Canadian Journal of Infectious Diseases and Medical Microbiology
Volume 2018 (2018), Article ID 7258672, 6 pages
https://doi.org/10.1155/2018/7258672

Research Article

Nasal and Pharyngeal Colonization by Bacterial Pathogens: A Comparative Study between Preclinical and Clinical Sciences Medical Students

Dharm Raj Bhatta, Deependra Hamal, Rajani Shrestha, Ranjana Parajuli, Nisha Baral, Supram Hosuru Subramanya, Niranjan Nayak, and Shishir Gokhale

Department of Microbiology, Manipal College of Medical Sciences, Pokhara, Nepal

Correspondence should be addressed to Dharm Raj Bhatta; ddharma2039@gmail.com

Received 18 February 2018; Revised 16 April 2018; Accepted 2 May 2018; Published 6 June 2018

Academic Editor: Giordano Dicuonzo

Copyright © 2018 Dharm Raj Bhatta et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Background. Upper respiratory tract is one of the commonest sites for microbial colonization. The colonized individuals are at risk of infections and can be a source of transmission of pathogens. Medical students are frequently exposed to a variety of infectious agents and more likely to get colonized by them. This study was aimed to determine the prevalence and to compare the colonization rates of nasal and pharyngeal bacterial pathogens among preclinical and clinical sciences medical students. Methods. This cross-sectional study was conducted among 100 preclinical and 100 clinical sciences medical students. Isolation, identification, and antibiotic susceptibility testing of the isolates were performed by standard microbiological techniques. Results. The nasal colonization by S. aureus and MRSA was 35% (70/200) and 19.5% (39/200), respectively. The nasal colonization by S. aureus and MRSA was significantly higher among clinical sciences students as compared to preclinical sciences students. Pharyngeal colonization by Haemophilus influenzae was significantly higher among clinical sciences students as compared to preclinical sciences students. The pharyngeal colonization by beta-hemolytic streptococci (nongroup A) was higher among preclinical sciences students than clinical sciences students. Conclusion. The nasal colonization by S. aureus and MRSA was higher among clinical sciences students. Pharyngeal colonization by potential bacterial pathogens was higher among clinical sciences students than preclinical students. Periodic screening of MRSA and potential throat pathogens of clinical sciences students and may reduce the incidences of nosocomial transmission of pathogens.

1. Introduction

Respiratory tract infections are one of the important causes of morbidity and mortality worldwide [1]. Upper respiratory tract, perpetually exposed to the environmental flora, is prone to get colonized with a variety of microbial agents. Bacterial pathogens such as Streptococcus pneumoniae, Streptococcus pyogenes, Haemophilus influenzae, Neisseria meningitidis, and Staphylococcus aureus often colonize the human upper respiratory tract. These pathogens get easily transmitted from colonized/infected individuals to healthy population via respiratory droplets or oropharyngeal secretions. Asymptomatic colonization by potential pathogens like Streptococcus pneumoniae, Streptococcus pyogenes, Haemophilus influenzae, and Neisseria meningitidis may lead to invasive infections and serious complications. The carrier rates of these pathogens vary depending upon socioeconomic status, environmental conditions, age, and antimicrobial therapy of the population [2]. Increasing resistance to antimicrobial agents and emergence of multidrug resistant (MDR) organisms makes the treatment of invasive infections challenging [3].

Transmission of respiratory pathogens in healthcare setting is determined by interaction with patients and microbial load in the hospital environment. Environmental quality of healthcare setting and concentration of airborne microbes depend on microbes expelled by patients and healthcare workers. In absence of adequate ventilation, microbes may persist in the hospital environment for variable durations. This enhances the risk for occupants, patients, and medical students who spend long hours in the hospital environment. The individuals involved in patient care and medical students of clinical sciences have greater chances of carrying pathogenic bacteria and can be a potential source of nosocomial infections [4–7].

This study was planned to determine the nasal and pharyngeal colonization by bacterial pathogens among undergraduate medical students and to compare the difference in the colonization rates among preclinical and clinical sciences medical students. We hypothesized that exposure to hospital environment would increase nasal and pharyngeal bacterial colonization among students of clinical sciences as compared to preclinical sciences students who have no such exposure to hospital environment. Similarly, higher antibiotic resistance pattern among isolates from clinical sciences students as compared to preclinical students is expected.

2. Materials and Methods

2.1. Study Design and Subjects

This cross-sectional prospective study was conducted over a period of five months from May 2017 to September 2017. Approval from the Institutional Ethical Committee (IRC) of Manipal College of Medical Sciences (MCOMS), Pokhara, Nepal, was obtained before the commencement of the study. All participants were enrolled after obtaining the written informed consent. Study population comprised 200 undergraduate medical students. The total available study population in one batch of preclinical sciences (Subset A) was 100 students. Therefore, whole population of one batch was included. Equal number of students from clinical sciences (Subset B) was taken for a comparative study after consulting a statistician. Basic and clinical sciences blocks are separated by a distance of 3.5 km. The students from both subsets do not share residential or mess arrangements and have very infrequent interactions.

2.1.1. Inclusion Criteria

Clinical science students with minimum two years of hospital exposure (interns) were included in Subset B. Preclinical sciences students without histories of hospitalization in the last six months were included in Subset A.

2.1.2. Exclusion Criteria

Clinical sciences students who were on long leave (>2 months) and preclinical sciences students with a history of hospitalization within the last six months were excluded from the study.

Demographic details including age, gender, nationality, hospital exposure, recent exposure to antibiotics, respiratory illness, smoking, chewing tobacco/gutka, and so on were collected by a structured questionnaire. The data of the related isolates from the Clinical Microbiology laboratory of Manipal Teaching Hospital were collected to determine the prevalence of respiratory pathogens among the patients for analysis during the study period.

2.2. Specimen Collection

One specimen from the anterior nasal cavity and one from the posterior pharyngeal wall (200 nasal swabs and 200 pharyngeal swabs) from 200 participants (100 from Subset A and 100 from Subset B) were collected. Specimens were obtained by rubbing both the anterior nares with the first swab and by swabbing the posterior oropharynx by the second swab.

2.3. Isolation and Identification of Bacterial Isolates

Specimens were inoculated immediately on 5% sheep blood agar and chocolate agar (Hi Media, Mumbai, India) plates at the point of collection. Inoculated plates were immediately transported to the laboratory and incubated at 37°C in a candle jar with increased CO₂ partial pressure. Identification of the isolates was performed by standard microbiological techniques such as colony morphology, Gram stain, the catalase test, the coagulase test, optochin sensitivity, bacitracin sensitivity, and the satelitism test [8].

2.4. Antibiotic Susceptibility Test

Antibiotic susceptibility testing of the isolates was performed on Mueller–Hinton agar (HI Media, Mumbai, India) by the Kirby–Bauer disc diffusion method [9]. Methicillin resistant Staphylococcus aureus (MRSA) was screened by the cefoxitin (30 µg) disc diffusion method [9].

2.5. Statistical Analysis

The correlation between variables was determined by the chi-square test using SPSS 11.5. A value ≤ 0.05 was considered significant.

3. Results

A total of 200 medical (MBBS) students comprising 100 students in Subset A (first year) and 100 in Subset B (interns) were enrolled in this study. The Subset A participants were 18–25 years of age, while Subset B were between 22 and 30 years of age. Demographic details of the students are shown in Table 1.

Table 1: Demographic and clinical details of the students.

Variable
Subset A () frequency
Subset B () frequency

Sex

Male
59
61

Female
41
39

Nationality

Nepali
62
58

Others (Indians, Sri Lankan, and Maldivian)
38
42

Antibiotic intake

Yes
05
04

No
95
96

Hospitalization

Yes
00
03

No
100
97

Respiratory infection

Yes
06
05

No
94
95

Smoking/tobacco intake

Yes
03
04

No
97
96

Bacteriological profile of nasal and pharyngeal swab cultures of Subset A and Subset B is shown in Table 2. The overall nasal colonization by S. aureus and MRSA was 35% (70/200) and 19.5% (39/200), respectively. The nasal colonization rate of S. aureus and MRSA was significantly higher ( values 0.003 and 0.001) among Subset B as compared to Subset A (Table 2). The isolates from the pharynx (Subset A and Subset B) were Haemophilus influenzae (12.5%), nongroup A beta-hemolytic streptococci (5.5%), S. aureus (5.5%), Streptococcus pneumoniae (4%), and Haemophilus parainfluenzae (3.5%). Pharyngeal colonization by Haemophilus influenzae was found significantly higher (p value 0.005) among Subset B as compared to Subset A (Table 2). Among the participants, 7.5% (15/200) were colonized with S. aureus in the nasal cavity along with other potential pathogens in the pharynx (Haemophilus influenzae, beta-hemolytic Streptococci, and Streptococcus pneumoniae).

Table 2: Distribution of bacterial isolates from nasal and pharyngeal specimens.

Organism
Nasal swab Subset A ()
Nasal swab Subset B ()
value

Staphylococcus aureus
25
45
0.003

Methicillin-resistant Staphylococcus aureus (MRSA)
10
29
0.001

Pharyngeal swab Subset A ()
Pharyngeal swab Subset B ()

Staphylococcus aureus
5
6
0.756

Methicillin-resistant Staphylococcus aureus (MRSA)
2
3
0.651

Haemophilus influenzae
6
19
0.005

Haemophilus parainfluenzae
3
4
0.700

Streptococcus pneumoniae
2
6
0.149

Beta-hemolytic streptococci
8
3
0.121

Significant association.

Out of 100 nasal swabs collected from Subset A, S. aureus was isolated from 25 (25%) participants, of which 10 (40%) were MRSA. The nasal carriage rate of S. aureus was 28.8% (17/59) and 19.5% (8/41) among male and female participants, respectively, which was statistically insignificant ( value 0.291). Similarly, the nasal carriage rate of MRSA was 13.5% (8/59) and 4.9% (2/41) among male and female participants, respectively. This difference was statistically insignificant ( value 0.155). Other bacterial flora isolated from nasal swabs includes Staphylococcus epidermidis, Micrococcus species, Enterococcus species, and aerobic spore bearer.

Bacteriological culture of nasal and pharyngeal specimens among Subset B showed similar bacterial isolates as in Subset A but relatively higher rate of colonization (Table 2). Nasal colonization by S. aureus among Subset B was 45% (45/100) with 29% (29/100) MRSA. The nasal carriage rate of S. aureus among male and female was 41% (25/61) and 41% (16/39), respectively. Similarly, the nasal MRSA colonization rate among participants was 26.2% (16/61) in male and 33.3% (13/39) in females. Antibiotic resistance pattern of S. aureus isolates from Subset A and Subset B is depicted in Table 3. No significant difference in the antibiotic resistance pattern of S. aureus isolates from Subset A and Subset B was observed. Antibiotic resistance pattern of pharyngeal isolates is depicted in Table 4.

Table 3: Antibiotic resistance pattern of Staphylococcus aureus isolates from nasal and pharyngeal specimens.

Antibiotic
Subset A () frequency (percentage)
Subset B () frequency (percentage)
value

Penicillin
27 (90%)
50 (98%)
0.107

Erythromycin
16 (53.3%)
38 (74.5%)
0.051

Ciprofloxacin
10 (33.3%)
21 (41.1%)
0.483

Gentamicin
01 (3.3%)
03 (5.8%)
0.609

Clindamycin
06 (20%)
11 (21.5%)
0.867

Ceftriaxone
06 (20%)
14 (27.4%)
0.453

Amikacin
01 (3.3%)
03 (5.8%)
0.609

Tetracycline
02 (6.6%)
06 (11.7%)
0.458

Vancomycin
00
00
—

Table 4: Antibiotic resistance pattern of pharyngeal isolates.

Organism (number)
Antibiotics (resistant percentage)

P
CIP
COT
C
CTR
AZM
E

Haemophilus influenzae (25)
—
1 (4%)
3 (12%)
1 (4%)
00
5 (20%)
—

Haemophilus parainfluenzae (7)
—
1 (14.3%)
1 (14.3%)
00
00
00
—

Beta-hemolytic streptococci (11)
00
00
00
—
00
—
—

Streptococcus pneumoniae (8)
3 (37.5%)
00
00
—
00
—
2 (25%)

Four isolates of beta-hemolytic streptococci (45.4%) were intermediate sensitive to penicillin. AZM: azithromycin, CIP: ciprofloxacin, CTR: ceftriaxone, COT: cotrimoxazole, C: chloramphenicol, E: erythromycin, P: penicillin.

Majority of students with nasal carriage of S. aureus had no history of antibiotic use in the past two weeks (95.8%), no history of hospitalization in the past six months (98.6%), no history of respiratory infections (92.9%), and no history of smoking/tobacco intake (95.7%). Similarly, majority of students with pharyngeal carriage of potential bacterial pathogens had no history of antibiotic use, hospitalization, respiratory infection, and smoking/tobacco intake.

4. Discussion

Burden of nosocomial infections is significantly higher in developing countries [10]. Healthcare professionals are considered important reservoirs for transmission of nosocomial pathogens. Another potential source of infections could be medical students particularly those involved in patient care. Human nasal cavity and pharynx are favorable anatomical sites for colonization by microbial agents. Therefore, it is important to screen healthcare workers and medical students for colonization by bacterial pathogens.

In our study, the nasal carriage rate of S. aureus among the clinical science student (Subset B) was 45% which is significantly higher than the preclinical science (Subset A) student (25%). Findings of our study are comparable with other studies with the colonization rate around 40% [11, 12]. In a similar study conducted among preclinical sciences students of Nepal, 15% of nasal carriage of S. aureus was reported [13]. However, similar studies from other countries have shown colonization rates ranging from 19% to 25% [14–16]. The nasal carriage rate of MRSA among Subset B in our study was 29% which is significantly higher than Subset A (10%). The MRSA colonization rate reported in 2016 by Ansari et al. from Nepal was lower (4%) than our findings [13]. Lower MRSA colonization rates ranging from 0% to 9.4% have been reported from other countries [14, 15, 17, 18]. Higher rates of S. aureus colonization among medical students of clinical sciences can be attributed to long-term exposure to hospital environment and regular interaction with patients. However, Syafina et al. reported higher S. aureus colonization among preclinical students as compared to clinical students [19]. Pathogens like MRSA survive for long durations due to their stability in the hospital environment. This enhances the risk of transmission and colonization. The MRSA colonization rates among healthcare workers in a particular setting depend on local prevalence of MRSA and infection control practices. High percentage of MRSA colonization among clinical students in our study could be associated with the high prevalence of MRSA (34.75%) among the clinical isolates of the Manipal Teaching hospital [20]. High prevalence of MRSA among the patients in healthcare setting increases the risk of colonization among the healthcare workers due to frequent interactions. Preclinical students on the other hand are away from the hospital environmental exposure and have lower S. aureus and MRSA colonization.

The carriage rate of S. aureus and MRSA among male students was found higher as compared to females which are comparable with other reports [15, 21, 22]. Older age has been considered as a possible factor for S. aureus colonization. The clinical science student of older age group is colonized more with S. aureus as compared to the younger age preclinical student.

Antibiograms of S. aureus isolated from Subset B showed higher but statistically insignificant resistance pattern as compared to Subset A (Table 2). This could be correlated with the fact that hospital strains are more resistant to commonly used antibiotics as compared to community strains [23, 24]. The antibiotic resistance pattern of the isolates is likely to change over a period of time due to changes in antibiotic prescription pattern. Increased antimicrobial resistance has been reported from the isolates of tertiary care teaching hospitals, possibly due to increased selective pressure arising from widespread antimicrobial use, high density of patients and healthcare workers, inadequate ventilation, and inadequate infection control policies. S. aureus isolates in our study were found more resistant to commonly used antibiotics as compared to report by Okamo et al. [15].

Upper respiratory tract colonization by bacterial pathogens increases the risk of invasive infections and transmission to the susceptible host. Microbial colonization is a complex process which involves colonization, elimination, and recolonization [25]. The overall pharyngeal colonization rate by bacterial pathogens was higher among Subset B as compared to Subset A but was statistically not significant except in case of H. influenzae. Higher rates of pharyngeal colonization among Subset B could be due to prolonged (>2 years) hospital environmental exposure and interactions with the variety of patients. The pharyngeal colonization rate of beta-hemolytic streptococci was higher among Subset A but statistically insignificant. Previous study from the same institution reported 65% colonization rate with Streptococcus pneumoniae and/or Haemophilus species among the healthcare workers which is higher than our findings [26]. Number of contributing factors could be associated with the nasal and pharyngeal microbial colonization. The common risk factors include younger age, winter, overcrowding, low socioeconomic status, and smoking. Low pharyngeal colonization rate in our study may be due to the fact that majority of the participants were nonsmokers belonging to middle and high income groups and specimens were collected in summer. The data from Clinical laboratory of Manipal Teaching Hospital, for corresponding months, revealed low rate of isolation of abovementioned organisms from the clinical samples. Lower prevalence of these pathogens among the patients could be related to lower pharyngeal carriage rates among the students. The nasal colonization rate of S. aureus was higher as compared to potential pathogens isolated from the pharynx. Pathogens like Streptococcus pneumoniae, Streptococcus pyogenes, and Haemophilus influenzae are delicate and get inactivated shortly after excretion and exposure to disinfectants. The survival time of these organisms in the hospital environment is shorter as compared to MRSA reflecting their poor transmission and low colonization rates.

The overall antibiotic resistance pattern of the pharyngeal isolates (Subset A and Subset B) revealed that most of the Haemophilus isolates were susceptible to commonly used antibiotics. Among Streptococcus pneumoniae isolates, 37.5% (3/8) were resistant to penicillin indicating the increasing resistance. Out of 11 beta-hemolytic streptococci, 45.4% (4/11) showed intermediate susceptibility to penicillin. This finding may be alarming for future emergence of penicillin-resistant strains. Finding of our study is comparable with study from India [27].

Screening of nasal and pharyngeal colonization among healthcare workers and medical students may help to predict the transmission of potential pathogens. The risk of transmission and dissemination of bacterial pathogens from one unit/ward to another is more with clinical sciences students as they undergo periodic rotational training program in various wards/units. The clinicians and other healthcare workers work in one particular unit and are less likely to spread the pathogens from one unit to another. Screening data can be important to minimize the transmission among high-risk patients like neonates, burn patients, postoperative patients, and ICU patients. In view of the above, survey of the hospital regarding the prevalence of MRSA and other potential pathogens in different units will help to tackle the situation. Based on the available data, hospital units can be classified as high-risk units (zone), moderate risk-units, and low-risk units. Awareness/orientation program may be needed after completion of the preclinical science study regarding the standard practices to minimize transmission and prevention of hospital-acquired infections. Regular screening program and restriction of colonized healthcare workers and medical students especially in high-risk units should be strictly implemented in order to reduce transmission of nosocomial pathogens.

The strength of our study lies in coverage of nasal and pharyngeal colonization by bacterial pathogens among medical students as most of the previous studies had limited findings of nasal colonization by S. aureus/MRSA only. Nasal and pharyngeal colonization among medical students could be a potential source of clonal spread of MRSA in the hospital. This has been amply emphasized in our study.

This study had some limitations. The study was conducted during the autumn/summer season; hence, seasonal variation in the colonization rate could not be studied. Molecular analysis of the potential pathogens was not done. The transmission of pathogens from medical students to patients, healthcare workers, and vice versa was not included in this study. The study was conducted among students of one medical college of Western Nepal, and results of the study cannot be generalized to students of other medical colleges.

5. Conclusion

Medical students of clinical sciences have higher rates of S. aureus and MRSA colonization. Higher colonization is perhaps due to prolonged hospital environmental exposure and interaction with patients. Pharyngeal colonization by potential pathogens was higher among the clinical sciences student. Higher rates of nasal and pharyngeal colonization among medical students can be threat for transmission of potential pathogens among patients and healthcare workers. Awareness among medical students about their role in transmission of pathogens and importance of universal precautions and hand hygiene would help in reducing the nosocomial infections.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors have no conflicts of interest.

Authors’ Contributions

Dharm Raj Bhatta as a principal investigator designed the study, collected and processed the specimen, analyzed the data, and drafted the manuscript. Deependra Hamal, Rajani Shrestha, Ranjana Parajuli, Nisha Baral, and Supram Hosuru Subramanya contributed in specimen collection, processing, and data analysis. Niranjan Nayak and Shishir Gokhale contributed in formulating objectives and refining manuscript. All authors have read and accepted the manuscript.

Acknowledgments

The authors are thankful to all the staffs of Microbiology Department, Manipal Teaching Hospital, Pokhara, Nepal, for their help and support. The authors would like to thank students of preclinical and clinical sciences for their participation in the study.

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