Skip to main content
IDCases logoLink to IDCases
. 2015 Oct 17;2(4):120–123. doi: 10.1016/j.idcr.2015.10.003

Infective endocarditis due to Bacillus cereus in a pregnant female: A case report and literature review

Mahek Shah a, Soumya Patnaik b,, Supakanya Wongrakpanich b, Yaser Alhamshari b, Talal Alnabelsi b
PMCID: PMC4712206  PMID: 26793477

Abstract

Incidence of infective endocarditis during pregnancy is around 0.006% with high maternal and fetal mortality. Bacillus cereus is an extremely rare cause for endocarditis in intravenous drug abusers (IVDA) or those with valvular disease or devices such as pacemakers. We report a case of B. cereus endocarditis, which, to the best of our knowledge, has never been reported in pregnancy. A 30-year-old, 25-week pregnant female presented with right shoulder pain, swelling and erythema on the lateral aspect of deltoid muscle from large abscess over her deltoid muscle. She was found to have a vegetation on the native tricuspid valve. Cultures from abscess fluid and blood cultures grew B. cereus, she was appropriately treated with antimicrobials and had favorable outcomes. There are <20 cases of B. cereus endocarditis reported but none during pregnancy. When cultures grow unusual organisms the case must be thoroughly investigated. This case illustrates a rare situation (endocarditis in pregnancy) with an unusual outcome (B. cereus) on an uncommon valve (tricuspid valve).

Abbreviations: ESR, erythromycin sedimentation rate; CRP, C-reactive protein; MIC, minimum inhibitory concentration

Keywords: Bacillus cereus, Infective endocarditis, Pregnancy, Intravenous drug use

Introduction

The occurrence of infective endocarditis during pregnancy is a very rare event with a reported incidence around 0.006%. Maternal mortality rate is documentated to be as high as 33% [1], [2]. Most of the deaths are secondary to heart failure or the presence of embolic events that complicate clinical course. Fetal mortality rates of up to 30% have also been reported [1].

Bacillus cereus is an extremely rare cause for endocarditis, and less than 20 cases reported so far. It is particularly seen in intravenous drug users (IVDU), those with underlying valvular disease or intravascular devices such as pacemakers and prosthetic valves [3]. We are reporting a case of B. cereus endocarditis in a young pregnant woman. To the best of our knowledge, B. cereus endocarditis has never been reported in pregnancy before.

As the most common tricuspid valve infective endocarditis in intravenous drug users is from Staphylococcus aureus infection, this case illustrates an unusual outcome (B. cereus) on an uncommon valve (tricuspid valve) in a rare situation (endocarditis in pregnancy).

Case report

A 30-year-old, 25-week pregnant female presented to the emergency room (ER) with right shoulder pain, which was progressively worse over a week with associated swelling and erythema on the lateral aspect of deltoid muscle. She has a long standing history of intravenous (IV) heroin and chronic methamphetamine use with tap water as diluents, as well as history of multiple hand abscesses.

At presentation, she was afebrile, hypotensive to 85/62 mmHg, tachycardic to 120/min, mildly tachypneic to 26/min, with normal oxygen saturation. Physical examination revealed poor oral dentition, and a large abscess over her deltoid muscle, from repeated intramuscular heroin injections. The abscess was incised and drained in the ER, and 100 mL of purulent fluid was obtained. Rest of her exam including the cardiovascular examination was unremarkable. White cell count (14.6 g/dL), ESR (55 mm/h) and CRP level (29 mg/L) were elevated. Her electrocardiogram was unremarkable, except for sinus tachycardia. There were no changes concerning for ischemic disease or conduction anomalies. She was started on methadone for control of opioid withdrawal and the fetus was closely monitored.

An extensive history about the technique of heroin use revealed that she often used her neck veins for access, disinfected the site of injection with alcohol swabs every time, used tap water as a diluent and denied using saliva or licking the needles at the time of use.

The patient was initially started on IV hydration with normal saline and was empirically started on IV daptomycin due to the growth of drug resistant organisms on cultures in the case of previous abscesses. A transthoracic echocardiogram showed a 0.3 cm × 0.4 cm vegetation on the native tricuspid valve along with mild tricuspid regurgitation. The rest of the heart chambers and valves were intact.

Cultures from abscess fluid grew B. cereus and Staphylococcus epidermidis. Multiple sets of blood cultures grew B. cereus. Antibiotic susceptibility tests revealed an elevated MIC for daptomycin and the patient was switched to IV vancomycin. The patient remained afebrile with stable vitals during the rest of her hospital stay. A decision was made to keep the patient on 6 weeks of IV vancomycin but the patient left against medical advice after completing five full weeks of treatment.

On a return visit to the hospital 4 weeks, the patient complained of vaginal discharge flu like symptoms for a week. Her blood cultures remained negative and the symptoms were attributed to opioid withdrawal. She was found to have elevated transaminases with an ALT of 1048 IU/L and AST of 480 IU/L but a work up for hepatitis was negative and the right upper quadrant ultrasound was within normal limits. Her LFTs trended down without intervention. The transaminitis was attributed to the presence of hepatotoxic agents in the street drugs that she had resumed after discharge. The patient did not have any signs or symptoms concerning for infection and was cleared for discharge.

She had an uncomplicated preterm vaginal delivery in her 37th week of gestation. Her infant was healthy at birth and on subsequent follow up.

Discussion

Bacillus infections have been recognized since the beginning of the 20th century and the nonanthrax species have increasingly been identified as pathogens [4], [5], [6], [7], [8]. B. cereus is a Gram-positive to Gram-variable aerobic or facultative anaerobic spore-forming rod that is ubiquitous in nature. Bacillus species have been demonstrated to be present in the hospital surroundings including equipment and mucous membranes of healthy individuals [4], [5]. The B. cereus group consists of six closely linked species: B. cereus, B. mycoides, B. pseudomycoides, B. thuringiensis, B. weihenstephanensis, and B. anthracis. Distinguishing between the individual species usually needs specialized in-laboratory molecular testing [9].

A majority of the human Bacillus infections are caused by B. cereus [3], [5], [10]. Clinical infections by B. cereus may be broadly classified as local infections, septicemia, central nervous system (CNS) infections including meningitis, respiratory infections, endocarditis or pericarditis and food poisoning caused by the production of a heat stable emetic and diarrheagenic toxin [7], [8], [11], [12], [13], [14]. A majority of the bacteremias with B. cereus are transient and clinically insignificant. Majority of the significant illnesses are seen in populations at risk such as IVDUs, patients on hemodialysis, neonates, immunocompromised patients and those with underlying malignancy [7], [14], [15], [16].

B. cereus is an unusual cause of endocarditis, usually associated with IVDUs, an underlying valvular disease or in association with implanted pacemakers and prosthetic valves (Table 1). All together, to the best of our knowledge, there are less than 20 cases of B. cereus endocarditis in literature but none have been documented in pregnancy [3]. The advancement in microbiological testing and increased awareness of its infectious potential allowed more cases of B. cereus endocarditis to be identified and reported. The first case of B. cereus endocarditis was reported in the 1970s in a patient with IVDU [17], [18]. In most previous cases of B. cereus endocarditis of the native valves in IV drug abusers, the patients responded well to antimicrobials alone and there was no need for surgery. Worse outcomes, poor antibiotic response and surgical intervention are more common in patients with prosthetic valves according to literature [19], [20], [21].

Table 1.

Characteristics of previously reported cases of Bacillus cereus endocarditis.

Author (year) Reference Valve involved Predisposing factors Remarks
Craig et al. (1974) Craig, C. P., W.-S. Lee, and M. Ho. 1974. Bacillus cereus endocarditis in an addict. Ann. Intern. Med. 80:418–419. Native (tricuspid valve) IVDU 18 year old with atrial septal defect
Lee et al. (1974) Lee, W., and M. Ho. 1974. Bacillus cereus endocarditis in an addict. Ann. Intern. Med. 80:418 Native (tricuspid valve) IVDU
Block et al. (1978) Block, C. S., M. L. Levy, and V. U. Fritz. 1978. Bacillus cereus endocarditis. S. Afr. Med. J. 53:556–557. Prosthetic valve (mitral valve) Prosthetic mitral valve
Tuazon et al. (1979) Tuazon CU et al., 1979. Serious infections from Bacillus sp. JAMA 241:1137–1140. Native (tricuspid valve) IVDU 3 Cases
Wanvarie et al. (1979) Wanvarie S, Rochanawatanon M. 1979. Bacillus cereus endocarditis. J. Med. Assoc. Thai. 62:34–38. Aortic valve Rheumatic heart disease
Weller et al. (1979) Weller PF, Nicholson A, Braslow N. 1979. The spectrum of Bacillus bacteremias in heroin addicts. Arch. Intern. Med. 139:293–294. No vegetation by echocardiogram IVDU
Oster at al (1982) Oster, H. A., and T. Q. Kong. 1982. Bacillus cereus endocarditis involving a prosthetic valve. South. Med. J. 75:508–50 Prosthetic valve Prosthetic aortic valve
Sliman et al. (1987) Sliman, R., S. Rehm, and D. Shlaes. 1987. Serious infections caused by Bacillus species. Medicine (Baltimore) 66:218–223. Right ventricular pacing wire History of rheumatic fever
Pacemaker
Steen et al. (1992)* Steen, M. K., L. A. Bruno-Murtha, G. Chaux, H. Lazar, S. Bernard, and C. Sulis. 1992. Bacillus cereus endocarditis: report of a case and review. Clin. Infect. Dis. 14:945–946 Prosthetic valve (aortic valve) Prosthetic aortic valve Mentions that there were 10 cases reported so far- 6 were IVDA, 1 had pacemaker, rest had valvular heart disease
Tomomasa et al. (1993) Tomomasa, T., K. Itoh, A. Matsui, T. Kobayashi, N. Suzuki, S. Matsuyama, and T. Kurome. 1993. An infant with ulcerative colitis complicated by endocarditis and cerebral infarction. J. Pediatr. Gasterenterol. Nutr. 17: 323–325. Native Immunosuppression Gastrointestinal instrumentation 12 month old infant in setting of diarrhea, ulcerative colitis and sepsis
Yamamura et al. (1994) Yamamura M, et al. 1994. A case of Bacillus cereus prosthetic valve endocarditis. Kyobu Geka 47:232–234. (In Japanese.) Mechanical mitral valve Prosthetic valve
Martin Cadenas et al. (1998) Martin Cadenas P, et al. 1998. Endocarditis by Bacillus cereus 1 in prosthetic mitral valve. Enferm. Infecc. Microbiol. Clin. 16:102–104. (In Spanish.) Mechanical mitral valve Prosthetic valve
Castedo et al. (1999) Castedo E, Castro A, Martin P, Roda J, Montero CG. 1999. Bacillus cereus prosthetic valve endocarditis. Ann. Thorac Surg. 68:2351–2352. Prosthetic valve (mitral valve) Prosthetic mitral valve
Cone et al. (2005) Cone LA, Dreisbach L, Potts BE, Comess BE, Burleigh WA. 2005. Fatal Bacillus cereus endocarditis masquerading as an anthrax-like infection in a patient with acute lymphoblastic leukemia: case report. J. Heart Valve Dis. 14:37–39. Native valve (mitral valve) Immunosupression Relapsing acute lymphoblastic leukemia with thigh abscess
Abusin et al. (2008) Abusin S, Bhimaraj A, Khadra S. 2008. Bacillus cereus endocarditis in a permanent pacemaker: a case report. Cases J. 1:95. Pacing wire Pacemaker
Thomas et al. (2012) Thomas BS, Bankowski MJ, Lau WK. Native valve Bacillus cereus endocarditis in a non intravenous- drug-abusing patient. J Clin Microbiol 2012;50:519–21. Native No IVDU
Barrund et al. (2012) Barrund O, Hidri N, Kim L et al. Pace-maker-associated Bacillus cereus endocarditis.
Diagnostic Microbiology infectious diseases 2012; 74L 313–315
Native Pacemaker
Oh et al. (2012) Oh DH, Kim MH, Kim YC et al. A case of native valve infective endocarditis caused by Bacillus cereus. Infection Chemotherapy 2012; 44: 310–314 Native (mitral valve) No IVDU
Ngow et al. (2013) Ngow HA, Khairina WMN. Bacillus cereus endocarditis in native aortic valve J Infect Chemother 2013; 19:154–157 Native (aortic valve) Former IVDU

The commonest sources leading to bacteremia in those with IV heroin abuse are colonization of the skin, contamination of injection equipment or paraphernalia, and organisms present in the heroin itself. In a study published in 1974, it was seen that 32% of street heroin samples and almost 50% of the injection drug paraphernalia grew Bacillus spp. on culture [7]. Other studies have shown the presence of Bacillus spp. in alcohol prep pads which may be used by these patients prior to injection [22]. We were unable to acquire the actual heroin samples or her equipment for testing but at least one of the above mentioned sources may have been the source of origin for the infection.

It is important to realize in clinical practice that B. cereus is a known blood culture contaminant and may be linked to contamination of ethanol solutions, hospital linen, culture media, hand gloves, and hospital construction material [23], [24], [25], [26], [27]. Another contributing factor is that Bacillus spp. grow easily on blood and chocolate agars at temperatures between 25 and 37 °C. Hence, a high suspicion should be maintained in the correct clinical setting especially in patients who continue to have multiple positive blood cultures. IVDUs with B. cereus bacteremia are at a high risk for developing aggressive endophthalmitis, panophthalmitis or acute keratitis that can lead to blindness within hours requiring enucleation of the eye [8], [26].

The choice of appropriate management of endocarditis in pregnancy can be challenging but prompt treatment is needed due to the high rates of maternal and fetal mortality associated with it [28], [29]. B. cereus unlike most B. anthracis isolates, produces beta lactamases and is usually resistant to Beta-lactam antimicrobials, including the third generation cephalosporins. Alternative antimicrobials that can be used are aminoglycosides, vancomycin, clindamycin or erythromycin [15], [16], however, their safety in pregnancy is debatable. Hence, their use should be considered with caution and on an individual basis. IV daptomycin is category B drug in pregnancy but since the organism had a high MIC (>4) for daptomycin, vancomycin (category C drug in pregnancy) was used instead which is known to be efficacious against B. cereus. Vancomycin may rarely be associated with sensorineural hearing loss or nephrotoxicity in the fetus after maternal use in the 2nd or 3rd trimester. Our patient tolerated the antibiotic well without any maternal or infant related adverse events even on follow up at 2 weeks postpartum.

Conclusion

A high suspicion for endocarditis must be maintained in patients with a history of IVDU and cultures growing unusual organisms, cases as such must be further investigated and early initiation of empiric antimicrobial therapy may improve outcomes. Early diagnosis of endocarditis in pregnancy may decrease the need for surgery in most cases. Pregnancy poses special challenges like optimal management of delivery and timing of surgery if indicated.

Conflict of interest statement

The authors declare that there are no conflicts of interest.

References

  • 1.Sliman R., Rehm S., Shlaes D.M. Serious infections caused by Bacillus species. Medicine (Baltim) 1987;66:218–223. doi: 10.1097/00005792-198705000-00005. [DOI] [PubMed] [Google Scholar]
  • 2.Drobniewski F.A. Bacillus cereus and related species. Clin Microbiol Rev. 1993;6:324–338. doi: 10.1128/cmr.6.4.324. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Logan N.A., Popovic T., Hoffmaster A. Bacillus and other aerobic endospore forming bacteria. In: Murray P.R., Baron E.J., Jorgensen J.H., editors. Manual of clinical microbiology. American Society for Microbiology Press; Washington, DC: 2007. p. 455. [Google Scholar]
  • 4.Barrie D., Wilson J.A., Hoffman P.N., Kramer J.M. Bacillus cereus meningitis in two neurosurgical patients: an investigation into the source of the organism. J Infect. 1992;25:291–297. doi: 10.1016/0163-4453(92)91579-z. [DOI] [PubMed] [Google Scholar]
  • 5.Tuazon C.U., Hill R., Sheagren J.N. Microbiologic study of street heroin and injection paraphernalia. J Infect Dis. 1974;129:327–329. doi: 10.1093/infdis/129.3.327. [DOI] [PubMed] [Google Scholar]
  • 6.Al-Hemidan A., Byrne-Rhodes K.A., Tabbara K.F. Bacillus cereus panophthalmitis associated with intraocular gas bubble. Br J Ophthalmol. 1989;73:25–28. doi: 10.1136/bjo.73.1.25. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Block C., Levy M., Fritz V. Bacillus cereus endocarditis – a case report. S Afr Med J. 1978;53:556–557. [PubMed] [Google Scholar]
  • 8.Craig C.P., Lee W.-S., Ho M. Bacillus cereus endocarditis in an addict. Ann Intern Med. 1974;80:418–419. doi: 10.7326/0003-4819-80-3-418. [DOI] [PubMed] [Google Scholar]
  • 9.Hsueh P.R., Teng L.J., Yang P.C., Pan H.L., Ho S.W., Luh K.T. Nosocomial pseudoepidemic caused by Bacillus cereus traced to contaminated ethyl alcohol from a liquor factory. J Clin Microbiol. 1999;37:2280. doi: 10.1128/jcm.37.7.2280-2284.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Centers for Disease Control and Prevention (CDC) Notes from the field: contamination of alcohol prep pads with Bacillus cereus group and Bacillus species – Colorado, 2010. Morb Mortal Wkly Rep. 2011;60:347. [PubMed] [Google Scholar]
  • 11.Coonrod J.D., Leadley P.J., Eickhoff T.C. Bacillus cereus pneumonia and bacteremia. Am Rev Respir Dis. 1971;103:711–714. doi: 10.1164/arrd.1971.103.5.711. [DOI] [PubMed] [Google Scholar]
  • 12.Banerjee C., Bustamante C.I., Wharton R., Talley E., Wade J.C. Bacillus infections in patients with cancer. Arch Intern Med. 1988;148:1769–1774. [PubMed] [Google Scholar]
  • 13.Riachard V., Van der Auwera P., Snoeck R., Daneau D., Meunier F. Nosocomial bacteremia caused by Bacillus species. Eur J Clin Microbiol Infect Dis. 1988;7:783–785. doi: 10.1007/BF01975049. [DOI] [PubMed] [Google Scholar]
  • 14.Tuazon C.U., Murray H.W., Levy C., Solny M.N., Curtin J.A., Sheagren J.N. Serious infections from Bacillus species. JAMA. 1979;241:1137–1140. [PubMed] [Google Scholar]
  • 15.Schemmer G.B., Driebe W.T., Jr. Posttraumatic Bacillus cereus endophthalmitis. Arch Ophthalmol. 1987;105:342–344. doi: 10.1001/archopht.1987.01060030062026. [DOI] [PubMed] [Google Scholar]
  • 16.Curtis J.R., Wing A.J., Coleman J.C. Bacillus cereus bacteremia. A complication of intermittent hemodialysis. Lancet. 1967;289(January (7482)):136–138. doi: 10.1016/s0140-6736(67)91036-7. [DOI] [PubMed] [Google Scholar]
  • 17.Oster H.A., Kong T.Q. Bacillus cereus endocarditis involving a prosthetic valve. South Med J. 1982;75:508–509. doi: 10.1097/00007611-198204000-00044. [DOI] [PubMed] [Google Scholar]
  • 18.Martin Cadenas P., Sanchez Alor G., Aguilar Ruiz J.C., Castedo E., Daza R., Mendaza P. Endocarditis by Bacillus cereus 1 in prosthetic mitral valve. Enferm Infecc Microbiol Clin. 1998;16:102–104. [PubMed] [Google Scholar]
  • 19.Yamamura M., Aoki K., Takanashi S., Tadokoro M., Furuta S., Mizokami T. [A case of Bacillus cereus prosthetic valve endocarditis] Kyobu Geka. 1994;47:232–234. [PubMed] [Google Scholar]
  • 20.Fekete T. Bacillus species and related genera other than Bacillus anthracis. In: Mandell G.L., Bennett J.E., Dolin R.M., editors. Principles and practice of infectious diseases. Churchill Livingston; New York City: 2010. p. 2727. [Google Scholar]
  • 21.Bottone E.J. Bacillus cereus, a volatile human pathogen. Clin Microbiol Rev. 2010;23:382. doi: 10.1128/CMR.00073-09. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Barrie D., Hoffman P.N., Wilson J.A., Kramer J.M. Contamination of hospital linen by Bacillus cereus. Epidemiol Infect. 1994;113:297. doi: 10.1017/s0950268800051724. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Noble R.C., Reeves S.A. Bacillus species pseudosepsis caused by contaminated commercial blood culture media. JAMA. 1974;230:1002. [PubMed] [Google Scholar]
  • 24.York M.K. Bacillus species pseudobacteremia traced to contaminated gloves used in collection of blood from patients with acquired immunodeficiency syndrome. J Clin Microbiol. 1990;28:2114. doi: 10.1128/jcm.28.9.2114-2116.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Loeb M., Wilcox L., Thornley D., Gun-Munro J., Richardson H. Bacillus species pseudobacteremia following hospital construction. Can J Infect Control. 1995;10:37. [PubMed] [Google Scholar]
  • 26.Farrar W.E., Jr. Serious infections due to “non-pathogenic” organisms of the genus Bacillus. Review of their status as pathogens. Am J Med. 1963;34:134–141. doi: 10.1016/0002-9343(63)90047-0. [DOI] [PubMed] [Google Scholar]
  • 27.Ward H., Hickman R.C. Bacterial endocarditis in pregnancy. Aust N Z J Obstet Gynaecol. 1971;11:189–191. doi: 10.1111/j.1479-828x.1971.tb00477.x. [DOI] [PubMed] [Google Scholar]
  • 28.Cox S.M., Hankins G.D., Leveno K.J., Cunningham F.G. Bacterial endocarditis: a serious pregnancy complication. J Reprod Med. 1988;33:671–674. [PubMed] [Google Scholar]
  • 29.Expert consensus document on management of cardiovascular disease during pregnancy. Eur Heart J. 2004;24:761–782. doi: 10.1016/s0195-668x(03)00098-8. [DOI] [PubMed] [Google Scholar]

Articles from IDCases are provided here courtesy of Elsevier

RESOURCES