Isolation of Schineria sp. from a man.

To the Editor: Schineria larvae has been isolated from maggots of the fly Wohlfahrtia magnifica (1), which cause myiasis in animals and people in Eurasia and northern Africa. In industrialized nontropical countries, a range of species in the order Diptera cause facultative myiasis in patients with neglected wounds (2). Since the recent description of S. larvae, Schineria sp. isolates and clones have been detected in diverse environmental and animal sources, but in all cases a relation with flies could be established. We describe a case of bacteremia due to Schineria sp. in a human patient with myiasis.

In July 2005, a 39-year-old homeless man with medical history of polyneuropathy related to alcohol abuse was examined at Montpellier Hospital, Montpellier, France, and found to be in poor general health and to have an abnormal electrocardiogram, mild fever (38[degrees]C), metabolic disorders, increased C-reactive protein (254 mg/L) and fibrinogen (18.23 [micro]mol/L), and a normal leukocyte count (7.8 x [10.sup.9]/L). Removal of his shoes and socks, which he had worn continuously for 2 months, showed advanced maceration of his feet (trench foot) with wounds invaded by maggots. The following organisms were found in wound samples: Proteus mirabilis, Providentia stuartii, group G Streptococcus, Streptococcus sp., and Enterococcus sp. Aerobic blood culture, after 2 days of incubation, was positive for a gram-negative rod, strain ADV1107. 05. Subculture on MacConkey medium showed positive reactions for oxidase, catalase, and gamma-glutamyltransferase. Positive malate reaction with API 20NE system (bioMerieux, Marcy l'Etoile, France) identified the strain as Oligella urethralis, whereas VITEK2 (bioMerieux) with ID-GN card failed to identify the strain. Disk diffusion assay showed the strain to be susceptible to [beta]-lactams, aminoglycosides, fluoroquinolones, tetracyclines, erythromycin, rifampin, and colistin but resistant to nalidixic acid and fosfomycin. Local therapy of debridement, bandaging, and sulfadiazin argentic, along with systemic antimicrobial therapy (ofloxacin 400 mg/day plus cefotaxime 6 g/day) for 2 weeks, led to clinical improvement and sterilization of the blood cultures. The local therapy was continued, and ofloxacin (400 mg/day) was prescribed for 15 days while the patient was in a rehabilitation center.

In October 2005, the patient was readmitted with the same symptoms. P. mirabilis, group A and group G streptococci, Morganella sp., Bacteroides fragilis, and Candida albicans were cultured from maggot-invaded wounds. Aerobic blood culture, after 1 day of incubation, was positive for strain ADV4155.05, which displayed the same phenotype as strain ADV1107.05 except for tetracycline resistance. Clinical improvement was observed after 2 weeks of the same local and systemic treatments as initially prescribed. The patient was transferred to an addiction care center and received oral antimicrobial therapy (ciprofloxacin 500 mg/day plus amoxicillin/clavulanic acid 3 g/day) for 20 days.

The 16S rDNA amplification and sequencing were performed with universal primers 27f and 1492r as described (3). The 1,414-bp sequences of the 2 isolates were identical and showed similarity level of 99.6% with the sequence of Schineria sp. 010793816 isolated from human urine (M. Vaneechoutte, pers. comm.) but only 98.3% with S. larvae L1/[68.sup.T] 16S rDNA. This finding differed from the biochemical identification and underlined the usefulness of sequencing to precisely identify gram-negative bacilli that assimilate only a few sugars. Phylogenetic analysis linked the 2 strains to the genus Schineria in the class Gamma Proteobacteria (Figure). However, whether the isolates are species S. larvae remains in doubt. Enterobacterial repetitive intergenic consensus-PCR and repetitive extragenic palindromic-PCR fingerprints (6) showed that the 2 strains were unrelated, thereby demonstrating that the second episode of bacteremia was a reinfection with a new strain and not a relapse.

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The 16S rDNA of our isolates is most related to an uncultured bacterium found in swine waste (7), but its presence in such an environment could be correlated with fly larvae proliferation. Because of the lifestyle of Schineria sp., thinking that the strains in our patient originated from his wounds' maggots is reasonable. Unfortunately, the maggots were thrown away and could be neither analyzed nor identified. Schineria sp. could not be cultivated from the patient's wounds, perhaps because of its close association to larvae or to the abundant associated flora. Despite the presence of virulent bacteria in the wounds, Schineria sp. was the sole bacterium recovered from blood during the 2 independent episodes of bacteremia, which suggests its invasive potential. Invasiveness may be enhanced by the maggots' acting as a vector as they move through the necrotic tissues toward the bloodstream. Invasiveness also may be a specific characteristic of the bacterium; phylogenetic methods placed the genus Schineria in a subgroup that included human pathogens Cardiobacterium, Francisella, Coxiella, and Legionella. Indeed, all the phylogenetic methods tested excluded Schineria spp. of the family Xanthomonadaceae (Figure), which conflicts with current classification (8).

No report has described bacteremia following myiasis with facultative parasites, but investigations of bacteria in reported myiasis cases have been conducted on cutaneous lesions and never on blood (9). Because of this association between maggots and risk for bacteremia, blood cultures should be performed for patients with myiasis and poor hygiene. Moreover, germ-free maggots bred for biosurgery use (10) should be checked, by molecular methods, for the absence of Schineria sp.

Laurent Roudiere, * Helene Jean-Pierre, ([dagger]) Christelle Comte, ([dagger]) Isabelle Zorgniotti, * Helene Marchandin, ([dagger]) and Estelle Jumas-Bilak *

* University Montpellier 1, Montpellier, France; and ([dagger]) Centre Hospitalier Universitaire de Montpellier, Montpellier, France

References

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(2.) Delhaes L, Bourel B, Scala L, Muanza B, Dutoit E, Wattel F, et al. Case report: recovery of Calliphora vicina first-instar larvae from a human traumatic wound associated with a progressive necrotizing bacterial infection. Am J Trop Med Hyg. 2001;64:159-61.

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(5.) Guindon S, Gascuel O. A simple, last, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol. 2003;52:696-704.

(6.) Versalovic J, Koeuth T, Lupski JR. Distribution of repetitive DNA sequences in eubacteria and application to fingerprinting of bacterial genomes. Nucleic Acids Res. 1991;19:6823-31.

(7.) Juteau P, Tremblay D, Villemur R, Bisaillon JG, Beaudet R. Analysis of the bacterial community inhabiting an aerobic thermophilie sequencing batch reactor (AT-SBR) treating swine waste. Appl Microbiol Biotechnol. 2004;66:115-22.

(8.) Saddler GS, Bradbury JF. Family I. Xanthomonadaceae fam. nov. In: Brenner DJ, Krieg NR, Staley JY, Garrity GM, editors. Bergey's manual of systematic bacteriology. 2nd ed. Vol. 2. New York: Springer; 2005. p. 63.

(9.) Mallon PW, Evans M, Hall M, Bailey R. Something moving in my head. Lancet. 1999;354:1260.

(10.) Nuesch R, Rahm Ca Rudin W, Steffen I, Frei R, Rufli T, et al. Clustering of bloodstream infections during maggot debridement therapy using contaminated larvae of Protophormia terraenovae. Infection. 2002;30:306-9.

Address for correspondence: Estelle Jumas-Bilak, University Montpellier 1, Laboratoire de Bacteriologie, EA 3755, Faculte de Pharmacie, 15 avenue Charles Flahault, BP14491, 34093 Montpellier, CEDEX 5 France; email: [e-mail]