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Low incidence of concurrent enteric infection associated with sporadic and outbreak-related human cryptosporidiosis in Northern Ireland.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Moore, J. E. Crothers, Lester J. Millar, Beverley Cherie Crothers, Elizabeth Xiao, Lihua |
| Copyright Year | 2002 |
| Abstract | Human cryptosporidiosis has emerged as an important gastrointestinal infection in the 1990s due to the ingestion of contaminated water and foodstuffs containing the protozoan parasite Cryptosporidium spp. (4, 9). This pathogen has particular clinical significance for immunocompromised persons, including AIDS patients and cancer patients receiving toxic chemotherapeutic drug regimens (4, 9). Concern relating to this parasite is founded on three parameters: (i) the causal agent of this infectious disease can be transmitted through contaminated water and food, (ii) when ingested, the causal agent is capable of causing a high degree of morbidity in healthy populations and mortality in vulnerable populations, and (iii) there is no effective antimicrobial treatment to eradicate this agent from the gastrointestinal tract in symptomatic individuals. To date, there have been very limited data describing the frequency and microbiological etiology of mixed enteric infections in the developed world, where an additional enteric pathogen has been isolated along with Cryptosporidium parvum. Hence, it was the aim of our investigation to retrospectively determine the frequency of mixed enteric infections with C. parvum and to determine the coinfecting organism in both sporadic and outbreak-related cryptosporidiosis. In 2000 and 2001, the Northern Ireland Public Health Laboratory processed 9,165 and 10,832 fecal specimens, respectively, which were from symptomatic patients and had been submitted mainly by general practitioners as well as from hospital wards. From these, Cryptosporidium sp. was detected by employment of the modified Ziehl-Neelsen acid-fast staining technique in 255 (2.8%) and 191 (1.8%) cases in 2000 and 2001, respectively, with the majority of cases involving children. The age distribution of cryptosporidial cases in 2000 was 46.7% for patients of 5 years, 18.4% for patients from 6 to 10 years, 9.8% for patients from 11 to 20 years, and 25.1% for patients of 20 years. In 2001, the age distribution was 34.0% for patients of 5 years, 16.2% for patients from 6 to 10 years, 6.3% for patients from 11 to 20 years, and 43.5% for patients of 20 years. During these 2 years, there were three waterborne outbreaks of cryptosporidiosis, as previously described (6). Correcting for the outbreaks, the prevalence of sporadic cases during this time was 2.0% (183 of 9,165) and 1.4% (147 of 10,832) for 2000 and 2001, respectively. In addition to undergoing conventional cryptosporidial microscopic analysis, all fecal specimens were concurrently examined for Campylobacter spp., serotypes of Salmonella enterica, Shigella spp., Escherichia coli O157:H7, and Yersinia enterocolitica, in accordance with previously published methodologies (2). In addition, fecal specimens were analyzed for Clostridium difficile by employment of the Oxoid Toxin-A kit in accordance with the manufacturer’s instructions (Oxoid Ltd., Basingstoke, England) and for other parasitic ova and cysts on request by the attending physician. The frequency and distribution of concurrent enteric infections with Cryptosporidium spp. are shown in Table 1, while the prevalence of bacterial fecal pathogens in stool specimens which were negative for Cryptosporidium spp. is shown in Table 2. Overall, in 446 episodes of cryptosporidiosis in the same number of patients over this 2-year period, there was 2.0% coinfection with another enteric pathogen and C. parvum, where Campylobacter sp. accounted for the most frequently isolated copathogen (1.1%; 5 of 446), followed by Salmonella (0.45%; 2 of 446) and others (0.45%; 2 of 446). Similarly, the Intestinal Infectious Disease study in England demonstrated 2.6% (1 of 39) coinfection with Campylobacter sp. and 2.6% (1 of 39) coinfection with Giardia lamblia (Giardia duodenalis) (2). This study also demonstrated a significantly higher incidence of cryptosporidiosis in rural areas than in urban areas and a higher incidence in the north of England than in the Midlands and the south of England. In addition, there has been a previous association between Cryptosporidium and Campylobacter infection in a waterborne outbreak in the north of England (5). The occurrence of mainly single-pathogen infection (98%) is of interest in trying to elucidate the potential reservoirs of this parasite in the local context. The three waterborne outbreaks produced only two cases of concurrent infection with an additional pathogen (Table 1). Furthermore, in all coinfection cases, with the exception of the patient with the positive Clostridium difficile toxin assay, none of the patients presented previously with a positive fecal specimen of the coinfecting organism. Although these outbreaks were associated with the contamination of final drinking water with animal and human feces, no other enteric pathogen was associated with the outbreaks. As animal feces and human sewage have previously been shown to be heavily contaminated with enteric pathogens (3, 7), as water has been shown to be an important vehicle in |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | http://jcm.asm.org/content/40/8/3107.full.pdf |
| PubMed reference number | 12149394v1 |
| Volume Number | 40 |
| Issue Number | 8 |
| Journal | Journal of clinical microbiology |
| Language | English |
| Access Restriction | Open |
| Subject Keyword | Acquired Immunodeficiency Syndrome CDISC SEND Biospecimens Terminology Campylobacter infection Coinfection Cryptosporidiosis Cryptosporidium parvum Cryptosporidium sp:PrThr:Pt:Stool:Ord:Acid fast stain Cyst Drinking Water Epstein-Barr Virus Infections Feces Gastrointestinal tract structure Giardia lamblia Ab.IgM:Titr:Pt:Ser:Qn Host-Pathogen Interactions Infection of digestive system Ingestion Mast/Stem Cell Growth Factor Receptor Kit, human Microbiological Morbidity - disease rate Neoplasms Ovum Paget's Disease, Mammary Parasite Encystment Pathogenic organism Patients Protozoa Reservoir Device Component Salmonella Scientific Publication Serotype Specimen Staining method Surgical Wound Infection Thioctic Acid Ward (environment) Water Pollution Yersinia enterocolitica disease transmission |
| Content Type | Text |
| Resource Type | Article |
