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. 2024 Jun 19;16(6):e62680. doi: 10.7759/cureus.62680

Identification of Yeast and Yeast-Like Fungi at a Tertiary Care Center: A Retrospective Study

Yogendra P Shelke 1, Ashwini A Tidake 2, Sarita Ugemuge 2, Prasanna Nakate 1, Suvarna Patil 1, Shailesh Lambhore 3, Nandkishor J Bankar 4,, Gulshan R Bandre 4
Editors: Alexander Muacevic, John R Adler
PMCID: PMC11258929  PMID: 39036264

Abstract

Background

Fungal infections pose a significant global health challenge. Despite their substantial impact, these ubiquitous fungi can become pathogenic but have not received adequate attention in public health, leading to infections that are often underestimated by the general public and healthcare professionals. Candida species and Cryptococcus species play a key role in these infections, with emerging multidrug resistance in Candida species posing considerable challenges. This study aimed to understand the prevalence of yeast and yeast-like infections, particularly in the COVID-19 era, and to assess the antifungal susceptibility pattern.

Methodology

A retrospective observational study was conducted at a rural tertiary care medical college in Maharashtra, India. Retrospective records of samples processed for fungal culture were analyzed in the microbiology department. Yeast identification and antifungal susceptibility were performed using the VITEK-2 automated system.

Results

Among 95 fungal isolates, 86 (90.52%) were yeast isolates, primarily non-albicans Candida (NAC) species. Candida albicans accounted for 41 (47.67%) yeast isolates. In 14 isolates, NAC species were not identified by the VITEK-2 system up to the species level. Isolates from urine samples contributed the highest percentage of 61% (58) of yeast isolates. C. albicans showed high sensitivity to most antifungal agents. Other Candida species, such as Candida famata, Candida parapsilosis, and Candida guilliermondii, were sensitive to all antifungal agents. Candida auris showed complete resistance to amphotericin B and fluconazole but sensitivity to other agents. Mixed sensitivity patterns were observed in Candida ciferri and Candida lusitaniae, with some resistance to voriconazole, caspofungin, and micafungin.

Conclusions

This study shows the increasing prevalence of yeast and yeast-like infections, particularly NAC, during the COVID-19 era. Improved yeast identification and susceptibility testing are crucial for guiding the appropriate treatment and mitigating the impact of these infections, emphasizing the need for comprehensive future studies in this area.

Keywords: yeast-like fungi, antifungal susceptibility, non-albicans candida, c. albicans, yeast

Introduction

Fungal infections pose a significant global health challenge, affecting approximately 150 million people annually and resulting in 1.7 million deaths [1]. Despite their substantial impact, fungal diseases, which are ubiquitous in the environment and can become pathogenic under specific conditions, have not received adequate attention in public health, leading to infections that are often underestimated by the general public and healthcare professionals [1,2]. Yeast is a unicellular fungus, with the pathogenic yeast genera Candida and Cryptococcus being the most common [3]. Candida species are responsible for approximately 90% of yeast infections worldwide [4]. The emergence of Candida auris, a multidrug-resistant yeast species discovered in 2009, highlights the growing threat posed by fungal pathogens, particularly in healthcare settings. C. auris is highly transmissible, capable of surviving on surfaces for >3 weeks, and is associated with severe infections and poor clinical outcomes [5,6].

Yeast infections have undergone significant changes, with non-albicans Candida (NAC) species now surpassing C. albicans as the main cause of candidiasis, particularly in the Asian continent [7,8]. Candida tropicalis, Candida glabrata, and Candida krusei are among the emerging NAC species driving this shift. In India, notable outbreaks have been linked to other yeast species such as Pichia anomala, Pichia fabianii, and Kodamaea ohmeri [9]. Furthermore, during the COVID-19 pandemic, fungal co-infections, especially involving Candida and Mucor, have become prevalent among affected individuals and are potentially exacerbated by the use of immunosuppressive therapies [10]. The objective of this retrospective observational study was to determine the prevalence of yeast and yeast-like infections, particularly in the era of COVID-19, and to assess the pattern of antifungal susceptibility.

Materials and methods

Study design and setting

This retrospective observational study was conducted to identify and analyze yeast and yeast-like isolates in a tertiary care rural medical college and hospital in Dervan, Maharashtra. All yeast and yeast-like isolates from January 2018 to December 2021 were included in the study, which involved the analysis of various clinical samples, their species types, and susceptibility. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines were followed in reporting this study.

Sample size

This study included all isolates over the study period. Therefore, the sample size was effectively all 95 fungal isolates identified and analyzed during the study period, including 86 yeast isolates and nine yeast-like isolates. Sample size calculations were not done as we analyzed the entire dataset.

Variables and data sources

Demographic factors such as patient age and sex and clinical details such as sample collection information and sample type were identified. Species-level identification and antifungal susceptibility patterns were performed using the VITEK-2 system (bioMérieux, Marcy-l’Etoile, France). The antifungal susceptibility panel included amphotericin B (AMP B), flucytosine, fluconazole, voriconazole, caspofungin, and micafungin. Data were obtained from the laboratory information system and extracted into Microsoft Excel version 21 (Microsoft Corp., Redmond, WA, USA) for further analysis.

Ethical considerations

No direct patient contact was involved in the study, and patient confidentiality was maintained through the anonymization of all data before analysis. Institutional ethical approval was not required.

Quantitative variables

Quantitative variables including patient age, minimum inhibitory concentration (MIC) (interpreted based on the Clinical and Laboratory Standards Institute breakpoints for each antifungal agent (version 2017, M60-Ed1)), and the percentage of isolates sensitive, resistant, or intermediate to each antifungal agent were determined.

Statistical methods

Descriptive statistics, including frequency and percentage distributions, were used to summarize the demographic and clinical characteristics of patients, as well as the distribution of fungal species and their antifungal susceptibility patterns. A linear regression model was used to assess the trend in the number of yeast and yeast-like isolates over the study period, with a specific focus on changes during the COVID-19 era (2020-2021). The susceptibility of isolates to each antifungal agent was determined and presented as the percentage of isolates sensitive, resistant, or intermediate to each agent.

Results

A total of 95 fungal isolates were identified during the study period, with nearly an equal distribution of female (48, 50.52%) and male (47, 49.47%) patients. Among these isolates, 86 (90.52%) were yeast isolates, predominantly comprising NAC species (45, 52.32%), and nine (9.47%) were yeast-like isolates, including Cryptococcus laurentii (six isolates) and Trichosporon asahii (three isolates) (Table 1).

Table 1. Summary of fungal isolates.

Category Female (%) Male (%) Total (%)
Total number of fungal isolates  48 (50.52%) 47 (49.47%) 95 (100%)
Yeast isolates 43 (50%) 43 (50%) 86 (90.52%)
Yeast-like isolates 5 (55.56%) 4 (44.44%) 9 (9.47%)
Non-albicans Candida (including Candida species where species-level identification was not done) 21 (46.67%) 24 (53.33%) 45 (52.32%)
Candida albicans 22 (53.66%) 19 (46.34%) 41 (47.67%)

In our study, C. albicans was the most prevalent species, including 43% of the total samples, with a significant presence in urine (26 isolates), sputum (11 isolates), blood (one isolate) and pus/tissue/wound swabs (three isolates). C. auris was comparatively rare, at 1% of the total, detected only in urine. Candida ciferri and C. tropicalis represented 6% and 9% of the samples, respectively, with occurrences in urine, sputum, and blood. Candida famata and T. asahii were 2% and 3% of the total, isolated in urine. Candida guilliermondii (3%) and Candida lusitaniae (5%) were identified in urine and other samples. Candida parapsilosis and Cryptococcus laurentii were identified in 5% and 6%, respectively, isolated in multiple sample types, including urine and sputum. Candida species not specified further were found in various samples, accounting for 15% of the total. Table 2 shows a diverse range of fungal species, with C. albicans being the predominant one in different clinical specimens.

Table 2. Distribution of yeast/yeast-like isolates isolated from various clinical samples.

ET = endotracheal

Species Sample Total (%)
Urine Sputum Blood Pus/Tissue/Wound swab Foley’s tip/Drain tip/Suction tip/ET suction Stool Retroperitoneal fluid
Candida albicans 26 11 1 3 0 0 0 41 (43%)
Candida auris 1 0 0 0 0 0 0 1 (1%)
Candida ciferri 2 2 0 2 0 0 0 6 (6%)
Candida famata 2 0 0 0 0 0 0 2 (2%)
Candida guilliermondii 3 0 0 0 0 0 0 3 (3%)
Candida lusitaniae 3 0 0 1 0 1 0 5 (5%)
Candida parapsilosis 2 0 2 1 0 0 0 5 (5%)
Candida species 8 3 0 0 2 0 1 14 (15%)
Candida tropicalis 4 2 1 1 1 0 0 9 (9%)
Cryptococcus laurentii 4 0 0 0 2 0 0 6 (6%)
Trichosporon asahii 3 0 0 0 0 0 0 3 (3%)

In the pre-COVID era (2018 and 2019), 25 (26%) isolates were identified, while in the COVID-19 era (2020 and 2021), 70 (74%) isolates were identified. A year-wise change in the trend of yeast and yeast-like isolates was observed. In the COVID-19 era (2020 and 2021), the number of cases of yeast and yeast-like infections increased. Figure 1 shows the linear regression analysis of the Candida cases. The blue points represent the actual data from each year, while the red line is the fitted linear regression model, showing a clear increasing trend in the number of cases over the years. Among 70 isolates in the COVID-19 era, 24% were found in samples taken from confirmed positive cases, either by antigen or real-time reverse transcription polymerase chain reaction (RT-PCR) tests.

Figure 1. Linear regression analysis of yearly Candida cases.

Figure 1

Blue points represent the number of cases, and the red line is the fitted linear regression model.

C. albicans showed high sensitivity to almost all antifungal agents during the study period and no difference was observed year-wise. For AMP B, 92.68% (38 isolates) were sensitive, while 7.32% (three isolates) were resistant. For flucytosine, all isolates (100%) were sensitive. Fluconazole sensitivity was observed in 97.56% (40 isolates), with only one isolate resistant (2.44%). High sensitivity was also observed for voriconazole at 97.56% (40 isolates), caspofungin at 97.56% (40 isolates), and micafungin at 97.56% (40 isolates). C. famata was completely sensitive to AMP B, flucytosine, voriconazole, caspofungin, and micafungin with 100% sensitivity across these antifungals. However, for fluconazole, 50% (one isolate) was resistant and 50% (one isolate) was not determined. All C. parapsilosis isolates were sensitive to AMP B, flucytosine, voriconazole, caspofungin, and micafungin, while fluconazole was not tested as it is intrinsically resistant. C. auris exhibited 100% resistance to AMP B, while being completely sensitive (100%) to flucytosine, voriconazole, caspofungin, and micafungin. It also showed complete resistance to fluconazole. C. ciferri had 83.33% (five isolates) sensitivity to AMP B and 16.67% (one isolate) resistance. For flucytosine, all isolates were sensitive. For fluconazole, 66.67% (four isolates) were not determined, 16.67% (one isolate) were resistant, and 16.67% (one isolate) were sensitive. Similar mixed patterns for voriconazole, caspofungin, and micafungin were observed, with some resistance observed. The C. guilliermondii isolates were completely sensitive (100%) to all antifungals, including AMP B, flucytosine, fluconazole, voriconazole, caspofungin, and micafungin. C. lusitaniae showed 100% sensitivity to AMP B, caspofungin, and micafungin. For flucytosine, 80% (four isolates) were sensitive and 20% (one isolate) were intermediate. For fluconazole, 40% (two isolates) were sensitive, 20% (one isolate) resistant, and 40% (two isolates) were not determined. Candida species were highly sensitive to all antifungals, with 92.86% (13 isolates) sensitivity to AMP B, voriconazole, caspofungin, and micafungin. The fluconazole results were completely sensitive at 100% (14 isolates) with no resistance observed. C. tropicalis showed high sensitivity to AMP B at 88.89% (eight isolates), flucytosine at 100% (nine isolates), voriconazole at 100% (nine isolates), caspofungin at 100% (nine isolates), and micafungin at 100% (nine isolates). For fluconazole, 77.78% (seven isolates) were sensitive, and 22.22% (two isolates) were not determined. C. laurentii isolates were entirely sensitive (100%) to AMP B, flucytosine, fluconazole, voriconazole, caspofungin, and micafungin, with no resistance observed. The T. asahii isolates were also completely sensitive (100%) to AMP B, flucytosine, fluconazole, voriconazole, caspofungin, and micafungin (Table 3).

Table 3. Antifungal susceptibility patterns.

R = resistant; S = sensitive; I = intermediate; AMP B = amphotericin B; ND = not determined

Species AMP B (R) n (%) AMP B (S) n (%) Flucytosine (I) n (%) Flucytosine (S) n (%) Fluconazole (ND) n (%) Fluconazole (R) n (%) Fluconazole (S) n (%) Voriconazole (R) n (%) Voriconazole (S) n (%) Caspofungin (R) n (%) Caspofungin (S) n (%) Micafungin (R) n (%) Micafungin (S) n (%)
Candida albicans 3 (7.32%) 38 (92.68%) 0 (0.0%) 41 (100.0%) 0 (0.0%) 1 (2.44%) 40 (97.56%) 1 (2.44%) 40 (97.56%) 3 (7.32%) 40 (97.56%) 1 (2.44%) 40 (97.56%)
Candida famata 0 (0.0%) 2 (100.0%) 0 (0.0%) 2 (100.0%) 1 (50.0%) 1 (50.0%) 0 (0.0%) 0 (0.0%) 2 (100.0%) 0 (0.0%) 2 (100.0%) 0 (0.0%) 2 (100.0%)
Candida parapsilosis 0 (0.0%) 5 (100.0%) 0 (0.0%) 5 (100.0%) 5 (100.0%) 0 (0.0%) 0 (0.0%) 0 (0.0%) 5 (100.0%) 0 (0.0%) 5 (100.0%) 0 (0.0%) 5 (100.0%)
Candida auris 1 (100.0%) 0 (0.0%) 0 (0.0%) 1 (100.0%) 0 (0.0%) 1 (100.0%) 0 (0.0%) 0 (0.0%) 1 (100.0%) 0 (0.0%) 1 (100.0%) 0 (0.0%) 1 (100.0%)
Candida ciferri 1 (16.67%) 5 (83.33%) 0 (0.0%) 6 (100.0%) 4 (66.67%) 1 (16.67%) 1 (16.67%) 2 (33.33%) 4 (66.67%) 1 (16.67%) 5 (83.33%) 2 (33.33%) 4 (66.67%)
Candida guilliermondii 0 (0.0%) 3 (100.0%) 0 (0.0%) 3 (100.0%) 0 (0.0%) 0 (0.0%) 3 (100.0%) 0 (0.0%) 3 (100.0%) 0 (0.0%) 3 (100.0%) 0 (0.0%) 3 (100.0%)
Candida lusitaniae 0 (0.0%) 5 (100.0%) 1 (20.0%) 4 (80.0%) 2 (40.0%) 1 (20.0%) 2 (40.0%) 0 (0.0%) 5 (100.0%) 0 (0.0%) 5 (100.0%) 0 (0.0%) 5 (100.0%)
Candida species 1 (7.14%) 13 (92.86%) 0 (0.0%) 14 (100.0%) 0 (0.0%) 0 (0.0%) 14 (100.0%) 1 (7.14%) 13 (92.86%) 1 (7.14%) 13 (92.86%) 0 (0.0%) 14 (100.0%)
Candida tropicalis 1 (11.11%) 8 (88.89%) 0 (0.0%) 9 (100.0%) 2 (22.22%) 0 (0.0%) 7 (77.78%) 0 (0.0%) 9 (100.0%) 0 (0.0%) 9 (100.0%) 0 (0.0%) 9 (100.0%)
Cryptococcus laurentii 0 (0.0%) 6 (100.0%) 0 (0.0%) 6 (100.0%) 0 (0.0%) 0 (0.0%) 6 (100.0%) 0 (0.0%) 6 (100.0%) 0 (0.0%) 6 (100.0%) 0 (0.0%) 6 (100.0%)
Trichosporon asahii 0 (0.0%) 3 (100.0%) 0 (0.0%) 3 (100.0%) 0 (0.0%) 0 (0.0%) 3 (100.0%) 0 (0.0%) 3 (100.0%) 0 (0.0%) 3 (100.0%) 0 (0.0%) 3 (100.0%)

Discussion

C. albicans, C. glabrata, C. parapsilosis, C. tropicalis, and C. krusei are the most common fungal species found on mucosal surfaces such as the skin and the respiratory, digestive, and urinary tracts. Over the last two decades, the incidence of yeast infections has increased dramatically due to increased cases of diabetes, the overuse of antibiotics, and immunosuppressive drugs such as steroids and human immunodeficiency virus infections. In the current COVID-19 era, the incidence of yeast infections has also increased [11]. Therefore, in this study, we retrospectively studied changes in the trends of isolating yeast and yeast-like species.

In our study, 86 (90.52%) of the 95 isolates were identified as yeast isolates, while nine (9.47%) were yeast-like isolates. Among yeast isolates, NAC species (52.32%) were predominant compared to C. albicans. A similar predominance of NAC was observed in a study by Sardi et al. [12].

C. laurentii (6%) emerged as a new danger, along with a few isolates of T. asahii (3%) in this study. Among these six C. laurentii isolates, four were recovered from confirmed cases of COVID-19. Surprisingly, most of the isolates were recovered from urine (four isolates), Foley’s tip (one isolate), and endotracheal tube secretions (one isolate). Only a few case reports are currently available. Londero et al. [13] reported on the relationship of C. laurentii with catheter-related infection, along with a change in nomenclature to Papiliotrema laurentiiC. laurentii is rare and commonly seen in immunosuppressed patients. Cutaneous and urinary tract infections were reported in case reports and case series by Molina-Leyva et al. [14] and Salazar-Leal et al. [15]. All T. asahii were recovered from urine samples taken from patients in the elderly age group. T. asahii with urinary tract infection was observed in a study by Khan et al. [16] in 2015 and Cronyn et al. [17] in 2021.

In this study, out of 86 yeast isolates, 41 were C. albicans and 45 were NAC. In 14 (31.11%) isolates, species-level identification was not performed. Among NAC in the species-level identifications, C. tropicalis (nine isolates), C. ciferri (six isolates), C. parapsilosis (five isolates), and C. lusitaniae (five isolates) emerged as common isolates. In different studies conducted throughout India and some outside India summarized in Table 4, NAC emerged as the leading cause of yeast infections, and in some studies, C. albicans was the most common isolate.

Table 4. Studies on the prevalence of yeast and yeast-like culture isolates.

Location Study type Prevalent isolates Reference
Indore, Madhya Pradesh Prospective cross-sectional Candidiasis prevalence was 0.86%. Non-albicans Candida isolates (65.9%) exceeded C. albicans (34.07%). Notably, C. tropicalis was 27.4%, C. glabrata 16.29%, C. krusei 15.55%, C. parapsilosis 5.92%, and C. lusitenia 0.74% [10]
Portugal Retrospective analysis A total of 906 diagnosed yeast infections, with the prominent species being C. albicans (69.6%), C. glabrata (7.6%), C. tropicalis (7.4%), C. parapsilosis, and C. krusei [18]
Kurnool, India Prospective investigation Among 64 Candida isolates, the predominant species were C. albicans (37.5%), followed by C. tropicalis (32.8%), C. krusei (20.3%), C. parapsilosis (6.2%), and C. glabrata (3.1%) [19]
Chennai, Tamil Nadu, India Prospective study A total of 250 Candida species were isolated, with 118 (47.2%) C. albicans, 64 (25.6%) C. tropicalis, 75 (30%) C. glabrata, 38 (15.2%) C. krusei, and 14 (5.6%) C. parapsilosis. Non-albicans Candida predominated (52.8%) over C. albicans [20]
Andhra Pradesh, India Prospective research A total of 53 Candida species were isolated; 64% were identified as C. albicans, while 35% were non-albicans Candida [21]
University of Florida, United States Retrospective analysis Out of 889 COVID-19 patients, 106 (12%) had candidiasis, and 14 (1.6%) specifically presented with oral candidiasis [22]
Bhopal, Madhya Pradesh, India Prospective cross-sectional C. tropicalis (46.79%) was the predominant species, followed by C. albicans (37.17%) and C. parapsilosis (9.61%). Non-albicans Candida species (62.82%) outnumbered C. albicans (37.17%) [23]
Silchar, Assam, India Prospective Investigation Out of 113 Candida species, 72.56% were non-albicans Candida, and 27.43% were C. albicans. Notably, C. glabrata constituted 32%, and C. tropicalis 30% of the non-albicans Candida isolates [24]
Aurangabad, Maharashtra, India Prospective Study A total of 164 Candida isolates, where C. albicans (40.8%) was the most common species, followed by C. tropicalis (29.3%), C. parapsilosis (9.7%), C. famata (9.1%), C. ciferrii (3.6%), and C. lusitaniae (3%) [25]

In this retrospective analysis, year-wise changes in the trend of isolating yeast and yeast-like isolates were observed. In the COVID-19 era (2020 and 2021), the number of cases of yeast and yeast-like infections increased. A similar incidence of yeast infections was reported in a retrospective study by Vijay et al. [26] in 2021. According to the Indian Council of Medical Research Annual Report Antimicrobial Resistance Research and Surveillance Network January 2020 to December 2020, the annual pattern of isolation indicated a consistent decrease in the isolation rate of C. tropicalis from 1% in 2016 to 0.76% in 2020, demonstrating a slight increase from 0.57% in 2019 to 0.76% in 2020. Simultaneously, the annual isolation rate for C. albicans decreased from 1% in 2016 to 0.56% in 2020. In contrast, there was an upward trajectory in the isolates of C. auris and C. parapsilosis from 2016 to 2020 [27].

Our study reports that the yearly isolation trend showed an increase in the isolation of yeast and yeast-like isolates. C. tropicalis (9%), C. ciferri (6%), C. parapsilosis (5%), and C. lusitaniae (5%) emerged as common isolates among NAC. In this study, of the 70 isolates identified during the COVID-19 era, 17 (24%) cases were positive, either by antigen or by RT-PCR test. This percentage of yeast infections is slightly higher than that reported in a retrospective analysis conducted in 2021 at the University of Florida by Katz et al. [22]. In another study, Silva et al. [28] found that most Candida species recovered from COVID-19 patients were isolated from the oropharynx, and Candida species and other yeasts were isolated from the respiratory tract in 21.4% of positive cases of COVID-19. However, in our study, out of 17 isolates of yeast and yeast-like fungi, 11 (65%) were isolated from urine samples of COVID-19-positive cases, and others were isolated from sputum, endotracheal secretion, and blood.

The limitation of this study is the lack of species-level identification for many of the NAC isolates, which may have led to an incomplete understanding of the specific types and behaviors of these fungi. Additionally, our study did not calculate morbidity and mortality rates associated with fungal infections, which limits our ability to fully assess their impact on patient health outcomes. Moreover, the absence of longitudinal follow-up restricts our understanding of the long-term effects of these infections. These gaps highlight the need for more comprehensive and detailed multicentered studies for a better understanding of fungal infection and its clinical significance and epidemiology.

Conclusions

There was an increase in the detection of yeast and yeast-like organisms, especially NAC, during the COVID-19 era, which indicates a change in the pattern of fungal infections, probably affected by the empirical antimicrobials and steroids during the COVID-19 pandemic. The isolation of commensal fungi highlights the importance of collecting paired samples from different sites or at different times to distinguish between colonization and infection. This approach improves accuracy, guides appropriate treatment decisions, and helps prevent unnecessary antifungal use, which can lead to resistance.

Disclosures

Human subjects: Consent was obtained or waived by all participants in this study.

Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.

Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following:

Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work.

Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work.

Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Author Contributions

Concept and design:  Gulshan R. Bandre, Yogendra P. Shelke

Drafting of the manuscript:  Gulshan R. Bandre, Shailesh Lambhore, Sarita Ugemuge, Ashwini A. Tidake

Critical review of the manuscript for important intellectual content:  Yogendra P. Shelke, Nandkishor J. Bankar, Prasanna Nakate, Suvarna Patil

Acquisition, analysis, or interpretation of data:  Nandkishor J. Bankar, Prasanna Nakate, Suvarna Patil, Shailesh Lambhore, Sarita Ugemuge, Ashwini A. Tidake

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