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- DOI 10.18231/j.ijmmtd.2024.027
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CrossMark
- Citation
Use of various substrate/ media for germ tube test (GTT) detection in Candida albicans and Candida dubliniensis from a tertiary care hospital
- Author Details:
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Santosh Kotgire *
-
Sunil Hatkar
Introduction
Candida species are the commonest fungal disease found in humans affecting mucosa, skin, nails, and internal organs of the body.[1] Candida species are commensals of the oral cavity, intestinal tract and vagina, with newborns being colonized soon after birth. In recent years, use of non-judicious antibiotics, corticosteroids, antineoplastic agents, immune suppressive drugs, widespread increased use of bone marrow and organ transplant, and unreasonable use of indwelling catheters have led to an increased incidence of the infections caused by Candida species.[1], [2]
Candida albicans is widely identified worldwide as being the most virulent yeast like fungi and in the majority of hospital based studies it has been found to be the most frequent cause of superficial and systemic mycosis.[1], [2] In 1955, Dublin ,Ireland a new species of Candida was isolated in a HIV infected individuals with oropharyngeal candidiasis which was named Candida dubliniensis, which was found to be closely related to C. albicans, as it shares many phenotypic properties, production of germ tube and chlamydospores formation.[1]
The gamut of candidiasis ranges from superficial infections of the vaginal and oral mucosae, to life-threatening invasive candidiasis with systemic involvement that proliferate via the bloodstream to internal organs of the body.[2], [3] The risk includes individuals admitted to intensive care units (ICUs), on dialysis, postsurgical patients; human immunodeficiency virus (HIV) infected hosts, elderly patients, premature infants and patients with hematological and terminal stage malignancies. [4]
Although various diagnostic methods are available for identification of Candida isolates such as morphological, molecular and biochemical modalities, but for rapid identification of Candida species in all mycology laboratories begins with the germ tube test.[1], [4]
The presumptive clinical identification of C.albicans and C. dubliniensis is usually based on its ability to produce germ tube when incubated at 370 c for 2 hours in pooled human serum.[5], [6] Germ tube formation was first reported and demonstrated by Reynold and Braude in 1956 and hence, the germ tube test is also known as a “Reynolds Braude Phenomenon”.
Infection occurs when there is hyphal growth and biofilm formation in the tissue. These mechanisms also allow resistance of C.albicans to traditional antifungal agents.[7]
Timely diagnosis is required in order to reduce mortality. Currently, Invasive Candidiasis (IC) is diagnosed through the findings of hyphae on microscopic examination or through a time- consuming culture.[8] Serological tests provide relatively faster and easier way to diagnose IC. β-d glucan (BDG) test is one widely used Candida serological test. However, it lacks specificity due to cross reaction with other fungi.[8] Other rapid assays have been developed to identify yeasts, and most of these methods are again extremely expensive and labor intense and may not be available routinely in all laboratories.[9]
The germ tube test (GTT) is a well-established, inexpensive, and easy to administer test used to identify C.albicans from other species (except Candida dubliniensis and Candida africana).[10] Various media can be used for induction of germ tube, each with unique compositions and function. Human serum is the most used medium for germ tube test. [2], [8] Its main limitation is the requirement of fresh human serum on a regular basis and potential biohazard. [2], [6], [8]
So the present study was conducted to assess the reliability of different media for germ tube test (GTT) production in Candida albicans and Candida dubliniensis isolated from various clinical samples.
Materials and Methods
Study design
Prospective cross-section study, conducted at Department of Microbiology, Indian Institute of Medical Science and Research Medical college from west-central part of Maharashtra
Study period
January 2022 to September 2022.
Identification and speciation
During nine months of present study, a total of 102 C.albicans and 09 C. dubliniensis strains were isolated from various clinical samples received at Department of Microbiology. All the isolate of Candida were identified and further speciated by conventional mycological methods such as Gram’s staining, culture on Sabouraud’s dextrose agar (SDA), germ tube test, chlamydospore formation on corn meal agar, sugar fermentation test, sugar assimilation test, and growth on Hi-chrome candida agar.[5], [11]
Different medium/substrate
Pooled human sera routinely used for detection of germ tube in clinical isolates of C.albicans and C.dubliniensis were compared with serum free medium such as Trypticase Soy Broth, YEPD (Yeast Extract Peptone Dextrose) broth, Muller-Hinton agar/broth and Peptone Water
Germ tube test (GTT) induction
Sabouraud’s dextrose agar was used to subculture all C.albicans and C.dubliniensis isolates and were incubated at 37°C for 24-48 hours. For Germ tube test detection, 2-3 colonies were picked up from fresh culture and light inoculum were made in 0.5ml of all serum free media mentioned above which were then transferred in 12×75 mm test tube. C.albicans ATCC 10231 and C. krusei were used as positive control and negative control with each batch of yeasts tested. [11], [12]
The serum free medium containing test tubes inoculated with C.albicans and C.dubliniensis were further incubated at 37°C in a water bath for 3 hours. Post that a drop of incubated suspension was placed on a glass slide and covered with coverslip. Evaluation of germ tube formation was done by Microscopic examination under 40X magnification for formation of germ tube. [5], [11], [12]
Typically, C. albicans reveals thin germ tubes, 3 to 4 mm in diameter and up to 20 mm long; unlike pseudohyphae that are not constricted at their point of origin. Observation of minimum five germ tubes in entire wet mount preparation was used as criterion for germ tube positivity. Negative results were confirmed by examining atleast 10X high power fields for the presence of germ tubes. [5], [11], [12]
Statistical analysis
Microsoft office 2016 was used for the analysis. Descriptive statistics like mean and percentages were used for the analysis.
Results and Observation
In the present study, the germ tube production for 102 C.albicans and 09 C dubliniensis isolates were evaluated by using five different media.
Details of the study can be seen in [Table 1]
|
S.No. |
Media/ Substrate |
Isolates with positive GTT |
Total (n=111) |
Percentage (%) |
|
|
Candida albicans (n=102) |
Candida dubliniensis (n=09) |
||||
|
01 |
Human pooled serum |
99 |
08 |
107 |
96.39 |
|
02 |
YEPD |
96 |
07 |
103 |
92.79 |
|
03 |
Trypticase soy broth |
85 |
04 |
89 |
80.18 |
|
04 |
Muller-Hinton broth |
72 |
03 |
75 |
67.56 |
|
05 |
Peptone water |
48 |
02 |
50 |
45.04 |
GTT- Germ tube test, YEPD- yeast extract peptone dextrose
For both the candida isolates human pooled serum showed 96.39% positivity followed by YEPD (yeast extract peptone dextrose) broth with 92.79% positivity, Trypticase soy broth showed 80.18% positivity , whereas Muller Hinton broth produced 67.56% positivity and least positivity was seen with Peptone water where only 45.04% of germ tube induction was observed.
Discussion
Many diagnostic mycology laboratories uses pooled human serum for germ tube detection. Germ tube test is widely considered, accepted, reliable and easy technique for quick presumptive identification of C.albicans and C. dubliniensis. Germ tube production by yeast cells indicates their morphological adaptation to filamentous forms under unfavourable conditions. [12], [13]
However, the use of pooled human serum has some disadvantages. Serum sample must be fresh or stored frozen and the inoculum size needs to be minimal (< 107 cells/ml) because heavy inoculum is known to hamper germ tube production.[14] The another major drawback in handling pooled human serum is the risk of transmission of infection with HIV or Hepatitis virus. Variableness in the performance noticed with different batches of serum and presence of biological inhibitors in pooled human sera might increase the chances of false negative results. [11], [12], [13], [14]
While study conducted by Mackenzie DWR [15] highlights that pooled human serum stored at 40C for 15 days reduces its ability to produce germ tubes by 50%.
Studies [9], [10], [11], [12] conducted with pooled human serum reported a 91-100% sensitivity 95–100% specificity for germ tube test, and the few other studies [5], [14] reported a sensitivity of 92.3%, 90%, and 35%, by using fetal bovine serum, rabbit serum, and horse serum respectively.
Hilmioglu et al.[16] conducted a study where they compared 12 fluids for GTT production, best results for GTT were obtained with fresh human serum, similarly human serum was found to be better in the study conducted Arora et al. [17] So in our present study also maximum number (96.39%) of C.albicans and C. dubliniensis strains produced germ tubes on pooled human serum and the possible reason may be due to the inhibitors present in the human serum, yeast cell concentration and storage condition of serum.
Our study highlights that around 92.79% of positivity were seen with YEPD ( Yeast Extract Peptone Dextrose) which correlates with a study conducted by KIM et al., [18] where demonstration of Germ tubes were seen within 30 minutes in YEPD at 390C but after 60 min in serum at 370C. Whereas study conducted by Bhumla et al.,[19] showed 81.25% production of germ tube production with YEPD and another study carried out by Abiroo Jan et al.,[20] showed 89.30% germ tube production but only in Candida albicans and no germ tube formation in candida dubliniensis.
Our study showed that with Trypticase Soya Broth both Candida isolates could produce germ tube in 80.18% strains which is similar to study carried out by of Arora DR et al., [17] and Makwana GE et al[21] where they reported trypticase soy broth to be less efficient than human serum in GTT production. In contrast to such findings, a study carried out by Joshi et al[11] and Deorukhkar et al., [12] recommended trypticase soy broth to be more effective option compared to pooled human serum for germ tube test for C.albicans and C. dubliniensis. So our study finding clearly showed that YEPD is best available media for germ tube production.
Muller-Hinton broth and Peptone Water revealed positive results in 67.56 % and 45.04% of C.albicans and C.dubliniensis isolates respectively in present study. Mattei AS et al.,[22] recommended Mueller Hinton broth or agar as a preferred media to human serum in germ tube production test . MA Atalay et al.,[23] reported 91.5% sensitivity using commercially available Muller Hinton Agar in the identification of C.albicans and C. dubliniensis, respectively. However, interestingly both the isolates of Candida showed low number of germ tube in Muller-Hinton Broth in our setting. An exact explanation of this phenomenon is unknown. In regards to peptone water many researchers[15], [16], [17] found out that, role of other media like RPMI-1640 broth, Sabouraud’s broth, animal serum and peptone water in GT formation was evaluated and found to be less productive.
In Peptone water only 45.04% strains of C.albicans and C. dubliniensis respectively could produce germ tubes, possible reason for low sensitivity may be due to the lower nutritive value of peptone water commensurate to other media. Similarly, Deorukhkar et al [12] also reported sensitivity of 69% in peptone water. So amongst all the non-serum based media our study suggest the less suited medium for germ tube production is peptone water
Conclusion
So our study clearly highlights that YPED broth is superior serum free media for germ tube production and ensuing rapid identification & presumptive differentiation of C.albicans and C. dubliniensis from other clinically significant Candida species without considerable time required for the preparation and testing of pooled human serum. Moreover, this medium is commercially available, is more stable, effective, is non biohazardous, convenient and cost effective alternative.
Source of Funding
None.
Conflict of Interest
None.
References
- F Bongomin, S Gago, R O Oladele, D W Denning. Global and multi-national prevalence of fungal diseases-estimate precision. J Fungi (Basel) 2017. [Google Scholar] [Crossref]
- CJ Clancy, MH Nguyen. Diagnosing Invasive Candidiasis. J Clin Microbiol 2018. [Google Scholar] [Crossref]
- ES Loreto, JSM Tondolo. . Fungal Infection 2019. [Google Scholar]
- SR Lockhart. Current Epidemiology of Candida Infection. Clin Microbiol Newsl 2014. [Google Scholar]
- EW Koneman, GD Robberts. . Practical Laboratory Mycology IIIrd edn 1985. [Google Scholar]
- M Henriques, S Silva. Candida Albicans Virulence Factors and Its Pathogenicity. Microorganisms 2021. [Google Scholar] [Crossref]
- C Hage, E Carmona, O Epelbaum, S Evans, L Gabe, Q Haydour. Microbiological Laboratory Testing in the Diagnosis of Fungal Infections in Pulmonary and Critical Care Practice. An Official American Thoracic Society Clinical Practice Guideline. Am J Respir Crit Care Med 2019. [Google Scholar]
- M Parra-Sánchez, IZY Breval, C Castro Méndez, S García-Rey, AL Vazquez, AÚ Iglesias. Candida albicans Germ-Tube Antibody: Evaluation of a New Automatic Assay for Diagnosing Invasive Candidiasis in ICU Patients. Mycopathologia 2017. [Google Scholar]
- M Ruhnke. Epidemiology of Candida albicans infections and role of non-Candida-albicans yeasts. Curr Drug Targets 2006. [Google Scholar]
- CD Sachin, K Ruchi, S Santosh. In vitro evaluation of proteinase, phospholipase and haemolysin activities of Candida species isolated from clinical specimens. Int J Med Biomed Res 2012. [Google Scholar] [Crossref]
- KR Joshi, JB Gavin, DA Bremner. The formation of germ tubes by Candida albicans in various peptone media. Sabouraudia 1973. [Google Scholar]
- SC Deorukhkar, S Saini, PA Jadhav. Evaluation of different media for germ tube production of Candida albicans and Candida dubliniensis. IJBAR 2012. [Google Scholar]
- CL Taschdjian, JJ Burchall, PJ Kozinn. Rapid identification of Candida albicans by filamentation on serum and serum substitutes. Am J Clin Pathol 1960. [Google Scholar] [Crossref]
- KR Joshi, DA Bremner, JB Gavin, PB Herdson, DN Parr. The formation of germ tubes by Candida albicans in sheep serum and trypticase soy broth. Am J Clin Pathol 1973. [Google Scholar]
- DWR Mackenzie. Serum tube identification of Candida albicans. J Clin Pathol 1962. [Google Scholar]
- S Hilmioglu, M Ilkit, Z Badak. Comparison of 12 liquid media for germ tube production of Candida albicans and C. tropicalis. Mycoses 2007. [Google Scholar]
- DR Arora, S Saini, Aparna, N Gupta. Evaluation of germ tube test in various media. Indian J Pathol Microbiol 2003. [Google Scholar]
- D Kim, WS Shin, KH Lee, JY Park, CM Koh. Rapid differentiation of Candida albicans from other Candida species using its unique germ tube formation at 39 degrees C. Yeasts 2002. [Google Scholar]
- U Bhumbla, A Gupta. A comparative study for production of germ tube in Candida albicans of various pulmonary samples, by different methods in a tertiary care hospital of south west Rajasthan. Int J Community Med Public Health 2021. [Google Scholar]
- A Jan, G Bashir, R Qadir, A Bashir, S Fomda. Aamir Yaqoob Hakak Modified Germ Tube Test: A Rapid Test for Differentiation of Candida Albicans from Candida Dubliniensis. Int J Contemp Med Res 2018. [Google Scholar]
- GE Makwana, H Gadhavi, M Sinha. Comparison of germ tube production by Candida albicans in various media. NJIRM 2012. [Google Scholar]
- AS Mattei, SH Alves, CB Severo, LD Guazzelli, FD Oliveira, LC Severo. Use of Mueller-Hinton broth and agar in the germ tube test. Rev Inst Med Trop Sao Paulo 2014. [Google Scholar]
- MA Atalay, AN Koc, OM Parkan, G Aydemir, F Elmali, H Sav. Can serums be replaced by Mueller-Hinton agar in germ tube test?. Niger J Clin Pract 2017. [Google Scholar]