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1.
MMWR Morb Mortal Wkly Rep ; 69(20): 618-622, 2020 May 22.
Article in English | MEDLINE | ID: mdl-32437343

ABSTRACT

Ceftriaxone-resistant Salmonella enterica serotype Typhi (Typhi), the bacterium that causes typhoid fever, is a growing public health threat. Extensively drug-resistant (XDR) Typhi is resistant to ceftriaxone and other antibiotics used for treatment, including ampicillin, chloramphenicol, ciprofloxacin, and trimethoprim-sulfamethoxazole (1). In March 2018, CDC began enhanced surveillance for ceftriaxone-resistant Typhi in response to an ongoing outbreak of XDR typhoid fever in Pakistan. CDC had previously reported the first five cases of XDR Typhi in the United States among patients who had spent time in Pakistan (2). These illnesses represented the first cases of ceftriaxone-resistant Typhi documented in the United States (3). This report provides an update on U.S. cases of XDR typhoid fever linked to Pakistan and describes a new, unrelated cluster of ceftriaxone-resistant Typhi infections linked to Iraq. Travelers to areas with endemic Typhi should receive typhoid vaccination before traveling and adhere to safe food and water precautions (4). Treatment of patients with typhoid fever should be guided by antimicrobial susceptibility testing whenever possible (5), and clinicians should consider travel history when selecting empiric therapy.


Subject(s)
Ceftriaxone/pharmacology , Disease Outbreaks , Drug Resistance, Microbial , Salmonella typhi/drug effects , Travel-Related Illness , Typhoid Fever/epidemiology , Typhoid Fever/microbiology , Adolescent , Adult , Aged , Ceftriaxone/therapeutic use , Child , Child, Preschool , Female , Humans , Infant , Iraq/epidemiology , Male , Middle Aged , Pakistan/epidemiology , Typhoid Fever/drug therapy , United States/epidemiology , Young Adult
2.
Tenn Med ; 103(4): 39-42, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20481249

ABSTRACT

Since joining the Centers for Disease Control and Prevention's (CDC) Foodborne Diseases Active Surveillance Network (FoodNet) in 1999, Tennessee has conducted active surveillance for foodborne pathogens including Shiga toxin-producing E. coli (STEC). The number of STEC infections has increased in recent years in the United States, including Tennessee, due partly to changes in clinical laboratories practices including non-culture based testing methods. Despite increased reporting, STEC infections are likely under-recognized in Tennessee. A 2007 statewide laboratory survey indicated that less than half of clinical laboratories test for STEC on-site. Among these, only nine reported using non-culture based methods. Only one clinical laboratory reported simultaneous culture for STEC O157 and testing with an assay that detects Shiga toxins for non-O157 STEC as recommended by the CDC. Adoption of CDC recommendations coupled with timely and complete reporting will enhance public health surveillance, outbreak investigations and interventions to prevent STEC infection.


Subject(s)
Clinical Laboratory Techniques , Escherichia coli Infections/epidemiology , Escherichia coli Infections/microbiology , Escherichia coli O157/isolation & purification , Escherichia coli O157/classification , Food Microbiology , Humans , Population Surveillance , Shiga Toxins/isolation & purification , Tennessee/epidemiology
3.
Antimicrob Agents Chemother ; 52(4): 1278-84, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18212096

ABSTRACT

Patients with typhoid fever due to Salmonella enterica serotype Typhi strains for which fluoroquinolones MICs are elevated yet that are classified as susceptible by the current interpretive criteria of the Clinical and Laboratory Standards Institute may not respond adequately to fluoroquinolone therapy. Patients from seven U.S. states with invasive Salmonella serotype Typhi infection between 1999 and 2002 were enrolled in a multicenter retrospective cohort study. Patients infected with Salmonella serotype Typhi isolates with ciprofloxacin MICs of 0.12 to 1 microg/ml (decreased ciprofloxacin susceptibility but not resistant to ciprofloxacin [DCS]) were compared with patients infected with isolates with ciprofloxacin MICs <0.12 microg/ml for fever clearance time and treatment failure. Of 71 patients, 30 (43%) were female and 24 (34%) were infected with Salmonella serotype Typhi with DCS; the median age was 14 years (range, 1 to 51 years). Twenty-one (88%) of 24 isolates with DCS were resistant to nalidixic acid. The median antimicrobial-related fever clearance times in the DCS and non-DCS groups were 92 h (range, 21 to 373 h) and 72 h (range, 19 to 264 h) (P = 0.010), respectively, and the fluoroquinolone-related fever clearance times in the DCS and non-DCS groups were 90 h (range, 9 to 373 h) and 64 h (range, 34 to 204 h) (P = 0.153), respectively. Four (17%) of 24 patients in the DCS group and 2 (4%) of 46 patients in the non-DCS group (relative risk, 2.5; 95% confidence interval, 1.2 to 5.1) experienced treatment failure. Associations persisted after adjustment for potential confounders. We demonstrate that patients infected with Salmonella serotype Typhi isolates with DCS show evidence of a longer time to fever clearance and more frequent treatment failure. Nalidixic acid screening does not detect all isolates with DCS.


Subject(s)
Anti-Bacterial Agents/pharmacology , Drug Resistance, Bacterial , Fluoroquinolones/pharmacology , Salmonella typhi/drug effects , Typhoid Fever/drug therapy , Adolescent , Adult , Anti-Bacterial Agents/therapeutic use , Child , Child, Preschool , Ciprofloxacin/pharmacology , Ciprofloxacin/therapeutic use , Cohort Studies , Female , Fluoroquinolones/therapeutic use , Foodborne Diseases/epidemiology , Hospitalization , Humans , Infant , Male , Microbial Sensitivity Tests/standards , Middle Aged , Population Surveillance , Retrospective Studies , Treatment Outcome , Typhoid Fever/microbiology , United States
4.
J Infect Dis ; 194(2): 222-30, 2006 Jul 15.
Article in English | MEDLINE | ID: mdl-16779729

ABSTRACT

BACKGROUND: A new multidrug-resistant (MDR) strain of Salmonella serotype Newport, Newport-MDRAmpC, has recently emerged. We sought to identify the medical, behavioral, and dietary risk factors for laboratory-confirmed Salmonella Newport infection, including that with Newport-MDRAmpC. METHODS: A 12-month population-based case-control study was conducted during 2002-2003 in 8 sites of the Foodborne Diseases Active Surveillance Network (FoodNet), with 215 case patients with Salmonella Newport infection and 1154 healthy community control subjects. RESULTS: Case patients with Newport-MDRAmpC infection were more likely than control subjects to have taken an antimicrobial agent to which Newport-MDRAmpC is resistant during the 28 days before the onset of diarrheal illness (odds ratio [OR], 5.0 [95% confidence interval {CI}, 1.6-16]). Case patients with Newport-MDRAmpC infection were also more likely to have eaten uncooked ground beef (OR, 7.8 [95% CI, 1.4-44]) or runny scrambled eggs or omelets prepared in the home (OR, 4.9 [95% CI, 1.3-19]) during the 5 days before the onset of illness. International travel was not a risk factor for Newport-MDRAmpC infection but was a strong risk factor for pansusceptible Salmonella Newport infection (OR, 7.1 [95% CI, 2.0-24]). Case patients with pansusceptible infection were also more likely to have a frog or lizard in their household (OR, 2.9 [95% CI, 1.1-7.7]). CONCLUSIONS: Newport-MDRAmpC infection is acquired through the US food supply, most likely from bovine and, perhaps, poultry sources, particularly among persons already taking antimicrobial agents.


Subject(s)
Bacterial Proteins/metabolism , Drug Resistance, Multiple, Bacterial , Food Microbiology , Salmonella Infections/epidemiology , Salmonella Infections/transmission , Salmonella/classification , Salmonella/isolation & purification , beta-Lactamases/metabolism , Animals , Anti-Bacterial Agents/pharmacology , Case-Control Studies , Cattle , Eggs/microbiology , Humans , Meat/microbiology , Odds Ratio , Risk Factors , Salmonella/drug effects , Salmonella/enzymology , Salmonella Infections/microbiology , United States/epidemiology
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