Methicillin-Resistant Staphylococcus aureus Carriage among Students at a Historically Black University: A Case Study

Background. Black people in the USA is afflicted with a higher rate of methicillin-resistant Staphylococcus aureus (MRSA) infection. This study determined the prevalence of MRSA carriage among black college students at a university setting. Methods. Hand and nasal swabs were collected and screened for MRSA by mannitol fermentation, coagulase, and DNase activities and their resistance to oxacillin. MRSA isolates were analyzed for antimicrobial resistance pattern, genetic profile for staphylococcal cassette chromosome mec (SCCmec) type, pulsed-field type, multilocus sequence type (ST), and the presence of Panton-Valentine leukocidin (PVL) gene. Results. MRSA was isolated from 1 of the 312 (0.3%) hand swabs and 2 of the 310 (0.65%) nasal swabs, respectively. All isolates lack multidrug resistance and have type IV SCCmec, characteristic of community-associated MRSA. These isolates were a ST8-MRSA-IVa-PVL(+) (USA300 strain), a ST8-MRSA-IVb-PVL(−), and a new MLST, ST2562-MRSA-IV-PVL(−), identified in this study. These isolates were thus not transmitted among students. Conclusion. We found a low rate of MRSA carriage among students in a black university. Our finding highlights the need of future study which involves multiinstitutions and other ethnic group to assess the association of black race with MRSA carriage.


Introduction
Staphylococcus aureus, a bacterium commonly isolated from humans, is an important causative agent for skin and so tissue infections, pneumonia, septic arthritis, endocarditis, osteomyelitis, and sepsis [1]. Methicillin-resistant Staphylococcus aureus (MRSA) strains resistant to -lactam antimicrobial agents have caused increased S. aureus infection and mortality [2,3]. Black people in the USA is afflicted with a higher rate of MRSA infection as indicated by studies of pediatric patients, community-onset skin and so tissue infections, right-sided endocarditis patients, and hospital patients [4][5][6][7][8][9][10]. A report by Klevens et al. [11] described signi�cant race disparity through a surveillance program in 2004-2005: incidence rates of invasive MRSA infection were consistently higher among blacks than whites in all age groups. Overall, infection rate was more than twice as high, and mortality rate was 80% higher for blacks than for whites. e reason for these racial disparities is not known.
It is well known that S. aureus carriage is a major risk factor for infection, and MRSA colonization as opposed to MSSA colonization is associated with an increased risk of infection [1][2][3]. A question needs to be answered is whether a higher rate of MRSA carriage occurs among blacks. National MRSA prevalence studies by the National Health and Nutrition Examination Survey Program (NHANES) [12][13][14] found that among noninstitutionalized US population the rates for MRSA carriage were 0.9% for white and 1.1% for black in 2001-2002, and 1.6% for both whites and blacks in 2003-2004 [14]. ese cross-sectional surveys identi�ed risk factors for MRSA carriage as healthcare facility exposure, age ≥60 years' females, diabetes, and household with income below poverty level. Some of the risk factors are also disproportionally associated with the blacks, making it difficult to discern the effect of race for MRSA carriage. Participants were recruited mostly from biology general education classes to better represent the student population. Samples were collected from those who authorized letter of informed consent. With separate swabs, a single sample was collected from each of the two body sites, nose and hand, from each participant. Swabs from each participant were coded with a numeric number that was followed by a letter H for hand swab, and a letter N for nasal swab, respectively. Cultures dried in an incidence of prolonged incubation were withdrawn from this study thus not all participants' nasal and hand samples were included. Repeated samples were excluded when indicated by information of participants. Health care facility exposure and antibiotic usage 6 months prior to sample collection were inquired, but answers were incomplete and inaccurate (e.g., incorrect apprehension of antibiotic usage) thus not included in this paper. For nasal sample collection, a sterile cotton-tipped swab was moistened by inserting into sterile 0.85% NaCl saline solution and then expressed out extra liquid. e moistened swab was then inserted into both anterior nares, one at a time with the same swab, and rotated gently against the inner surface. e swab was withdrawn and immediately streaked on a mannitol salt agar (MSA, BD, Sparks, MD, USA). Skin samples from hand were collected with a moisten swab prepared as described for nasal sampling, by gently rubbing a 1 cm 2 area of �ngertips of one hand, the swab was then immediately streaked on a MSA. MSA plates were incubated at 35 ∘ C for up to 48 hours. Nasal and skin samples were collected from 364 participants, of these 347 were black students. Among the cultures lost in the incubation incidence, 35 hand and 37 nose cultures were from the black students. Data from the 312 skin and 310 nose samples from black students are analyzed in this paper.

MRSA Screening.
One or two (if obvious difference in color) white or yellow or cream-colored colonies on MSA plate with yellow surrounding (indicative of fermentation) were subcultured on trypticase soy agar (TSA). Each subculture was subjected to Gram stain followed by microscopic examination. Only mannitol-fermenting, gram-positive cocci were screened for oxacillin resistance using oxacillin screen agar (BD, Sparks, MD) which contains 0.6 g/mL oxacillin and 40 mg/mL NaCl. Following the manufacturer's instruction, isolates were grown in trypticase soy broth (TSB) at 37 ∘ C for 4-6 hours and diluted to 0.5 McFarland standard with TSB. en ten microliter of the inoculate suspension was deposited onto an oxacillin screen agar and smeared in a 1 inch 2 area with a sterile cotton-tipped swab. S. aureus ATCC 29213 (oxacillin susceptible) and S. aureus ATCC 43300 (oxacillin resistant) were included for quality control. e plates were incubated at 35 ∘ C for 24 hours and observed for growth.
Isolates which formed visible colonies on oxacillin screen agar were tested for coagulase activity by tube coagulase test (Fluka Analytical, Buchs, Switzerland) using rabbit plasma with EDTA following the manufacturer's instruction. S. aureus ATCC 43300 and Escherichia coli ATCC 25922 were included as positive and negative controls, respectively. Oxacillin-resistant coagulase-positive isolates were tested for deoxyribonuclease (DNase) activity using DNase test agar (BD, Sparks, MD, USA). Isolates were transferred onto DNase test agar and incubated at 35 ∘ C for 24 hours. Following incubation, the plates were �ooded with 1 N HCl. A clear zone around the area of growth indicated DNase activity. Oxacillin-resistant, coagulase-positive, and DNase-positive isolates were identi�ed as MRSA.

Antimicrobial Susceptibility Pattern by Disc Diffusion
Assay. Antibiotic testing was performed using standard NCCLS methods for antimicrobial disk susceptibility [15]. Antibiotics tested included penicillin (10 IU), cipro�oxacin (5 g), clindamycin (2 g), erythromycin (15 g), doxycycline (30 g), tetracycline (30 g), trimethoprim/sulfamethoxazole (1.25/23.75 mcg), and vancomycin (30 g) (BD, Sparks, MD). Brie�y, MRSA isolates were grown in TSB for 4-6 hours to reach or to be diluted to 0.5 McFarland standard with TSB. A sterile cotton-tipped swab was moistened in the standardized suspension and then streaked on Mueller-Hinton agar (BD, Sparks, MD). Antibiotic discs were positioned on the surface of the inoculated plate. Aer incubating at 35 ∘ C for 18 hours, the diameter of zone of inhibition was measured, and susceptibility was determined according to the de�nition by manufacturer. S. aureus ATCC 25923 was included in the tests for quality control.

Erythromycin Induced Clindamycin Resistance-D Test.
MRSA isolates were grown in TSB at 37 ∘ C for 4-6 hours, diluted to 0.5 McFarland standard with TSB, and streaked on TSA containing 5% sheep blood. Antimicrobial discs of erythromycin (15 g) and clindamycin (2 g) were placed 17 mm apart from edge to edge on inoculated plate. e plates were incubated at 35 ∘ C for 18 hours and then photographed and visually inspected.

SCCmec
Typing. Sequences speci�c for SCCmec type I to V and mecA, respectively, were detected by multiplex PCR on an iCycler (Bio-Rad) using primers (Operon, Huntsville, AL, USA) and conditions described by Zhang et al. [16]. Strains of known SCCmec types, JCSC4744 (type IVa) and JCSC2172 (type IVb), were included in PCR for comparison. PCR amplicons were analyzed by electrophoresis through 2% agarose gel (Fisher, Fair Lawn, NJ, USA).

PFGE.
Isolates were genetically typed using PFGE aer digestion with SmaI following a standardized protocol [17]. PFGE-generated DNA �ngerprints were digitized and analyzed with BioNumerics Ver. 3.5 (Applied Maths, Sint-Martens-Latem, Belgium) by using a position tolerance of 1.0 and an optimization of 1.0. Cluster analysis was performed by the unweighted pair group method, using arithmetic averages (UPGMA), and DNA relatedness was calculated on the basis of the Dice coefficient. Isolates were considered to be genetically related if their macrorestriction DNA patterns differed by ≤7 bands and the Dice coefficient of correlation was ≥75% [18]. e prototypic pulsotype strains NRS 382, NRS 383, NRS 384, NRS 123, NRS 385, NRS 386, and NRS 387 for USA100, USA200, USA300, USA400, USA500, USA700, and USA800, respectively, were obtained through the Network on Antimicrobial Resistance in S. aureus (NARSA).

MLST.
Sequences of internal fragments of 7 housekeeping genes, arcC, aroE, glpF, gmk, pta, tpi, and yqiL of each MRSA isolate were ampli�ed by PCR as described by Enright et al. [19]. PCR amplicons were puri�ed and nucleotide sequence determined for both strands at Beckman Coulter Genomics (Beverley, MA, USA). e sequences were then trimmed so that they correspond exactly to the region that used to de�ne the alleles. e trimmed sequences of each strain were submitted to the S. aureus database (http:// saureus.mlst.net/) to obtain allelic pro�le.

Detection of PVL Gene.
Sequence speci�c for the junction region of the contiguous, cotranscribed lukS-PV and lukF-PV genes was detected by PCR with primers (Operon, Huntsville, AL, USA) and conditions described by Lina et al. [20]. PCR amplicons were analyzed by electrophoresis through 2% agarose gel.

Survey Participants.
Student population during the survey period was an average of 4,796 headcounts, of which 94% was of black race. Students' demographic source was 70% instate and 30% out-of-state. Date of birth was collected from 211 participants between fall 2006 and spring 2007, of which 205 (97%) aged 18-25 years.

MRSA Carriage.
Since S. aureus can be isolated from multiple skin locations but the nose is the primary reservoir for replication and spread to other body areas [2], we investigated MRSA carriage at nares and hand for comparison. Hands were chosen mainly because it is convenient site to sample and would less likely cause concern to students. ree hundred and twelve skin (hand) swabs and 310 nasal swabs from black students were included in this study. Of these, 1 MRSA isolate (237H) was obtained from skin swabs (0.3%), but the nasal swab of the same participant (237N) was among the dried MSA cultures in the initial screening thus not included in this study. Two MRSA isolates (81N and 240N) were obtained from nasal swabs (0.65%), but the hand swabs of these same participants (81H and 240H) were negative for

Antimicro�ial Suscepti�ility Pro�le.
All 3 MRSA isolates were found resistant to penicillin and ampicillin, two (81N and 240N) were also resistant to erythromycin, but all were susceptible to cipro�oxacin, clindamycin, doxycycline, tetracycline, trimethoprim-sulfamethoxazole, and vancomycin ( Table 2). ese have the drug-resistance pattern of community-associated MRSA (CA-MRSA) strains. Clindamycin is a main choice for treating CA-MRSA skin and so-tissue infections. Some CA-MRSA isolates, however, have the potential to become resistant to clindamycin [21]. We conducted D test for the 2 erythromycin resistant, but clindamycin-susceptible isolates strains, (81N and 240N) and found that one strain (81N) was positive for erythromycininduced clindamycin resistance.

MRSA Molecular Analysis.
All 3 MRSA isolates carried type IV SCCmec, IV for 237H, IVa for 240N, and IVb for 81N ( Figure 1). is is consistent with their lack of multidrug resistance.

Discussion
SCCmec is a mobile genetic element that carries the methicillin-resistance gene mecA. Currently, eleven major types of SCCmec have been identi�ed [22]. Type I, II, and III carry additional drug-resistance gene and oen found in healthcare-associated MRSA (HA-MRSA) strains; type IV  and V carry no additional drug-resistance gene and are CA-MRSA strains [3,22]. All 3 isolates carry type IV SCCmec, characteristic of CA-MRSA. MRSA strains have been established by PFGE as USA100 to USA1200, and multilocus sequence typing (ST) based on allelic pro�le of seven housekeeping genes. In this study, we identi�ed one USA300 strain which is also ST8, a CA-MRSA strain as a primary cause for staphylococcal skin and so tissue infection. e other 2 isolates are not so typical: 81N is a ST8 and related to USA700; 237H clusters with USA100 and was a ST2562, a new MLST strain.
From 312 skin (hand) swabs and 310 nasal swabs, 1 MRSA (0.3%) isolate was obtained from skin swabs and 2 (0.65%) from nasal swabs. Given the high rate of MRSA infection among the blacks [4][5][6][7][8][9][10][11], the nasal carriage rate initially surprised us, a rate lower than the black and white (1.6%) as found in the national prevalence survey during 2001-2004 [14]. However, a lower rate of carriage was conceivable for the population of our study. First, our study subjects were university students aged mostly 18-25 (see Section 3.1) at the time of sample collection; therefore, some of the known risk factors such as children, age greater than 60, and educational level below high school diploma were eliminated in our study.
Further, living in crowded household and having household members of MRSA-colonized persons have been found to increase the risk of becoming colonized by MRSA [3,[23][24][25][26]. Students can be contaminated by MRSA by a household member who is infected or a carrier through person to person contact, contact of surfaces, or contaminated household items and become a carrier. Living in the university dormitory limits the students' chance of such contacts with household member. erefore, when students lose their transiently carried MRSA strain, they may have a reduced chance to be retransmitted by a household member.
Other studies on nasal carriage of MRSA among college students had reported varied �ndings. In a Hawaii college in 2005, 3 of 100 students and faculty members (3%) carried MRSA [27]; in a Texas college in 2007-2008, 15 of 203 students (7.4%) carried MRSA, and the associated risk factor was determined as hospitalization within 12 months [28]; at 2 higher-learning institutions in Tennessee in 2009, investigation of student athletes found 4 of 124 (3.2%) in one institution, and 1 of 153 (0.65%) in another, carried MRSA [29].
However, the carriage rates are difficult to compare given the range of variables and the limited sample sizes.
ere have been reports describing a lower rate of nasal carriage of S. aureus in persons of African origin. Millian et al. in a 1960 study found that S. aureus carriage in African American female and male aged 18-69 were 19.5% (of 67) and 9.7% (of 72), whereas in their white counterparts were 36.7% (of 147) and 38.4% (of 271), respectively [30]. Nobel in a study of British school children aged 5-14 at an immigrant community in 1974 found nasal carriage among black children was 30% whereas among their white counterparts was 41%, a less striking but similar trend [31]. On the contrary, Lamikanra et al. in a survey of Nigerian students from primary school to university in 1985 found that S. aureus carriage as high as 56.4% [32]. Yet, the surveys by NHANES found S. aureus carriage in the USA was 25% in blacks and 33.3% in whites during 2001-2002; and 22% in blacks and 30.7% in whites during 2003-2004 [14]. is recent data indicates a more than 8% lower S. aureus carriage rate in blacks than in whites, lending supporting evidence to the notion of lower S. aureus carriage among black people.
A lower rate of S. aureus colonization could mean a higher risk for MRSA colonization or infection. For example, studies in the health care setting in 1960s suggested that an individual with persistent nasal carriage of S. aureus is generally protected against the acquisition of new S. aureus strains, while intermittent S. aureus carriers, in contrast, may be at risk of acquiring drug-resistant S. aureus [33]. Stevens et al. [23] found that skin infection took longer to develop in methicillin-sensitive S. aureus carriers (2.9 year) than MRSA carriers (0.8 years) and non-S. aureus carriers (2.2 years), supporting such hypothesis. Persons of noncarrier for S. aureus may suffer low level of S. aureus infection and it would be an advantage before the drug-resistance era. However, with the rise and wide spread of drug-resistant S. aureus the noncarrier has reduced barrier to the colonization of exposed S. aureus and can be at higher risk of being transmitted a MRSA strain and become infected [2]. is seems also a plausible factor for a higher rate of MRSA infection among the black population. But further investigation is needed.
Our study has several limitations. First, our results represented a convenience sample from a single institution, therefore, it cannot be generalized or used to predict prevalence in other settings. Second, we could not conduct a controlled study that would require the participants of an equivalent student population of other ethnic group. ird, it should be noted that our data was collected during 2006-2007, but MRSA prevalence data for the same period could not be found for comparison. Forth, we did not screen for methicillin-sensitive S. aureus which would offer additional data to understand S. aureus carriage among people of African origin. Fih, there is a growing evidence that CA-MRSA may preferentially colonize other parts of the body such as throat and inguinal areas [3,26,[34][35][36][37]. As illustrated by Miller et al. [26] in a survey of 3 body sites, nasal, oropharynx, and inguinal areas, nasal sample only revealed 49% of MRSA carriage of the combination of the 3 body sites. In the absence of additional oropharynx and inguinal specimens, the rate of MRSA carriage in our study was certainly underestimated. Our �nding nonetheless highlights the need of future study which involves multiinstitutions and other ethnic group to assess the association of black race with MRSA carriage.
In conclusion, our study found nasal carriage rate of MRSA among the black college students was 0.65%, and skin carriage in hand was 0.3%, a lower nasal carriage rate than that found among whites and blacks by the NHANES surveys. All three isolates are CA-MRSA as indicated by type IV SCCmec and nonmultidrug resistance. eir distinct molecular pro�les do not indicate transmission among students. �on��ct of �nterests e authors have no con�ict of interests to declare.