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PEDIATRICS Vol. 107 No. 4 April 2001, pp. 775-776

EXPERIENCE AND REASON:
Bacteremic Infection With Pediococcus: Vancomycin-Resistant Opportunist



    ABSTRACT
Top
Abstract
Introduction
Discussion
References

Pediococci are recently recognized Gram-positive human pathogens, resistant to vancomycin and generally susceptible to penicillin. Infection in adults has been seen in patients with chronic underlying conditions as well as those with previous abdominal surgery. Two previous infants with congenital gastrointestinal malformations requiring surgical correction have been reported with sepsis attributable to Pediococcus sp. We report a third infant born with gastroschisis who developed Pediococcus bacteremia and meningitis 3 months after surgery, and speculate regarding the role of probiotics in the pathogenesis of this infection.

 Key words:  Pediococcus, vancomycin resistance, bacteremia, lactobacilli, gastroschisis, probiotics.

Pediococci, recently recognized human pathogens, are members of the lactic acid-producing family of facultatively anaerobic bacteria.1,2 This group of organisms, which also includes Lactobacillus and Leuconostoc species, importantly is resistant to vancomycin and may be misidentified as viridans streptococci.3,4 We present an infant born with gastroschisis who developed Pediococcus sp septicemia, and probable meningitis, to alert pediatricians to these pathogens and their apparent association with underlying gastrointestinal abnormalities.


    CASE REPORT

A 34-week gestation female was delivered by cesarean section to a 22-year-old, group B streptococcal bacteriuric woman. The pregnancy was complicated by the presence of fetal gastroschisis. The infant had Apgar scores of 4 and 9, at 1 and 5 minutes, respectively. She was intubated and ventilated; intravenous fluids were begun. Blood cultures were obtained and parenteral ampicillin and gentamicin initiated.

Physical examination on admission to the neonatal intensive care unit revealed an infant weighing 2108 g, a head circumference of 31.5 cm, and length of 44.5 cm. Her exteriorized bowel was wrapped with saline-soaked lap pads. At 2 hours of age, repair of the infant's gastroschisis, release of constricting Ladd's bands, resection of ischemic, atretic ascending colon, and placement of colostomy, and Broviac catheter were performed.

At 2 days of life, the infant was taken back to the operating room, where additional necrotic colon and distal ileum were resected. Antibiotics were changed to vancomycin, cefotaxime, and clindamycin, which were administered for a total of 10 days. Enteral feedings with Pregestimil (Mead Johnson, Evansville, IN) were begun on the infant's ninth day of life, but interrupted on multiple occasions because of bilious emesis and gastrointestinal hemorrhage.

On day 43 of life, blood culture yielded Enterococcus faecalis, for which the infant received 10 days of ampicillin and gentamicin therapy. When she was 2 months old, stool culture revealed no normal enteric Gram-negative rods. Oral lactobacilli (Bacid) from capsules were added to her formula in an attempt to reintroduce normal bowel flora. Two episodes of coagulase-negative staphylococcal sepsis were treated with vancomycin and subsequent replacement of the Broviac catheter.

At 3 months of age, the infant now without a Broviac catheter in place, developed lethargy and irritability, marked icterus associated with elevated direct bilirubin (peak: 10.9 mg/dL) and alanine aminotransferase (peak: 268 units/L), and metabolic acidosis. Lumbar puncture, after initiation of antibiotics, showed cloudy cerebrospinal fluid (CSF) with 43 white blood cells/mm3 (42% segmented and 32% band forms), protein of 47 mg/dL, and glucose of 60 mg/dL. Gram-positive cocci, sensitive (by Kirby-Bauer disk diffusion test) to chloramphenicol and clindamycin, intermediate to penicillin (minimal inhibitory concentration [MIC] = 1 µg/mL) and resistant to vancomycin (MIC >1 µg/mL) and ceftriaxone (MIC >1 µg/mL), were isolated from blood culture. The organisms were catalase-, pyrrolidone carboylyl peptidase-, and arginine dihydrolase-negative; bile eusculin- and group D streptococcal antigen-positive. They were identified as Pediococcus sp. The CSF was sterile. The infant received 21 days of intravenous ampicillin and gentamicin with normalization of her neurologic examination and improved hepatic function. Intercurrent pseudomembranous enterocolitis was treated with a 10-day course of metronidazole. She was discharged from the hospital on oral formula at 159 days of age, weighing 4416 g.

Subsequent culture of 2 Bacid capsules' contents obtained from the hospital pharmacy yielded Lactobacillus acidophilus and E faecium, the latter susceptible to vancomycin. A sample of the Pregestimil formula was sterile.


    DISCUSSION
Top
Abstract
Introduction
Discussion
References

Pediococcus spp are Gram-positive, catalase- and oxidase-negative cocci that may be either alpha -hemolytic or nonhemolytic.3 Because of their reaction with group D streptococcal antisera, they may be overlooked and erroneously identified as streptococci. Suspicion should be aroused, however, by their susceptibility to penicillin and ampicillin (and generally aminoglycosides) and resistance to vancomycin.1-5

Originally thought to be clinically insignificant, pediococci have been associated with human infection since 1987.1 Of the 14 previously reported cases of bacteremia,6-11 only 2 were in children.7,10 A 2-week-old infant had jejunoileal atresia and a 2-month-old had gastroschisis, as did the 3-month-old in this report. Infection in adults has also been seen in individuals with previous abdominal surgery and tube-feedings, as well as with chronic underlying conditions including cancer, diabetes, pulmonary and cardiovascular disease, and, most recently, pregnancy. We strongly suspect that our infant had concomitant Pediococcus meningitis based on her CSF pleocytosis and symptomatology, which resolved with antibiotic therapy. This diagnosis remains speculative because her CSF was obtained after initiation of antimicrobials and was sterile.

Pediococci are found on fermenting vegetables and in silage, dairy products, and beer. They have been used in the processing and preservation of selected meats, vegetables, cheeses, and soy products.6,7 Human isolates have been obtained from saliva, stool, urine, sputum, wounds, abscesses, and blood.7,11 We attempted to delineate the source of our patient's Pediococcus, but we were unsuccessful. Culture of the Pregestimil was sterile. Cultures of the contents of 2 lactobacillus (Bacid) capsules (as had been added to her formula), however, revealed L acidophilus as well as E faecium. The latter isolate was of initial concern because of its increasing association with both nosocomial infection and high-level vancomycin resistance.4 Fortunately, this isolate was vancomycin-susceptible. Unfortunately, however, the original formulae and capsules administered to this patient were not available for these cultures, performed 5 months after the episode of Pediococcus bacteremia, 2 months after the infant's discharge. Lactobacillus casei sps rhamnosus has previously been shown to decrease the incidence of traveler's diarrhea, duration and severity of rotavirus diarrhea, and incidence and duration of antibiotic-associated diarrhea.12 We urge caution, however, in using commercially available probiotics in children and adults with gastrointestinal abnormalities, pending additional study. We would also suggest that frequent use of vancomycin in hospitalized, seriously ill patients may lead to increased recovery of vancomycin-resistant organisms, including pediococci. Knowledge of their unusual antimicrobial susceptibility pattern will facilitate bacterial identification, allow institution of appropriate antibiotic therapy, and prevent initiation of costly isolation procedures, as are used for vancomycin-resistant enterococci.


    ACKNOWLEDGMENTS

We thank Marcia L. Lincoln and Dr Kenneth Ryan of the University Medical Center Microbiology Laboratory in Tucson, Arizona, and Richard Luoma, Lynn Williamson, and Patricia Fisher of Benefis HealthCare Microbiology Laboratory in Great Falls, Montana, for their assistance with laboratory studies. Amy O'Brien aided in manuscript preparation.

Leslie L. Barton, MD
Department of Pediatrics
and Steele Memorial Children's Research Center
University of Arizona
Tucson, AZ 85724-5073

Evelyn D. Rider, MD
Ronald W. Coen, MD
Benefis HealthCare and Great Falls Clinic
Great Falls, MT 59405


    FOOTNOTES

Received for publication Mar 23, 2000; accepted May 16, 2000.

Reprint requests to (L.L.B.) 1501 N Campbell Ave, Box 245073, Tucson, AZ 85724-5073. E-mail: llb{at}peds.arizona.edu


    ABBREVIATIONS

CSF, cerebrospinal fluid; MIC, minimal inhibitory concentration.


    REFERENCES
Top
Abstract
Introduction
Discussion
References
  1. Colman G, Efstratiou A Vancomycin-resistant leuconostocs, lactobacilli and now pediococci. J Hosp Infect 1987; 10:1-3 [CrossRef][Medline]
  2. Ruoff KL, Kuritzkes DR, Wolfson JS, Ferraro MJ Vancyomycin-resistant gram-positive bacteria isolated from human sources. J Clin Microbiol 1988; 26:2064-2068 [Abstract/Free Full Text]
  3. Riebel WJ, Washington JA Clinical and microbiologic characteristics of pediococci. J Clin Microbiol 1990; 28:1348-1355 [Abstract/Free Full Text]
  4. Nelson RRS Intrinsically vancomycin-resistant Gram-positive organisms: clinical relevance and implications for infection control. J Hosp Infect 1999; 42:275-282 [CrossRef][Medline]
  5. Swenson JM, Facklam RR, Thornsberry C Antimicrobial susceptibility of vancomycin-resistant Leuconostoc, pediococcus, and Lactobacillus species. Antimicrob Agents Chemother 1990; 34:543-549 [Abstract/Free Full Text]
  6. Golledge CL, Stingemore N, Aravena M, Joske D Septicemia caused by vancomycin-resistant Pediococcus acidilactici. J Clin Microbiol 1990; 28:1678-1679 [Abstract/Free Full Text]
  7. Mastro TD, Spika JS, Lozano P, Appel J, Facklam RR Vancomycin-resistant Pediococcus acidilactici: nine cases of bacteremia. J Infect Dis 1990; 161:956-960 [Medline]
  8. Corcoran GD, Gibbons N, Mulvihill TE Septicaemia caused by Pediococcus pentosaceus: a new opportunistic pathogen. J Infect 1991; 23:179-182 [CrossRef][Medline]
  9. Sire JM, Donnio PY, Mesnard R, Pouëdras P, Avril JL Septicemia and hepatic abscess caused by Pediococcus acidilactici. Eur J Clin Micribiol Infect Dis 1992; 11:623-625
  10. Atkins JT, Tillman J, Tan TQ, Demmler GJ Pediococcus pentosaceus catheter-associated infection in an infant with gastroschisis. Pediatr Infect Dis J 1994; 13:75-76 [Medline]
  11. Sarma PS, Mohanty S Pediococcus acidilactici pneumonitis and bacteremia in a pregnant woman. J Clin Microbiol 1998; 36:2392-2393 [Free Full Text]
  12. Vanderhoof JA, Whitney DB, Antonson DL, Hanner TL, Lupo JV, Young RJ Lactobacillus GG in the prevention of antibiotic-associated diarrhea in children. J Pediatr 1999; 135:564-568 [CrossRef][Medline]

Pediatrics (ISSN 0031 4005). Copyright ©2001 by the American Academy of Pediatrics



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