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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)
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!
Most of the manuscripts are published within 3 to 4 months of their submission if they are found to be suitable after the review process. JCDR is published bimonthly and the accepted articles were usually published in the next issue. Recently, due to the increased volume of the submissions, the review process has become slower and it ?? Section can take from 4 to 6 months for the articles to be reviewed. The journal has an extensive author support system and it has recently introduced a paid expedited review process. The journal also mentions the average time for processing the manuscript under different submission systems - regular submission and expedited review.
Strengths of the journal: The journal has an online first facility in which the accepted manuscripts may be published on the website before being included in a regular issue of the journal. This cuts down the time between their acceptance and the publication. The journal is indexed in many databases, though not in PubMed. The editorial board should now take steps to index the journal in PubMed. The journal has a system of notifying readers through e-mail when a new issue is released. Also, the articles are available in both the HTML and the PDF formats. I especially like the new and colorful page format of the journal. Also, the access statistics of the articles are available. The prepublication and the manuscript tracking system are also helpful for the authors.
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Overall, the publishing process with JCDR has been smooth, quick and relatively hassle free and I can recommend other authors to consider the journal as an outlet for their work."

Dr. P. Ravi Shankar
KIST Medical College, P.O. Box 14142, Kathmandu, Nepal.
On April 2011

Dear team JCDR, I would like to thank you for the very professional and polite service provided by everyone at JCDR. While i have been in the field of writing and editing for sometime, this has been my first attempt in publishing a scientific paper.Thank you for hand-holding me through the process.

Dr. Anuradha
On Jan 2020

Important Notice

Case report
Year : 2009 | Month : August | Volume : 3 | Issue : 4 | Page : 1682 - 1684 Full Version

Spectrum of Nocardiosis –A report of three cases

Published: August 1, 2009 | DOI:

*(MD),Associate professor,**(MSc) ,(Ph.D), Professor,***(MSc), Assistant professor Department of Microbiology. Fr. Muller Medical College Kankanady Mangalore-575002

Correspondence Address :
Dr. Meena Dias, Asso. Prof.,
Dept. of Microbiology,
Fr. Muller Medical College,
Kankanady, Mangalore-575002
Phone-0824 2238273


Nocardiosis is caused by soil borne aerobic actinomycetes in immunocompromised hosts as well as in persons without any predisposing factors. We report here, three cases of culture proven Nocardia asteroides infection. Two cases were reported from immunocompetent individuals and the last one from an HIV patient.


Nocardia asteroides, Immunocompetent, Immunocompromised

Nocardiosis is a localized or disseminated opportunistic infection caused by a soil borne aerobic actinomycete. The organism enters through the respiratory tract (1). Members of this genus consist of delicately branching gram positive, partially acid fast, aerobic actinomycetes (2). The organism grows readily on blood agar, Sabouraud’s agar, or in other simple media in 2 to 5 days. Pathogenic species of Nocardia are found in house dust, beach sand, garden soil and swimming pools (3).
N.asteroides is the predominant human pathogen besides N. brasiliensis, N.otitidiscaviarum and N.farcinica(3). A review of literature showed an increasing incidence and the changing spectrum of nocardiosis in recent years. Although nocardiosis is prevalent in immunosuppressed patients like organ transplant recipients and those infected with HIV, the recent years have witnessed its increased incidence in healthy immunocompetentpatients(2),(4),(5),(6),(7),(8),(9),(10). We report here, three culture proven cases of nocardiosis caused by N.asteroides, two in an immunocompetent and one in an immunocompromised individual.

Case 1
An 8 months old male baby was admitted to the paediatric ward with a history of fever, cough and breathlessness of 20 days duration. A diagnosis of pneumonia was made and he was treated with cefotaxime and amikacin. There was remarkable improvement with the treatment and he was discharged after 10 days of admission. About a month later, the child came back with similar complaints. The child was pale and febrile. Respiratory system examination revealed decreased breath sounds and crepitations. Other systems were normal. Chest roentgenogram and computerized tomography showed right lobe consolidation with multiple loculated empyema . Ultrasound of abdomen showed consolidation of the lung with encysted empyema. Haemoglobin was 8.1 gm% and total WBC count was 32,300 cells/cu mm with a differential count showing 67% polymorphs, 32% lymphocytes and 1% eosinophils. ESR was 90 mm at the end of the 1st hour. Peripheral smears showed the diagnosis of microcytic hypochromic anaemia. Malarial parasites were not found. Gastric aspiration was negative for AFB. Screening for HIV and HBsAg gave negative results.
Right mini thoracotomy was done and the pus sample was sent for microbiological investigation.
Gram stain of the pus showed numerous polymorphonuclear lymphocytes and gram positive, branched, beaded filaments which were partially acid fast by the modified acid fast stain and hence, aroused the suspicion of Nocardia species. Cultures on Brain heart infusion blood agar, Blood agar and Lowenstein Jensen media grew dry, irregular, adherent white colonies when incubated aerobically at 37Âş C for 48 hours. The isolate was identified as N.asteroides, based on biochemical characterization. It was catalase positive, produced urease, did not decompose casein and tyrosine, did not liquefy gelatin and did not grow in the presence of 0.4 % gelatin. The blood culture was negative for Nocardia. Histopathology of the pus showed an acute inflammatory infiltrate with no evidence of tuberculosis. Postoperatively, the patient was started on Amoxyclav I.V and was later put on cotrimoxazole following the culture reports. His condition improved dramatically. The child was discharged with the advice to continue cotrimoxazole for the next 3 months. The follow up of over one year revealed complete resolution of the infection without any signs of recurrence.

Case 2
Pus collected from the wound of a 23 year old male with osteomyelitis of the thumb was subjected to microbiological investigation. General examination and routine laboratory tests were normal. HIV antibody and HbsAg tests were negative. Gram’s stain of the pus from the wound showed gram positive, filamentous bacteria which were found to be acid fast by the modified acid fast stain. Blood agar and Sabouraud’s dextrose agar grew dry, wrinkled, chalky white colonies which were identified as N. asteroides based on biochemical tests (Table/Fig 1). A course of cotrimoxazole was administered for 3 weeks. He improved dramatically.

Case 3
An old man aged 65 years presented with a history of low grade fever, cough and expectoration since 15 days. Respiratory system examination revealed bilateral bronchial breath sounds. Other systems were normal. The WBC count was 16,500/cu mm with a differencial neutrophil count of 92%.ESR was 100 mm at the end of the 1st hour. Chest X-ray showed bilateral opacity. The HIV antibody test was positive. Gram’s stain of the sputum showed numerous polymorphonuclear lymphocytes with gram positive, branched filaments which were found to be acid fast by the modified acid fast staining method. N.asteroides was isolated in pure culture. Earlier, he was started on anti tubercular treatment based on X-ray findings, but based on the culture reports, the patient was started on cotrimoxazole. He showed remarkable improvement at the time of discharge. He was discharged with the advice to continue the same treatment for the next 3 months. The patient was lost for follow-up.


Nocardiosis was described for the first time in humans by Eppinger (1890) after Edmond Nocard (1888), a veterinarian noted an aerobic actinomycete in bovine farcy in cattle on the island of Guadeloupe (7).Since then, the classification of the Nocardia species has undergone several changes. Based on their cell wall components, particularly cell envelope lipid, peptidoglycan compositions and DNA relatedness; they were reclassified as aerobic bacteria (3).
Nocardiosis is an acute, sub acute or chronic suppurative infection with a tendency to remissions and exacerbations, which initially may mimic pneumonia, tuberculosis, carcinoma or lung abscess(1). Similar findings were observed in our patients; one patient mimicked pneumonia and the other tuberculosis. Infection occurs in all ages, even in neonates (1),(2),(3),(6) and the male to female ratio is 3:1 (1),(2),(3),(6) .
Nocardiosis is chiefly an opportunistic infection, particularly found in patients with lymphoreticular neoplasms and chronic pulmonary disorders, in organ transplant recipients and in those who had a long term treatment with corticosteroids. Suppression of cellular immunity appears to play an important role in the establishment of Nocardia infections (1)[,(3).However, Nocardial infection also occurs without concurrent diseases or therapies. In recent years, many cases have been reported in immunocompetent individuals (4),(7),(8),(9),(10).In Curry’s analysis of 455 cases, 39% of the patients did not have any preexisting illness, trauma or immunosuppressive therapy (2). In India, Tendolkar et al (6) recorded similar findings. Their study showed no obvious predisposing factors in about 5 cases and male preponderance of infections.
Nocardiosis should be suspected in patients who present with pulmonary lesions or cerebral abscesses. Nocardial lesions in lungs or other organs in the body erode the blood vessels and disseminate to involve other sites (2),(3),(10).Nocardiosis in the CNS usually follows pulmonary Nocardiosis. Nocardiosis is uncommonly reported in patients who are infected with HIV despite the profound T cell immunosuppression that occurs during infection, the frequency of infection being 1.8 % in adults with HIV (11).The reason may be due to the under reporting of cases, as it is mistaken as pulmonary tuberculosis (1),(5),(12)or malignancy in CNS Nocardiosis (10).This was noticed in one of our patients, where he was started on anti tubercular drugs based on radiological suspicion, though sputum for AFB was negative. It is important to consider Nocardiosis in the differential diagnosis of pulmonary diseases which do not respond to ATT and in which the sputum is negative for AFB.
A high index of suspicion, followed by aggressive laboratory diagnosis and effective treatment, is ecessary to bring down the mortality rate in patients with Nocardiosis.


Schiff TA, McNeil MM, Brown JM. Cutaneous Nocardia farcinica infection in a nonimmunocompromised patient: Case report and review. Clin Infect Dis 1993; 16:756-60.
Lerner PI: Nocardia species: In principles and practice of infectious disease. 4th edition Mandel, Douglass, Bennet. Eds (Churchill Livingston) 1995:2273-80.
Curry WA. Human Nocardiosis. A clinical review with selected case reports. Arch Intern Med.1980; 140:818-826.
Lerner IP. Nocardiosis. Clin Infect Dis. 1996; 22:891-905.
Dinulos JG, Darmstadt GL, Wilson CB, Krengel WF, Burns JL. Nocardia asteroides septic arthritis in a healthy child. Paediatr Infect Dis J. 1999; 18:308-310.
Gaude GS, Hemashettar BM, Bagga AS, Chatterjii R. Clinical Profile of pulmonary Nocardiosis. Indian J Chest Dis Allied Sci. 1999; 41:153-7.
Tendolkar U, Deodhar L, Khatri M. Prevalence of Nocardiosis and use of modified Thayer Martin Medium Ind. J. Pathol Microbiol 1994; 37:395-401.
Mihwac Pak and Seth Rivera. Nocardiosis in an otherwise immunocompetent pregnant female. Chest 2005; 128(4)
Benes J, Viechova J, Picha D, Horova B and Zatloukal P. Disseminated Nocardia asteroides infection in an immunocompetent woman following an arm injury. Infection 2003; 31:112-14.
Dias M,Nagarathna S,Mahadevan A,Chandramouli BA,Chandramuki A.Nocardial brain abscess in an immunocompetent host. Indian J Med Microbiol .2008; 26:274-7.
Uttamchandani RB, Daikos GL, Reyes RR et al. Nocardiosis in 30 patients with advanced human immunodeficiency virus infection: clinical features and outcome. Clin Infect Dis 1994; 18:348-53.
Subhash HS, Christopher DJ, Roy A, Cherian AM. Pulmonary nocardiosis in human immunodeficiency virus infection: a tuberculosis mimic. J. Postgrad Med 2001; 47(1):30-2.
Javaly K, Horowitz HW, Wormser GP. Nocardiosis in patients with HIV infection. Report of two cases and review of literature. Medicine 1992; 71(3):128-38.

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