TRICHOSPORONOSIS – AN ASSOCIATION WITH CLINICAL FACTORS AND ITS OUTCOME

T. PREMAMALINI1*, S.V. RAJYOGANANDH2, R. VIJAYAKUMAR3, ANUPMA JYOTI KINDO4, S.K. MARAK RUNGMEI5
1Department of Microbiology, Sri Ramachandra Medical College and Research Institute, Chennai, 600116, Tamil Nadu, India
2Department of Microbiology, Sri Ramachandra Medical College and Research Institute, Chennai, 600116, Tamil Nadu, India
3Department of Microbiology, Sri Ramachandra Medical College and Research Institute, Chennai, 600116, Tamil Nadu, India
4Department of Microbiology, Sri Ramachandra Medical College and Research Institute, Chennai, 600116, Tamil Nadu, India
5Department of Microbiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India
* Corresponding Author : drtpremamalini@gmail.com

Received : 16-03-2018     Accepted : 20-03-2018     Published : 30-03-2018
Volume : 10     Issue : 3       Pages : 1078 - 1082
Int J Microbiol Res 10.3 (2018):1078-1082
DOI : http://dx.doi.org/10.9735/0975-5276.10.3.1078-1082

Keywords : Trichosporonosis, risk factors, indwelling device
Conflict of Interest : None declared
Acknowledgements/Funding : Author thankful to Sri Ramachandra Medical College and Research Institute, Chennai, 600116, Tamil Nadu
Author Contribution : All author equally contributed

Cite - MLA : PREMAMALINI, T., et al "TRICHOSPORONOSIS – AN ASSOCIATION WITH CLINICAL FACTORS AND ITS OUTCOME ." International Journal of Microbiology Research 10.3 (2018):1078-1082. http://dx.doi.org/10.9735/0975-5276.10.3.1078-1082

Cite - APA : PREMAMALINI, T., RAJYOGANANDH, S.V., VIJAYAKUMAR, R., KINDO, ANUPMA JYOTI, MARAK RUNGMEI, S.K. (2018). TRICHOSPORONOSIS – AN ASSOCIATION WITH CLINICAL FACTORS AND ITS OUTCOME . International Journal of Microbiology Research, 10 (3), 1078-1082. http://dx.doi.org/10.9735/0975-5276.10.3.1078-1082

Cite - Chicago : PREMAMALINI, T., S.V. RAJYOGANANDH, R. VIJAYAKUMAR, ANUPMA JYOTI KINDO, and S.K. MARAK RUNGMEI. "TRICHOSPORONOSIS – AN ASSOCIATION WITH CLINICAL FACTORS AND ITS OUTCOME ." International Journal of Microbiology Research 10, no. 3 (2018):1078-1082. http://dx.doi.org/10.9735/0975-5276.10.3.1078-1082

Copyright : © 2018, T. PREMAMALINI, et al, Published by Bioinfo Publications. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.

Abstract

Introduction: The genus Trichosporon usually cause superficial mycoses, but recently they have emerged as an important pathogen causing invasive infections in immuno-compromised patients. Invasive Trichosporonosis is mainly documented in patients with associated risk factors and co-morbid conditions like haematological malignancies, cardiac or renal disease, intravenous or central line catheter, prosthetic devices and implants, prior antibiotic therapy, stay in Intensive care unit. Objective: This study was undertaken to assess the risk factors and co-morbid conditions associated with Trichosporonosis and its clinical outcome. Materials and Methods: We considered around 72 clinical isolates for the study that were, dry yeast like colonies, urease positive, showed blastoconidia and arthroconidia in gram stain, and were suspected to belong to the genus Trichosporon. Later, they were confirmed genotypically using Trichosporon specific PCR. The demographic and clinical details were collected from all the patients for the study. Results: About 66% of the affected patients were males, with male to female ratio 2:1. All our patients had any one of associated risk factor. Indwelling catheter was present in most of the patients (97.2%) in our study. Bladder catheterisation was the predominant risk factor among patients who grew Trichosporon sp. in urine sample (83.7%). Majority of the patients (52.8%) had associated bacterial infections. Discussion and conclusion: The associated risk factors increase the colonisation of this genus by breaking mucosal barrier, later leading to establishment of infection.

References

1. Chagas-Neto T.C., Chaves G.M. and Colombo A.L. (2008) Mycopathologia, 166, 121-132
2. Haupt H.M., Merz W.G., Beschorner W.E., Vaughan W.P. and Saral R. (1983) Journal of Infectious Diseases, 147, 199-203.
3. Cox G.M. and Perfect J.R.(1998) Topley and Wilson’s microbiology and microbial infections-medical mycology, 9thed, 461–84.
4. Walling D.M., McGraw D.J., Merz W.G., Karp J.E. and Hutchins G.M. (1987) Reviews of Infectious Diseases, 9 , 1013–19.
5. Rodrigues Gda S., de Faria R.R., Guazzelli L.S., Oliveira Fde M., Severo L.C. (2006)RevistaIberoamericana de Micología, 23, 85-89.
6. Gueho E., Improvisi L., de Hoog G.S., Dupont B. (1994) Mycoses , 37, 3-10.
7. Girmenia C., Pagano L., Martino B., D'Antonio D., Fanci R., Specchia G., Melillo L., Buelli M., Pizzarelli G., Venditti M. and Martino P. (2005) Journal of Clinical Microbiology , 43, 1818-28.
8. Krzossok S., Birck R., Henke S., Hof H., van der Woude F. J. & Braun C. (2004) Clinical Nephrology, 62, 66–68.
9. Rastogi V.L. and Nirwan P.S. (2007) Indian Journal of Medical Microbiology, 25, 59–61.
10. Chitasombat M.N., Kofteridis D.P., Jiang Y., Tarrand J., Lewis R.E. and Kontoyiannis D.P. (2012) Journal of Infection, 64, 68–75.
11. Ahmad S., Al-Mahmeed M., Khan Z.U. (2005) Journal of Medical Microbiology, 54, 639–46.
12. Taj-Aldeen S.J., Al-Ansari N., El Shafei S., Jacques F. Meis., Ilse Curfs-Breuker, Bart Theelen and Teun Boekhout (2009) Journal of Clinical Microbiology, 47, 1791-9.
13. Kontoyiannis D.P., Torres H.A., Chagua M., Hachem R., Tarrand J.J., Bodey G.P. and Raad I.I. (2004) Scandinavian Journal of Infectious Diseases, 36, 564–9.
14. Suzuki K., Nakase K., Kyo T., Kohara T., Sugawara Y., Shibazaki T., Oka K., Tsukada T. and Katayama N. (2010) European Journal of Haematology, 84, 441–7.
15. McGinnis M.R. (1994) Mycology. In Clinical Microbiology Procedures Handbook, 6, 6.1.1–6.1.6.1.12.
16. De Hoogs G.S., Guarro J., Gene J. and Figueras M.J. (2000) Atlas of clinical fungi, 2nd ed. Guanabara, Rio de Janeiro, Brazil.
17. Magalhaes A.R., Mondino S.S., Silva Md. and Nishikawa M.M. (2008) Memórias do Instituto Oswaldo Cruz, 103(8), 786-90.
18. Ramraj Vijayakumar, Sidhartha Giri and Anupma Jyoti Kindo (2012) Journal of Laboratory Physicians, 4(1), 1–4.
19. Sugita T., Nishikawa A. and Shinoda T. (1998) Journal of Clinical Microbiology, 36(5), 1458-60.
20. Fleming R.V., Walsh T.J. and Anaissie E.J. (2002) Infectious Disease Clinics of North America, 16(4), 915-933.
21. Walsh T.J., Groll A., Hiemenz J., Fleming R, Roilides E. and Anaissie E. (2004) Clinical Microbiology and Infections, 10 (1), 48-66.
22. Colombo AL., Melo AS., Crespo Rosas RF., Salomao R., Briones M., Hollis RJ., Messer SA. and Pfaller MA. (2003) Diagnostic Microbiolgy and Infectious Diseases, 46(4), 253-257.
23. Febre N., Silva V., Medeiros E.A.S., Wey S.B., Colombo A.L. and Fischman O. (1999) Journal of Clinical Microbiology, 37, 1584–86.
24. Silva V., Zepeda G. and Alvareda D. (2003) RevistaIberoamericana de Micología, 20, 21-3.
25. Paramananthanmariappan, Gordon Smith, Simon V. Bariol, Sami A Moussa and David A.Tolley (2005) Journal of urology, 173 (5), 1610-14
26. Sheng-Yuan Ruan and Jung-Yien Chien Po-Ren Hsueh. (2009) Clinical Infectious Diseases, 49 (1), e11–e17.
27. Khanna R., Oreopoulos D.G., Vas S., McNeely D. and McCready W. (1980) British Medical Journal, 280, 1147–48.
28. Wei Sun, Jianrong Su, Shuzhen Xu and Donghui Yan (2012) Journal of Medical Microbiology, 61, 1750–57.
29. Wolf D.G., Rama Falk, Moshe Hacham, Bart Theelen, Teun Boekhout, Gloria Scorzetti, Mervyn Shapiro, Colin Block, Ira F. Salkin and Itzhack Polacheck (2001) Journal of Clinical Microbiology, 39, 4420–25.
30. Pradhan S., Agrawal E., Murthy R. and Tomar R. (2017) International Journal of Medical Research and Review, 5 (03), 285-292.