Volume 18, Number 1—January 2012
Intestinal Toxemia Botulism in 3 Adults, Ontario, Canada, 2006–2008
Five cases of intestinal toxemia botulism in adults were identified within an 18-month period in or near Toronto, Ontario, Canada. We describe findings for 3 of the 5 case-patients. Clinical samples contained Clostridium botulinum spores and botulinum neurotoxins (types A and B) for extended periods (range 41–61 days), indicative of intestinal toxemia botulism. Patients’ clinical signs improved with supportive care and administration of botulinum antitoxin. Peanut butter from the residence of 1 case-patient yielded C. botulinum type A, which corresponded with type A spores found in the patient’s feces. The food and clinical isolates from this case-patient could not be distinguished by pulsed-field gel electrophoresis. Two of the case-patients had Crohn disease and had undergone previous bowel surgery, which may have contributed to infection with C. botulinum. These cases reinforce the view that an underlying gastrointestinal condition is a risk factor for adult intestinal toxemia botulism.
Botulism is a neuroparalytic condition, typified by cranial nerve palsies that may be followed by descending symmetrical flaccid paralysis, which can lead to respiratory arrest and, in some instances, death (1). Intestinal toxemia botulism is an infectious form of botulism in which illness results from ingesting spores, which is followed by spore germination and intraluminal production of botulinum neurotoxins over an extended period (2). Intestinal toxemia botulism is rarely reported in adults; <20 cases have been described in the literature since the first reports in 1980 and 1981 (3,4). The rarity of this condition contributes to its obscurity, an obscurity that may negatively affect those infected through a lack of rapid diagnosis and treatment. Countries with published case reports of intestinal toxemia botulism in adults are the United States (3–10), Italy (11,12), Iceland (9), and Japan (13). The etiologic agents involved in intestinal toxemia botulism in adults are Clostridium botulinum types A, B, and F (6–9,13,14) and, more rarely, C. baratii type F (10), and C. butryicum type E (11,12).
Although considered a rare condition, intestinal toxemia botulism was reported in 5 adults in or near Toronto, Ontario, Canada, during November 2006–May 2008. We report the clinical, laboratory, and epidemiologic findings for 3 of the 5 case-patients. Details pertaining to the clinical course of illness of 1 of the patients were previously published in a case report (15). In this case series, we document 3 cases of adult intestinal toxemia botulism, which occurred in a small geographic area in a short period, and provide further evidence for the potential role of host factors, such as Crohn disease, previous bowel surgery, and short bowel syndrome, which may predispose a person to intestinal toxemia botulism.
We reviewed case investigation files from the Ontario Ministry of Health and Long-Term Care and the local public health units in or near Toronto. Physicians involved in the cases provided clinical summaries. Consent to publish information pertaining to the diagnosis of intestinal toxemia botulism was obtained from the 3 case-patients. Two additional cases were reported in November 2006 and May 2008; however, consent was not obtained from those patients.
Serum, stool, gastric aspirate, and enema samples were assayed for botulinum toxin by using the mouse bioassay (16). Stool and enema specimens were cultured for C. botulinum as described (16). Botulinum neurotoxin was identified by neutralization with specific antitoxin types A, B, E, and F obtained from the Centers for Disease Control and Prevention (Atlanta, GA, USA). C. botulinum was identified and differentiated from other botulinum toxin–producing clostridia on the basis of Gram stain reaction, morphologic features, motility, lipase and lecithinase reactions on egg yolk agar, sugar fermentations, esculin hydrolyis, gelatin liquefaction, and production of botulinum neurotoxin. Pulsed-field gel electrophoresis (PFGE) was done as described (17). Cases of adult intestinal toxemia botulism were confirmed by detection of C. botulinum in stool specimens over prolonged periods in conjunction with clinical observations consistent with botulism. One of these cases has been reported separately as a case study (15).
A 63-year-old woman was admitted to a hospital on November 22, 2006, after a 2-day history of abdominal pain, blurred vision, diarrhea, dysarthria, dysphagia, horizontal binocular diplopia, imbalance, and weakness in the arms and hands. No recent infections, wounds, or antimicrobial drug use were reported. After admission to the hospital, she experienced respiratory arrest, for which intubation and ventilation were required. The patient’s medical history included Crohn disease, bowel surgery, short bowel syndrome, hypertension, breast cancer, nephrolithiasis, and small fiber polyneuropathy (motor function was normal on nerve conduction studies 6 years earlier). A pathology report from 20 years earlier noted acute and chronic inflammation of the patient’s large and small bowels. No acute wounds or punctures were apparent on examination.
The neurologic examination showed a normal level of consciousness and mental state; reduced pupillary light responses; bilateral, symmetrical ophthalmoplegia; bilateral ptosis; bifacial lower motor neuron weakness; moderate proximal and distal symmetrical limb weakness; absent tendon reflexes; and flexor plantar responses. Muscle tone was decreased; neither atrophy nor fasciculation occurred, and sensation was intact. Results of routine blood and urine tests showed only a mild elevation of the serum amylase level. Botulism was strongly suspected. However, other conditions that affect the central nervous system, including the brainstem and cranial nerves, were considered. Results of tests for syphilis, Lyme disease, West Nile virus infection, acetylcholine receptor antibodies, and IgG against GQ1b were negative.
Results of cerebrospinal fluid studies, including cytology and viral PCR studies, were also normal. A magnetic resonance imaging scan of the brain had unremarkable findings. Electrodiagnostic studies showed mildly reduced compound motor action potential amplitudes and normal sensory responses. Posttetanic facilitation was marked, with a 700% increase in compound motor action potential amplitudes. Electromyography showed that lower limb muscles were electrically silent. Enema fluid, stool, and gastric aspirate specimens were positive for type A botulinum neurotoxin and viable C. botulinum type A spores, with organisms persisting in stool for 61 days. Botulinum antitoxin was administered in the evening of November 23, 2006.
The environmental investigation found that the patient ate a limited diet of tea, bagels, peanut butter, occasional honey, and weekly Chinese take-out food. An opened jar of peanut butter from the patient’s residence yielded positive test results for C. botulinum type A spores, containing ≈14 C. botulinum spores/kg.
Both heated and nonheated samples from the enema fluid were positive for C. botulinum type A, indicating the presence of spores. Analysis of clinical and peanut butter isolates by PFGE indicated identical PFGE patterns (Figure).
The patient was still mechanically ventilated as of December 15, 2006, and required regular sedation. Once sedation wore off, the patient experienced random, spastic-like, nonpurposeful movements of all extremities. Her condition improved over the next 6 months, and she could walk by the time she was discharged.
Bulbar symptoms developed in a 50-year-old woman with ophthalmoparesis on February 7, 2007, and her symptoms worsened until she was admitted to the hospital on February 10, 2007, with complete ophthalmoplegia, dysphagia, and quadriparesis. The patient’s medical history included a diagnosis of Crohn disease in 1979 and 4 previous bowel resections with ileocolonic anastomosis, complicated by enterocutaneous fistulas (in 1986, 1995, 2001, and 2002). She had no wounds, and no chest or abdominal pains were reported before the onset of symptoms. The patient experienced oropharyngeal discomfort and difficulty speaking but was able to respond to questions with a yes or no. A repeat computed tomography scan was carried out, and results were normal. Lumbar puncture was conducted for full studies, including tests for West Nile virus. Over the next 24 hours, she had a decreased level of consciousness, a depressed Glasgow coma scale score, tachycardia, and difficulty breathing, with eventual respiratory failure requiring ventilation support.
The neurologic examination showed minimal orbicularis oculi contractions and quadriparesis with normal reflexes. The differential diagnoses being considered for this case-patient included the following: viral encephalitis, meningitis, brain stem lesion, myasthenia gravis, and infectious agents, specifically, C. botulinum and enteric organisms linked to Guillain-Barré syndrome, such as Campylobacter, Salmonella, and Shigella spp. The initial assessment by the consulting neurology team was that of Miller Fischer variant of Guillain-Barré syndrome and Eaton-Lambert syndrome or acute motor axonal neuropathy. Electromyography studies showed myopathic-like motor unit action potential. Results of a Tensilon test were negative. Additional tests, including a test for antibody against acetylcholine, and repeat electromyography studies with high frequency stimulation were negative (no incremental response and a negative acetylcholine antibody test results), which indicated that myasthenia gravis and Eaton-Lambert syndrome were unlikely. A presumptive diagnosis of botulism from intestinal toxemia, based in part on the patient’s history of Crohn disease and previous bowel surgeries, was made on February 13, 2007. The patient received botulinum antitoxin on February 23, 2007. She remained dependent on a ventilator for 5 months and had a percutaneous endoscopic gastrostomy tube for feeding, leading to line sepsis on 2 occasions, ventilator-assisted pneumonia, and a tracheostomy.
The patient’s food history included consumption of toast with peanut butter, coffee, chicken soup, and home-prepared beef tacos with grated cheese, lettuce, tomatoes, and salsa. Before the onset of symptoms, the patient consumed peanut butter daily. An opened jar of peanut butter from the home yielded positive test results for C. botulinum type A.
Of 7 serum samples, the first sample was positive for botulinum neurotoxin; however, the quantity was insufficient for serotype determination. Subsequent serum sample test results were negative for botulinum neurotoxin. Type A botulinum toxin was detected in the first stool specimen, which was collected on February 21, 2007. All subsequent stool specimen test results were negative for botulinum toxin. Test results for 5 of 8 stool specimens were positive for either C. botulinum type A or type B spores over 56 days. Three subsequent stool samples collected in May 2007 yielded negative test results for C. botulinum.
The patient was transferred to a rehabilitation hospital on June 17, 2007, where she required nightly ventilation support and received therapy for swallowing and speech as well as physiotherapy and occupational therapy. In September 2007, ventilator support was gradually withdrawn; the patient learned to eat on her own and was discharged, but she continued to receive outpatient therapy for an additional 3 months. During a follow-up visit in June 2009, the patient was walking independently, and a respiratory evaluation showed normal ventilatory capacity of forced expiratory volume of 2.58 L, 99% of predicted normal inspiratory muscle strength, and only minimal expiratory muscle weakness.
A 45-year-old man with no known history of gastrointestinal problems and otherwise healthy was admitted to the hospital on January 8, 2008, with a distended abdomen and blurry vision (15). The patient’s abdomen continued to distend, and bowel sounds were diminished despite nasogastric suctioning. No recent infections or antimicrobial drug therapy were noted. The distended abdomen signaled a possible bowel obstruction, and scans confirmed the presence of an obstruction with unknown cause. A neurologic consultation was necessary after 5 days to assess the patient’s worsening neurologic symptoms. Guillain-Barré syndrome and myasthenia gravis were initially considered, but results of a nerve conduction study were classic for botulism. Botulism was suspected on January 14, 2008, on the basis of neurophysiologic findings, coupled with the clinical observations suggestive of botulism.
Clinical samples were subsequently sent for analysis, and through consultation with the physician, neurologist, and public health practitioners, it was determined that the patient would still benefit from antitoxin, even though it had been more than 24 hours since the onset of symptoms. Antitoxin was administered the evening of January 14, 2008. The patient remained hospitalized until February 27, 2008, when clinical symptoms improved. C. botulinum type B was detected in the patient’s stool at weeks 2 and 8 after the onset of symptoms. Botulinum neurotoxin was not detected in the stool extracts. Resulting of testing of both heated samples were positive for C. botulinum type B, indicating the presence of spores in the sample. Two subsequent fecal samples at weeks 11 and 15 yielded negative test results for C. botulinum. The persistence of C. botulinum type B over a period of 41 days supported the diagnosis of intestinal toxemia botulism. The patient had a history of eating primarily commercial canned food, although no specific types were reported, and none of the patient’s contacts were reported to be ill.
Diagnosis of intestinal toxemia botulism was determined through repeated detection of botulinum neurotoxins, viable C. botulinum, or both in clinical samples over extended periods. Colonization with C. botulinum persisted in case-patients 1, 2, and 3 for 61, 56, and 41 days, respectively. In addition to the persistence of organisms in stool samples, the diagnoses were supported by the presence of clinical features compatible with botulism (Table). In previously published reports, C. botulinum was present in stool specimens for periods ranging from 2 to 119 days (9). Two additional cases of intestinal toxemia botulism in adults were identified in close proximity and time to the 3 cases reported here; however, consent was not obtained to publish the findings pertaining to these cases.
Intestinal toxemia botulism in adults is described in detail in earlier reports (3), and Arnon summarized 10 previous cases (2). Since the summary of Arnon, 3 cases have been reported in Italy (11), and a case occurred in Japan in 1999 (13). Previously cited risk factors for intestinal toxemia botulism in adults include structural and functional gastrointestinal abnormalities, including Crohn disease (8), surgical alterations of the intestine (6,9), Meckel diverticulum (12,18), and modified intestinal flora caused by prolonged antimicrobial drug therapy (6–10,13). Two of the patients described in this report had Crohn disease and previous bowel surgery. In addition, case-patient 1 also had short bowel syndrome. Unlike the first 2 case-patients, case-patient 3 was previously healthy and had no history of gastrointestinal problems. Three other published reports of intestinal toxemia botulism in adults occurred in patients with no preexisting medical conditions or antimicrobial drug use reported. These cases occurred in Kentucky, USA (9); Iceland (9); and Japan (13). The initial symptoms of acute abdominal distension and small bowel obstruction experienced by case-patient 3 are uncommon and suggest that the differential diagnosis for small bowel obstruction in an otherwise healthy patient should include botulism (15).
Several factors could lead to underdiagnosis of intestinal toxemia botulism. Symptoms of botulism are similar to other conditions affecting the central nervous system, and botulism may be misdiagnosed as Guillain-Barré syndrome, myasthenia gravis, Eaton-Lambert syndrome, stroke syndromes, or tick paralysis (1,19). Similar to botulism in infants, cases of intestinal toxemia botulism in adults occur sporadically and may be missed unless the physician has seen a case of botulism previously. Two cases of foodborne botulism, both attributed to carrot juice, had been identified in the same region only 2 months before the first case of intestinal toxemia botulism described here (20), perhaps contributing to a period of higher awareness of botulism cases.
Given that intestinal toxemia botulism in adults is rare, the identification of multiple cases in a small geographic area in a short period is unusual. Two cases of intestinal toxemia botulism in adults, caused by C. butyricum which produced type E neurotoxin, were reported in Italy (11,12). The cases in Italy occurred in 2 communities ≈30 km apart and were separated by 12 months (12).
Two of the case-patients described in our report had Crohn disease and prior bowel surgery. Such conditions are consistent with previously published cases, providing further evidence that host susceptibility may play a substantial role in this disease. Although intestinal toxemia botulism is a rare disease worldwide, it is a serious disease that causes substantial illness and high health care costs. Public health practitioners and physicians investigating suspected botulism cases should thoroughly consider the patient’s medical history, particularly for underlying gastrointestinal conditions that may make them susceptible to intestinal toxemia botulism.
Ms Sheppard was an MPH student at the University of Guelph, Guelph, Ontario, Canada, at the time this research was conducted. Her research interests include the epidemiology of enteric and infectious diseases.
We thank the public health practitioners at Toronto Public Health, Niagara Region Public Health, Durham Region Health Department, Hamilton Public Health Services, Andrea Ellis, and Rachel Rodin for their contributions to the case investigations; and Jeremy Sobel and Stephen Arnon for consultation throughout the investigations.
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Suggested citation for this article: Sheppard YD, Middleton D, Whitfield Y, Tyndel F, Haider S, et al. Intestinal toxemia botulism in 3 adults, Ontario, Canada, 2006–2008. Emerg Infect Dis [serial on the Internet]. 2012 Jan [date cited]. http://dx.doi.org/10.3201/eid1801.110533