Notes from the Field: Shigella with Decreased Susceptibility to Azithromycin Among Men Who Have Sex with Men — United States, 2002–2013
Katherine E. Heiman, MPH1, Maria Karlsson, PhD1, Julian Grass, MPH1, Becca Howie1, Robert D. Kirkcaldy, MD2, Barbara Mahon, MD1, John T. Brooks, MD3, Anna Bowen, MD1 (Author affiliations at end of text)
Bacteria of the genus Shigella cause approximately 500,000 illnesses each year in the United States. Diarrhea (sometimes bloody), fever, and stomach cramps typically start 1–2 days after exposure and usually resolve in 5–7 days.* For patients with severe disease, bloody diarrhea, or compromised immune systems, antibiotic treatment is recommended, but resistance to traditional first-line antibiotics (e.g., ampicillin and trimethoprim-sulfamethoxazole) is common. For multidrug-resistant cases, azithromycin, the most frequently prescribed antibiotic in the United States (1), is recommended for both children and adults (2,3). However, not all Shigellae are susceptible to azithromycin (4–6). Nonsusceptible isolates exist but are not usually identified because there are no clinical laboratory guidelines for azithromycin susceptibility testing. However, to monitor susceptibility of Shigellae in the United States, CDC's National Antimicrobial Resistance Monitoring System (NARMS) has, since 2011, routinely measured the azithromycin minimum inhibitory concentration (MIC) for every 20th Shigella isolate submitted from public health laboratories to CDC, as well as outbreak-associated isolates. All known U.S. Shigella isolates with decreased susceptibility to azithromycin (DSA-Shigella), and the illnesses caused by them, are described in this report.
DSA-Shigella is defined as a Shigella isolate with an azithromycin MIC >16 µg/mL (4). Twenty-nine DSA-Shigella isolates were identified through routine NARMS testing. Additional isolates from 2002–2013 were identified through a previous NARMS study (n = 3) (4), requests to public health officials (n = 2), and retrospective testing of available isolates with pulsed-field gel electrophoresis (PFGE) patterns indistinguishable from DSA-Shigella isolates (n = 21).
Among 55 patients from 17 states infected with DSA-Shigella (36 S. flexneri, 18 S. sonnei, one S. boydii), age ranged from 1 to 89 years (median: 42 years); 44 (80%) were men, and seven (13%) were children (aged <18 years). Of 35 patients for whom information was available, 23 (66%) were white, 11 (31%) were black, and one (3%) was Asian/Pacific Islander (two patients self-identified as white and Hispanic and one as Hispanic only). All but one patient resided in an urban area; one child and none of 29 adults for whom information was available reported international travel. Four patients were part of a recognized shigellosis outbreak (5). The median duration of illness was 11 days (n = 17). Of patients for whom information was available, 46% (12 of 26) had bloody diarrhea, 50% (16 of 32) had fever, and 45% (19 of 42) were hospitalized. Eighty-one percent (13 of 16) of men for whom information was available were human immunodeficiency virus (HIV)–positive, and 79% (11 of 14) identified as gay, bisexual, or other men who have sex with men (collectively referred to as MSM). Four men reported recent high-risk sexual practices, including anonymous sexual contact (n = 1), sexual contact without a barrier (n = 2 anal-genital; n = 1 oral-anal), and many sexual partners (n = 1); five had a history of syphilis.
All isolates harbored mphA or ermB macrolide resistance genes that are commonly plasmid-encoded. Fifty-three percent (29 of 55) were resistant to five or more classes of antibiotics, and 4% (2 of 55) were resistant to ciprofloxacin. NARMS data indicated that isolates were not susceptible to the drug used for treatment in seven of 19 patients, including three treated with azithromycin.
DSA-Shigella infections are occurring in the United States. Although some of the infections occurred among children, who are often treated with azithromycin for shigellosis, these data suggest that MSM, especially HIV-infected MSM, are currently at greater risk for infection with DSA-Shigella. Shigellosis is more common and can be more severe among HIV-infected persons with CD4 cell counts <200/mm3 (7). Clinical failure of azithromycin was recently reported in a Dutch HIV-infected patient with shigellosis (6). Clinicians should be aware that MSM and HIV-positive persons with shigellosis might be infected with Shigella strains with reduced susceptibility to azithromycin. Clinicians should culture stool specimens of MSM and HIV-infected men experiencing diarrhea and determine antimicrobial susceptibility of Shigella to antibiotics other than azithromycin to help guide treatment, if needed. Meticulous handwashing and reducing fecal-oral exposures during sexual contact can reduce risk for infection (7).
The number of cases presented in this report is likely a substantial underestimate because NARMS routinely tests only 5% of Shigella isolates submitted to public health laboratories, and targeted testing using PFGE might miss cases because Shigella is highly mutable and plasmid-encoded macrolide resistance genes are mobile. Additionally, because NARMS began routinely measuring susceptibility to azithromycin in 2011, and recent isolates were more likely to be available for retrospective analysis, these data provide no information about trends. To better track illnesses and guide patient management, clinical laboratory guidelines for azithromycin susceptibility testing among Enterobacteriaceae are urgently needed.
State and local health departments in California, District of Columbia, Georgia, Hawaii, Iowa, Illinois, Indiana, Massachusetts, Michigan, Nevada, New York City, Ohio, Pennsylvania, South Dakota, Texas, Virginia, and Washington.
1Division of Foodborne, Waterborne, and Environmental Diseases, National Center for Emerging and Zoonotic Infectious Diseases, CDC; 2Division of STD Prevention, National Center for HIV, Hepatitis, STD, and TB Prevention, CDC; 3Division of HIV/AIDS Prevention, National Center for HIV, Hepatitis, STD, and TB Prevention, CDC (Corresponding author: Anna Bowen, firstname.lastname@example.org, 404-639-4636)
- Hicks L, Taylor T. U.S. outpatient antibiotic prescribing, 2010. N Engl J Med 2013;368:1461–2.
- American Academy of Pediatrics. Shigella infections. In: Red book: 2012 report of the Committee on Infectious Diseases. Pickering LK, ed. 29th edition. Elk Grove Village, IL: American Academy of Pediatrics; 2012:645–7.
- World Health Organization. Guidelines for the control of shigellosis, including epidemics due to Shigella dysenteriae type 1. Geneva, Switzerland: World Health Organization; 2005. Available at http://whqlibdoc.who.int/publications/2005/9241592330.pdf.
- Howie RL, Folster JP, Bowen A, Barzilay EJ, Whichard JM. Reduced azithromycin susceptibility in Shigella sonnei, United States. Microb Drug Resis 2010;16:245–8.
- Karlsson MS, Bowen A, Reporter R, et al. Outbreak of infections caused by Shigella sonnei with reduced susceptibility to azithromycin in the United States. Antimicrob Agents Chemother 2013;57:1559–60.
- Hassing RJ, Melles DC, Goessens WHF, Rijnders BJA. Case of Shigella flexneri infection with treatment failure due to azithromycin resistance in an HIV-positive patient [Letter]. Infection 2014; February 2, 2014 [Epub ahead of print].
- Panel on Opportunistic Infections in HIV-Infected Adults and Adolescents. Guidelines for the prevention and treatment of opportunistic infections in HIV-infected adults and adolescents: recommendations from the Centers for Disease Control and Prevention, the National Institutes of Health, and the HIV Medicine Association of the Infectious Diseases Society of America. Atlanta, GA: US Department of Health and Human Services, CDC; 2014. Available at http://aidsinfo.nih.gov/contentfiles/lvguidelines/adult_oi.pdf.
* Additional information available at http://www.cdc.gov/nczved/divisions/dfbmd/diseases/shigellosis.
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