CC BY-NC-ND 4.0 · J Lab Physicians 2022; 14(03): 343-347
DOI: 10.1055/s-0042-1744236
Case Report

Granulicatella adiacens as an Unusual Cause of Empyema: A Case Report and Review of Literature

1   Department of Microbiology, All India Institute of Medical Sciences, Bhubaneswar, India
2   Department of Microbiology and Infection Control, Vikash Multispeciality Hospital, Bargarh, Odisha, India
,
Baijayantimala Mishra
1   Department of Microbiology, All India Institute of Medical Sciences, Bhubaneswar, India
,
Satyajeet Sahoo
3   Department of Pulmonary Medicine, All India Institute of Medical Sciences, Bhubaneswar, India
,
1   Department of Microbiology, All India Institute of Medical Sciences, Bhubaneswar, India
› Author Affiliations
 

Abstract

Granulicatella adiacens, a nutritionally variant Streptococcus (NVS), is part of the normal commensal flora of human mouth, genital, and intestinal tracts and rarely causes disease. It has been mostly reported from bacteremia and endocarditis cases, but rarely can cause vertebral osteomyelitis, pancreatic abscess, otitis media, and endovascular, central nervous system, ocular, oral, bone and joint, and genitourinary infections. Due to requirement of fastidious culture conditions and non-specific colony morphology, serious diagnostic difficulties may arise in cases of NVS infections. Here, we are reporting a rare fatal infection of G. adiacens presented with empyema complicated to sepsis and necrotizing fasciitis.

Clinicians should be aware of the pathogenic potential of Granulicatella adiacens (a normal commensal flora of human mouth, genital and intestinal tracts). Appropriate supplemented media and a reliable detection system should be used to identify these fastidious organisms. We present this rare case to bring awareness among clinicians regarding such a rare but potentially fatal infection.


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Introduction

Granulicatella adiacens is a nutritionally variant Streptococcus (NVS). Pyridoxine or other additional agents supplementation into standard media is required for its laboratory isolation.[1] Taxonomically, these bacteria were transferred from Streptococcus to a separate genus Abiotrophia [2] and later, on the basis of 16S rRNA gene sequencing this genus was divided into the genera Abiotrophia and Granulicatella (species Granulicatella adiacens, G. elegans, and G. balaenopterae).[3]

Granulicatella is part of the normal commensal flora of human mouth, genital and intestinal tracts and rarely causes disease. Granulicatella adiacens has been mostly reported to cause bacteremia and endocarditis, but rarely can cause vertebral osteomyelitis, pancreatic abscess, otitis media and endovascular, central nervous system, ocular, oral, bone and joint and genitourinary infections.[4]

Infections due to nutritionally variant Streptococcus may have a high mortality rate because of difficulties in robust and reliable diagnosis and therapeutic failures. In a recent survey, mortality rate in nutritionally variant Streptococcus infections was found to be 9.0%.[5] For treatment of Abiotrophia and Granulicatella endocarditis and other serious infections, penicillin or ceftriaxone is the drug of choice as per the American Heart Association (AHA) guidelines.[6] Through this article, we present a review and our experience of a rare case of empyema caused due to G. adiacens complicated to sepsis and necrotizing fasciitis and ultimately death.


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Materials and Methods

Case History

A 68-year-old male patient presented with left side chest pain and pain in lower limbs to the emergency department. On examination, the body temperature was 38.5°C, blood pressure 78/50 mm Hg, and pulse rate was 93/min. On chest examination, heart sounds were normal but respiratory rate was 28/min, vesicular breath sound and crepitations were present in the left chest. He was a known case of type 2 diabetes mellitus, hypertension and osteoarthritis of knee joints. He was alcoholic. Chest X-ray showed left-sided encysted pleural effusion. The patient was diagnosed with left-sided empyema with ruptured baker's cyst and septic shock. On ultrasound-guided aspiration, thick pus was aspirated and sent for biochemical analysis, bacteriological culture and sensitivity, Ziehl–Neelsen stain and CBNAAT (Cartridge-based nucleic acid amplification test). Simultaneously, one set of blood (BACT/ALERT FA Plus and BACT/ALERT FN Plus) and urine samples were sent for bacteriological culture. The patient was diagnosed as a case of left-sided empyema with septic shock and transferred to the ICU for management. Intercostal chest tube was placed and fluid was drained. The patient was managed with intravenous saline infusion and empirical antibiotic (inj. cefuroxime) was started. Laboratory findings showed an increased total leukocyte count (18,580/mm3), absolute neutrophil count (17,290 mm3), increased C-reactive protein (CRP 11.2 mg/dL), and hemoglobin level was 11.2 g/dL. Fasting blood sugar was 201 g/dL and serum uric acid was 8.9 mg/dL. Kidney function test was also deranged with serum urea level 102 mg/dL and creatinine 1.2 mg/dL. Pleural pus grew minute colonies on sheep blood agar after 48 hours, which were gram-positive cocci in small chains, catalase-negative, and subsequently identified as Granulicatella adiacens using the VITEK2 system (bioMérieux, France) using Gram positive (GP) identification card with 98% probability index. Antimicrobial susceptibility was performed using the E-test method (HiMedia, Mumbai, India) and MICs in µg were reported according to the EUCAST Clinical Breakpoints.[7] The isolate was sensitive to benzylpenicillin (MIC: 0.002 μgm/ml), ampicillin (0.016 μgm/ml), ampicillin sulbactam (0.016 μgm/ml), ceftriaxone (0.002 μgm/ml), teicoplanin (0.016 μgm/ml), vancomycin (0.016 μgm/ml) and linezolid (0.5 μgm/ml) and resistant to gentamicin (MIC >16 μgm/ml) and cotrimoxazole (MIC > 40 μgm/ml). After 5 days of incubation, blood culture also grew same organism with same sensitivity pattern. Urine culture was sterile. There was no significant improvement from the first presentation, except reduced drain fluid from intercostal site. As per the culture report, the empirical antibiotic was changed to inj. ceftriaxone and inj. linezolid. On the fifth day of targeted therapy, pleural pus was still there although minimal, and was sent for bacterial culture was sterile. But on the seventh day of hospitalization, the patient developed right lower limb necrotizing fasciitis with myonecrosis. Fasciotomy was done and it revealed necrotic muscles of lower leg posterior compartment with hematoma in the intra-muscular compartment. Unfortunately, the patient passed away on twelfth day of hospitalization due to acute myocardial infarction.


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Discussion

We did the literature search over past 10 years (2011–2020) using search engines PubMed using the MeSH term, “Granulicatella adiacens.” Case reports with only monomicrobial infection due to G. adiacens were included in the review. All articles published in English were included in this analysis.

We reviewed 77 literatures on the subject (G. adiacens) over the past 10 years (2011–2020). Using the inclusion and exclusion criteria, 24 literature were found relevant and included in the review.[8] [9] [10] [11] [12] [13] [14] [15] [16] [17] [18] [19] [20] [21] [22] [23] [24] [25] [26] [27] [28] [29] [30] [31] Clinical details of all published literature are compiled in the [Table 1]. As per the review of literature of last 10 years, G. adiacens is found to be the cause of various infections such as bacteremia, endocarditis, osteomyelitis, septic arthritis, discitis, prosthetic joint infections, carbuncle, bacterascites (spontaneous bacterial peritonitis), dacryocystitis, and abscess. Out of these, 13 isolated from blood (4 bacteremia, 8 endocarditis, 1 septic arthritis), 10 from synovial fluid/pus (6 prosthetic joint infection, 2 osteomyelitis, 2 discitis), one each from dacryocystitis, bacterascites, and carbuncle. Further extending search in PubMed using MeSH terms such as “empyema” and “Granulicatella” found only one case report of empyema (pleural pus) caused by Granulicatella elegans.[32] None of them were from empyema pus and blood simultaneously except our present report of G. adiacens. All cases were reported from abroad, except three from India: one from New Delhi (suprapatellar abscess), one from Odisha (carbuncle), and the present study from Bhubaneswar, Odisha (empyema pus and blood). To the best of our knowledge, the present study is the first case report of thoracic empyema caused by G. adiacens complicated to necrotizing fasciitis and sepsis.

Table 1

Clinicoepidemiological details of infections caused by Granulicatella adiacens

Infections caused by Granulicatella adiacens

Year

Geographical location

Age/sex

Clinical diagnosis

Clinical samples

References

Bacteremia

2011

Charlottesville, Virginia

89 y/F

Multiple trauma victim with bacteremia

Blood

8

2011

New Haven, Connecticut, USA

1 d/Mch

Early onset neonatal sepsis

Blood

9

2013

Rome, Italy

7 y/F

Shone syndrome (coarctation of aorta, mitral stenosis and subvalvular aortic stenosis) with Bacteremia

Blood

10

5 y/M

Infundibular pulmonary stenosis with Bacteremia.

Blood

Endocarditis

2013

San Diego, CA, U.S.A.

50 y/M

Bivalvular (mitral and aortic valves) endocarditis

Blood

11

2013

Kerala, India

63 y/M

Infective endocarditis

Blood

12

2015

Australia

57 y/M

Subacute Bacterial endocarditis with type II mixed cryoglobulinemia

Blood

13

2016

Tokyo, Japan

67 y/F

Infective endocarditis with Sjogren's syndrome with oral complications

Blood

14

2019

Columbia, USA

44 y/F

Endocarditis, osteomyelitis, brain abscess

Blood

15

2019

Switzerland

32 y/F

Cardiac implantable electronic device related infection and bioprosthesis endocarditis

Blood

16

2019

U.S.A.

82 y/M

Bilateral lower extremity purpuric rash and complete heart block secondary to infective endocarditis

Blood

17

2020

Farmington CT, United States

46 y/M

Infective endocarditis and glomerulonephritis

Blood

18

Prosthetic joint infection

2013

Paris, France

55 y/M

Prosthetic joint infection (knee) after dental treatment

Knee fluid aspirate

19

2016

Peterborough, Cambridgeshire, PE3 9GZ, UK

81 y/M

Prosthetic joint infection (hip)

Pus aspirate from hip

20

2017

Marseille, France

75 y/M

Prosthetic joint infection (hip)

Synovial fluid

21

65 y/M

Prosthetic joint infection (knee)

Synovial fluid

44 y/F

Prosthetic joint infection (hip)

Surgical biopsy sample

2017

Eau Claire, WI, USA

64 y/M

Prosthetic joint infection (knee)

Synovial fluid

22

Osteomyelitis

2016

Swedish Neuroscience Institute

46 y/M

Vertebral osteomyelitis

Vertebral body biopsy tissue

23

2018

Kitakyushu, Japan.

10 y/F

Mandibular osteomyelitis

Bone marrow fluid

24

Septic arthritis

2019

Iowa City, Iowa

5 y/M

Ruptured appendicitis and retrocecal abscess presenting as atraumatic knee pain

Blood

25

Discitis

2013

Tokyo, Japan

48 y/F

Pyogenic discitis

Blood and disk biopsy sample

26

2020

Rome, Italy

51 y/M

Spondylodiscitis (L1-L2 and L5-S1 discs)

disk biopsy sample

27

Dacryocystitis

2015

Morgantown, WV 26505, USA

46 y/F

Dacryocystitis

Purulent material from lacrimal sac

28

Bacterascites

2015

Charlottesville, VA 22908, USA

50 y/M

Large distended abdomen (ascites)

Ascitic fluid

29

Abscess

2018

New Delhi, India

30 y/M

Suprapatellar abscess

Aspirated pus from Knee joint swelling

30

18 y/M

Elbow abscess

Pus swab

Carbuncle

2012

Odisha, India

56 y/M

Carbuncle, multiple discharging sinus over right scapular region

Pus

31

Empyema

2016

South Africa

30 y/F

Empyema underlying TB and HIV

Caused by Granulicatella elegans

Pleural pus

32

Empyema

2020

Odisha, India

68 y/M

Empyema underlying diabetes mellitus and alcoholism

Pleural pus and Blood

Present study

Necrotizing fasciitis is a destructive and rapidly progressive soft tissue infection with significant morbidity and mortality. It may necessitate surgical intervention and may progress to systemic involvement, septic shock, and multiorgan failure without intervention. Although the exact cause of necrotizing fasciitis in the present case is not clear, as clinical sample could not be sent for microbiological investigations. But association with G. adiacens infection cannot be ruled out as there is one published report of cervical necrotizing fasciitis due to polymicrobial cause including G. adiacens following dental extraction and its surgical management.[33]

Due to requirement of fastidious culture conditions and non-specific colony morphology, serious diagnostic difficulties may arise in cases of NVS infections. Commercial blood culture media contain pyridoxal and support the growth of NVS. However, in the present case, the bacteria isolated from pleural pus and blood samples grew on commercial 5% sheep blood agar (without any additional supplement) as cited in other reports.[31]

With evolvement of the newer advanced laboratory systems, that is, the MALDI-TOF (VITEK MS, Bruker MS) system and the VITEK 2 system, NVS can be identified up to the species level. In our case also, the isolate was identified using the VITEK 2 system.

As NVS are parts of normal commensal flora of human mouth, genital and intestinal tracts, their exact pathogenic role is unclear. Proteins secreted by these species may act as virulence determinants for interaction with the host. The secretome of G. adiacens is well documented in infective endocarditis and oral infections. More importantly, G. adiacens secretome comprised several putative virulence proteins, which enhance bacterial colonization and virulence through their multifunctional roles.[34] [35] Granulicatella and Abiotrophia spp. have the ability to bind to fibronectin and other extracellular matrix proteins and this binding ability appears to correlate with their degree of infectivity.[36]

Thus, clinicians should be aware of the pathogenic potential of these organisms. They can be easily overlooked because of their poor growth or no-growth on conventional solid media. NVS should be suspected when Gram stain shows microbial cells but cultures are negative. Due to the difficulties in identification of these bacteria, it is crucial for microbiology staff to be vigilant to prevent misidentification. For culture-negative cases, molecular test or Matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOFMS) would be a faster and reliable method for identification. The difficulty in identifying these organisms leads to delays in diagnosis. In addition, the results of susceptibility testing may not be accurate or reliable. Therefore, appropriate supplemented media and a reliable detection system should be used to identify these fastidious organisms.


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Conflict of Interest

None declared.

Acknowledgments

We would like to thank Mrs. Alakananda Mahapatra, laboratory technician, for technical help.

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  • 7 European Committee on Antimicrobial Susceptibility Testing. Breakpoint Tables for Interpretation of MICs and 7. Zone Diameters, Version 7.1, 'e European Committee on Antimicrobial Susceptibility Testing, Birmingham, UK, 2017 http://www.eucast.org
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  • 16 Sendi P, Wustmann K, Büchi AE. et al. Cardiac implantable electronic device-related infection due to Granulicatella adiacens . Open Forum Infect Dis 2019; 6 (04) ofz130 DOI: 10.1093/ofid/ofz130.
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  • 19 Mougari F, Jacquier H, Berçot B. et al. Prosthetic knee arthritis due to Granulicatella adiacens after dental treatment. J Med Microbiol 2013; 62 (Pt 10): 1624-1627 DOI: 10.1099/jmm.0.058263-0.
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  • 22 Pingili C, Sterns J, Jose P. First case of prosthetic knee infection with Granulicatella adiacens in the United States. IDCases 2017; 10: 63-64 DOI: 10.1016/j.idcr.2017.08.003.
  • 23 York J, Fisahn C, Chapman J. Vertebral osteomyelitis due to Granulicatella adiacens, a nutritionally variant streptococci. Cureus 2016; 8 (09) e808 DOI: 10.7759/cureus.808.
  • 24 Mizuki K, Morita H, Hoshina T. et al. Chronic mandibular osteomyelitis caused by Granulicatella adiacens in an immunocompetent child. J Infect Chemother 2019; 25 (05) 376-378
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Address for correspondence

Ashoka Mahapatra, MD
Microbiology, Department of Microbiology, All India Institute of Medical Sciences
Bhubaneswar, 751019
India   

Publication History

Article published online:
13 April 2022

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  • References

  • 1 Christensen JJ, Facklam RR. Granulicatella and Abiotrophia species from human clinical specimens. J Clin Microbiol 2001; 39 (10) 3520-3523
  • 2 Kawamura Y, Hou XG, Sultana F, Liu S, Yamamoto H, Ezaki T. Transfer of Streptococcus adjacens and Streptococcus defectivus to Abiotrophia gen. nov. as Abiotrophia adiacens comb. nov. and Abiotrophia defectiva comb. nov., respectively. Int J Syst Bacteriol 1995; 45 (04) 798-803
  • 3 Collins MD, Lawson PA. The genus Abiotrophia (Kawamura et al.) is not monophyletic: proposal of Granulicatella gen. nov., Granulicatella adiacens comb. nov., Granulicatella elegans comb. nov. and Granulicatella balaenopterae comb. nov. Int J Syst Evol Microbiol 2000; 50 (Pt 1): 365-369
  • 4 Cerceo E, Christie JD, Nachamkin I, Lautenbach E. Central nervous system infections due to Abiotrophia and Granulicatella species: an emerging challenge?. Diagn Microbiol Infect Dis 2004; 48 (03) 161-165
  • 5 Cargill JS, Scott KS, Gascoyne-Binzi D, Sandoe JAT. Granulicatella infection: diagnosis and management. J Med Microbiol 2012; 61 (Pt 6): 755-761
  • 6 Baddour LM, Wilson WR, Bayer AS. et al; American Heart Association Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease of the Council on Cardiovascular Disease in the Young, Council on Clinical Cardiology, Council on Cardiovascular Surgery and Anesthesia, and Stroke Council. Infective endocarditis in adults: diagnosis, antimicrobial therapy, and management of complications: a scientific statement for healthcare professionals from the American Heart Association. Circulation 2015; 132 (15) 1435-1486
  • 7 European Committee on Antimicrobial Susceptibility Testing. Breakpoint Tables for Interpretation of MICs and 7. Zone Diameters, Version 7.1, 'e European Committee on Antimicrobial Susceptibility Testing, Birmingham, UK, 2017 http://www.eucast.org
  • 8 Gardenier JC, Hranjec T, Sawyer RG, Bonatti H. Granulicatella adiacens bacteremia in an elderly trauma patient. Surg Infect (Larchmt) 2011; 12 (03) 251-253
  • 9 Bizzarro MJ, Callan DA, Farrel PA, Dembry LM, Gallagher PG. Granulicatella adiacens and early-onset sepsis in neonate. Emerg Infect Dis 2011; 17 (10) 1971-1973
  • 10 De Luca M, Amodio D, Chiurchiù S. et al. Granulicatella bacteraemia in children: two cases and review of the literature. BMC Pediatr 2013; 13: 61
  • 11 Garibyan V, Shaw D. Bivalvular endocarditis due to Granulicatella adiacens . Am J Case Rep 2013; 14: 435-438
  • 12 Shailaja TS, Sathiavathy KA, Unni G. Infective endocarditis caused by Granulicatella adiacens . Indian Heart J 2013; 65 (04) 447-449 DOI: 10.1016/j.ihj.2013.06.014.
  • 13 Sim BW, Koo RM, Hawkins C, Bowden F, Watson A. Granulicatella adiacens subacute bacterial endocarditis as the underlying cause of type II mixed cryoglobulinaemia. BMJ Case Rep 2015; 2015: bcr2014206091 DOI: 10.1136/bcr-2014-206091.
  • 14 Morita F, Hirai Y, Suzuki K. et al. Infective endocarditis and Sjögren's syndrome diagnosed simultaneously. IDCases 2016; 7: 6-8 DOI: 10.1016/j.idcr.2016.11.003.
  • 15 Patil SM, Arora N, Nilsson P, Yasar SJ, Dandachi D, Salzer WL. Native valve infective endocarditis with osteomyelitis and brain abscess caused by Granulicatella adiacens with literature review. Hindawi Case Reports in Infectious Diseases 2019; DOI: 10.1155/2019/4962392.
  • 16 Sendi P, Wustmann K, Büchi AE. et al. Cardiac implantable electronic device-related infection due to Granulicatella adiacens . Open Forum Infect Dis 2019; 6 (04) ofz130 DOI: 10.1093/ofid/ofz130.
  • 17 Halford B, Piazza MB, Berka H, Taylor C. Blocking a rash diagnosis: a rare case of infective endocarditis. BMJ Case Rep 2019; 12 (03) e226213 DOI: 10.1136/bcr-2018-226213.
  • 18 Shaik A, Roeuth D, Azmeen A. et al. Granulicatella causing infective endocarditis and glomerulonephritis. IDCases 2020; 21: e00792 DOI: 10.1016/j.idcr.2020.e00792.
  • 19 Mougari F, Jacquier H, Berçot B. et al. Prosthetic knee arthritis due to Granulicatella adiacens after dental treatment. J Med Microbiol 2013; 62 (Pt 10): 1624-1627 DOI: 10.1099/jmm.0.058263-0.
  • 20 Aweid O, Sundararajan S, Teferi A. Granulicatella adiacens prosthetic hip joint infection after dental treatment. JMM Case Rep 2016; 3 (03) e005044 DOI: 10.1099/jmmcr.0.005044.
  • 21 Quénard F, Seng P, Lagier JC, Fenollar F, Stein A. Prosthetic joint infection caused by Granulicatella adiacens: a case series and review of literature. BMC Musculoskelet Disord 2017; 18 (01) 276 DOI: 10.1186/s12891-017-1630-1.
  • 22 Pingili C, Sterns J, Jose P. First case of prosthetic knee infection with Granulicatella adiacens in the United States. IDCases 2017; 10: 63-64 DOI: 10.1016/j.idcr.2017.08.003.
  • 23 York J, Fisahn C, Chapman J. Vertebral osteomyelitis due to Granulicatella adiacens, a nutritionally variant streptococci. Cureus 2016; 8 (09) e808 DOI: 10.7759/cureus.808.
  • 24 Mizuki K, Morita H, Hoshina T. et al. Chronic mandibular osteomyelitis caused by Granulicatella adiacens in an immunocompetent child. J Infect Chemother 2019; 25 (05) 376-378
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