Literature DB >> 28883956

Prevalence of Nasal colonization with Staphylococcus aureus in 4 cities in Peru.

Joan Neyra1, Michael Ellis2, Claudio Rocha1, Juan Silvera3, Moisés Apolaya3, Maruja Bernal1, Rina Meza1, Enrique Canal1, Yocelinda Meza1, David Blazes4.   

Abstract

BACKGROUND: Antimicrobial resistance (AMR) is a growing public health threat around the world and is not well characterized in the developing setting. Specifically, there is a lack of information regarding nasal colonization with S. aureus and methicillin-resistant Staphylococcus aureus (MRSA) in Latin America and Peru.
METHODS: This is the report of the baseline findings of a prospective cohort study followed up over 1 year at four geographically and ecologically distinct Peruvian Air Force bases in order to determine S. aureus nasal colonization prevalence and risk factors. Additionally, all MRSA isolates underwent molecular analysis which included pulsed-field gel electrophoresis and determination of virulence and resistance genes.
RESULTS: We enrolled 756 military personnel. Anterior nares colonization with Staphylococcus aureus was detected in 73 of 756 participants (9.7 %) and MRSA was detected in 2 of 756 (0.3 %). Colonization rates differed significantly (P = 0.02) between geographic enrollment sites: Talara-4.3 %, Iquitos-9.1 %, Arequipa-14.0 % and Lima-11.3 %. Risk factors for S. aureus colonization included being male and a reported history of respiratory disease.
CONCLUSION: Overall, we found low prevalence of S. aureus and MRSA nasal colonization in this Peruvian military population. These findings contribute to the overall epidemiological understanding of S. aureus and MRSA in Latin America. The colonization rates which varied based on geographical location warrants further study.

Entities:  

Keywords:  Antimicrobial resistance; Methicillin-resistant Staphylococcus aureus; Military personnel

Year:  2016        PMID: 28883956      PMCID: PMC5531008          DOI: 10.1186/s40794-016-0025-x

Source DB:  PubMed          Journal:  Trop Dis Travel Med Vaccines        ISSN: 2055-0936


Background

The increasing prevalence of methicillin-resistant Staphylococcus aureus is a global problem, affecting military and non-military populations around the world. MRSA was first documented in 1960, and until the late 1990s, its presence was confined largely to hospital settings with occasional outbreaks. Since then, the number of outbreaks and infections caused by MRSA, specifically community–associated methicillin-resistant Staphylococcus aureus (CA-MRSA) strains increased steadily [1, 2]. USA300 genotype is the predominant CA-MRSA strain recovered from outbreak investigations in U.S. and different countries in Europe and Asia, such as Japan [3], constituting a common cause of community associated skin and soft tissue infections (SSTIs). Nasal colonization with Staphylococcus aureus or MRSA is a risk factor for subsequent infection by these bacteria [4, 5]. In non-Latin American populations, colonization status varies with approximately 20–30 % persistently colonized and 20 % is intermittently colonized [6-8]. Colonization is facilitated by the anatomy of the nasal vestibule and the resistance of S. aureus to microbicide peptides in the mucus [9]. Nasal colonization appears to change during one’s lifetime. Colonization begins shortly after birth, decreases during the first 5 years and then it increases until 50 % are carriers between 6 and 12 years; and finally it decreases as children mature and become adults [10]. In the military setting, Staphylococcus aureus infections complicate combat-related injuries and produce skin and soft-tissue infections during deployments or training. Among U.S. soldiers, MRSA SSTIs represent a considerable burden, and nasal colonization is a risk factor for subsequent disease [1, 11–14]. For example, the cumulative incidence of SSTIs after 10 weeks of follow-up at training facilities in U.S. military trainees was 38 % in MRSA-colonized subjects while in non-colonized it was only 2 % [11]. The Centers for Disease Control and Prevention’s (CDC) 2013 report on antibiotic resistant pathogens listed MRSA as one of the most serious threats, causing 80,461 severe infections and 11,285 deaths per year in the U.S., leading to a heavy burden of the healthcare system [15]. Similarly, the 2014 WHO Global Health Report on Antimicrobial Resistance reported that in all the WHO regions, MRSA prevalence of infections was above 20 % and increased the risk of death and the associated healthcare costs [16, 17]. In Latin America, a surveillance network for resistant bacterial infections was organized in 1998 under Pan American Health Organization (PAHO) sponsorship; collecting data from specific national and regional hospitals with adequate laboratory infrastructure and resources. However, there is little information regarding the prevalence in other areas, so the geographic extent and the characteristics of MRSA infections in Latin America are not well described in terms of prevalence, isolates, and risk factors [18]. Our current knowledge indicates that four MRSA clones are the most prevalent in Latin America: Brazilian, Pediatric, Cordobes/Chilean and New York/Japan, with marked differences in virulence, antimicrobial resistance profile and geographical distribution [19]. In Peru, current information about MRSA is mostly limited to case reports or series from hospital-based samples from reference hospitals with appropriate protocols for lab procedures and resources. Unfortunately, these studies do not inform us about the prevalence of S. aureus nasal colonization nor the epidemiological characteristics in the community, especially in young at-risk populations such as military personnel. Our work was the first study to systematically determine the prevalence and the molecular characteristics of nasal colonization with Staphylococcus aureus and MRSA among a Peruvian military population in multiple cities in Peru. Herein, we report the baseline results of this study.

Methods

Study design

We conducted a prospective cohort study with 1 year of follow-up among active duty military personnel from four bases one in each region of the Peruvian Air Force (Lima, Arequipa, Talara, and Iquitos). This is the report of the baseline findings of this cohort. The study population included male and female military active duty personnel, between age 18 and 59 years, stationed at these bases with different climate characteristics (Iquitos is located in the jungle; Talara, in the northern desert coast, Lima at the central coast with mild to warm temperatures depending on the season, and Arequipa, which is located at high altitude in the southern highlands, with a dry and relatively cold climate). See Fig. 1.
Fig. 1

Map of Peru showing the location of the four sites. Lima, the capital city of Peru is located at the central desert coast; Talara, in the northern desert coast; Arequipa, in the southern highlands; and Iquitos is located in the northeastern jungle (Image taken from Google Earth)

Map of Peru showing the location of the four sites. Lima, the capital city of Peru is located at the central desert coast; Talara, in the northern desert coast; Arequipa, in the southern highlands; and Iquitos is located in the northeastern jungle (Image taken from Google Earth)

Study procedures

We enrolled military personnel from four large bases in each Air Force region. After we obtained written informed consent, each participant completed a self-administered questionnaire about demographic and risk factors and provided a nasal swab. Investigators obtained a sample from the vestibular area of each of the nares, using BD BBL CultureSwabs® (BD Diagnostic, Sparks MD). Each nasal swab specimen was placed in a refrigerated container and later stored in a refrigerator at 4 °C until the time of the shipping to Naval Medical Research Unit-6 lab (NAMRU-6). Once they arrived at NAMRU-6 Bacteriology lab, the time gap between sample collection and plating was 1 month.

Lab procedures

Labeled swabs were shipped to the Naval Medical Research Unit N° 6 (NAMRU-6) located at Lima, Peru. Nasal culture specimens were placed in 5 ml of tryptic soy broth (TSB) supplemented with 6.5 % NaCl and incubated for 18-24 h at 35 °C. After that time, a 75 microL aliquot was plated onto mannitol salt agar. Plates were incubated for up to 48 h at 37 °C and inspected for yellow colonies characteristic of S. aureus. Identified isolates were sub cultured onto tryptic soy agar with 5 % sheep blood. Subsequent colonies underwent catalase and coagulase testing per Micro Lab Standard Operational Procedures (SOP) at NAMRU-6. All confirmed S. aureus isolates collected from the nasal swabs were shipped to Uniformed Services University (USU)’s Laboratory where they underwent susceptibility testing using disk diffusion tests for identifying MRSA strains, following the standards established by the Clinical and Laboratory Standards Institute [20]. Additionally, all MRSA strains underwent pulsed field gel electrophoresis (PFGE) procedures. Using polymerase chain reaction (PCR) we detected Panton-Valentine Leukocidin (PVL), arginine catabolic mobile element (ACME), staphylococcal chromosome cassete (SCCmec) type, presence of toxic shock syndrome toxin (TST), gene ileS-2 for resistant to mupirocin (mupA), and tolerance to chlorhexidine (qacA/B) using standard protocols.[7].

Statistical analysis

Overall and baseline colonization status are described based on gender, rank, base of recruitment, age group, time of service in the Peruvian Air Force (≤10 years, 11–20 years, > 20 years), type of activities, smoking status, previous hospitalizations in the last 12 months, previous deployments, use of antibiotics in the last 12 months, previous SSTIs in the last 12 months, previous respiratory diseases, use of corticosteroids in the last 12 months, place of residence, medical conditions; and is reported as numbers and proportions with two-sided 95 % confidence intervals. We also report the prevalence rate of nasal colonization with MRSA strains and the results of the antimicrobial susceptibility for those isolates positive to Staphylococcus aureus. We used a logistic regression model to determine the association with the variables listed above. The Institutional Review Boards at USU (Bethesda, MD, USA), and NAMRU-6 (Lima Peru) approved the research protocol.

Results

Demographic and clinical characteristics

We enrolled 756 participants. The mean age of the participants was 30.3 ± 11.5 years, but almost 60 % of our study population was younger than 30 years. Slightly more than 80 % were male and 61 % of the participants had more than 10 years of military service. Almost 90 % of the study population included Non-Commissioned officers and troops, and their occupations included administrative (32.5 %), instructional (36.5 % and combat (29.2 %) activities. We found that 20.1 % of the participants had a reported medical condition. Of them, 10 % reported gastrointestinal diseases, 5.4 % reported a skin disease, 2.6 % reported a respiratory disease, and 1.1 % reported an infectious disease. More than a third of the participants (34.8 %) reported the use of antibiotics during the previous year; of these, 52 % (136) gave a specific antibiotic. In addition, 20.2 % reported the use of corticosteroids; and 11.6 % of the enrolled participants were hospitalized during the previous year. Regarding the diagnosis of any SSTI during the previous year, only 5.8 % reported a SSTI. Smoking was common: 34.2 % were current smokers, 16.7 % were past smokers, and 45.6 % reported never smoking (Table 1).
Table 1

Demographic characteristics of study participants

VariableFrequency (N = 756)Percentage (%)
Age
 18 – 29 years45059.5
 30 – 39 years9512.6
 40 – 49 years15120.0
 50 years or more607.9
Time of service
 10 years or less46361.2
 11 – 20 years10313.6
 20 years or more19025.1
Sex
 Female14619.3
 Male61080.7
Rank
 Officers8411.1
 Non-Commissioned Officers36848.7
 Troops30440.2
Base of recruitment
 Iquitos25333.5
 Arequipa16421.7
 Talara16221.4
 Lima17723.4
Administrative activities
 No51067.5
 Yes24632.5
Instruction activities
 No48363.9
 Yes27336.1
Combat activities
 No53570.8
 Yes22129.2
Number of activities
 Not related10614.0
 Unique58076.7
 Multiple709.3
Place of residence
 Barracks25033.1
 Inside the base11415.1
 Outside the base39251.9
Medical conditions
 No60479.9
 Yes15220.1
Number of medical conditions
 None60479.9
 One disease11815.6
 More than one disease344.5
Use of antibiotics in the previous year
 No42756.5
 Yes26334.8
 Unknown668.7
Use of corticosteroids in the previous year
 No53670.9
 Yes15320.2
 Unknown678.9
Hospitalized during the previous year
 No64585.3
 Yes8811.6
 Unknown233.0
Diagnosis of SSTIs during the previous year
 No67188.8
 Yes445.8
 Unknown415.4
Smoking status
 Never34545.6
 Past smoker12616.7
 Current smoker25934.2
Demographic characteristics of study participants

Baseline nasal colonization with Staphylococcus aureus and MRSA

The baseline nasal colonization prevalence among the 756 enrolled participants was 9.7 %. There were two periods of recruitment, in October-November 2013 (655 participants) and April-August 2014 (101 participants), and the baseline nasal colonization rates for each period were similar (9.8 % vs. 8.9 %, p = 0.7853, Z-statistic for comparison of two proportions). The overall rate of colonization with MRSA was 0.3 % during the study period (2 of 756). These isolates were collected during the 6 month visit at Arequipa, one in a participant enrolled in October 2013 and a second from a different participant who was enrolled in in May 2014). Molecular analysis of these MRSA isolates demonstrated that they possessed SCCmec type IV and qacA/B (chlorhexidine tolerance), but lacked genes for PVL, mupirocin resistance, and toxic shock syndrome toxin (TST). Table 2 shows statistically significant associations between prevalence of nasal colonization at baseline and demographic and clinical variables. Those participants between 18 and 29 years old and 40 to 49 years old had a higher prevalence of nasal colonization (10.2 % vs. 11.3 %); while, the prevalence was lower than 7 % for other age groups. Nasal colonization was greater in male than female (10.3 vs. 6.8 %, p = 0.201). The troops had 11.5 % of nasal baseline nasal colonization, higher than officers or non-commissioned officers (9.5 % vs. 8.2 %). There was a statistically significant difference in the distribution of nasal colonization by base of recruitment (p = 0.023); Talara had the lowest baseline prevalence (4.3 %) compared to the other three bases that had similar rates (Iquitos-9.1 %, Arequipa-14.0 % and Lima-11.3 %). Those who lived on base but not in the barracks had the lowest prevalence (5.3 %) but this was not significantly (p = 0.198) different from those who lived at the barracks (11.2 %) and those who lived off the base (9.9 %).
Table 2

Prevalence of baseline nasal colonization among the different variables under study (N = 756)

VariableBaseline Nasal colonization (%, 95 % CI) P value
Positive (n = 73)Negative (n = 683)
Age
 18 – 29 years10.2 (7.4 – 13.0)89.8 (86.9 – 92.6)0.537a
 30 – 39 years6.3 (1.4 – 11.2)93.7 (88.8 – 98.6)
 40 – 49 years11.3 (6.2 – 16.3)88.7 (83.7 – 93.8)
 50 years or more6.7 (0.3 – 13.0)93.3 (86.9 – 99.7)
Time of service
 10 years or less10.6 (7.8 – 13.4)89.4 (86.6 – 92.2)0.334
 11 – 20 years5.8 (1.3 – 10.4)94.2 (89.6 – 98.7)
 20 years or more9.5 (5.3 – 13.7)90.5 (86.3 – 94.7)
Sex
 Female6.8 (2.7 – 10.9)93.2 (89.0 – 97.3)0.201
 Male10.3 (7.9 – 12.7)89.7 (87.3 – 92.1)
Rank
 Officers9.5 (3.2 – 15.8)90.5 (84.2 – 96.8)0.340
 Non-Commissioned Officers8.2 (5.3 – 10.9)91.8 (89.0 – 94.7)
 Troops11.5 (7.9 – 15.1)88.5 (84.9 – 92.1)
Base of recruitment
 Iquitos9.1 (5.5 – 12.6)90.9 (87.4 – 94.5)0.023
 Arequipa14.0 (8.7 – 19.4)85.9 (80.6 – 91.3)
 Talara4.3 (11.8 – 7.5)95.7 (92.5 – 98.8)
 Lima11.3 (6.6 – 15.9)88.7 (84.0 – 93.4)
Number of activities
 Not related10.4 (4.5 – 16.2)89.6 (83.8 – 95.5)0.587
 Unique9.1 (6.8 – 11.5)90.9 (88.5 – 93.2)
 Multiple12.9 (4.9 – 20.8)87.1 (79.2 – 95.1)
Number of medical conditions
 None9.9 (7.5 – 12.3)90.1 (87.7 – 92.5)0.122
 One disease6.1 (1.7 – 10.5)93.9 (89.5 – 98.3)
 More than one disease17.6 (4.6 – 30.7)82.4 (69.3 – 95.4)
Respiratory diseases the previous year
 No9.1 (7.0 – 11.2)90.9 (88.8 – 92.9)0.002
 Yes30.0 (9.4 – 50.6)70.0 (49.4 – 90.6)
Use of antibiotics the previous year
 No9.1 (6.4 – 11.9)90.9 (88.1 – 93.6)0.598
 Yes11.0 (7.2 – 14.8)88.9 (85.2 – 92.8)
 Unknown7.6 (11.3 – 14.0)92.4 (85.9 – 98.9)
Use of dicloxacillin previous year
 No9.3 (7.2 – 11.4)90.7 (88.6 – 92.8)0.005
 Yes33.3 (5.4 – 61.2)66.7 (38.8 – 94.6)
Use of corticosteroids the previous year
 No8.9 (6.5 – 11.4)91.0 (88.6 – 93.5)0.432
 Yes12.4 (7.2 – 17.7)87.6 (82.3 – 92.8)
 Unknown8.9 (2.1 – 15.9)91.0 (84.1 – 97.9)
Hospitalized during the previous year
 No9.6 (7.3 – 11.9)90.4 (88.1 – 92.7)0.971
 Yes10.2 (3.8 – 16.6)89.8 (83.4 – 96.2)
 Unknown8.7 (0.0 – 20.5)91.2 (79.5 – 100)
Diagnosis of SSTIs during the previous year
 No9.5 (7.3 – 11.8)90.5 (88.2 – 92.7)0.848
 Yes9.1 (0.5 – 17.7)90.9 (82.3 – 99.5)
 Unknown12.2 (5.2 – 22.4)87.8 (77.6 – 97.9)
Smoking status
 Never8.1 (5.2 – 11.0)91.9 (88.9 – 94.8)0.297
 Past smoker12.7 (6.9 – 18.5)87.3 (81.5 – 93.1)
 Current smoker10.4 (6.7 – 14.2)89.6 (85.8 – 93.3)
Place of residence
 Barracks11.2 (7.3 – 15.1)88.8 (84.9 – 92.7)0.198
 Inside the base5.3 (1.1. – 9.4)94.7 (90.6 – 98.9)
 Outside the base9.9 (6.9 – 12.9)90.1 (87.1 – 93.0)

aWe used the Fisher’s exact test. For the rest of the variables, we used the Pearson chi square test

Prevalence of baseline nasal colonization among the different variables under study (N = 756) aWe used the Fisher’s exact test. For the rest of the variables, we used the Pearson chi square test Having a respiratory disease increases the prevalence of nasal colonization (30 %) compared with those without respiratory disease (9.1 %, p = 0.002). Smoking did not affect the prevalence of nasal colonization; the rates were similar among those who never smoked (8.1 %), previous smokers (12.7 %) and currently smokers (10.4 %) (p = 0.300) (Table 3).
Table 3

Potential risk factors associated with baseline nasal colonization with Staphylococcus aureus

VariableNUnadjusted ORAdjusted OR (95 % CI) P-value
Use of antibiotics during the previous year
 No400RefRef
 Yes2381.21.4 (0.8 – 2.6)0.283
Hospitalization during the previous year
 No566RefRef
 Yes721.01.0 (0.4 – 2.4)0.980
Diagnosis of SSTI during the previous year
 No600RefRef
 Yes380.50.4 (0.1 – 1.8)0.237
Sex
 Female122RefRef
 Male5161.82.4 (1.0 – 5.7)0.043
Base of recruitment
 Talara144RefRef
 Iquitos2072.52.5 (0.9 – 6.5)0.065
 Lima1492.82.7 (0.9 – 7.3)0.051
 Arequipa1383.94.5 (1.7 – 11.9)0.002
Smoking status
 Never smoked312RefRef
 Past smoker1071.71.6 (0.8 – 3.5)0.204
 Current smoker2191.21.1 (0.6 – 2.1)0.756
Respiratory diseases
 No619RefRef
 Yes193.54.5 (1.4 – 14.7)0.014
Time of service 6380.990.97 (0.94 – 0.99)0.030
Potential risk factors associated with baseline nasal colonization with Staphylococcus aureus Among those who used antibiotics during the last year, the nasal colonization prevalence at baseline was not different among those who used them (11.0 %) or not (9.1 %). However, when we analyzed the use of dicloxacillin the previous year, those who reported its use had a 33.3 % prevalence of nasal colonization, compared with those who did not report its use (9.3 %, p = 0.005). Regarding the use of corticosteroids, those who used them the previous year, had a prevalence of 12.4 %, which was similar to those who did not use them (8.9 %), (p=: 0.432). In terms of hospitalization during the previous year, the rates were similar among those who were hospitalized (10.2 %) and those who were not (9.6 %) (p = 0.971). Similarly there was no difference in prevalence between those who had the diagnosis of SSTIs during the last year (9.1 %) and those who did not (9.5 %). The identified risk factors for S. aureus colonization included being male and a reported history of respiratory disease; while time of service had a slight protective effect.

Antimicrobial susceptibility of positive isolates and MRSA isolates

NAMRU-6 and USUHS labs processed 183 positive Staphylococcus aureus samples from the participants during the study period (1 year). Antimicrobial susceptibility is reported in Table 3. The highest resistance was to erythromycin (16.4 %). In addition, 6.6 % had an inducible resistance to clindamycin. All isolates were susceptible to ceftaroline, trimethoprim-sulfamethoxazole, vancomycin, and linezolid (Table 4).
Table 4

Antimicrobial susceptibility of 183 Staphylococcus aureus isolates

AntibioticNumber (%) of samples
SusceptibleResistantIntermediate
Clindamycina 179 (97.8)4 (2.2)-
Erythromycin153 (83.6)30 (16.4)-
Doxycycline180 (98.4)-3 (1.6)
Linezolid183 (100)--
Oxacillin181 (98.9)2 (1.1)-
Rifampin183 (100)--
TMP-SMX b 183 (100)--
Vancomycin183 (100)--
Gentamicin177 (96.7)6 (3.3)-
Levofloxacin182 (99.5)1 (0.5)-
Ceftaroline183 (100)--

a 6.6 % of the samples showed inducible resistance to clindamycin

bTMP-SMX, trimethoprim-sulfamethoxazole

Antimicrobial susceptibility of 183 Staphylococcus aureus isolates a 6.6 % of the samples showed inducible resistance to clindamycin bTMP-SMX, trimethoprim-sulfamethoxazole

Discussion

Baseline prevalence

There are only a few studies of nasal colonization in active duty military populations, primarily from the US and one from China, but none in Peru or Latin America. These studies found that the prevalence of colonization in American recruits was 31 % [11], while the Chinese military found a different rate depending if individuals were deployed to urban (24.6 %) or suburban military centers (16.1 %) [21]. In both cases, the prevalence was higher than what we found at baseline in our study population (9.7 %). Only two previous studies were performed in community settings in Peru. One study included only children from Cajamarca and found a prevalence of 11.9 % [22], while the second included inhabitants of an impoverished community of Lima, and found that among adults of different ages the prevalence of nasal colonization ranged from 20.4 to 39.6 % [23]. These two previous studies in Peru are comparable with others studies performed in Latin American countries that showed that the nasal colonization rates with Staphylococcus aureus in community settings was quite varied. In adult populations, the nasal colonization rates in Brazil ranged between 32.7 % [24] and 40.8 % [25]; while among Colombian medical students the rate was 25 % [26]. The prevalence we obtained in the Peruvian military was closer to the prevalence rate reported among adult students in Nigeria (14 %) and healthcare workers in Nicaragua (6.7 to 11.6 %) [27, 28]. In Peru, 3 MRSA strains from Peruvian citizens returning from abroad were characterized in 2011, one was ST30 and the other two were ST8 clones which are related to the USA300 clone [29]. We found differences in the prevalence of nasal colonization based on the site of the geographical site if study enrollment. Of the four sites, Lima is the capital city of Peru (approximately 10 million inhabitants), while Arequipa (900,000 inhabitants) and Iquitos (420,000 inhabitants) are the most important urban centers in the highlands and the jungle and had higher prevalence rates; while Talara, which is a smaller city than the other three (101,000 inhabitants), had only 4.3 %. This colonization prevalence differences may be attributed to a number of factors including climate and ecology, population size, or access to healthcare. An important aspect of population size is that it generally suggests differences in commercial movement, and therefore access to common antibiotics that are still sold without a medical prescription at small pharmacies and drugstores. Additionally, the distribution of antibiotics to each military health facility is based on the most prevalent diseases and the size of the base, which are larger in Lima, Arequipa and Iquitos where administrative and operational regional offices are located, and therefore exceed the population assigned to Talara, which is only an operational base. The increased exposure to antibiotics in Lima, Iquitos and Arequipa might favor the development of nasal colonization with Staphylococcus aureus by eliminating other commensal bacteria colonizing the human nares; unfortunately information regarding the most used antibiotics at each of the bases or local areas is currently unavailable. Dicloxacillin is an antibiotic belonging to the beta lactam family that is used extensively for the treatment of SSTIs. We had expected that the use of dicloxacillin might reduce the rates of nasal colonization with Staphylococcus aureus, but we found the opposite. Possibly, the normal microbiota in the anterior nares is more susceptible than Staphylococcus aureus to dicloxacillin, therefore favoring the Staphylococcus aureus growth. Another possible reason can be the misuse of this antibiotic, which is usually prescribed for 7 to 14 days, but if the dose and time of prescription were not adequate, the antibiotic might have limited effect. We were not able to collect information regarding the dose, time of prescription, where the antibiotics were purchased, or if the treatment was completed. We identified only two participants with MRSA and therefore our overall prevalence of MRSA colonization during the study period was 0.3 % (2 of 756). These isolates possessed SCCmec type IV which is the characteristic mobile genetic element carrying the mecA gene (methicillin-resistance) found most commonly in CA-MRSA strains. Our MRSA colonization prevalence was close to those reported in previous studies in Peru and Latin America, where it ranges from 0.6 to 1.8 % [23, 30, 31] in communities; however these proportions are lower than those observed in developed countries like US or Europe. In terms of military populations, our results reflect that MRSA nasal colonization is lower than rates reported in US military populations (3 %), while the Chinese study did not detect any MRSA [11, 21]. Our questionnaire was not designed to provide more specific historical information regarding the type of SSTI and treatments prescribed, dose and timing of antibiotics and corticosteroids, time of hospitalization, place, and antibiotics used during this time, which could have given us more detailed information regarding these risk factors. Also, given that this was a self-administered questionnaire, there is the potential for recall bias. In addition, it is possible that some participants did not understand the questions asked or did not know the medical terms used; therefore they left the questions blank. In addition, it is possible that sample handling could have affected the recovery of positive S. aureus isolates, specifically during the sampling procedure due to discomfort of the participants that led to movements of the head and a poor quality sample, and the limited available timeframe we had for doing it. Different climate conditions at each site may have affected also the recovery due to the use of a refrigerated container that could not have kept a low temperature at all times. We believe our results can serve as a proxy to understanding of the nasal colonization with Staphylococcus aureus in the community. We found that these isolates have a remarkable antimicrobial susceptibility with very little resistance when compared with other populations. This susceptibility may allow us an optimization of the current treatment of different infections where Staphylococcus aureus is a common etiologic agent. This standardization should help to reduce the indiscriminate exposure to more expensive and broader spectrum antibiotics that should be left as second or third line options, which are more expensive and increase the risk of adverse reactions.

Conclusions

In summary, we found a low prevalence of baseline nasal colonization with Staphylococcus aureus (9.7 %) and MRSA (0.3 %) in an active duty military population in Peru. Our results increase the current knowledge about Staphylococcus aureus nasal colonization in Peru and Latin America. Further study exploring the geographically differences in S. aureus nasal colonization warrants further investigation.

Abbreviations

AMR, Antimicrobial resistance; MRSA, methicillin-resistant Staphylococcus aureus; SCCmec, staphylococcal cassette chromosome mec
  27 in total

1.  The changing pattern of methicillin-resistant staphylococcus aureus clones in Latin America: implications for clinical practice in the region.

Authors:  Eduardo Rodríguez-Noriega; Carlos Seas
Journal:  Braz J Infect Dis       Date:  2010-12       Impact factor: 1.949

Review 2.  Community-associated methicillin-resistant Staphylococcus aureus.

Authors:  Thomas R Wallin; H Gene Hern; Bradley W Frazee
Journal:  Emerg Med Clin North Am       Date:  2008-05       Impact factor: 2.264

3.  Low prevalence of methicillin-resistant Staphylococcus aureus nasal carriage in urban and rural community settings in Bolivia and Peru.

Authors:  Alessandro Bartoloni; Lucia Pallecchi; Connie Fernandez; Antonia Mantella; Eleonora Riccobono; Donata Magnelli; Dario Mannini; Marianne Strohmeyer; Filippo Bartalesi; Higinio Segundo; Joaquin Monasterio; Hugo Rodriguez; César Cabezas; Eduardo Gotuzzo; Gian Maria Rossolini
Journal:  Int J Infect Dis       Date:  2012-12-21       Impact factor: 3.623

Review 4.  The role of nasal carriage in Staphylococcus aureus infections.

Authors:  Heiman F L Wertheim; Damian C Melles; Margreet C Vos; Willem van Leeuwen; Alex van Belkum; Henri A Verbrugh; Jan L Nouwen
Journal:  Lancet Infect Dis       Date:  2005-12       Impact factor: 25.071

Review 5.  Methicillin-resistant Staphylococcus aureus strain USA300: origin and epidemiology.

Authors:  Fred C Tenover; Richard V Goering
Journal:  J Antimicrob Chemother       Date:  2009-07-16       Impact factor: 5.790

6.  Molecular identification and antimicrobial susceptibility of Staphylococcus aureus nasal isolates from medical students in Cartagena, Colombia.

Authors:  Alfonso Bettin; Ceyla Causil; Niradiz Reyes
Journal:  Braz J Infect Dis       Date:  2012 Jul-Aug       Impact factor: 1.949

Review 7.  Staphylococcus aureus: determinants of human carriage.

Authors:  J U E Sollid; A S Furberg; A M Hanssen; M Johannessen
Journal:  Infect Genet Evol       Date:  2013-04-22       Impact factor: 3.342

8.  Nasal colonization of and clonal transmission of methicillin-susceptible Staphylococcus aureus among Chinese military volunteers.

Authors:  Fen Qu; Enbo Cui; Tongsheng Guo; Haijing Li; Suming Chen; Liming Liu; Wang Han; Chunmei Bao; Yuanli Mao; Yi-Wei Tang
Journal:  J Clin Microbiol       Date:  2009-11-04       Impact factor: 5.948

9.  Natural history of community-acquired methicillin-resistant Staphylococcus aureus colonization and infection in soldiers.

Authors:  Michael W Ellis; Duane R Hospenthal; David P Dooley; Paula J Gray; Clinton K Murray
Journal:  Clin Infect Dis       Date:  2004-09-02       Impact factor: 9.079

10.  [The frequency and antibiotic susceptibility of Staphylococcus aureus from nasal swabs in an suburban marginal population in Lima, Peru].

Authors:  Edgar Carmona; Seyzo Sandoval; Coralith García
Journal:  Rev Peru Med Exp Salud Publica       Date:  2012-06
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