Volume 6, Number 4—August 2000
Antimicrobial Resistance in Salmonella Enteritidis, Southern Italy, 1990-1998
During 1990 to 1998, we identified multidrug-resistant isolates of Salmonella Enteritidis in southern Italy. Plasmids containing class I integrons and codifying for synthesis of extended-spectrum ß-lactamases were detected. Active surveillance for resistance to antimicrobial agents is needed to guard against the possible spread of resistant clones.
In the last decade, the incidence of Salmonella Enteritidis infections has increased in many countries. In Europe, this serotype now predominates among Salmonella isolates from humans (1). In southern Italy, identification of S. Enteritidis has increased steadily since 1990, in parallel with increases throughout Europe. After a temporary decline in 1995 and 1996, isolation rates from both sporadic cases and foodborne outbreaks increased. During 1998, records from the Center for Enteric Pathogens in southern Italy show identification rates of approximately 45% in all human Salmonella isolates and 61% in isolates from patients hospitalized for enteritis. In the Enteritidis serotype, resistance to antimicrobial drugs is rare, but resistance to antibacterial agents has been increasing in some Mediterranean countries (2).
We conducted a retrospective study of antimicrobial drug resistance patterns of S. Enteritidis isolates identified from human, animal, and environmental sources in southern Italy from 1990 to 1998. We also investigated mechanisms of resistance at the molecular level.
From 1990 to 1998, 1,889 strains of S. Enteritidis were referred to the Center for Enteric Pathogens, Palermo, southern Italy: 86% were of human origin, 2.9% from infected animals (mainly poultry), 6.7% from sewage plant effluents and surface water, and 4.4% from foods (mainly eggs and egg-based dishes). All strains were biochemically identified by standard tests and were serotyped for somatic and flagellar antigen identification. Phage types were determined with 10 typing phages (3).
Forty-four (2.3%) of the 1,889 strains tested were resistant to at least one antibiotic; we examined patterns of antibiotic resistance, phage types, and plasmid profiles of these 44 strains (Table). Resistance to ampicillin, alone or associated with other ß-lactams, and tetracycline, alone or associated with aminoglycosides, sulfonamides, and trimethoprim, were the most commonly encountered phenotypes among the S. Enteritidis isolates studied. Of the 17 tetracycline-resistant strains, nine and eight, respectively, had transferrable plasmids of 80 and 30 MDal.
Six strains isolated from pediatric patients with enteritis (three in 1992, 1994, and 1996 in Sicily and three in 1997 in Calabria) were resistant to ampicillin, aztreonam, cephalotin, third-generation cephalosporins, and sulfonamides by the Kirby-Bauer method (7). Two of the 1997 isolates were also resistant to chloramphenicol. The double-disk synergy test was positive for all six isolates, suggesting the production of ESBL. In five cases, plasmids of 38, 70, and 80 MDal were shown by conjugation to mediate the complete pattern of resistance. In one strain identified in 1992, a 30-MDal plasmid was detected, but the resistance traits could not be transferred to recipient cells.
Six isolates of S. Enteritidis carried integrons with inserted regions of DNA of 0.8 to 2.5 kb (Table). Transconjugant Escherichia coli from these strains was also positive, indicating that the integrons were carried on plasmids. DNA fragments of approximately 2.0 kb were obtained from ESBL-producing strains.
During the 9-year study, a small proportion of resistant strains was found within Enteritidis, 2.3% showing resistance to at least one antimicrobial drug and 0.9% to three or more. Prevalence in southern Italy was similar to that in other European countries, such as England and Wales (8) and the Czech Republic (9); however, it was lower than prevalence detected from 1987 to 1993 in Greece, where up to 67.4% of strains of S. Enteritidis from human and nonhuman sources were resistant to antibiotics and the resistance rate increased steadily until 1991 (2). No temporal trend or possible association with source was investigated in resistance patterns identified in southern Italy because resistant strains are rare and usually from human sources.
The unusual characteristics of antimicrobial resistance of some S. Enteritidis isolates highlight the problem of emergence of drug resistance in a common serotype of Salmonella, transmitted in popular food items and often implicated in foodborne outbreaks. We identified six ESBL-producing isolates from epidemiologically unrelated cases, a rare finding (10-12). All six strains were isolated from community-acquired enteritis cases in otherwise healthy children, who had no recent history of hospitalization or antimicrobial therapy. This observation is not consistent with the hypothesis that multidrug-resistant clones are selected or resistance determinants are acquired as a consequence of antibiotic treatment. Moreover, the presence of integrons in strains isolated as long ago as 1991 is of particular concern because of the ability of these elements to disseminate resistance traits by intra- and inter-specific gene transfer (13,14).
Although most isolates identified in southern Italy were susceptible, some aspects of the epidemiology of S. Enteritidis are cause for concern. Active monitoring of S. Enteritidis strains for resistance to antibacterial drugs seems crucial because of the public health implications of a potential spread of resistant clones.
Dr. Mammina is a physician in the Department of Hygiene and Microbiology "G. D'Alessandro" of the University of Palermo. Her research interests focus on the molecular epidemiology of bacterial diseases, with an emphasis on enteric pathogens and tuberculosis.
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Suggested citation: Nastasi A, Mammina C, Cannova L. Antimicrobial Resistance in Salmonella Enteritidis, Southern Italy, 1990-1998. Emerg Infect Dis [serial on the Internet]. 2000, Aug [date cited]. Available from http://wwwnc.cdc.gov/eid/article/6/4/00-0415
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