Journal of Clinical and Diagnostic Research, ISSN - 0973 - 709X

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Aug 2018




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Thanking you
With sincere regards
Dr. Rajendra Kumar Ghritlaharey, M.S., M. Ch., FAIS
Associate Professor,
Department of Paediatric Surgery, Gandhi Medical College & Associated
Kamla Nehru & Hamidia Hospitals Bhopal, Madhya Pradesh 462 001 (India)
E-mail: drrajendrak1@rediffmail.com
On May 11,2011




Dr. Shankar P.R.

"On looking back through my Gmail archives after being requested by the journal to write a short editorial about my experiences of publishing with the Journal of Clinical and Diagnostic Research (JCDR), I came across an e-mail from Dr. Hemant Jain, Editor, in March 2007, which introduced the new electronic journal. The main features of the journal which were outlined in the e-mail were extensive author support, cash rewards, the peer review process, and other salient features of the journal.
Over a span of over four years, we (I and my colleagues) have published around 25 articles in the journal. In this editorial, I plan to briefly discuss my experiences of publishing with JCDR and the strengths of the journal and to finally address the areas for improvement.
My experiences of publishing with JCDR: Overall, my experiences of publishing withJCDR have been positive. The best point about the journal is that it responds to queries from the author. This may seem to be simple and not too much to ask for, but unfortunately, many journals in the subcontinent and from many developing countries do not respond or they respond with a long delay to the queries from the authors 1. The reasons could be many, including lack of optimal secretarial and other support. Another problem with many journals is the slowness of the review process. Editorial processing and peer review can take anywhere between a year to two years with some journals. Also, some journals do not keep the contributors informed about the progress of the review process. Due to the long review process, the articles can lose their relevance and topicality. A major benefit with JCDR is the timeliness and promptness of its response. In Dr Jain's e-mail which was sent to me in 2007, before the introduction of the Pre-publishing system, he had stated that he had received my submission and that he would get back to me within seven days and he did!
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On April 2011
Anuradha

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On Jan 2020

Important Notice

Case report
Year : 2012 | Month : February | Volume : 6 | Issue : 1 | Page : 123 - 125 Full Version

Rhodutorula Meningitis in a HIV-2 Seropositive Patient: A Case Report


Published: February 1, 2012 | DOI: https://doi.org/10.7860/JCDR/2012/.1856
Ashish Khanna, Menka Khanna, Aruna Aggarwa l

1. MD, Assistant Professor, Department of Microbiology , SGRDIMSR, Amritsar (Punjab). 2. MD, Associate Professor, Department of Pathology , SGRDIMSR, Amritsar (Punjab). 3. MD, Professor and Head of Department (Dean Academics), (I/C ICTC–Integerated Testing and councilling centre set up by NACO) Department of Microbiology, SGRDIMSR (Punjab).

Correspondence Address :
Dr Ashish khanna
538, Basant Avenue
Amritsar-143001, Punjab (India)
Phone: 9465128936; 091-0183-2562919
Email- ashish_538@yahoo.co.in

Abstract

Rodutorula, a common saprophyte has recently emerged as an opportunistic pathogen in immunocompromised patients. Meningitis caused by Rodurorula species in HIV-1 infected patients have been reported rarely but rodutorula infection in HIV-2 infected patient has not been reported till date. We present a case of meningitis caused by Rodutorula rubra in a patient infected with HIV-2 virus. The diagnosis of the patient was confirmed by cell cytology, gram staining and culture of the CSF. Contamintion was ruled out by repeated culturing from different samples from the same patient. Therapy with Amphotericin B showed good results and the patient was discharged after recovery.

Keywords

Opportunistic infections, Human immunodeficiency virus, Rhodotorula species, Meningitis

Introduction
Improvement in the therapeutic and diagnostic capabilities with the advent of invasive surgical procedures and immunosupression predispose to a number of opportunistic pathogens. Most of the fungal infections are caused by the common fungal pathogens such as the Candida species, the Aspergillus species, Histoplasma capsulatum, Blastomyces dermatitidis, Coccidioides immitis and Cryptococcus neoformans. The Rhodotorula species, although they were common saprophytes uptil now, recently have been reported to cause opportunistic infections (1). Rare cases of fungaemia which are associated with catheters, endocarditis, peritonitis, meningitis and endophthalmitis have been reported in the literature, as being caused by this yeast (2).We are presenting here a case of human immunodeficiency virus (HIV-2) infection in a patient who presented to the emergency with a history of fever of one week’s duration, with an altered sensorium. The diagnosis of meningitis is confirmed by cell cytology, India ink preparation, gram staining and the culture of cerebrospinal fluid, which grew Rhodotorula species. The patient was successfully treated with Amphotericin B. Meningitis, which is caused by the Rhodotorula species, is very rare, with only 2-3 cases being reported in the literature, that too, in the patients who were suffering from HIV-1 (1),(2),(3),(4),(5).

Case Report

A 45-year old female was admitted with high grade fever of one week’s duration. The fever was associated with rigors and chills. The patient also complained of neck pain, headache and vomiting since one day. On examination, the patient was found to be febrile (102F) with an altered sensorium. The neck rigidity and Kernig’s sign were positive. Investigations revealed the haemoglobin level to be 11gm%, TLC to be 14300/cmm, blood glucose to be 86mg/ dl, urea to be 21mg/dl and creatine to be 1.1mg/dl. The X-ray of the chest was normal and the blood culture was sterile after 48 hour of incubation at 37°C. Lumber puncture was performed after doing the fundoscopy. CSF was collected under asceptic conditions in a sterile container and it was sent for Case Report Microbiology Section cytological, biochemical and microbiological examinations. The cell cytology showed a WBC count of 60 cells / cmm, with a mixture of neutrophils and lymphocytes. The CSF protein level was 82mg/dl and the sugar level was 45mg/dl. In the Microbiology laboratory, bacteriological and fungal cultures were put up. Various staining methods like ZN staining, gram staining and India ink staining were performed. ZN staining revealed no acid fast bacilli. Gram staining showed inflammatory cells along with budding yeast cells of size, 4-8 micron metres. India ink preparation showed encapsulated budding yeast cells with a clear halo around them. The latex agglutination test for the cryptoccocal antigen was negative. The patient was found to be reactive to HIV-2 antibodies with Coombs AIDS RS ( Span Diagnostics) , Bidot (J Mitra) and Retroquick ( Qualpro diagnostics). On the 2nd day the bacteriological culture was found to be sterile. On the 3rd day, the fungal culture yielded a mucoid red growth on SDA at 37°C and at 20°C. The gram staining of the the growth revealed budding yeast cells. LCB was made from the growth, which showed budding yeast cells. One more tube of SDA in which another sample of the same patient was inoculated on the 3rd day before starting the anti-fungal treatment, again revealed the same findings. Further, the nitrate assimilation test and inositol assimilation were carried out, which were negative with the test strain. The CD4 count was 396cells/dl. CT was not carried out as the as the patient was very poor. These findings, along with the biochemical tests, helped us to diagnose the pathogen as Rhodutorula rubra. Repeated isolation from a different sample from the same patient helped us to rule out contamination. The patient was started on Amphotericin B (1mg/kg/day), she showed improvement in her condition within 3-4 days and she recovered fully within 7-10 days. After 10 days of Amphotericin therapy, the patient was put on a maintainance dose of Itraconazole 400 mg, once a day for three months. ART was not given as her CD4 count was adequate according to the NACO guidelines. After the therapy, the patient recovered fully within two weeks and so, no repeat sample was taken. She was followed up to six months and showed no recurrence.

Discussion

The advent of the AIDS syndrome and the widespread use of broad spectrum antibiotics and immunosuppressive drugs have led to the increased incidence of fungal infections in humans. The genus, Rhodutorula includes 38 species which are mostly found in environmental sources like shower curtains, bath tubs and tooth brushes. Members of the Rhodutorula genus, which were generally considered to be non pathogens, are nowadays being recovered from humans from the skin, lungs, conjunctiva, urine and CSF (2). However the Rhodutorula species have been implicated as a cause of meningitis, endocarditis, ventriculitis, peritonitis, central venous catheter infection and keratitis. The genus, Rhodutorula is an encapsulated pigmented yeast. Microscopically, the unicellular cells are spherical in shape, their size varies from 4-6 μm and they are surrounded by capsules. Ascospores are absent in this fungus. Rhodutorula rubra is the most common species which is isolated from clinical samples, followed by Rhodutorula glutinis. The red colonies which are formed are due to the presence of the carotenoid pigment, torularhodin. The Rhodutorula species can be easily confused with the Cryptococcus species, but the carotenoid pigment and the biochemical tests help in differentiating them. The Rhodutorula species have low virulence and low mortality. Fatal cases have been documented on autopsy. They are common saprophytes of the skin, urine and faeces, but they are rarely isolated from blood and CSF (6). HIV-2 is mostly confined to western Africa and a prevalence of 10% has been reported from some settings in Africa (7). The incidence of HIV-2 is very low in the Indian sub-continent. The first case of HIV-2 in India was reported in 1991 by Rubsamen- Waigmann (8),(9). It is less pathogenic than HIV-1 and rates of disease development in the HIV-2 infection are much lower than those of HIV-1. There is a long term disease non-progression in HIV-2 (10). In an autopsy study which was conducted in Cote d’Ivoire, which comprised 154 people who were infected with HIV-1 and 40 people who were infected with HIV-2, severe CMV encephalitis was observed, which was more common in people who were infected with HIV-2 (11). Similarly, in our case also, opportunistic fungal infections were seen with a higher CD-4 count than was the case normally with the HIV-1 infection. As the CD-4 count was more than 350 cells/dl, ART was not started as per the NACO guidelines. Moreover, more clinical data is needed to determine the more effective treatment and the optimal timing of ART in HIV-2 infection, as studies on HIV-2 are comparatively less in number. Relapse with Rhodutorula meningitis was reported by Gyaurgieva et al, which was treated with itraconazole therapy (4). The infection with this rare yeast could be underreported due to its similarity with Cryptococcus neoformans. In our case, the possibility of contamination was ruled out as CSF is a sterile fluid and growth was obtained twice on SDA medium which contained antibiotics, from different samples from the same patient. Thus, the Rhodotorula species was considered to have a pathogenic role in causing meningitis in the present case.

References

1.
Thakur K, Singh G, Agrawal S, Rani L. Meningitis which was caused by Rhodutorula rubra in an human immunodeficiency virus infected patient. Indian J Med Microbiol 2007; 25: 166-68.
2.
Felipe FT , Silva FC. Rhodutorula infection; A systemic review of 128 cases from the literature. Rev Iberoam Micol 2008;25 :135-40.
3.
Shinde RS, Mantus BC, Patil G, Parande MV, Parande AM. Meningitis due to Rhodutorula glutinis in an HIV infected patient. Indian J Med Microbiol 2008;26(4): 375-97.
4.
Gyaurgieva OH, Bogomolova TS, Peacock C, Beaumel A, Djomand G, Ngbichi JM et al. The mortality and the pathology of an HIV- infected patient. J Med Vet Mycol 1996; 34:357-59.
5.
Lanzafame M, De Checchi G, Parinello A, Trevenzoli M, Cattelan AM. Rhodutorula glutinis related meningitis. J Clin Microbiol 2001; 39: 410.
6.
Lo Re V III, Fishman NO, Nachamkin I. Recurrent catheter related Rhodutorula rubra infection. Clin Microbiol Infect 2003 (9) : 897-900.
7.
Schim van der loeff MF, Aaby P. Towards a better understanding of the epidemiology of HIV-2. AIDS 1993:13 Suppl A : S 69-84.
8.
Murugan S, Anburajan R. Prevalence of the HIV-2 infection in southern Tamil Nadu. Indian J Sex Transm Dis 2007; 28: 113.
9.
Rubsamen- Waigmann H, Briesen HV, Maniar JK, Rao PK, Scholz C, Pfutzner A. The spread of HIV-2 in India. Lancet 1991; 337:550-1.
10.
Marlink R, Kanki P, Thior I , Travers K, Eisen G, Siby T et al. The reduced rate of disease development after the HIV-2 infection as compared to HIV-1. Science 1994;265:1587–90.
11.
Lucas SB, Honnou A, Peacock C, Beaumel A, Djomand G, Ngbichi JM et al. The mortality and the pathology of the HIV infection in a west African city. AIDS 1993; 7: 1569-79.

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ID: JCDR/2012/3411.3822:1856

FINANCIAL OR OTHER COMPETING INTERESTS: NONE.

Date of Submission: Jul 10, 2011
Date of Peer Review: Nov 26, 2011
Date of Acceptance: Dec 20, 2011
Date of Publishing: Feb 15, 2012

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