J Med Microbiol 57 (2008), 1247-1250; DOI: 10.1099/jmm.0.2008/001719-0
© 2008 Society for General Microbiology
ISSN 1473-5644
Rising prevalence of enteric fever due to multidrug-resistant Salmonella: an epidemiological study
Surinder Kumar,
Meher Rizvi
and
Nidhika Berry
Department of Microbiology, Maulana Azad Medical College, Bahadur Shah Zafar Marg, New Delhi, India
Correspondence
Meher Rizvi
rizvimeher{at}yahoo.co.in
Received 11 March 2008
Accepted 17 June 2008
A prospective study of the prevalent aetiology of enteric fever was undertaken at a tertiary care hospital in North India at intervals of every 3 years. Salmonella spp. were isolated from 174 (7 %) patients. Amongst these, 140 (80 %) patients were infected by Salmonella enterica subspecies enterica serovar Typhi (S. Typhi) and 16 (9 %) by S. enterica serovar Paratyphi A; the remaining 11 % were infected by other S. enterica serogroups, Typhimurium, Paratyphi C and Senftenberg, and other group E salmonella. A significantly greater number of S. Typhi were isolated in the summer and monsoon months. Multidrug resistance (resistance to chloramphenicol, ampicillin and co-trimoxazole) sequentially increased from 34 % in 1999 to 66 % in 2005. Increasing resistance was also noticed to the other antibiotics, especially to the cephalosporins. Moreover 8 % of the S. Typhi isolates were found to be presumptive extended spectrum β-lactamase producers. There was a gradual development of resistance to fluoroquinolones over the 7 years. No resistance was observed to fluoroquinolones in 1999, while in 2005 4.4 % resistance was observed to sparfloxacin, 8.8 % resistance to ofloxacin and a high resistance, 13 %, to ciprofloxacin. This is an alarming development and it is of paramount importance to limit unnecessary use of fluoroquinolones and third generation cephalosporins so that their efficacy against salmonella is not jeopardized further.
Abbreviations: ESBL, extended spectrum β-lactamase.
Present address: Department of Microbiology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, India. 
 |
INTRODUCTION
|
|---|
Typhoid fever is an important cause of morbidity and mortality in many developing countries, with an estimated 33 million cases worldwide (Edelman & Levine, 1986). In Asia, the mean incidence of enteric fever is estimated to be 900 per 100 000 people per annum (Ivanoff, 1994). Enteric fever is endemic in all parts of India and still constitutes a significant health hazard. The resistance of Salmonella enterica subspecies enterica serovar Typhi (S. Typhi) to chloramphenicol was first reported in India from Kerala, where a substantial outbreak took place in 1972 (Paniker & Vimla, 1972). Since then multidrug-resistant strains of S. Typhi have escalated into a worldwide problem (Ackers et al., 2000; Jesudasan & John, 1990; Kamili et al., 1993; Madhulika et al., 2004). The steadily increasing multidrug resistance in S. Typhi strains is a cause of grave concern in India, where such strains are endemic in many parts. A prospective study was planned to assess the antimicrobial susceptibilities of all salmonella species isolated from blood. The study was conducted over 3 non-consecutive years (1999, 2002 and 2005) spanning a 7 year period.
|
METHODS
|
|---|
The study was carried out from January to December in the years 1999, 2002 and 2005, in the 1500 bed Lok Nayak Hospital, New Delhi (India). Blood samples were collected from febrile patients prior to initiation of antibiotic therapy. These samples, 5–10 ml from adults and 2–3 ml from children, were collected by venepuncture using aseptic technique, and inoculated directly into blood culture bottles containing 50 ml brain heart infusion broth. The samples were processed according to standard recommended techniques (Koneman et al., 1997). A detailed clinical and treatment history was elicited from all of the patients. The bottles were incubated at 37 °C for 7 days and examined daily for bacterial growth. Subcultures were performed on the first, second, third, fifth and seventh day of incubation on 5 % sheep blood agar and MacConkey agar. Suspected non-lactose fermenting colonies were screened biochemically and their identity confirmed serologically.
Antibiotic sensitivity was tested by the Kirby–Bauer technique according to Clinical and Laboratory Standards Institute guidelines (Bauer et al., 1966). The following antibiotics (Himedia) were used: amoxicillin (10 µg), ampicillin (10 µg), chloramphenicol (30 µg), nalidixic acid (30 µg), cefotaxime (10 µg), cefuroxime (30 µg), ceftriaxone (10 µg), cefpodoxime (30 µg), co-trimoxazole (25 µg), gentamicin (10 µg), netilmicin (10 µg), ciprofloxacin (5 µg), ofloxacin (5 µg), sparfloxacin (5 µg), azithromycin (15 µg) and amoxicillin/clavulanic acid (20/10 µg). Presumptive extended spectrum β-lactamase (ESBL) producers were screened by combined disc test, as well as by double disc synergy test, using discs of amoxicillin/clavulanic acid, amoxicillin, cefoperazone sulbactam, cefoperazone, ceftriaxine and cefotaxime. The discs of substrates were kept at a distance of 15 mm from the inducers (amoxicillin/clavulanic acid and cefoperazone sulbactam). A difference of >5 mm in the zone of inhibition of the cephalosporin versus the inducer was a marker of a presumptive ESBL producer. Statistical analysis was performed using the chi-square test and Student’s paired t-test.
|
RESULTS AND DISCUSSION
|
|---|
A total of 5565 patients entered the study, of which 174 (3.1 %) in all had bacteraemia due to Salmonella spp. The majority of isolates, 157 (90.2 %), were from children and 17 (9.8 %) were isolated from adults (Table 1
). The cases were predominantly in the 6–15 year age group, representing 40.2 % of the total. An unusual feature was that there were as many as 7 (4 %) neonates from whom S. Typhi was isolated, the youngest being merely 8 days old. This is believed to be the first ever report of enteric fever in an 8-day-old neonate. More than half (55.7 %) of the patients were males.
S. Typhi, totalling 140 (80.5 %) isolates, predominated. There were 16 isolates (9.2 %) that were S. enterica serovar Paratyphi (S. Paratyphi) A, and 18 (10.3 %) isolates that were other Salmonella serogroups: 5 (2.9 %) S. enterica serovar Typhimurium (S. Typhimurium), 2 (1.1 %) S. Paratyphi C, 3 (1.7 %) S. enterica serovar Senftenberg, 3 (1.7 %) other group E salmonella and 5 (2.9 %) Salmonella serogroups other than groups A, B, C, D and E .
It was observed that a large number, 120 (69.0 %), of the cases of enteric fever clustered in the hot months of April, May and June, and in the monsoon season, with a larger peak in the summer and a smaller peak in the monsoon season (Fig. 1). The number of cases decreased during autumn and winter. During the summer and monsoon months the water supply and sanitation systems are under a great strain in Delhi, which could account for the higher incidence in these months.
Multidrug resistance in S. Typhi (resistance to ampicillin, chloramphenicol and co-trimoxazole) was observed in 74 (52.9 %) of the isolates. On studying the trend over the 7 year period, multidrug resistance increased from 16 (34 %) isolates in 1999 to 28 (58 %) isolates in 2002, and rose to 30 (66 %) isolates in 2005, along with a rising resistance to all the other drugs (Table 2). S. Paratyphi A did not exhibit any resistance to chloramphenicol (Table 3). Only one (6.3 %) isolate was resistant to co-trimoxazole. However, 9 (56.3 %) isolates were resistant to ampicillin. S. Typhimurium expressed 100 % resistance to ampicillin. S. Senftenberg and other group E serotypes shared similar resistance patterns: 33.3 % resistance to chloramphenicol and 66.7 % to ampicillin. S. Typhi exhibited extremely high, 59 (42.1 %) isolates, resistance to amoxicillin/clavulanic acid. Amongst the cephalosporins, the least, 8 (5.7 %) isolates, resistance was demonstrated against cefotaxime followed by 17 (12.1 %) isolates with resistance to ceftriaxone and cephalexin, and a high resistance, 20 (14.3 %) isolates, to cefpodoxime, and 22 (15.7 %) isolates with resistance to cefuroxime. Resistance to amoxicillin/clavulanic acid has increased significantly over the years studied. This high level of resistance to β-lactam β-lactamase inhibitor could be due to hyperproduction of class A β-lactamases such as TEM-1 or SHV-1. The most common inhibitor-resistant enzymes are derivatives of TEM-1. It is unlikely that all these organisms are ESBL producers, as most of the isolates are still sensitive to the third generation cephalosporins. This has also been suggested by Jesudasan & John (1990).
We feel that in the Indian scenario, with the high level of resistance to amoxicillin/clavulanic acid, this β-lactam β-lactamase combination is a poor inducer for the detection of ESBL producers. We recommend cefoperazone/sulbactam (1 : 1) as a better inducer for screening purposes. A total of 8 % isolates were identified as presumptive ESBL producers. Ceftriaxone proved to be a better substrate than cefpodoxime, cefotaxime and cefoperazone. Presumptive ESBL production increased from none in 1999 to 8 % in 2005 in S. Typhi. We also observed a gradual increase in resistance among the fluoroquinolones, with least resistance, 4 (2.9 %), to sparfloxacin, and a higher resistance to ofloxacin, 6 (4.3 %), and the highest resistance, 14 (10 %), to ciprofloxacin. A total of 9 (6.4 %) isolates were resistant to azithromycin. Nalidixic acid was used for the screening of fluoroquinolone resistance. Its resistance closely mirrors resistance to ciprofloxacin (Table 2
). We feel that individual fluoroquinolones should be tested separately as this study shows different sensitivity patterns among the three quinolones tested, which was confirmed by the patients recovering from the infection despite some being resistant to nalidixic acid. Incremental drug resistance was observed over the years. In 2005, multidrug resistance had increased to 66 % from 34 % in 1999, which is alarming. In our study emergence of resistance to fluoroquinolones was noticed. There have been varying reports from other parts of India. Some studies from India have reported no resistance to ciprofloxacin (Kabra et al., 2000; Ciraj et al., 1999), while others have reported development of resistance to ciprofloxacin and norfloxacin (Rathish et al., 1995; Gaind et al., 2006). Our study with the newer quinolones yielded lower resistance to them than to ciprofloxacin. Thus newer fluoroquinolones appear to be a better option than ciprofloxacin. There was a statistically significant rise in resistance from 1999 to 2005 against chloramphenicol, co-trimoxazole, ampicillin, ofloxacin and ciprofloxacin (P<0.003, P<0.001, P<0.05, P<0.05 and P<0.01, respectively).
Ciprofloxacin was significantly more effective in treating multiresistant typhoid fever than ceftriaxone. Although the sensitivity profile does not show much difference between the two (Table 3), in 27 patients in whom ceftriaxone was used as the drug of first choice, fever did not subside. Ciprofloxacin was successfully resorted to in these cases. Failure of ceftriaxone in these cases could be attributed to ESBL production, and hyperproduction of TEM and SHV type of β-lactamases. No treatment failure occurred in the 73 cases where ciprofloxacin was used as a drug of first choice. Similar results have been reported in other studies (Mirza et al., 1995; Wallace et al., 1993). Although fluoroquinolones are not advised for use in children in many countries, they have been used for treating typhoid with few side effects (Gupta, 1994). It was noticed that none of the other Salmonella serogroups exhibited triple drug resistance. Among them maximum resistance was observed against ampicillin. These point to divergent lines of antibiotic resistance.
Although in our study S. Paratyphi A was not the leading cause of enteric fever, there are reports of increasing isolation rates of S. Paratyphi A from India as well as Asia (Sood et al., 1999; Ochiai et al., 2005). The emergence of S. Paratyphi A has an important implication – licensed typhoid fever vaccines (Vi polysaccharide and live oral Ty21a) are not protective against S. Paratyphi A infections. The emergence of this serotype may portend a decline in the usefulness of these vaccines in controlling enteric fever in the future. New vaccination strategies should include bivalent vaccines that protect against both S. Typhi and S. Paratyphi A (Ochiai et al., 2005).
At present, similar treatment strategies may work for both organisms but with the recent escalation of drug resistance in S. Paratyphi A future enteric fever prevention strategies in Asia must focus on it too (Harish et al., 2004). It is clear that multidrug-resistant strains of S. Typhi have become firmly entrenched in various parts of the Indian subcontinent. In our opinion ofloxacin and sparfloxacin are better options then ciprofloxacin and cephalosporins. Urgent consideration should be given to what should be the most appropriate first line therapy for enteric fever in the subcontinent.
|
REFERENCES
|
|---|
Ackers, M. L., Puhr, M. D., Tauxe, R. V. & Mintz, E. D. (2000). Laboratory based surveillance of Salmonella serotype Typhi infections in the United States: antimicrobial resistance on the rise. JAMA 283, 2668–2673.[Abstract/Free Full Text]
Bauer, A. W., Kirby, W. M. M., Sherris, J. C. & Truck, M. (1966). Antibiotic susceptibility testing by standardized single disc method. Am J Clin Pathol 45, 493–496.[Medline]
Ciraj, A. M., Seetha, K. S., Gopalkrishna, B. K. & Shivananda, P. G. (1999). Drug resistance pattern and phage types of Salmonella Typhi isolates in Manipal, South Karnataka. Indian J Med Sci 53, 486–489.[Medline]
Edelman, R. & Levine, M. M. (1986). Summary of an international workshop on typhoid fever. Rev Infect Dis 8, 329–349.[Medline]
Gaind, R., Paglietti, B., Murgia, M., Dawar, R., Uzzau, S., Cappuccinelli, P., Deb, M., Aggarwal, P. & Rubino, S. (2006). Molecular characterization of ciprofloxacin resistant Salmonella enterica serovar Typhi and Paratyphi A causing enteric fever in India. J Antimicrob Chemother 58, 1139–1144.[Abstract/Free Full Text]
Gupta, A. (1994). Multi-drug resistant typhoid fever in children: epidemiology and therapeutic approach. Pediatr Infect Dis J 13, 134–140.[Medline]
Harish, B. N., Madhulika, U. & Parija, S. C. (2004). Isolated high level ciprofloxacin resistance in Salmonella enterica subsp. enterica serotype Paratyphi A. J Med Microbiol 53, 819[Free Full Text]
Ivanoff, B. (1994). Typhoid fever: global situation and WHO recommendations. In Proceedings of the 2nd Asia Pacific Symposium on Typhoid Fever and Other Salmonellosis, p. 39. Bangkok: Infectious Disease Association of Thailand.
Jesudasan, M. V. & John, T. J. (1990). Multiresistant Salmonella typhi in India. Lancet 336, 252[Medline]
Kabra, S. K., Madhulika, Talati, A., Soni, N., Patel, S. & Modi, R. R. (2000). Multidrug-resistant typhoid fever. Trop Doct 30, 195–197.[Medline]
Kamili, M. A., Ali, G., Shah, M. Y., Khan, R. S. & Alladaquab, G. Q. (1993). Multiple drug resistance typhoid fever outbreak in Kashmir valley. Indian J Med Sci 47, 147–151.[Medline]
Koneman, E. W., Allen, S. D., Janada, W. M., Schreckenberger, P. C. & Winn, W. C. (1997). Guidelines for the collection, transport, processing, analysis and reporting of cultures from specific specimen sources. In Colour Atlas and Textbook of Diagnostic Microbiology, 5th edn, pp. 153–162. New York: Lippincott.
Madhulika, U., Harish, B. N. & Parija, S. C. (2004). Current pattern in antimicrobial susceptibility of Salmonella Typhi isolates in Pondicherry. Indian J Med Res 120, 111–114.[Medline]
Mirza, S. H., Beeching, N. J. & Hart, C. A. (1995). The prevalence and clinical features of multi-drug resistant Salmonella Typhi infection in Baluchistan, Pakistan. Ann Trop Med Parasitol 89, 515–519.[Medline]
Ochiai, R. L., Wang, X. Y., von Seidlein, L., Yang, J., Bhutta, Z. A., Bhattacharya, S. K., Agtini, M., Deen, J. L. & Wain, J. (2005). Salmonella Paratyphi A rates, Asia. Emerg Infect Dis 11, 1764–1766.[Medline]
Paniker, C. K. J. & Vimla, K. N. (1972). Transferable chloramphenicol resistance in Salmonella Typhi. Nature 239, 109–110.[Medline]
Rathish, K. C., Chandrashekar, M. R. & Nagesha, C. N. (1995). An outbreak of multi-drug resistant typhoid fever in Bangalore. Indian J Pediatr 62, 445–448.[CrossRef][Medline]
Sood, S., Kapil, A., Dash, N., Das, B. K., Goel, V. & Seth, P. (1999). Paratyphoid fever in India: an emerging problem. Emerg Infect Dis 5, 483–484.[Medline]
Wallace, M. R., Yousif, A. & Mahroos, G. (1993). Ciprofloxacin versus ceftriaxone in the treatment of multi-drug resistant typhoid fever. Eur J Clin Microbiol Infect Dis 12, 907–910.[CrossRef][Medline]
This article has been cited by other articles:
|
|
|
|
 
E. I. Broughton, M. Ip, C. L. Coles, and D. G. Walker
Higher hospital costs and lengths of stay associated with quinolone-resistant Salmonella enterica infections in Hong Kong
J. Public Health Med.,
June 14, 2009;
(2009)
fdp057v1.
[Abstract]
[Full Text]
[PDF]
|
|
|
TOP
INTRODUCTION
METHODS
