High prevalence of spirochetosis in cholera patients, Bangladesh.
Because anecdotal evidence has indicated frequent cholera and intestinal spirochetosis coinfection in Bangladesh, we studied both diseases in this study. Intestinal spirochetosis has negative effects on domestic swine and poultry industries (3). In humans, 1%-64% of colonic specimens demonstrate intestinal spirochetosis, with the highest prevalence in developing countries and immunocompromised populations (4). The etiologic agents of intestinal spirochetosis are members of the genus Brachyspira (formerly Serpulina and Treponema). B. pilosicoli isolated from humans cause disease in pigs and in chicken models of infection (5,6). B. aalborgi isolated from humans do not colonize animals (7). Surveillance of intestinal spirochetosis requires molecular tools because culture has limited sensitivity caused by the fastidious nature of Brachyspira spp. (8). Patients with symptomatic intestinal spirochetosis have chronic diarrhea or soft feces (4,9,10); these clinical signs may resolve with antimicrobial drug therapy (9). Histologic analysis of intestinal biopsy specimens showed densely packed spirochetes attached by 1 end to colonic epithelium, forming a false brush border (11). Invasion of colonic epithelial cells and bleeding may occur (4,12). Virulence mechanisms remain poorly understood. Research on a vaccine to protect pigs against intestinal spirochetosis has begun. However, there is no vaccine for protection against intestinal spirochetosis in humans.
Co-infection of cholera patients with additional pathogens has focused on enterotoxigenic Escherichia coli (ETEC); 13% of cholera patients in Bangladesh are co-infected with ETEC (13). The potential for pathogenic synergy between V. cholerae and other pathogens has been proposed but not investigated.
We defined the frequent presence of spirochetes in feces of patients with cholera. A 3-step method was used to establish the distribution of spirochetes in rice-water stool: 1) the presence of spirochetes in rice-water stool was determined by using dark-field microscopy; 2) the diversity of Brachyspira spp. within a subset of these patients was quantified by 16S rDNA analysis; and 3) the genetic diversity within the most abundant species was determined by analysis of NADH oxidase (nox).
Rice-water stool samples were collected from symptomatic cholera patients ([greater than or equal to]15 years of age with no history of antimicrobial drug therapy) during the spring cholera outbreak of 2006 in Dhaka, Bangladesh, at the International Centre for Diarrheal Disease Research, Bangladesh, as part of a larger study (14). Samples were examined by dark-field microscopy for V. cholerae and other bacteria, and the presence of V. cholerae, lytic vibriophage, and ETEC was determined by using standard methods (14). Samples were preserved at 4[degrees]C in formalin, or cell pellets were resuspended in phosphate-buffered saline and 15% glycerol and stored at -80[degrees]C. Analysis showed that 36% (23/64) of samples that were positive for only V. cholerae also harbored spirochetes (online Technical Appendix, panels A-F, available from www.cdc.gov/EID/content/15/4/571-Techapp.pdf). Spirochetes were also found in 4/11 and 5/15 samples that harbored ETEC alone or both ETEC and V. cholerae, respectively. When we removed ETEC-positive samples as potential confounders, the presence of spirochetes was independent of lytic vibriophage in V. cholerae-positive stool samples (online Technical Appendix, panel G), which is in contrast to the documented trend concerning non-V. cholerae bacteria in rice-water stool (14). The ratio of spirochetes to V. cholerae was [approximately equal to]1 and independent of lytic vibriophage (online Technical Appendix, panel H).
In the second step, 10 samples were chosen for molecular analysis on the basis of a large amount of spirochetes. Samples were heated (99[degrees]C for 10 min), and standard PCR for a diagnostic segment of the 16S rDNA gene (15) was performed by using genus Brachyspira-specific primers (5'-GTCTTAAGCATGCAAGTC-3' and 5'-AACAGGCTAATAGGCCG-3'). Products were cloned and sequenced bidirectionally (GenBank accession nos. FJ599620-FJ599639). B. pilosicoli was the most common species, found in all 10 samples (online Technical Appendix, panel I). B. aalborgi was the second most common species (7 samples). A second set of panspecific 16S rDNA degenerate primers (5'-GTTTGATYCTGGCTYAGARCKAACG-3' and 5'-CCSSTACGGMTACCTTGTTACG-3') confirmed the presence of Brachyspira spp. and suggested that spirochetes of other genera were not present. The added resolution of nox analysis also identified B. hyodysenteriae at lower abundance.
Culture, purification, and microscopy of B. pilosicoli from glycerol stocks was used to cross-validate the molecular approach. Standard fastidious anaerobe agar (FAA) supplemented with bovine blood (10%), spectinomycin (400 [micro]g/mL), and polymyxin B (5 [micro]g/mL) was determined empirically to be the optimal medium for isolation of spirochetes. Dilutions of glycerol stocks from each patient were plated on FAA agar; single colonies were best obtained with an FAA overlay. Plates were incubated for 21 days at 37[degrees]C in an atmosphere of 94% H2 and 6% CO2. Most colonies gave rise to sigmoidal spiral cell morphotypes similar to the morphotype of the American Type Culture Collection (ATCC) (Manassas, VA, USA) control strain for B. pilosicoli. Additional controls were ATCC B. hyodysenteriae, Helicobacter pylori, and Borrelia burgdorferi. Subsequent molecular analysis of patient isolates confirmed them as B. pilosicoli. Consistent with previous studies, B. aalborgi was not cultured from patient samples.
In the third step, 5 samples were analyzed by using nox sequence comparisons that yield higher phylogenetic resolution. DNA was extracted and a nox segment was amplified by using degenerate primers (5'-GCYGGHACATGGGCDGCAAAAAC-3' and 5'-CAAATACRCAAATAGCRTTAG-3'). Products were cloned and sequenced bidirectionally (GenBank accession nos. FJ599589-FJ599619). B. pilosicoli was the most common nox sequence found. A phylogenetic tree (Figure) demonstrated that individual patients harbored clonal lines of B. pilosicoli (patients B, D, and E) or more diverse strains (patient A). Overall, B. pilosicoli strains found in cholera patients were extremely diverse relative to the known outgroup species, which indicates the potential for detection of new species related to intestinal spirochetosis.
It has been casually observed for a century that stool from cholera patients harbors spirochete-like bacteria. We now define the major agents present as B. pilosicoli and B. aalborgi. More than one third of the cholera patients had spirochetes in their stools at densities equal to those of V. cholerae. The pathophysiology of intestinal spirochetosis in this setting and its relevance to human health remain unknown. Epidemiologic analysis of intestinal spirochetosis has so far relied on retrospective studies of colonic tissue collected for reasons secondary to the disease (4). We recommend a community-based prospective study of stool samples from healthy persons and patients with diarrhea by using the techniques described herein; animal reservoirs should be identified as a potential point of control. In the context of V. cholerae infection, we hypothesize that spirochetes may be present before V. cholerae infection and exacerbate the already devastating clinical course of cholera.
This study was supported by National Institutes of Health (NIH) grant AI055058 to A.C. E.J.N. is a recipient of the Fogarty/ Ellison Fellowship in Global Health awarded by the Fogarty International Center at NIH (D43 TW005572). A.C. is an investigator of the Howard Hughes Medical Institute.
Dr Nelson is a medical student at Tufts University School of Medicine. His research interests include relationships between host, pathogen, and bacteriophages in cholera.
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Use of trade names is for identification only and does not imply endorsement by the Public Health Service or by the U.S. Department of Health and Human Services.
Eric J. Nelson, Angela Tanudra, Ashrafuzzaman Chowdhury, Anne V. Kane, Firdausi Qadri, Stephen B. Calderwood, Jenifer Coburn, and Andrew Camilli
Address for correspondence: Andrew Camilli, Department of Molecular Biology and Microbiology, Howard Hughes Medical Institute-Tufts University School of Medicine, 136 Harrison Ave, Boston, MA 02111, USA; email: email@example.com
Author affiliations: Howard Hughes Medical Institute-Tufts University School of Medicine, Boston, Massachusetts, USA (E.J. Nelson, A. Camilli); Medical College of Wisconsin, Milwaukee, Wisconsin, USA (A. Tanudra, J. Coburn); Tufts Medical Center, Boston (A. Tanudra, A.V. Kane, J. Coburn); Jahangirnagar University, Dhaka, Bangladesh (A. Chowdhury); International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka (F. Qadri); Massachusetts General Hospital, Boston (S.B. Calderwood); and Harvard Medical School, Boston (S.B. Calderwood)
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|Author:||Nelson, Eric J.; Tanudra, Angela; Chowdhury, Ashrafuzzaman; Kane, Anne V.; Qadri, Firdausi; Calderwo|
|Publication:||Emerging Infectious Diseases|
|Date:||Apr 1, 2009|
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