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Journal of Clinical Microbiology, January 2009, p. 245-246, Vol. 47, No. 1
0095-1137/09/$08.00+0     doi:10.1128/JCM.01452-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Controlled Evaluation of Bactec Peds Plus/F and Bactec Lytic/10 Anaerobic/F Media for Isolation of Salmonella enterica Serovars Typhi and Paratyphi A from Blood{triangledown}

Megan E. Reller,1* Anita K. M. Zaidi,2 Shazia Sultana,2 Shazia Azeem,2 Beenish Hanif,2 Shahida Qureshi,2 Rumina Hasan,2 Zulfiqar Bhutta,2 Rehana Akhter,3 and Donald A. Goldmann1

Department of Medicine, Children's Hospital Boston, Boston, Massachusetts,1 Departments of Pediatrics and Pathology, Aga Khan University, Karachi, Pakistan,2 National Institute for Child Health, Karachi, Pakistan3

Received 29 July 2008/ Returned for modification 2 September 2008/ Accepted 6 November 2008


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ABSTRACT
 
We compared anaerobic lytic (AL) and pediatric aerobic resin-containing (Peds Plus/F) blood culture media for the isolation of Salmonella enterica serotype Typhi or Paratyphi A from children. The yields from AL and Peds Plus/F media were the same with equal volumes of blood, but recovery was faster from AL medium than Peds Plus/F medium (10.7 and 16.4 h, respectively) (P < 0.001).


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TEXT
 
Salmonella enterica serotype Typhi causes an estimated 16 million illnesses per year with 600,000 deaths globally (9). S. enterica serotypes Typhi and Paratyphi A are the most-common causes of community-acquired bacteremia in South Asia; children are affected disproportionately, with high mortality under age 5 years (1, 7, 11). Enteric (typhoid) fever cannot be clinically distinguished from other causes of acute febrile illness in areas of endemicity (9). Accurate microbiological diagnosis currently depends on culture of blood, since culture of bone marrow is rarely done now and most children are treated as outpatients. The Bactec Peds Plus/F (PP; BD Diagnostics-Diagnostic Systems, Sparks, MD) bottle, an aerobic blood culture medium with resins, is a commercial pediatric bottle commonly used worldwide. The standard recommendation for culturing blood in a single PP bottle is based on its demonstrated superior recovery of pathogens such as Streptococcus pneumoniae and the infrequency of anaerobic pathogens in children in North America (14).

We hypothesized that the optimal pediatric bottle for North America might not be best for South Asia and that an anaerobic lytic bottle might theoretically be better for the recovery of S. enterica serotypes Typhi and Paratyphi A in areas of the world where Salmonella organisms are the most-common pathogens recovered from blood. Although Salmonella bacteria are facultative anaerobes, isolates requiring strict anaerobic conditions for growth have been reported (6). Furthermore, the historic superiority of culture of bone marrow (sensitivity, 80% to 95%) over culture of blood (sensitivity, 60% to 80%) has been attributed to recovery of intracellular bacilli from mononuclear phagocytes (5, 9, 12). Recent studies from Vietnam suggest that ~66% of bacteria in blood are also harbored within phagocytes, and thus, lysis of circulating macrophages in blood might improve the yield of blood cultures (9). Because inadequate blood sampling is frequent in pediatrics and could confound the comparison of media, we undertook a volume-controlled evaluation of PP versus Bactec lytic/10 anaerobic/F (AL) (BD Diagnostics-Diagnostic Systems) media to assess the yield and time to detection of Salmonella from the blood of children. For our study site, we chose Karachi, Pakistan, since S. enterica serotypes Typhi and Paratyphi A are the most-common causes of pediatric bacteremia in Pakistan (2) and the presence of a state-of-the-art clinical microbiology laboratory at Aga Khan University Hospital enabled the comparison of these media. The study was approved by ethical review boards at both the Children's Hospital Boston and Aga Khan University.

(This work was presented in part as abstract 48 at the 55th Annual Meeting of the American Society for Tropical Medicine and Hygiene, Atlanta, GA, 13 November 2006 [10a].)

Children from ≥1 to 15 years of age with suspected enteric fever (history of ≥3 days of undifferentiated fever, no hospitalization in the previous 3 days, and a documented temperature of ≥38°C) presenting to the Aga Khan University Hospital, a primary care clinic in a low-income community, or to Karachi's large public sector referral children's hospital (National Institute for Child Health) were eligible if assessed by usual providers to require a blood culture and if consent could be obtained during daytime hours by the study doctor. Age-appropriate volumes of blood (3 ml for 1- to 3-year-olds and 4.5 ml for >3- to 15-year-olds) were obtained by a single aseptic venipuncture. Equal volumes of blood were inoculated into each of paired, preweighed PP and AL bottles. When bone marrow cultures were indicated clinically, aspirated bone marrow was divided between a second set of PP and AL bottles.

Paired bottles were transported within 3 h of collection to the Aga Khan Hospital's clinical microbiology laboratory, where they were weighed to the nearest 0.01 g before being loaded into a Bactec 9240 series automated blood culture instrument. Contaminants were assessed according to published criteria (13). Paired volumes were considered to be equal if within 50% of each other for volumes of <5 ml and within 20% of each other for volumes of ≥5 ml (10) The gold standard for diagnosis of enteric fever was isolation of S. enterica serotype Typhi or Paratyphi A from either bottle or both, since Salmonella bacteria are always pathogenic when recovered from blood. Salmonella isolates were identified biochemically and were typed with specific antisera (2). Statistical analyses were performed with STATA 9 statistical software; McNemar's modified chi-square test was used to assess yield and the Wilcoxon matched-pairs signed-rank test for time to detection.

Of 817 paired blood cultures submitted from 817 patients over 12 months, 46 (5.6%) grew pathogens (39 S. enterica serotype Typhi and 7 S. enterica serotype Paratyphi A) and 36 (4.4%) grew contaminants (including coagulase-negative staphylococci and gram-positive rods). No isolates of Streptococcus pneumoniae or Haemophilus influenzae were found. The two media were comparable for the recovery of S. enterica serotypes Typhi and Paratyphi A (Table 1). The median volume of blood cultured in the PP and AL bottles was 1.86 ml (intraquartile range, 1.53 to 2.33) and 1.96 ml (intraquartile range, 1.67 to 2.45), respectively. All isolates were recovered from <5 ml of blood (maximum of 4.90 ml in the PP and 4.12 ml in the AL), so Table 1 represents comparable volumes within 50%. If only sets that are within 20% are considered to be equal volumes, 17 isolates grew in both bottles and 2 each in PP or AL only. When recovered from both bottles, the median times to detection of S. enterica serotype Typhi and S. enterica serotype Paratyphi A were 16.4 h (interquartile range, 11.8 to 22 h) for PP and 10.7 h (interquartile range, 8.8 to 16 h) for AL, respectively (P < 0.001). Of the 10 patients who had both bone marrow and blood cultures, 2 had S. enterica serotype Typhi isolated only from bone marrow and not from blood in either PP or AL bottles; the other 8 were negative. Multidrug (ampicillin, chloramphenicol, and co-trimoxazole) resistance was found in 15 of 39 (38.5%) isolates of Salmonella enterica serotype Typhi and none of the 7 isolates of S. enterica serotype Paratyphi A. All isolates were susceptible to ceftriaxone and ciprofloxacin by current CLSI interpretive criteria (3), although resistance to nalidixic acid was found in 18 (46.2%) S. enterica serotype Typhi isolates and 2 (28.6%) S. enterica serotype Paratyphi A isolates.


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  		TABLE 1. Comparative yields of Salmonella from PP and AL blood culture bottles

In conclusion, we found that S. enterica serotypes Typhi and Paratyphi A were the most frequent isolates from blood in Pakistani children with suspected enteric fever, which suggests that our clinical criteria for enrollment were specific for enteric fever in this population. We found that the AL bottle was not superior to PP for the recovery of S. enterica serotypes Typhi and Paratyphi A, although it achieved results faster. Because we enriched our sample with those suspected clinically to have enteric fever and enrolled at two hospitals during 12 months, our sample size for S. enterica serotype Typhi was larger than is usually reported for any one organism in a study designed to compare two different media (15). One must choose a medium formulation based on the total spectrum of pediatric bloodstream pathogens in a population. Since the anaerobic lytic medium and other lytic media that contain saponin have been shown to have reduced recovery of S. pneumoniae (4), and pneumococci do cause pediatric bacteremia in Pakistan (8), we conclude that PP would be a better overall choice for the evaluation of pediatric bacteremia in Pakistan, as it is in North America.


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ACKNOWLEDGMENTS
 
This work was made possible by a Burroughs Wellcome Fund-The Ellison Medical Foundation-American Society of Tropical Medicine and Hygiene Postdoctoral Fellowship in Tropical Infectious Diseases and a Glaser Foundation Glaser Pediatric Research Scholar Award (M.E.R.).

We thank BD Diagnostics-Diagnostic Systems for donating blood culture bottles and the microbiology staff at the Aga Khan University Hospital for their assistance.


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FOOTNOTES
 
* Corresponding author. Present address: Medical Microbiology Division, Department of Pathology, Meyer B1-193, The Johns Hopkins Hospital, 600 N. Wolfe St., Baltimore, MD 21287-7093. Phone: (410) 955-5077. Fax: (410) 614-8087. E-mail: mreller1{at}jhmi.edu Back

{triangledown} Published ahead of print on 12 November 2008. Back


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Journal of Clinical Microbiology, January 2009, p. 245-246, Vol. 47, No. 1
0095-1137/09/$08.00+0     doi:10.1128/JCM.01452-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.




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