Kavitha.
Y1, Mohan S2, Anandi V3, Babu H4
1Dr.
Kavitha.Y, Associate Professor, 2Dr. Mohan S, Senior Associate Professor,
3Dr. Anandi V, Professor, These three authors are affiliated with Department
of Microbiology, Vinayaka Missions Medical College & Hospital, Karaikal-609609,
Vinayaka missions research foundation (Deemed to be University) 4Dr.
Harish Babu, Assistant Professor, Department of Obstetrics and Gynecology, Vinayaka
Missions Medical College & Hospital, Karaikal- 609609 Vinayaka missions
research foundation (Deemed to be University), Karaikal- 609609 Puducherry, India
Corresponding
Author: Dr. Mohan S, Address- Department of Microbiology, VMMC & H, Karaikal, Vinayaka
missions research foundation (Deemed to be University). Karaikal- 609609, Puducherry,
India. E-mail Address: drmohanmmc@gmail.com
Abstract
Introduction: Candida species are opportunistic pathogens
which cause a wide variety of infections in humans ranging from trivial
intertriginous infection to fatal candidemia. Vulvo vaginal candidiasis (VVC) is an acute inflammatory disease and a
frequent reason for gynaecological consultations. The present study
aimed at determining prevalence of Candida species from VVC and to speciate
isolated Candida with antifungal susceptibility profile among non pregnant
women. Materials and Methods: This
was a cross sectional study conducted over a period of six monthsin the
department of microbiology and Obstetrics and Gynecology. Swabs collected from
patients were subjected to microscopy (Gram s stain) and culture on Sabouraud’s
dextrose agar. Species level was identified by using chrome agar. Antifungal susceptibility testing:
Antifungal susceptibility testing was performed by NCCLS M44 -A Disc diffusion
method. Results: A total of 209 high vaginal swabs were
collected from non pregnant women. 71 patients high vaginal swabs
yielded growth of Candida species and accounted for 33.97%. Most commonly
isolated species were Candida albicans 31 (43.66%) followed by Candida
tropicalis 27(38.03%) and Candida glabrata 13(18.31%). All species were found
to be susceptible to Amphotericin B. Among
commonly used antifungals, clotrimazole was found to be most susceptible. But,
C.glabrata species was least susceptible to frequently used antifungals. Conclusion: Candida albicans was the
most commonly isolated species.CHROMagar is
rapid, technically simple and cost effective compared to time consuming
technically demanding expensive conventional methods. Performing antifungal susceptibility is useful in
choosing appropriate antifungal in treating vulvo vaginal
candidiasis.
Key words: Vulvo vaginal
candidiasis, Candida albicans, CHROM agar
Author Corrected: 30th August 2018 Accepted for Publication: 3rd September 2018
Introduction
Vulvo vaginal candidiasis (VVC) is an acute inflammatory disease
and a frequent reason for gynecological consultation as it can affect up to 75%
of women of child-bearing age[1]. Clinical signs and symptoms include intense
pruritus, vaginal discharge, anerythematous vulva and dyspareunia [2]. Until recently, the problem of
vaginal candidiasis was often ignored, or treated as an insignificant problem
forthe female population. It received more focus onlyafter Herman Gardner said:
“Vaginitis can cause moreinconvenience than any other gynaecological disease. In
addition, many mental and emotional problems are associated with vaginitis “[3].
There
are many risk factors for development of vulvovaginalcandidiasis, like vaginal
ecosystem, pregnancy, hormonalcontraception, diabetes, stress recent
antibioticuse, dietary practices, gastrointestinal colonization by theorganism,
clothing and weaken immune-compromised system[4].
VVC
is most often caused byCandida albicans, however, other species of Candidasuch
as Candida glabrata, Candida parapsilosis, and Candida tropicalis are
emerging [5]. Azole antifungals are being frequently being used to treat
infections caused by Candida species Recently
studies reported that intrinsic azole resistance in some Candida
species as well as development of high-level azole resistance is a problem of
critical importance in the clinical setting [6]. Mostof the studies done
previously focused on immunocompromised subjects, especially pregnant women,
with few studies on other wise immunocompetent women.
The present study aimed at determining prevalence of
Candida species from VVC and to speciate isolated Candida with antifungal
susceptibility profile among non pregnant women.
Material
and Methods
This
was a cross sectional study conducted over a period of six months in the
departmentof microbiology in collaboration with the department of Obstetrics
and Gynaecology of Vinayaka mission’s medical college and
hospital. Study population consisted of non pregnant women attending OPD of
Obstetrics and Gynaecology. Verbal consent was obtained from the women before
sample collection. Clinical examination was performed of each participant and
recorded signs of vaginal abnormalities. A pair of highvaginal swabs were
obtained from the posterior vaginal fornix of the subjects aseptically with the
help of a vaginal speculum. Swabs collected from patients were subjected to
microscopy (Gram s stain) and culture on Sabouraud’s dextrose agar.
Species
identification: CHRO Magar was used for preliminary identification of yeast and
to detect mixed infections. Candida species were differentiated by colonial
morphology and colors, which were generated by a chromogenic in the agar,
asdescribed by Wortman et al[7].
Antifungal
susceptibility testing: Antifungal susceptibility testing was performed by
NCCLS M44 - A Disc diffusion method.
Inoculum
was prepared by picking five distinct colonies of approximately 1 mm in
diameter from 24 h old culture of Candida species. Colonies were suspended in 5
ml of sterile saline and its turbidity was adjusted visually with the
transmittance to that produced by a 0.5 McFarland standard. Inoculation of test
plates were done with a sterile cotton swab dipped into the suspension. The
dried surface of a sterile Mueller-Hinton + GMB (glucose and methylene blue)
agar plate was inoculated by evenly streaking the swab over the entire agar
surface. Anti fungal disks were dispensed onto the surface of inoculated agar
plate. Plates were incubated at 350 C and examined after 20-24
hours. The zone of inhibition was measured and the results were recorded as
susceptible/resistant[8]. Patients aged between 15-45 years and non-pregnant
were included in the study. Immunocompromised patients, menstruating women and
patients who were taken antifungal therapy in past two weeks (before sample
collection) were excluded. Statistical analysis was done by simple percentage
method.
Results
A total of 209 high vaginal swabs
were collected from non pregnant women aged between 15-45 years attending with
any vulvovaginal
candidiasis symptoms (itching, soreness, vaginal secretions, inflammation,
rashes etc.). Of the 209 patients included in the study, 71 patients high
vaginal swabs yielded growth of Candida species and accounted for 33.97%.
Majority of the patients yielded growth were ranged between 26-35 years and
accounted for 54% followed by 16-25 years which showed 30%. Least growth was
seen in the patients between the age group of 36-45 years which accounted for
14% (Table.1).
Table-1:
Age wise distribution of Candida growth on SDA medium
Age |
Growth
on SDA |
15-25 |
22 (30%) |
26-35 |
39(54%) |
36-45 |
10 (14%) |
Table-2:
Candida species isolated from high vaginal swabs.
Candida species |
Number (%) |
Candida albicans |
31 (43.66%) |
Candida tropicalis |
27 (38.03%) |
Candida glabrata |
13 (18.31%) |
Total |
71 (100%) |
Most
commonly isolated species were Candida albicans 31 (43.66%) followed by Candida
tropicalis 27(38.03%) and Candida glabrata 13(18.31%) (Table.2)
Table-3: Antifungal
susceptibility of Candida species isolated.
Candida species |
Clotrimazole |
Fluconazole |
Miconazole |
Amphotericin B |
Candida albicans(n=31) |
22(70.96%) |
11(35.48%) |
19(61.29%) |
100(100%) |
Candida tropicalis (n=27) |
15(55.55%) |
7(25.92%) |
13(48.14%) |
100(100%) |
Candida
glabrata(n=13) |
3(23.07%) |
3(23.07%) |
5(38.46%) |
100(100%) |
Discussion
In
the present study infection rate of vulvovaginal candidiasis was found to be 33.97%.
But according to the study conducted by Enweani et al[9]V VC in
non-pregnant women was 40.6% which is high compared to the present study. Eckert
et al [10]found 25% of VVC among non pregnant women.The
prevalence of vaginal candidiasis reported by different studies was 16.5%,
21.31%, and 19%[11,12,13]. This relatively low prevalence of vaginal
candidiasis among women in other studies probably due to to adequate knowledge,
good personal hygiene, and normal levels of estrogens and corticoids[14].
In the present study, Candida species was
predominantly isolated in the age group of 26-35 years which accounted for 54%.
This may be due to high sexual activity, poor personal hygiene, the use of
contraceptives, and drug abuse among this age-group. Alo et al[15] reported a
higher prevalence of C. albicans (33.33%) within the age bracket of
36–40 years, while those between 20 and 25 years had the lowest prevalence
(20.42%).
In the present study, low Candida infection was
found in age group 36-45 years which accounted for 14%. This finding is in line
with a previous report by Okungbowa et al[16] who reported prevalence of 10%
and 2% within the age-groups of 36–45 and over 46 years, respectively. They
reported that this was probably due to the possible increase in vaginal
immunity with age as they have decreased levels of estrogen and corticoids, and
thus are resistant to Candida infections.
In
the present study, Candida albicans31
(43.66%) was the most predominant
species isolatedfollowed by Candida tropicalis
27(38.03%) and Candida glabrata 13(18.31%), similar to other study
by Grigoriou et al, the most commonly
isolated species from the patients was C. albicans. According to Habibipour R, [17]C. albicans (81.3%) predominantly and
then C. glabrata (11%), C. tropicalis (4.4%) and C. kuresi (2.2%)
were isolated from VVC. A similar distribution of Candida spp. Similar
observation was found by other authors [18,19].
C.
albicansadheres to vaginal epithelial cells in
significantly highernumbers than do other Candida species [20]. Vaginitis
induced by non-albicans species is clinically indistinguishable from
that caused by C. albicans[21]. The reason for the increase in incidence
of VVC caused by non-albicans species is thought to be single-dose
antifungal treatment, low-dosage azole-maintenance regimens, and the use of
over-the-counter antimycotics[22].
In the present study, all three species of Candida were
least susceptible to fluconazole and no Candida species showed resistance to
amphotericinB. Few strains of Candida species exhibited multi drug resistance
to routinely used antifungals. Relatively low levels of fluconazole resistance
were observed in all species of Candida isolated.Resistance to fluconazole is of
great concern as it is the most common azole used for the treatment of
candidiasis including VVC. Fluconazole is available in both intravenous and
oral formulations with high bioavailability and is more cost-effective than
other antifungal agents.
As per
study by Mishra et al[23] all C. glabrata, 50% C. tropicalis
and 12% C. albicans isolates were found to be resistant to
fluconazole.But, another study by Khan M et al observed,C. krusei
showed 100% resistance to fluconazole[24]. It is worth mentioning that the
non-albicans species had the highest levels of resistance compared to C.
albicans.C.glabrata was the least susceptible to the tested antifungals.Although amphotericin B iseffective
against most strains of Candida spp., its usage is limited due to the nephro
toxicity associated with it.
Conclusion
Candida albicans was the most
commonly isolated species followed by C.tropicalis. Among commonly used
antifungals, clotrimazole was found to be most susceptible. But, C.glabrata
species was least susceptible to frequently used antifungals. Hence, species
level identification is required to choose appropriate antifungal and chrom
agar medium will helpful to mycology laboratories for rapid identification of
clinically important candida spp.
Contributions
by Authors
1. Dr.
Harish Babu: Clinical examination of patients and specimen collection.
2. Dr.
Kavita: Study design and microbiology work up.
3. Dr.
Anandi and Dr. Mohan: Collection of review literature and manuscript
preparation.
Information added to existing knowledge:Usually
involvement of C.albicans is frequent in causing vulvovaginal candidiasis and
other species cause vulvovaginal candidiasis infrequently. But in our study,
isolation rate of C.tropicalis is almost equal to C.albicans.
References
1. Sobel JD. Pathogenesis and treatment of recurrent vulvovaginal candidiasis. Clin Infect Dis. 1992 Mar;14 Suppl 1:S148-53.[pubmed]
2.
Borges S, Silva J, Teixeira P. The role of lactobacilli and probiotics
in maintaining vaginal health. Arch Gynecol Obstet. 2014
Mar;289(3):479-89. doi: 10.1007/s00404-013-3064-9. Epub 2013 Oct 30. [pubmed]
3. Sobel JD, Faro S, Force RW, et al. Vulvovaginal
candidiasis: epidemiologic, diagnostic, and therapeutic considerations. Am J
Obstet Gynecol. 1998 Feb;178(2):203-11.[pubmed]
4.
Ahmad A, Khan AU. Prevalence of Candida species and potential risk
factors for vulvovaginal candidiasis in Aligarh, India. Eur J
ObstetGynecolReprod Biol. 2009 May;144(1):68-71. doi:
10.1016/j.ejogrb.2008.12.020. Epub 2009 Mar 3.[pubmed]
5. Jindal N, Gill P, Aggarwal A. An epidemiological study of
vulvovaginal candidiasis in women of childbearing age. Indian J Med Microbiol.
2007 Apr;25(2):175-6.[pubmed]
6. Flowers SA, Colón B, Whaley SG, et al. Contribution of
clinically derived mutations in ERG11 to azole resistance in Candida albicans.
Antimicrob Agents Chemother. 2015 Jan;59(1):450-60. doi: 10.1128/AAC.03470-14.
Epub 2014 Nov 10.[pubmed]
7.
Wortman JR, Gilsenan JM, Joardar V, The 2008 update of the Aspergillus
nidulans genome annotation: a community effort. Fungal Genet Biol. 2009
Mar;46 Suppl 1:S2-13. doi: 10.1016/j.fgb.2008.12.003. Epub 2008 Dec 25.[pubmed]
8. Wayne,
P.A.: Method for Antifungal Disk Diffusion Susceptibility Testing of Yeasts,
NCCLS document M44 -A (2004).
9.
Enweani IB, Gugnani HC, Okobia R, Ojo SB. Effect of contraceptives on
the prevalence of vaginal colonization with Candida species in Edo
State, Nigeria. Rev IberoamMicol. 2001 Dec;18(4):171-3.[pubmed]
10. Eckert LO, Hawes SE, Stevens CE, et al. Vulvovaginal candidiasis:
clinical manifestations, risk factors, management algorithm. Obstet Gynecol.
1998 Nov;92(5):757-65.[pubmed]
11.
Mahadani JW, Dekate RR, Shrikhande AV.Cytodiagnosis of discharge per
vaginum. Indian J Pathol Microbiol. 1998 Oct;41(4):403-11.[pubmed]
12.
Nandan D, Gupta YP, Krishnan V, et al. Reproductive tract infection in
women of reproductive age group in Sitapur/Shahjahanpur District of
Uttar Pradesh. Indian J Public Health. 2001 Jan-Mar;45(1):8-13.[pubmed]
13.
Aring BJ, Mankodi PJ, Jasani JH. Incidence of vaginal candidiasis in
leucorrhoea in women attending in OPD of gynecology and obstetrics department.
Int J Biomed Adv Res. 2012;3(12):867–869.
14.
Fernández Limia O, Lantero MI, Betancourt A, et al. Prevalence
of Candida albicans and Trichomonas vaginalis in pregnant women in
Havana City by an immunologic latex agglutination test. MedGenMed. 2004
Oct 15;6(4):50.[pubmed]
15.
Alo MN, Anyim C, Onyebuchi AK, Okonkwo EC. Prevalence of asymptomatic
co-Infection of candidiasis and vaginal trichomoniasis among pregnant women in
Abakaliki, South-Eastern Nigeria. J Nat Sci Res. 2012;2(7):87–91.
16.
Okungbowa FI, Isikhuemhen OS, Dede AP. The distribution frequency of
Candida species in the genitourinary tract among symptomatic
Individuals in Nigerian cities. Rev IberoamMicol. 2003 Jun;20(2):60-3.[pubmed]
17.
Habibipour R. Prevalence Rate of Vulvovaginal Candidiasis and Identification
ofCandida Species inWomen in Referred to Hamedan Hospitals 2013-2014,West of
Iran. Zahedan J Res Med Sci. 2013; 18(3):6250.
18.
Corsello S, Spinillo A, Osnengo G, et al. An epidemiological survey of
vulvovaginal candidiasis in Italy. Eur J ObstetGynecolReprod Biol. 2003
Sep 10;110(1):66-72.[pubmed]
19.
Nazeri M, Mesdaghinia E, Moravej SAR, Atabakhshiyan R, SoleymaniF. Prevalence
of vulvovaginal candidiasis and frequency of Candidaspecies in women [in
Persian]. J Mazandaran Univ Med Sci.2012;21(86):254–62.
20.
Simões JA, Giraldo PC, Faúndes A. Prevalence of
cervicovaginal infections during gestation and accuracy of clinical
diagnosis. DOI:10.1155/S1064744998000246
21. Bauters TG, Dhont MA, Temmerman MI, Nelis HJ. Prevalence
of vulvovaginal candidiasis and susceptibility to fluconazole in women. Am J
Obstet Gynecol. 2002 Sep;187(3):569-74.[pubmed]
22.Reed BD. Risk factors for Candida vulvovaginitis. ObstetGynecolSurv. 1992 Aug;47(8):551-60. [pubmed]
23.
Mishra M, Agrawal S, Raut S, et al. Profile of yeasts isolated from
urinary tracts of catheterized patients. J Clin Diagn Res. 2014
Feb;8(2):44-6. doi: 10.7860/JCDR/2014/6614.4003. Epub 2014 Feb 3.[pubmed]