Skip directly to local search Skip directly to A to Z list Skip directly to navigation Skip directly to site content Skip directly to page options
CDC Home

Volume 4, Number 2—June 1998

Synopsis

Campylobacter jejuni Strains from Patients with Guillain-Barré Syndrome

Ban Mishu Allos*, Frank T. Lippy*, Andrea Carlsen*, Ronald G. Washburn†, and Martin J. Blaser*‡
Author affiliations: *Vanderbilt University School of Medicine,; ‡The Department of Veterans Affairs Medical Center, Nashville, Tennessee, USA; †The Bowman Gray School of Medicine, Winston-Salem, North Carolina, USA

Suggested citation for this article

Abstract

Guillain-Barré syndrome (GBS), an acute demyelinating peripheral neuropathy, may be triggered by an acute infectious illness; infection with Campylobacter jejuni is the most frequently reported antecedent event. In Japan, O:19 is the most common serotype among GBS-associated C. jejuni strains. To determine whether serotype O:19 occurs among GBS-associated strains in the United States and Europe, we serotyped seven such strains and found that two (29%) of seven GBS-associated strains from patients in the United States and Germany were serotype O:19. To determine whether GBS-associated strains may be resistant to killing by normal human serum (NHS), we studied the serum susceptibility of 17 GBS- and 27 enteritis-associated strains (including many O:19 and non-O:19 strains) using C. jejuni antibody positive (pool 1) or negative (pool 2) human serum. Using pool 1 serum we found that one (6%) of 18 serotype O:19 strains compared with 11 (42%) of 26 non-O:19 strains were killed; results using pool 2 serum were nearly identical. Finally, 8 O:19 and 8 non-O:19 strains were not significantly different in their ability to bind complement component C3. Serotype O:19 C. jejuni strains were overrepresented among GBS-associated strains in the United States and Germany and were significantly more serum-resistant than non-O:19 strains. The mechanism of this resistance appears unrelated to C3 binding.

Guillain-Barré syndrome (GBS) is an acute demyelinating polyneuropathy characterized by an immunologic attack upon peripheral nerve myelin (1,2). The trigger for this immune attack is unknown; however, GBS is frequently preceded by an acute infectious illness (3). In recent years, infection with Campylobacter jejuni has emerged as one of the most common antecedent events associated with GBS. Up to 40% of patients with GBS have culture or serologic evidence of C. jejuni infection when neurologic symptoms begin (4-6). The many variants of GBS—including acute motor axonal neuropathy, acute inflammatory demyelinating neuropathy, and Miller Fisher syndrome—have also been associated with preceding C. jejuni infection (7-9).

C. jejuni infections are common in the United States, affecting approximately 1% of the population each year (10). Typically, they cause a self-limited gastrointestinal illness characterized by diarrhea, abdominal pain, and fever. However, approximately 1 in 2,000 C. jejuni infections may be complicated by GBS (11). Because C. jejuni infections occur far more commonly than GBS, either host (12) or strain (5,13) characteristics may determine which infected persons contract GBS. Several reports from Japan showed that a particular serotype, O:19, was overrepresented among C. jejuni strains isolated from GBS patients (5,13). Among 12 Japanese patients with GBS and culture-confirmed C. jejuni infection, 10 (83%) were infected with strains of O:19, a serotype that accounts for only 2% of randomly selected C. jejuni isolates in Japan (5). However, in England, none of four C. jejuni strains isolated from patients with GBS were serotype O:19 (6). Other Campylobacter serotypes predominate among GBS patients in other parts of the world. All nine C. jejuni strains isolated from GBS patients in South Africa were serotype O:41 (14); this serotype accounts for fewer than 2% of isolates from South African children with uncomplicated enteritis. With Lior typing (a serotyping system based upon heat-labile antigens), all four GBS-associated C. jejuni strains in Germany were serotype O:11 (15).

Whether the predominance of O:19 strains among GBS patients is limited to Japan is not clear. Furthermore, the reason for the O:19 overrepresentation among Japanese GBS strains is unknown, but their resistance to host bacterial clearance mechanisms is one possibility. C. jejuni strains vary in their susceptibility to the bactericidal activity in normal human serum (NHS) (16). Bacteria that are more resistant to nonspecific serum killing may elicit more extensive specific responses to eliminate the organism; such elicited immune responses may have the potential of greater tissue injury and myelin damage.

To determine whether C. jejuni serotype O:19 is an important cause of GBS outside Japan, we serotyped GBS-associated strains from the United States and Germany. To investigate the immunologic response to GBS-associated C. jejuni strains, we performed two additional sets of experiments. First, we examined the susceptibility of C. jejuni strains to NHS. Our hypothesis was that GBS-associated Campylobacter strains, more specifically O:19 strains, are more serum-resistant than those from patients with uncomplicated enteritis. To further characterize the mechanism of resistance, we determined whether C. jejuni strains isolated from GBS patients differ in their capacity to bind complement component C3.

Statistical Analysis

We determined mean values, standard deviations, odds ratios, p-values, paired T-tests, 95% confidence limits, and interquartile ranges. Software included Lotus 123 and EpiInfo (a statistical software package designed by the Centers for Disease Control and Prevention [CDC]).

Serotyping of Strains

Seven GBS-associated strains were serotyped with the O (formerly heat-stable) serotyping scheme of Penner and Hennessy (17) and the heat-labile serotyping scheme of Lior (18). Serotyping was conducted (19) at the CDC Campylobacter Reference Laboratory. A GBS-associated strain was defined as one isolated from a patient with GBS (n = 6) or from a patient infected during an outbreak in which at least one infected person contracted GBS (n = 1). Four strains were from patients in the United States, and three were from patients in Germany; four of these were isolated from women.

Serotype O:19 was present in one of four U.S. GBS-associated C. jejuni isolates and one of three German isolates. Thus, 2 (29%) of 7 GBS-associated C. jejuni isolates from patients in the United States and Germany were O:19. The O and heat-labile serotypes of the seven GBS-associated strains are shown in Table 1.

Serum Bactericidal Assays

We studied 44 GBS- and enteritis-associated strains from all over the world. We divided C. jejuni isolates into two major groups. Group 1 (17 GBS-associated strains) was divided into two subgroups. Subgroup 1A (GBS-associated/type O:19) consisted of seven C. jejuni O:19 isolates: three from the United States, three from Japan, and one from Germany. Subgroup 1B (GBS-associated/non-O:19 serotype) consisted of 10 C. jejuni isolates with serotypes other than O:19: three from the United States, two from Germany, and five from England. Group 2 (27 enteritis-associated strains from patients with uncomplicated enteritis but no known GBS association) was also divided into two subgroups. Subgroup 2A (not GBS-associated/type O:19) consisted of 11 C. jejuni O:19 isolates: 10 from the United States and one from Japan. Subgroup 2B (not GBS-associated/non-O:19 serotype) consisted of 16 C. jejuni isolates from U.S. patients with serotypes other than O:19. Serum-resistant C. fetus strain 23D and its spontaneous serum-susceptible mutant, 23B, were used as controls (20).

Strains were grown on trypticase soy blood agar plates (BBL Cockeysville, MD, USA) at 37oC for 48 hours in an incubator containing 10% CO2, 5% O2, and 85% N2. The bacteria were harvested in 0.15M saline and centrifuged at 8,000 g for 15 minutes. The supernatant was discarded, the pellet was resuspended in 300 µl of saline, and 10-fold serial dilutions were performed in saline. From the 10-4, 10-5, and 10-6 dilutions, 400 µl aliquots of cells were added to 1.2 ml of Hanks balanced salt solution (HBSS).

Two sources of NHS were used in these assays. Pool 1 consisted of serum from five healthy adults that was pooled, aliquotted, and frozen at -70°C. The level of C. jejuni antibodies in pool 1 serum was determined by enzyme-linked immunosorbent assay (ELISA) (4). The optical density ratio (ODR) for immunoglobulin G (IgG) was 5.14; the ODR for IgM was 0.66. Documentation of previous C. jejuni infection was not required to be included in this pool. In contrast, pool 2 consisted of serum from two healthy adults with only low-titer antibody. The ODR for pool 2 serum in the IgG assay was 0.37; and the ODR in the IgM assay was 0.30. As a control, the NHS was heated to 56oC for 30 minutes (heat inactivated NHS [HINHS]) to ablate all complement activity.

The assay to determine susceptibility to NHS was performed in sterile, disposable 96-well microtiter U-bottom plates (Falcon MICROTEST III, Becton Dickinson & Co., Franklin Lakes, NJ, USA). From each of the bacterial suspensions, a 150 µl aliquot was added to duplicate wells. In addition, 50 µl of NHS or HINHS (diluted to 40% with HBSS) was added; the final serum concentration in the suspension was 10%. After the assay plate was incubated at 37oC for 1 hour, 50 µl of the suspension from each well was poured onto blood agar plates and incubated for 48 hours; the number of CFUs was then calculated. The difference between the counts for cells incubated with NHS and HINHS was expressed as median log10 kill for each strain; greater than 1 log10 kill was considered a serum-susceptible strain (21). If less than 1 log10 kill occurred, the strain was considered serum-resistant. The identical procedure was performed using pool 1 and pool 2 serum.

The resistance of the 44 C. jejuni strains studied to killing by NHS is shown in Table 2. Of these strains, 12 (27%) were resistant to killing by C. jejuni antibody-positive pool 1 serum and 10 (23%) were resistant to killing by C. jejuni antibody-negative pool 2 serum; thus, as described previously (22), antibodies to C. jejuni had little impact on serum-killing. The GBS-associated strains were no more likely to be resistant to serum-killing than were the strains from patients with uncomplicated enteritis. However, O:19 strains were significantly more likely than other C. jejuni serotypes to resist serum-killing, regardless of GBS-association and serum pool used (Table 2). In serum pool 1, only 1 of 18 O:19 strains was serum-susceptible compared with 11 (42%) of 26 non-O:19 strains (odds ratio = 12.5, p = 0.008). Similarly, in serum pool 2, no O:19 strain was serum-susceptible compared with 10 (38%) of the non-O:19 isolates.

125I-C3 Binding Assays

Eight strains from Group 1 (four randomly selected from each subgroup) and eight from Group 2 (four randomly selected from each subgroup) were grown on blood agar plates as described above. C. fetus strains 23D and 23B again served as controls and the assays were conducted (21). In brief, bacteria from each plate were harvested in 1.5 ml of HBSS and were centrifuged at 8,000 g for 15 minutes; the pellet was resuspended in 0.5 ml HBSS and adjusted to OD450 = 3.0. For each strain studied, a suspension of 4 µl 125I-C3 (with 20,000 cpm to 65,000 cpm) and 2.5 µl of either NHS or HINHS from pool 2 and 100 µl of the bacteria-HBSS suspension were incubated at 37oC for 15 minutes. 125I-C3 was prepared in the laboratory of one of the authors (RGW) (21). The suspensions were then centrifuged twice at 175xg for 5 minutes, the pellet was resuspended in HBSS, and the supernatant was discarded. The bottom 5 mm (containing the pellet) of each tube was clipped, and emissions were determined in a gamma counter. The counts in the negative control mixtures containing HINHS were subtracted from the NHS counts. An assay was considered valid only if the net pellet counts (NHS minus HINHS) for control strain 23B were at least four times higher than for 23D. To control for nonspecific binding, the counts for each strain studied were expressed as the ratio of net counts relative to the serum susceptible control (23B). Each strain was assayed two to four times.

Mean binding of serum-susceptible control strain 23B was 497 cpm, whereas mean binding of serum-resistant control strain 23D was 54. The mean ratio of C3-binding for strain 23D to 23B of 0.114 was as expected (21). In contrast, the mean ratio for C3 binding to C. jejuni strains in comparison with strain 23B was 0.022 to 0.464 (mean 0.216). The eight O:19 strains were not significantly different from the eight non-O:19 strains in their ability to bind 125I-C3 (Table 3).

Conclusion

This study of GBS patients in the United States and Germany confirms the observation made in Japan that serotype O:19 is overrepresented among patients with C. jejuni-induced GBS. Of 298 randomly collected Campylobacter isolates from patients with enteritis in the United States, only 3% were serotype O:19 (19). A similarly low prevalence of O:19 strains is found in all parts of the world, including North and South America, Asia, and Europe (5,6,19,23). Although specific serotyping surveys have not been done in Germany, it is unlikely that serotype O:19 is more frequent among German C. jejuni isolates. Thus, the GBS-associated strains in our study were more than 11 times as likely to belong to this serotype (p = 0.03). Although the association among GBS and C. jejuni serotype O:19 was not as marked as in Japan (where more than 80% of GBS-associated isolates are O:19), this serotype clearly is overrepresented among GBS-associated strains in other countries. We conclude that the association of O:19 strains with GBS is not just a local phenomenon in Japan but likely reflects a fundamental characteristic of O:19 strains. O-serotype 2 and heat-labile serotype 4, which were common among the GBS strains, are commonly represented among infected persons in the United States (23).

Despite the frequency of Campylobacter infections in GBS patients, such strains are difficult to obtain for several reasons. First, in most C. jejuni-infected patients, stools are clear before neurologic symptoms begin. Second, most neurologists do not culture stool samples when GBS is first diagnosed. And finally, even if a stool culture is ordered and Campylobacter is present, few microbiology laboratories save their isolates; by the time the case is reported, the strain has been discarded. Thus, these seven strains represent one of the largest collections of GBS-associated strains described. Additionally, these are likely to be representative of the population of GBS-associated C. jejuni strains. Unless serotype O:19 strains persist in stools longer, are more easily cultured, or are less likely to be discarded by microbiology laboratories (and no data support any of these possibilities), these strains probably are not different in any systematic way from other GBS-associated isolates.

Most C. jejuni strains are susceptible to killing by human serum (22), but because we studied highly selected strains (most either serotype O:19 or from GBS patients), a high proportion of strains in this investigation were resistant. In this context, the finding that C. jejuni strains from GBS patients were no more likely than the strains from patients with uncomplicated enteritis to be serum resistant is not surprising. Even when the analysis was limited only to serotype O:19 strains, no differences were found between GBS- and enteritis-associated strains. However, serotype O:19 strains were substantially less serum-susceptible than strains of other serotypes and were 12 times as likely to be serum-resistant. Although serotype O:19 represents only a small percentage of C. jejuni strains from patients with uncomplicated enteritis in the United States or Japan, it is the most common serotype identified in GBS patients in both locales. The relatively small variation in serum susceptibility of the O:19 strains is consistent with the close genetic relationship observed among these strains (24).

To better understand the basis for the relative serum-resistance among the O:19 strains, we compared their ability to bind C3 in relation to non-O:19 strains. Because C3 binding occurs after activation by either the alternative or classical complement pathways, it is a screen for differences in these early steps. The serum-resistance of C. fetus is explained by the inability of C3 to bind to the cell surface (25). In contrast, C3 binding is normal in serum-resistant Salmonella, but the C5-9 membrane attack complex does not insert properly (26). In the present study, the lack of substantial C3 binding differences among O:19 and non-O:19 C. jejuni strains suggests that the early steps in complement activation are similar among strains. However, clear differences in serum-susceptibility bespeak either rapid inactivation of C3 or reduced assembly or function of the membrane attack complex in the more resistant strains. Future studies should address this point.

The increasing awareness of the importance of C. jejuni infection in triggering GBS is another example of how previously well-described diseases have emerged as sequelae of acute infectious illnesses. This study attempts to begin to characterize the nature of this association; however, there is much to learn about how an acute gastrointestinal infection results in ascending paralysis. One fact is quite clear: many more people are infected with C. jejuni than contract GBS subsequently. Perhaps some persons are predisposed to contracting GBS after infection with campylobacters that might cause only uncomplicated enteritis in another patient. Conversely, as we have suggested in this paper, some strains may be more likely than others to trigger GBS. No associations between human leukocyte antigen (HLA) types and GBS have been found (27,28). However, in Great Britain and Japan, an association between HLA type and C. jejuni-associated GBS has been suggested (9,29). Perhaps some combination of familial susceptibility, HLA type, strain serotype, or other host or strain characteristics together play a role in the pathogenesis of C. jejuni-induced GBS.

The relative serum-resistance of O:19 strains correlates with mechanism. Furthermore, the relevance of these in vitro assays to the susceptibility of organisms in vivo cannot be known with certainty. We speculate that the relative insensitivity of these strains to the lytic effects of complement allows them to trigger a heightened specific immunologic response. We further speculate that this heightened immunologic response leads to injury of peripheral nerve structures. Since only a small fraction of infections caused by C. jejuni O:19 lead to GBS (estimated incidence 1 in 158) (30), additional factors also must be involved in vivo.

Ban Mishu Allos is an assistant professor of medicine in the Division of Infectious Diseases, Department of Medicine and the Department of Preventive Medicine at Vanderbilt University School of Medicine in Nashville, Tennessee. Her clinical work relates to HIV and other infectious diseases; her research has focused on foodborne illness in general and Campylobacter jejuni as a cause of Guillain-Barré syndrome in particular.

Acknowledgments

We thank Charlotte Patton for serotyping the strains and Manfred Kist for supplying the strains from Germany.

This work was supported by grant NIH-1-K08-NS01709 of the NINDS, NIH (BMA); NIH grant KO4-AI01036 (RGW); and the Medical Research Service of the Department of Veterans Affairs (MJB).

References

  1. Hughes RAC. Guillain-Barré Syndrome. London: Springer-Verlag; 1990.
  2. Asbury AK, Johnson PC. Pathology of peripheral nerves. Philadelphia: WB Saunders; 1978.
  3. Winer JB, Hughes RAC, Anderson MJ, Jones DM, Kangro H, Watkins RFP. A prospective study of acute idiopathic neuropathy II. Antecedent events. J Neurol Neurosurg Psychiatry. 1988;51:6138. DOIPubMed
  4. Mishu B, Ilyas AA, Koski CL, Vriesendorp F, Cook SD, Mithen FA, Serologic evidence of previous Campylobacter jejuni infection in patients with the Guillain-Barré syndrome. Ann Intern Med. 1993;118:94753.PubMed
  5. Kuroki S, Saida T, Nukina M, Haruta T, Yoshioka M, Kobayashi Y, Campylobacter jejuni strains from patients with Guillain-Barré syndrome belong mostly to Penner serogroup 19 and contain B-N-acetylglucosamine residues. Ann Neurol. 1993;33:2437. DOIPubMed
  6. Rees JH, Soudain SE, Gregson NA, Hughes RAC. Campylobacter jejuni infection and Guillain-Barré syndrome. N Engl J Med. 1995;333:13749. DOIPubMed
  7. Allos BM. Campylobacter jejuni infection as a cause of the Guillain-Barré syndrome. Infect Dis Clin North Am. 1998;12:17384. DOIPubMed
  8. Ho TW, Mishu B, Li CY, Gao CY, Cornblath DR, Griffin JW, Guillain-Barré syndrome in northern China: relationship to Campylobacter jejuni infection and anti-glycolipid antibodies. Brain. 1995;118:597605. DOIPubMed
  9. Yuki N, Taki T, Takahashi M, Saito K, Yoshino H, Tai T, Molecular mimicry between GQ1b ganglioside and lipopolysaccharide of Campylobacter jejuni isolated from patients with Fisher's syndrome. Ann Neurol. 1994;36:7913. DOIPubMed
  10. Tauxe RV. Epidemiology of Campylobacter jejuni infections in the United States and other industrialized nations. In: Nachamkin I, Blaser MJ, Tompkins LS, editors. Campylobacter jejunicurrent strategy and future trends. Washington: American Society for Microbiology; 1992. p. 9-19.
  11. Allos BM, Blaser MJ. Potential role of lipopolysaccharides of Campylobacter jejuni in the development of Guillain-Barré syndrome. J Endotoxin Res. 1995;2:2378.
  12. Rees JH, Vaughan RW, Kondeatis E, Hughes RAC. HLA-class II alleles in Guillain-Barré syndrome and Miller Fisher syndrome and their association with preceding Campylobacter jejuni infection. J Neuroimmunol. 1995;62:537. DOIPubMed
  13. Fujimoto S, Yuki N, Itoh T, Amako K. Specific serotype of Campylobacter jejuni associated with Guillain-Barré syndrome. J Infect Dis. 1992;165:183.PubMed
  14. Lastovica AJ, Goddard EA, Argent AC. Guillain-Barré syndrome in South Africa associated with Campylobacter jejuni O:41 strains. J Infect Dis. 1997;Suppl 2:S13943. DOIPubMed
  15. Enders U, Karch H, Toyka KV, Heesemann J, Hartung HP. Campylobacter jejuni and Guillain-Barré syndrome. Ann Neurol. 1994;35:249. DOI
  16. Blaser MJ, Perez-Perez G, Smith PF, Patton CM, Tenover FC, Lastovica AJ, Extraintestinal Campylobacter jejuni and Campylobacter coli infections: host factors and strain characteristics. J Infect Dis. 1986;153:5529.PubMed
  17. Penner JL, Hennessy JN. Passive hemagglutination technique for serotyping Campylobacter fetus subsp. jejuni on the basis of soluble heat-stable antigens. J Clin Microbiol. 1980;2:7327.
  18. Lior H, Woodward DL, Edgar JA, Laroche LJ, Gill P. Serotyping of Campylobacter jejuni by slide agglutination based on heat-labile antigenic factors. J Clin Microbiol. 1982;15:7618.PubMed
  19. Patton CM, Nicholson MA, Ostroff SM, Ries AA, Wachsmuth IK, Tauxe RV. Common somatic O and heat-labile serotypes among Campylobacter strains from sporadic infections in the United States. J Clin Microbiol. 1993;31:152530.PubMed
  20. Blaser MJ, Smith PF, Hopkins JA, Heinzer I, Bryner JH, Wang WLL. Pathogenesis of Campylobacter fetus infections. Serum resistance associated with high molecular weight surface proteins. J Infect Dis. 1987;155:696709.PubMed
  21. Gonzales-Valencia G, Perez-Perez GI, Washburn RG, Blaser MJ. Susceptibility of Helicobacter pylori to the bactericidal activity of human serum. Helicobacter. 1996;1:2833. DOIPubMed
  22. Blaser MJ, Smith PF, Kohler PF. Susceptibility of Campylobacter isolates to the bactericidal activity of human serum. J Infect Dis. 1985;151:22735.PubMed
  23. Patton CM, Wachsmuth IK. Typing schemesare current methods useful? In: Nachamkin I, Blaser MJ, Tompkins LS, editor. Campylobacter jejunicurrent strategy and future trends. Washington: American Society for Microbiology; 1992. p. 110-28.
  24. Fujimoto S, Allos BM, Patton CM, Blaser MJB. Restriction fragment length polymorphism analysis and random amplified polymorphic DNA analysis of Campylobacter jejuni strains isolated from patients with Guillain-Barré syndrome. J Infect Dis. 1997;176:11058. DOIPubMed
  25. Blaser MJ, Smith PF, Repine JE, Joiner KA. Pathogenesis of Campylobacter fetus infection. J Clin Invest. 1988;81:143444. DOIPubMed
  26. Joiner KA, Hammer CH, Brown EJ, Cole RJ, Frank MM. Studies on the mechanism of bacterial resistance to complement-mediated killing. I. Terminal complement components are deposited and released from Salmonella minnesota S218 without causing bacterial death. J Exp Med. 1982;155:80919. DOIPubMed
  27. Hillert J, Osterman PO, Olerup O. No association with HLA-DR, -DQ, or -DP alleles in Guillain-Barré syndrome. J Neuroimmunol. 1991;31:6772. DOIPubMed
  28. Winer JB, Briggs D, Welsh K, Hughes RAC. HLA antigens in the Guillain-Barré syndrome. J Neuroimmunol. 1988;18:136. DOIPubMed
  29. Yuki N, Fujimoto S, Yamada S, Tsujino Y, Kinoshito A, Itoh T. Serotype of Campylobacter jejuni, HLA, and the Guillain-Barré syndrome. Muscle Nerve. 1992;:9689.PubMed
  30. Allos BM, Blaser MJ. Campylobacter jejuni infection and the Guillain-Barré syndrome: mechanisms and implications. International Journal of Medical Microbiology, Virology, Parasitology, and Infectious Diseases. 1994;281:5448.

Tables

Suggested citation: Allos BM, Lippy FT, Carlsen A, Washburn RG, Blaser MJ. Campylobacter jejuni Strains from Patients with Guillain-Barré Syndrome. Emerg Infect Dis [serial on the Internet]. 1998, Jun [date cited]. Available from http://wwwnc.cdc.gov/eid/article/4/2/98-0213.htm

DOI: 10.3201/eid0402.980213

Top of Page

Table of Contents – Volume 4, Number 2—June 1998

Comments to the EID Editors

Please contact the EID Editors via our Contact Form.

 

Past Issues

Select a Past Issue:

Art in Science - Selections from Emerging Infectious Diseases
Now available for order



CDC 24/7 – Saving Lives, Protecting People, Saving Money. Learn More About How CDC Works For You…

USA.gov: The U.S. Government's Official Web PortalDepartment of Health and Human Services
Centers for Disease Control and Prevention   1600 Clifton Rd. Atlanta, GA 30333, USA
800-CDC-INFO (800-232-4636) TTY: (888) 232-6348 - Contact CDC–INFO