 25.8 | 6.0-21.0 | mg/dL |
| Creatinine | 0.7 | 0.6-1.4 | mg/dL |
| Calcium | 8.5 | 8.8-11.1 | mg/dL |
| Total protein | 6.2 | 5.9-8.4 | g/dL |
| Albumin | 2.7 | 3.2-5.2 | g/dL |
| Bilirubin total | 0.35 | 0.00-1.20 | mg/dL |
| Alkaline phosphatase | 77 | 40-129 | U/L |
| Aspartate aminotransferase | 27 | Oct-50 | U/L |
| Alanine aminotransferase | 36 | Oct-50 | U/L |
Discussion
P. pullorum is a gram-negative bacterium belonging to the genus Paenochrobactrum, which falls under the family Brucellaceae. It was first described in 2010 by Kämpfer et al., after isolating from the poultry environment [3]. The genus Paenochrobactrum consists of three classified species including Paenochrobactrum gallinarii, Paenochrobactrum glaciei, P. pullorum, and unclassified Paenochrobactrum including Paenochrobactrum sp., Paenochrobactrum sp. BAB-4388, Paenochrobactrum sp. BAB-4391, Paenochrobactrum sp. DB-12, Paenochrobactrum sp. VRE47B1_13_1E, Paenochrobactrum sp. VRE69B1_13_1E [4]. P. pullorum is a rod-shaped, non-spore-forming, non-motile, oxidase-positive, and has a specific ability to fix atmospheric nitrogen, thus having a potential role in agriculture [5-7]. P. pullorum infections are uncommon but can arise, particularly in patients with comorbidities or exposure to environmental sources sheltering the bacterium. Though it is typically susceptible to ciprofloxacin and trimethoprim-sulfamethoxazole, appropriate antibiotic selection guided by susceptibility testing is essential for successful outcomes [3]. There is limited information available on the pathogenic potential of P. pullorum in humans and more research is needed to understand its pathogenic mechanisms and clinical significance in human disease.
Conclusions
This case report highlights the significance of considering unusual pathogens like P. pullorum in the differential diagnosis of bacteremia, particularly in patients with environmental exposures. Timely identification and appropriate antibiotic therapy are essential for successful outcomes.
The authors have declared that no competing interests exist.
Author Contributions
Concept and design: Pradeep Kumar Mada
Acquisition, analysis, or interpretation of data: Pradeep Kumar Mada
Drafting of the manuscript: Pradeep Kumar Mada
Critical review of the manuscript for important intellectual content: Pradeep Kumar Mada
Human Ethics
Consent was obtained or waived by all participants in this study
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