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Methicillin-susceptible, doxycycline-resistant Staphylococcus aureus, Cote d'Ivoire.

We report 2 outbreaks of Panton-Valentine leukocidin--positive, doxycycline-resistant, methicillin-susceptible Staphylococcus aureus infections in French soldiers operating in Cote d'Ivoire. In a transssectional survey, nasal carriage of this strain was found in 2.9% of 273 soldiers about to be sent to Cote d'Ivoire and was associated with prior malaria prophylaxis with doxycycline.

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Staphylococcus aureus strains that produce Pantonlentine leukocidin (PVL) have been shown to be associated with community-acquired infections such as skin and soft tissue infections and necrotizing pneumonia (1). A limited number of PVL-positive, methicillin-resistant S. aureus (MRSA) clones have recently emerged globally (2) and have been described as causing epidemic community-acquired infections (3,4). In contrast, PVL-positive, methicillin-susceptible S. aureus (MSSA) corresponds to many diverse clones (5) that may cause sporadic infections with limited dissemination. We describe severe staphylococcal infections due to a clone of doxycycline-resistant, PVL-positive (doxyR-PVL+) MSSA in soldiers who served in Cote d'Ivoire.

The Study

During 2004 and 2005, 4 soldiers with recurrent cutaneous infections related to doxycycline-resistant MSSA (DoxyR-MSSA) visited the Centre Hospitalier Universitaire in Clermont-Ferrand, France. The soldiers belonged to 2 companies, A and B, based at different places in France (Clermont-Ferrand and Brives, respectively), and had been to Cote d'Ivoire at 2 distinct periods. In October 2005, a health warning was sent to French military authorities. We conducted retrospective interviews of soldiers in company A and performed a transsectional nasal carriage survey of 273 soldiers in company B, who were about to be sent to Cote d'Ivoire. We defined case-patients as soldiers who had had at least 1 cutaneous infection during or after their time in Cote d'Ivoire. Information was collected from company A case-patients by telephone interview and, for hospitalized soldiers, chart review.

When available, staphylococcal strains were sent to the French National Reference Centre for Staphylococci in Lyon, France. Sequences specific for staphylococcal enterotoxin genes (sea-e, seh, sek, sem, sel, and seo), the PVL genes (lukS-PV-lukF-PV), and accessory gene regulator alleles (agr 1-4) were detected by PCR (6-8). Fingerprinting by pulsed-field gel electrophoresis, spa typing, and multilocus sequence typing were performed as described (9).

Company A comprised 70 French soldiers who had taken doxycycline, 100 mg per day, for malaria prophylaxis while in Cote d'Ivoire (August-November 2003). During their 3 weeks in training camp, each soldier stayed in 1 of 4 rooms. Of 13 soldiers who stayed in room 3, 8 (61.5%) reported having had at least 1 cutaneous infection while in Cote d'Ivoire, compared with none of 2 soldiers in room 1, 1 (8%) of 13 in room 2, and 7 (18%) of 39 in room 4. Two soldiers (1A and 2A) visited our clinic in November 2004 for treatment of abscesses that required surgical debridement for 1 year. For each patient, doxyR-MSSA was isolated from the abscess in a site acting as a reservoir (nasal or perianal skin). Their conditions were successfully treated with topical application of mupirocin to the reservoir site. No recurrence occurred after a year. Another soldier from company A (patient 3A) was found to be an asymptomatic nasal carrier of doxyR-MSSA. His wife (patient 4A) experienced several recurrent doxyR-MSSA abscesses, including 1 that was debrided at our hospital in January 2004.

In company B, [approximately equal to]70 soldiers had served in Cote d'Ivoire during October 2004-February 2005 and stayed for 6 weeks in the same training camp that company A stayed in the year before. Two soldiers (IB and 2B) visited our hospital. Patient 1B was hospitalized with furunculosis and osteomyelitis of the left femoral diaphysis 5 months after attending training camp (and 1 month after he returned to France). Surgically removed bone samples contained S. aureus isolates that had profile characteristics similar to those obtained from furuncles (Figure). Patient 2B visited our clinic in March 2005 for recurrent axillary abscesses due to the same clone of MSSA. He did not experience recurrence after MSSA eradication from the nasal and axillary reservoirs. In September 2005, recurrent furunculosis developed in a third soldier (3B), who had not gone to Cote d'Ivoire but who was in close contact with soldiers returning from there. In April 2005 and December 2005, doxyR-MSSA--related recurrent abscesses developed in his wife and their 5-year-old child.

[FIGURE OMITTED]

To estimate the prevalence of PVL-positive MSSA carriage in soldiers, nasal culture specimens were collected on May 9 and 10, 2005, from 273 soldiers in company B (a total of 1,100 soldiers) who were about to be sent to Cote d'Ivoire. Of these 273 soldiers, 98 (35.9%) were colonized with S. aureus. Among them, 28 (10%) were carriers of PVL--doxyR-MSSA and 8 (2.9%) were carriers of PVL+doxyR-MSSA. These PVL+doxyR-MSSA isolates belonged to the same clone as those found in patients 2A, 1B, and 2B. All the MSSA isolates were considered to belong to the same clone as they shared a large core of common genetic characteristics (Figure). All PVL+doxyR-MSSA carriers had been to Cote d'Ivoire and had taken doxycycline for malaria prophylaxis (Table).

Conclusions

We characterized 2 outbreaks caused by the same clone of PVL+doxyR-MSSA. These outbreaks occurred in 2 military companies that served in Cote d'Ivoire at different times and whose soldiers received doxycycline for malaria prophylaxis. This epidemic MSSA clone was responsible for infections traditionally associated with PVL, mainly skin and soft tissue infections, but also deep-seated infections such as severe osteomyelitis. Since these outbreaks, several similar cases affecting different companies who had been to Cote d'Ivoire have been reported to the French military authorities (Figure). Another striking feature was the spread of the clone within families after the soldiers' return from Cote d'Ivoire. This virulent clone has already disseminated to different continents. Analysis of the database of the French National Reference Centre for Staphylococci (which contains the characteristics of [approximately equal to]5,000 S. aureus strains worldwide) found 25 methicillin susceptible isolates with identical toxin gene content and agr type from unrelated patients from Africa, Polynesia, and France (data not shown).

Our study has limitations. The investigation conducted in company A was retrospective, so we could not control for other pathogens. Recall bias may have occurred, and the incidence of cutaneous infections in company A could have been underestimated. However, epidemiologic links between case-patients were well established. Only case-patients who visited our hospital were documented, but they enabled recognition of the outbreaks. Recent similar cases in soldiers who visited our hospital for PVL+doxyR-MSSA cutaneous infections after their return from Cote d'Ivoire confirm that the strain is still disseminating and is strongly associated with a stay in that country (Figure).

The infecting MSSA is remarkable in its resistance to doxycycline, which may favor selection of a preexisting PVL+doxyR-MSSA in cartier soldiers who are given a prophylactic dose of doxycycline. Because the 2 companies had no contact with each other before, during, and after their stay in Cote d'Ivoire, we think that the S. aureus clone persists in Cote d'Ivoire. Transmission may have occurred through the persistence of the strain in the environment of the training camp in Cote d'Ivoire, where hygiene conditions were poor (4 rooms, 3 showers, 3 lavatories for [approximately equal to]70 soldiers). However, the relatively high prevalence of PVL-positive MSSA carriage found in our study suggests that nasal carriage may play an important role in transmission of these highly virulent microorganisms.

References

(1.) Lina G, Piemont Y, Godail-Gamot F, Bes M, Peter MO, Gauduchon V, et al. Involvement of Panton-Valentine leukocidin--producing Staphylococcus aureus in primary skin infections and pneumonia. Clin Infect Dis. 1999;29:1128-32.

(2.) Vandenesch F, Naimi T, Enright MC, Lina G, Nimmo GR, Heffernan H, et al. Community-acquired methicillin-resistant Staphylococcus aureus carrying Panton-Valentine leukocidin genes: worldwide emergence. Emerg Infect Dis. 2003;9:978-84.

(3.) Boubaker K, Diebold P, Blanc DS, Vandenesch F, Praz G, Dupuis G, et al. Panton-Valentine leukocidin and staphyloccoccal skin infections in schoolchildren. Emerg Infect Dis. 2004; 10:121-4.

(4.) Favero MS. Outbreaks of community-associated methicillin-resistant Staphylococcus aureus skin infections. Infect Control Hosp Epidemiol. 2003;24:787.

(5.) Chini V, Petinaki E, Foka A, Paratiras S, Dimitracopoulos G, Spiliopoulou I. Spread of Staphylococcus aureus clinical isolates carrying Panton-Valentine leukocidin genes during a 3-year period in Greece. Clin Microbiol Infect. 2006; 12:29-34.

(6.) Lina G, Piemont Y, Godail-Gamot F, Bes M, Peter MO, Gauduchon V, et al. Involvement of Panton-Valentine leukocidin--producing Staphylococcus aureus in primary skin infections and pneumonia. Clin Infect Dis. 1999;29:1128-32.

(7.) Diep BA, Sensabaugh GF, Somboona NS, Carleton HA, Perdreau-Remington E Widespread skin and soft-tissue infections due to two methicillin-resistant Staphylococcus aureus strains harboring the genes for Panton-Valentine leucocidin. J Clin Microbiol. 2004; 42:2080-4.

(8.) Dufour P, Gillet Y, Bes M, Lina G, Vandenesch F, Floret D, et al. Community-acquired methicillin-resistant Staphylococcus aureus infections in France: emergence of a single clone that produces Panton-Valentine leukocidin. Clin Infect Dis. 2002;35:819-24.

(9.) Gillet Y, Issartel B, Vanhems P, Fournet JC, Lina G, Bes M, et al. Association between Staphylococcus aureus strains carrying gene for Panton-Valentine leukocidin and highly lethal necrotising pneumonia in young immunocompetent patients. Lancet. 2002;359: 753-9.

Address for correspondence: Olivier Lesens, Maladies Infectieuses et Tropicales, CHU Clermont-Ferrand, Hotel Dieu, 63000, Clermont-Ferrand, France; email: olesens@chu-clermontferrand.fr

Dr Lesens is an infectious diseases consultant in the Department of Infectious Diseases, Hotel Dieu, Clermont-Ferrand. His scientific interests are epidemiology of S. aureus and vancomycin-resistant enterococci.

Olivier Lesens, * Rachel Haus-Cheymol, ([dagger]) Philippe Dubrous, ([double dagger]) Catherine Verret, ([dagger]) Andre Spiegel, ([dagger]) Richard Bonnet, * Michele Bes, ([section]) Henri Laurichesse, * Jean Beytout, * Jerome Etienne, ([section]) Rene Migliani, ([paragraph]) Jean Louis Koeck, ([double dagger]) and the Working Group on Cutaneous Infections in the Army

* Centre Hospitalier Universitaire, Clermont-Ferrand, France; ([dagger]) Ecole du Val de Grace, Paris, France; (double dagger]) Hopital d'Instruction des Armees Robert-Picque, Bordeaux, France; ([section]) Universite Lyon 1, Lyon, France; and ([paragraph]) Institut de Medecine Tropicale du Service de Sante des Armees, Le Pharo, Marseille-Armees, France
Table. Factors associated with nasal carriage of Staphylococcus
aureus in 273 soldiers (company B) who were about to be sent to
Cote d'Ivoire

 PVL-DoxyR
 PVL+DoxyR S. aureus
 S. aureus ([double
 ([dagger]) dagger])
Variable (n = 8) (n = 34)

Age, y 24.3 25.9
Male (%) 87.5 97.1
Living with health care worker (%) 25.0 26.5
Living with children <16 y (%) 50.0 61.8
Hospitalization within 1 year (%) 0.0 17.6
Fight sport practice# (%) 0.0 5.9
Previous mission in malaria-endemic 100.0 91.2
 area (%)
Previous mission in Cote d'Ivoire (%) 100.0 88.2
Previous doxycycline intake (%) 100.0 88.2

 DoxyS p value
 S. aureus ([paragraph])
 ([section]) (PVL+ vs.
Variable (n = 56) PVL-)

Age, y 24.5 NS
Male (%) 100.0 NS
Living with health care worker (%) 12.5 NS
Living with children <16 y (%) 53.6 NS
Hospitalization within 1 year (%) 17.8 NS
Fight sport practice# (%) 7.1 NS
Previous mission in malaria-endemic 37.5 <0.001
 area (%)
Previous mission in Cote d'Ivoire (%) 30.4 <0.001
Previous doxycycline intake (%) 32.1 <0.001

 p value
 ([paragraph])
 (PVL+DoxyR vs.
Variable PVL-DoxyR)

Age, y NS
Male (%) NS
Living with health care worker (%) NS
Living with children <16 y (%) NS
Hospitalization within 1 year (%) NS
Fight sport practice# (%) NS
Previous mission in malaria-endemic NS
 area (%)
Previous mission in Cote d'Ivoire (%) NS
Previous doxycycline intake (%) NS

* PVL, Panton-Valentine leukocidin; DoxyR, doxycycline resistant;
DoxyS, doxycycline susceptible; NS, not significant.

([dagger]) All methicillin-susceptible S. aureus (MSSA).

([double dagger]) 28 MSSA and 6 methicillin-resistant S. aureus
(MRSA).

([section]) 55 MSSA and 1 MRSA, all PVL-negative.

([paragraph]) Fisher exact test.

# Military exercises that involve physical contact.
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Article Details
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Title Annotation:DISPATCHES
Author:Lesens, Olivier; Haus-Cheymol, Rachel; Dubrous, Philippe; Verret, Catherine; Spiegel, Andre; Bonnet,
Publication:Emerging Infectious Diseases
Article Type:Clinical report
Geographic Code:4EUFR
Date:Mar 1, 2007
Words:1920
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