key: cord-1012347-g6lsrat1 authors: Khatri, Akshay M.; Rai, Shipra; Shank, Caroline; McInerney, Alissa; Kaplan, Blanka; Hagmann, Stefan H. F.; Kainth, Mundeep K. title: A tale of caution: prolonged Bacillus clausii bacteraemia after probiotic use in an immunocompetent child date: 2021-02-24 journal: Access Microbiol DOI: 10.1099/acmi.0.000205 sha: 87f93d04c9d773c2d02600bb1015b9ea7c6d0c94 doc_id: 1012347 cord_uid: g6lsrat1 INTRODUCTION: Bacillus clausii as a probiotic supplement is increasingly used in both adult and paediatric patient populations. There is limited awareness about potential adverse effects. CASE PRESENTATION: We report a case of prolonged (111 days) B. clausii bacteraemia after brief probiotic use in a 17-month-old immunocompetent child, without a definite focus of infection and in the absence of predisposing risk factors or underlying co-morbidities. We identified seven probiotic use-associated cases of prolonged B. clausii bacteraemia (mean duration [range] 64 days [14–93 days] where data were available) in the literature, all with underlying co-morbidities. CONCLUSION: B. clausii probiotic preparations may cause prolonged bacteraemia, rendering patients with underlying co-morbidities as well as those with unrecognized risk factors vulnerable for significant infectious complications. Probiotics are 'live microorganisms that, when administered in adequate amounts, confer a health benefit to the host' [1] . The use of probiotic supplements in the USA is steadily rising -National Health Interview Surveys reported increased prebiotic and probiotic use in adults (0.4-1.6 %) and children (0.3-0.5 %) from 2007 to 2012 [2] . Common probiotic preparations contain bacteria (Lactobacillus, Bifidobacterium, Bacillus, Enterococcus, Streptococcus) and fungi (Saccharomyces boulardi) [1] . Bacillus clausii is a Gram-positive, aerobic, endosporeforming, facultatively alkaliphilic rod-shaped bacterium [3] . The spores germinate into vegetative forms that colonize the small intestine and can persist in faeces for up to 12 days after administration [4] . In fasting conditions, spore germination can occur rapidly, within 3 h of incubation, producing persistent bacterial growth [5] . The spores are heat stable and can survive in environments with poor nutrition, dehydration and low pH [6] . The B. clausii-containing probiotic Enterogermina (Sanofi-Aventis S.p.A.) was registered in 1958 and has been available over-the-counter since 1999 [4] . In Asia, B. clausii probiotics have been used for acute diarrhoeal illnesses [7, 8] . However, there are rare reports of adverse effects due to probiotics [1] . We describe the prolonged persistence of B. clausii bacteraemia after probiotic use in an immunocompetent child. A 17-month-old girl, born full term and with no significant past medical history, was admitted to our hospital for persistent fevers and positive blood cultures. Prior to admission, she had travelled with her family to western India for 26 days in early 2020. While abroad, she was hospitalized for 2 days with non-bloody, non-bilious emesis and non-bloody diarrhoea. Testing revealed a negative malarial parasite smear and C-reactive protein (CRP) of 18 mg l −1 [normal range (N): <5.0 mg l −1 ]. She was discharged on oral cefixime and a probiotic containing B. clausii 2 billion spores per capsule (Enterogermina; Sanofi-Aventis S.p.A.), OPEN ACCESS which she continued for 4 days. She had intermittent fevers (highest temperature 38.3 °C) for the remainder of her trip. She presented to our paediatric emergency department 1 day after return to the USA for evaluation of persistent fevers; however, on arrival, she was afebrile and haemodynamically stable, with a normal physical exam. Laboratory testing revealed a white blood cell (WBC) count of 14 510 µl −1 (N: 6000-17 000 µl −1 ), platelet count of 586 000 µl −1 (N: 150 000-400 000 µl −1 ), CRP of 10.1 mg l −1 and erythrocye sedimentation rate (ESR) of 51 mm h -1 (N: 0-20 mm h -1 ). Urinalysis was negative. Respiratory viral panel (RVP) testing of a nasopharyngeal swab revealed Coronavirus (non-SARS-CoV-2) infection. Blood cultures grew a Gram-positive bacillus after 2 days of incubation, so empiric ceftriaxone was initiated. The organism was identified as B. clausii by matrix-assisted laser desorption/ionization-time of flight MS (Beckman Coulter) and was confirmed by the state reference laboratory. She had 19 blood cultures growing B. clausii during her 31-day hospitalization. Empiric ceftriaxone was switched to ampicillin, due to reports of ampicillin's efficacy against B. clausii [3] . Antimicrobial susceptibility was derived using Clinical and Laboratory Standards Institute guidelines -the isolate was susceptible to ceftriaxone, gentamicin, levofloxacin and vancomycin (Table 1) [9] . Persistent bacteraemia prompted addition of levofloxacin, with gentamicin added for synergy. Ampicillin was discontinued after further sensitivity testing was indeterminate and replaced with intravenous vancomycin, while continuing gentamicin and levofloxacin. Oral vancomycin was added to target bacteria from germinating intraluminal spores. She had an extensive evaluation for source and risk factors predisposing to persistent bacteraemia. Urine cultures revealed no growth. Repeat RVP testing was negative. Multiple transthoracic echocardiograms were negative for endocarditis. Abdominal ultrasound was unremarkable. Magnetic resonance imaging (MRI) of chest/abdomen/pelvis revealed no acute abnormalities, with patent arterial and venous vasculature. Brain MRI was unremarkable. Lower extremity ultrasound was negative for deep vein thrombosis. Positron emission tomography scanning did not reveal a source of infection. Vitamin A and zinc levels were normal; however, zinc/multivitamin supplementation was started to prevent micronutrient deficiency and bacterial translocation. Immunology was consulted to rule out underlying immunodeficiency. Evaluation revealed normal quantitative immunoglobulins and protective titres to tetanus, diphtheria, measles, mumps, rubella and Streptococcus pneumoniae (consistent with normal humoral immunity). Assessment of cellular immunity revealed a normal lymphocyte immunophenotype (normal CD4+ and CD8+ T cells and CD19+ B cells) and normal lymphocyte function (based on phytohaemagglutinin/ pokeweed mitogen response). Complement assays including total complement (CH50), alternate pathway (AH50) and mannose binding lectin were normal. Phagocytic evaluation revealed normal dihydrorhodamine (DHR), glucose-6phosphate-dehydrogenase and myeloperoxidase staining. B. clausii bacteraemia has been previously described in only a few patients with underlying illnesses [10] [11] [12] [13] . A 5-month-old child with congenital heart disease and malnutrition developed recurrent B. clausii bacteraemia (persisting for more than 10 days in each instance) and subsequently succumbing to multidrug-resistant Klebsiella pneumoniae sepsis with multiorgan failure [10] . B. clausii bacteraemia was also noted in three adults with advanced lung cancer and ischaemic colitis [11] . Prolonged bacteraemia for 70 and 93 days respectively was reported in two adults after valve replacement, despite antimicrobial therapy [12] . Lastly, an adult diabetic patient, who had received antibiotics and probiotics for a surgical-site infection, developed B. clausii bacteraemia that resolved after 2 weeks with teicoplanin [13] . F, female; IV, intravenous; M, male; na, not available; PO, oral; WBC, white blood cell. *An approximate duration of 58 days was derived after review of the case report. The patient had received probiotics at 3 months of age and he presented with sepsis 3 weeks later. He again presented for surgery at 5 months of age and was found to have bacteraemia recurrence, lasting at least 3 weeks. To the best of our knowledge, this is the first case of B. clausii bacteraemia occurring in an immunocompetent paediatric patient. The reason for bacteraemia lasting more than 100 days, while on combined antimicrobial therapy, is unknown. The evaluation did not reveal any previously undiagnosed co-morbidity, as seen in previously reported cases [10] [11] [12] [13] . Our suspicion for an intravascular source or immunocompromised state was low, given negative comprehensive workup, haemodynamic stability and rapid symptom resolution. In some cases, bacteraemia following probiotic use is postulated to occur secondary to intestinal bacterial translocation, particularly in the setting of pre-existing intestinal pathology (such as diarrhoea or anatomical gut alterations) [1] . In our case we hypothesize that a persistent intra-luminal focus of B. clausii spores germinated over time and allowed prolonged or recurrent bacterial translocation through the bowel wall, which was facilitated by the antecedent diarrhoea illness. The median (range) duration of bacteraemia noted in the reviewed cases (including our case) was 70 days (14-111 days) ( Table 2 ), supporting our hypothesis of an intra-luminal focus of germinating B. clausii spores with intermittent bacterial translocation. Such transmigration can occur regardless of a patient's immune status [13] . Probiotic organisms have antimicrobial resistance genes, which facilitate their concurrent administration with antibiotics -thus, treating infections caused by probiotic organisms is challenging [14, 15] . The chromosomally located, nontransferable erm gene in B. clausii produces a macrolidelincosamide-streptogramin-B phenotype, which results in macrolide resistance [16] . Additionally, B. clausii has been shown to possess intrinsic resistance to penicillins, cephalosporins, aminoglycosides and macrolides [17] . Marketed in India for use in paediatric diarrhoeal illness, the probiotic used by our patient contains four different B. clausii strains [18] . The strains are named according to their antibiotic resistance: 'O/C' resistant to chloramphenicol; 'N/R' resistant to novobiocin and rifampin; 'T' resistant to tetracycline; and 'SIN' resistant to neomycin and streptomycin [18] . All four strains were sensitive to multiple antibiotics (including penicillins, glycopeptides, quinupristin, dalfopristin, linezolid and fluoroquinolones) and resistant to cefuroxime, ceftriaxone, cefotaxime and cefepime [3] . In our patient, B. clausii was resistant to penicillin, rifampin and clindamycin, while sensitivity to ampicillin could not be determined. Antimicrobial resistance was also noted in some of the prior reported cases (Table 1) . There are mixed data available regarding the efficacy of B. clausii probiotics. A systematic review of six trials showed that B. clausii helped decrease hospitalization duration by 1 day [7] . Another multi-centre study found that B. clausii compared to zinc administration helped to decrease diarrhoea duration and mean daily stool output; however, the group receiving zinc had worsening diarrhoea (compared to no intervention), making interpretation of these results unclear [8] . In pre-term infants, B. clausii failed to show a significant effect on incidence of late-onset sepsis [19] . Until now, the safe administration of probiotics has focused on potentially avoiding them in patients with compromised immune systems or underlying serious illnesses [1, 15] . In one review, it has been proposed to give probiotics cautiously in patients with a single major risk factor (immunocompromised status, prematurity), or with more than one minor risk factor (presence of central venous catheter, probiotic administration through jejunostomy, underlying heart anomaly, disrupted intestinal epithelial integrity, probiotics with high mucosal adhesion/known pathogenicity or use of broad-spectrum, probiotic-resistant antibiotics) [1] . In contrast, our case highlights the concerning finding that probiotics can cause bacteraemia in healthy individuals. How often this occurs and its related clinical consequences are not clear. The paucity of reporting so far could be either due to the bacterium's low pathogenicity, or to the tendency to regard Bacillus species as blood culture contaminants [20] . Given the ever-increasing worldwide probiotic usage, clinicians should be vigilant about the concerning potential of B. clausii-containing probiotics to cause prolonged bacteraemia, even in immunocompetent hosts. Additional investigations are needed to evaluate risk factors and help elucidate mechanisms that lead to gastrointestinal translocation of these bacteria. This work received no specific grant from any funding agency. Probiotic use in clinical practice: what are the risks? 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Persistent bacteriemia due to Bacillus clausii. Poster presented at: 29th European Congress of When good bacteria behave badly: a case report of Bacillus clausii sepsis in an immunocompetant adult Antibiotic resistance in probiotic bacteria Spores of Poly-antibiotic resistant Bacillus Clausii Characterization of a new ermrelated macrolide resistance gene present in probiotic strains of Bacillus clausii Antibiotic resistance: the pros and cons of probiotics Molecular characterization and identification of Bacillus clausii strains marketed for use in oral bacteriotherapy Bacillus clausii for prevention of late-onset sepsis in preterm infants: a randomized controlled trial Updated review of blood culture contamination The authors gratefully acknowledge Dr Sujatha Rajan, our paediatric infectious disease colleague, for her valuable insight on this case. The authors declare that there are no conflicts of interest The research met our institutional definition of a case report (a medical chart review of three or fewer patients), and thus institutional research board review was not needed. The parents of our patient reviewed the manuscript prior to submission. Informed consent was obtained from the father of the patient. Five reasons to publish your next article with a Microbiology Society journal 1 . The Microbiology Society is a not-for-profit organization. 2. We offer fast and rigorous peer review -average time to first decision is 4-6 weeks. 3. Our journals have a global readership with subscriptions held in research institutions around the world. 4. 80% of our authors rate our submission process as 'excellent' or 'very good'. 5. Your article will be published on an interactive journal platform with advanced metrics.Find out more and submit your article at microbiologyresearch.org.