Methicillin-Resistant Staphylococcus aureus,

Little is known about the epidemiology of methicillin-resistant Staphylococcus aureus (MRSA) in most Pacific Island nations. Relatively high rates of MRSA have been reported in Polynesian people living outside the Pacific Islands. To determine the prevalence and characteristics of MRSA, we assessed wound swabs from 399 persons with skin and soft tissue infection living in Samoa. MRSA was isolated from 9% of study participants; 34 of the 196 S. aureus isolates were MRSA. Five MRSA genotypes were identified; the 3 most common were USA300, the Queensland clone, and a sequence type 1 MRSA strain that shares <85% homology with the sequence type 1 MRSA strain common in the region (WA MRSA-1). The Southwest Pacific MRSA clone was identified but accounted for only 12% of MRSA isolates. The high prevalence of MRSA in Samoa provides impetus for initiatives to improve antimicrobial drug resistance surveillance, infection control, and antimicrobial drug use in Pacific Island nations.

I nfections caused by methicillin-resistant Staphylococcus aureus (MRSA) have become a global health concern during the past 2-3 decades. The epidemiology of MRSA has demonstrated marked geographic variation in the prevalence and genotypes of MRSA (1,2), and recent reports from many parts of the world indicate that the prevalence and diversity of MRSA continue to increase (3,4). Studies of the global epidemiology frequently have not included MRSA obtained from persons living in developing nations.
The prevalence and genetic variation of MRSA infection in most Pacifi c Island nations remain unknown. The only study of MRSA in the Pacifi c was conducted after a report in 2004 of an increased incidence of MRSA infection in Polynesian people in Hawaii (5). This study showed that most MRSA infections in Hawaii were caused by the USA300 MRSA strain (6).
Relatively high rates of MRSA infection have been reported in Polynesian people living outside the Pacifi c Islands region, including in Alaska, Australia, and New Zealand, and have been attributed to infection with the Southwest Pacifi c clone of MRSA (sequence type [ST] 30 SCCmec type IV, also referred to as Western Samoan phage pattern [WSPP] MRSA or the Oceania strain) (7)(8)(9)(10). The Southwest Pacifi c clone of community-associated MRSA was identifi ed in New Zealand in 1992 (11). The fi rst isolate and many subsequent isolates of this strain were from persons in New Zealand who had some association with Samoa. The Southwest Pacifi c MRSA clone has now spread as far as Europe and South America (4,12). This MRSA strain has been postulated to have arisen from a pandemic penicillin-resistant S. aureus strain, known as phage type 80/81, that caused serious hospital-and community-acquired infections during the 1950s (13).
Samoa is an independent nation in the Southwest Pacifi c, with a population of ≈180,000 persons (Samoan Statistics Department, www.spc.int/prism/wstest/index. htm; Figure). Samoa has a small and developing economy predominantly comprising remittances from Samoan persons living overseas, agriculture, and tourism. The gross domestic product per capita was US $2,987.90 in 2008 (http://data.un.org). Life expectancy in Samoa is 74.9 years for women and 68.5 years for men, and the infant mortality rate is ≈22.3 per 1,000 live-born infants. The publicly funded National Health Service is based at the national

Methicillin-Resistant
Staphylococcus aureus, Samoa, 2007Samoa, -2008 referral hospital in Apia; in addition, Samoa has 7 district hospitals (14). Several outreach and integrated community health services provide primary health care services, such as clinics and vaccinations. Samoa gained independence from New Zealand in 1962; a large Samoan population resides in New Zealand. In New Zealand, infections caused by S. aureus, whether methicillin susceptible or resistant, are more common in Maori and Polynesian persons than in other ethnic groups (15)(16)(17). Antimicrobial drug resistance is routinely monitored in New Zealand through testing of bacterial isolates from specimens taken for diagnostic purposes. In 2008, 9% of S. aureus isolates were methicillin resistant, but this rate varied considerably among different parts of the country, with rates as high as 13%-16% in hospitals in the Auckland area (18).
In Samoa, as in many other developing countries, antimicrobial drug resistance is not systematically monitored. The microbiology service at the main public hospital in Apia performs antimicrobial drug susceptibility testing only when specifi cally requested by the treating doctor. This testing is infrequent, and the results are not regularly collated (V. Kini, pers. comm.). Testing for antimicrobial drug susceptibility requires equipment, resources, and a high level of expertise and quality assurance-requirements that are beyond the means of many laboratories in the developing world. If a high rate of antimicrobial drug resistance exists in Samoa, it would substantially affect this relatively poor country with relatively high rates of infectious diseases. We performed a systematic study to assess the prevalence and characteristics of MRSA isolated from wound swabs from persons with skin and soft tissue infection living in Samoa.

Methods
During the summer of 2007-2008, a study investigator (J.A.S.) collected S. aureus isolates from persons with skin and soft tissue infection. Review of patient notes was used to identify hospital patients who had skin lesions. All ambulatory patients who attended a clinic during the visit by J.A.S. and any family members who accompanied them were asked if they had a skin lesion. All persons with a skin lesion were invited to participate in the study; <5 persons declined to participate. At hospitals, participants included inpatients and outpatients, but this information was not recorded. No attempt was made to categorize infections as hospital acquired or community acquired, although the source of the wound was recorded.
All participants had skin and soft tissue infection, but this infection was not always the primary reason for contact with health services. Skin and soft tissue infection was defi ned as increasing pain, warmth, induration, erythema, or purulent discharge. Swabs were collected twice from patients who had separate lesions on the upper and lower body. If a patient had >1 infected site in the same region (e.g., upper body), only the larger lesion was swabbed.
Patient data collected included demographic information (age, sex, occupation, and village of residence) and recent exposure to health services (use of antimicrobial drugs in the last month and contact with health services in last 3 months). We attempted to include persons of different ages, both sexes, and various occupations.
The Lower South Ethics Committee in New Zealand, and the Health Research Council in Samoa gave ethical approval for the study. Participants were given an information sheet about the research and a small card explaining, in Samoan, how to take care of wounds. The study investigator explained the purpose of the study in Samoan, and the consent form was printed in Samoan and in English.
Swabs were taken after the wound was cleaned with sterile water. Swabs were placed into Amies transport media (Fort Richard Laboratories, Auckland, New Zealand), stored on ice, and transported to the laboratory at 1 of the 2 main hospitals. All swabs were processed within 12 hours after collection. Swabs were spread onto sheep blood agar containing aztreonam (6 mg/L) and incubated for 16-24 hours. A catalase test was performed on colonies suspected to be S. aureus, and catalase-positive colonies were identifi ed by using a latex agglutination test (BBL Staphyloslide Latex Test, Becton Dickinson, Sparks, MD, USA). S. aureus isolates were transported on a nutrient agar slope to LabPLUS (Auckland, New Zealand).
In New Zealand, antimicrobial drug susceptibility testing was performed by using disk diffusion for penicillin, and agar dilution breakpoint testing for cotrimoxazole, doxycycline, erythromycin, gentamicin, oxacillin, and vancomycin in accordance with Clinical and Laboratory Standards Institute methods and interpretive standards (19-21). MRSA isolates were tested by disk diffusion for susceptibility to ciprofl oxacin and clindamycin, including inducible clindamycin resistance. Additional fusidic acid and mupirocin disk diffusion susceptibility testing was performed when required to assist with identifi cation of MRSA strains.
MRSA isolates were tested for the genes encoding for Panton-Valentine leukocidin (PVL) by PCR (22). Multilocus sequence typing (23); spa typing (24); and if necessary, pulsed-fi eld gel electrophoresis (PFGE) of SmaI-digested genomic DNA were used to identify and characterize MRSA strains. StaphType software version 1.5 (Ridom GmbH, Würzburg, Germany) was used to assign spa types. We compared spa types by using the BURP (based upon repeat pattern) algorithm and excluding spa types with <5 repeats and setting a maximum cost of 4 between members of a spa group cluster. PFGE banding patterns were analyzed with BioNumerics software version 5.1 (Applied Maths, Saint-Martens-Latern, Belgium) by using the Dice coeffi cient and unweighted pair group method with arithmetic averages, at settings of 0.5% optimization and 1.5% position tolerance.
Categorical data are expressed as proportions and 95% confi dence intervals (CIs), calculated by the modifi ed Wald method. Statistical signifi cance of comparative categorical data was examined by using the χ 2 test.

Results
A total of 423 swabs were obtained from skin and soft tissue infections of 399 persons at 8 locations on the 2 main islands of Samoa (Upolu and Savai'i) and a smaller island, Manono. The 8 locations were the main public hospital in Apia (the capital on Upolu), the main public hospital on Savai'i, 5 district hospitals around the main islands, and community-based clinics on Manono.
Infections in skin and soft tissue were in wounds from falls, cuts, dog bites, car accidents, and burns; as well as boils and carbuncles. Many were described as po'u, a Samoan term for idiopathic tropical ulcer. Twenty-four persons each had swabs from 2 separate lesions. Even though we did not categorize infections as hospital acquired or community acquired, we were able to infer likely place of acquisition from the description of the wound: 20 (5%) of 399 represented infections of surgical sites, which were hospital acquired; 335 (84%) represented communityacquired infections, such as impetigo; po'u; boils; or infections of wounds resulting from dog bites, machete cuts, or assaults. We were not able to further classify the remaining 44 (11%) infections.
Participants lived in 165 villages around Samoa. We detected S. aureus in participants from 102 villages. In terms of place of domicile, MRSA was widespread throughout Samoa and was isolated from persons from 27 villages. There did not appear to be any geographic clustering associated with residence close to the main public hospital in Apia, although MRSA was more likely to be isolated from residents of Upolu, the main island on which Apia is located, than from residents of Savai'i, the less-populated and less-developed island. MRSA was isolated from 11% of participants from Upolu, but from only 3% of participants from Savai'i. Of the 153 MSSA isolates from 187 participants, 124 (81%) isolates were resistant to penicillin, but resistance to any other antimicrobial drug was uncommon. Of the 34 MRSA isolates, 22 were resistant only to β-lactams. Of the remaining 12 MRSA, 8 were ciprofl oxacin and erythromycin resistant, 2 were erythromycin resistant with inducible clindamycin resistance, and 2 were ciprofl oxacin resistant. All MRSA isolates were susceptible to cotrimoxazole, doxycycline, gentamicin, and vancomycin, and none had constitutive clindamycin resistance.
Except for the MRSA isolates identifi ed as type ST1 by multilocus sequence typing, all other MRSA belonged to a known MRSA strain ( Table 2). Seven of the 9 ST1 isolates had indistinguishable PFGE profi les. The ST1 MRSA isolates had 82% homology by PFGE typing with another ST1 MRSA strain common in the region (the Australian WA MRSA-1).
Antimicrobial drug resistance profi le was associated with strain ( Table 2). All isolates of the USA300 strain were ciprofl oxacin resistant, and most also were erythromycin resistant. All of the Queensland clone and Southwest Pacifi c clone MRSA, and 8 of the 9 ST1 MRSA isolates, were resistant only to β-lactams.

Discussion
Considerable concern exists internationally about increasing levels of antimicrobial drug resistance (25). Consequences include treatment failure, the need to use newer antimicrobial drugs to achieve treatment goals, the adverse effects frequently associated with these newer drugs, increased expenditure, and longer hospital stays. In developing countries, such as Samoa, an additional concern exists: when resistance to less expensive antimicrobial drugs becomes widespread, the more expensive antimicrobial drugs are simply not available (26). As in many other developing countries (27), use of antimicrobial drugs is extremely high in Samoa. More than 60% of all prescriptions dispensed in hospitals and private pharmacies include an antimicrobial drug (28). No current data are available on the prevalence of antimicrobial drug resistance in Samoa. In other countries, high levels of antimicrobial drug use correlate with high levels of resistance (29). In addition, inadequate dosing and poor adherence by patients may also increase the development of resistance (25). Anecdotal evidence indicates these practices also are common in Samoa.
In Samoa, children <5 years of age were more likely than persons in other age groups to have skin and soft tissue infection caused by S. aureus; however, the prevalence of MRSA infections were similar in children, adults, and elderly persons. Participants who had reported recent antimicrobial drug use were less likely to have S. aureus, but their prevalence of MRSA did not differ signifi cantly from those who did not report recent antimicrobial drug use. The lack of association between MRSA prevalence and health care exposure or antimicrobial drug use was surprising; however, the data on antimicrobial drug use  may not be entirely reliable. A previous study found that many Samoans are unclear about which medicines were antimicrobial drugs (30). Most of the health care exposure reported in our study related to primary care exposure, and most of the MRSA strains isolated are typically associated with community acquisition (31). Even though most participants had community-onset skin and soft tissue infection, more detailed information about diagnosis and place of acquisition would have been valuable. Few data are available on the prevalence of MRSA in the community in nonindustrialized countries. The World Health Organization has identifi ed a need to strengthen monitoring of antimicrobial drug prescriptions and resistance and has funded pilot programs to achieve this (25,32). In this study in Samoa, MRSA was isolated from 9% of all participants, and 18% of participants from whom S. aureus was isolated had MRSA. Although we attempted to include a wide range of persons in the study, we cannot be sure that some groups in our sample were not overrepresented or underrepresented. Carrying out such research is diffi cult in a country such as Samoa, where research and laboratory infrastructure are not ideal. Ability to speak Samoan, knowledge of Samoan culture, and previous experience of living in Samoa were essential for the success of the project.
We found that the diversity of MRSA isolates in Samoa that caused skin and soft tissue infection was similar to that in Denmark, a country of >5 million persons (3). We expected that isolates of the Southwest Pacifi c clone MRSA would be the predominant MRSA strain, but these were in the minority. The high prevalence of USA300 and Queensland clone MRSA might refl ect the amount of travel between Samoa and the United States and Australia, respectively. The Queensland clone is now common in the Australian states of New South Wales and the Northern Territory in addition to Queensland (33). However, the large number of isolates of the Samoa ST1 MRSA clone and the isolation of almost equal numbers of 3 different MRSA clones suggest that the situation may not be that simple.
The Samoa ST1 MRSA isolates were distinct by both PFGE and spa typing from the community-associated ST1 MRSA strain commonly found in Australia and New Zealand, WA MRSA-1 (33). The Samoa ST1 MRSA isolates shared only 82% homology by PFGE with WA MRSA-1. WA MRSA-1 isolates are typically spa type t127, which does not cluster by BURP analysis with the spa types (t1853 and t6080) of the Samoa ST1 MRSA. In addition, the WA MRSA-1 strain is characterized by fusidic acid resistance and often also mupirocin or erythromycin resistance, whereas the Samoa ST1 MRSA isolates generally were resistant only to β-lactams. The Samoa ST1 MRSA isolates also were distinct from the USA400 ST1 MRSA strain with which they shared only 80% homology by PFGE. The Samoa ST1 MRSA strain might have originated in the Pacifi c. However, MRSA with spa type t1853 have also been isolated in New Zealand, mainly from patients in the Auckland area, since at least 2008 (34).
Three of the 5 strains that we identifi ed among MRSA isolates in Samoa (the USA300, Queensland, and Southwest Pacifi c strains) typically are associated with community acquisition (31). The Samoa ST1 MRSA strain is also likely to be predominantly associated with communityacquired infections. ST1 is recognized as a prominent genetic background of community-associated MRSA (35). The Samoa ST1 MRSA shares >80% homology by PFGE typing with 2 other ST1 community-associated MRSA strains: WA MRSA-1 and USA400. WA MRSA-1 caused the fi rst cases of community-associated MRSA infection in previously healthy persons in Western Australia in the early 1990s, and USA400 was the strain isolated from the fi rst cases of community-acquired MRSA in the United States (31). The Samoa ST1 MRSA strains are not multiresistant, another feature typical of community-associated MRSA strains. On the other hand, none of the isolates of this strain carried the PVL genes, which are commonly found in community-associated MRSA. However, WA MRSA-1 is also PVL negative. Clearly, further characterization of the Samoa ST1 MRSA is warranted.
Evidence suggests that community-associated MRSA strains, particularly USA300, are more easily transmitted and might be more virulent than other S. aureus strains (31). In North America, approximately one third of persons with community-acquired USA300 MRSA infection require hospital admission (36). Moreover, communityassociated MRSA is no longer just a problem in the community; it also has become a common cause of health care-associated infections (37). Hospital-acquired USA300 infections are more likely than community-acquired USA300 infections to be invasive and be associated with treatment failures (36). Thus, increases in the prevalence, severity, and complexity of diseases caused by globally successful community-associated MRSA strains are likely to be associated with increased illness, death, and cost. Economic analyses have consistently demonstrated that MRSA infections are associated with higher cost than are MSSA infections; although these studies have focused primarily on the costs associated with hospital care (38). None of these studies have investigated the consequences of MRSA in the developing world, yet the effects of disease are considerable (39).
Although reducing MRSA infection in the Samoan community is desirable, no controlled trials have demonstrated effective means of reducing communityassociated MRSA infections in a community setting.
Recommendations to reduce transmission of communityassociated MRSA include washing hands, caring for and covering wounds, not sharing contaminated personal items, appropriately disposing of contaminated waste, and appropriately prescribing antimicrobial drugs (40). Any interventions have substantial resource implications for a developing nation but must start with reliable surveillance of antimicrobial drug susceptibility, which is essential to monitor, control, and manage antimicrobial drug resistance. Thus, there is a clear need to assist developing countries with performing quality antimicrobial drug susceptibility testing and surveillance.
The results of our study, together with future surveillance efforts, can be used to provide information for local prescribing; the prevalence of MRSA in Samoa is high, and empiric prescription of antimicrobial drugs needs to account for this high prevalence. For example, we advocate that any patient in Samoa suspected to have serious, invasive S. aureus infection have adequate cultures and antimicrobial drug susceptibility testing performed. S. aureus infection in such a patient should be treated with vancomycin and a β-lactamase-stable penicillin drug until laboratory results are available. Patients with uncomplicated skin and soft tissue infections requiring antimicrobial drug treatment should receive cotrimoxazole or, if the patient cannot tolerate sulfonamides, clindamycin. Boils or furuncles should be treated by drainage, infection control, and wound care, with antimicrobial drugs reserved for complications.
We identifi ed a wide range of genotypes of MRSA that were causing wound infections in a small Pacifi c Island nation. Our hope is that this study will provide a starting point for future research into antimicrobial drug resistance in the Pacifi c and provide impetus for initiatives to improve antimicrobial drug use in Pacifi c Island nations. Antimicrobial drug resistance is a global concern that does not respect national boundaries; consequently, countries need to assist each other in addressing the problem.