Anilkumar Gopinathan

Radionuclides and radiation indices of high background radiation area in Chavara-Neendakara placer deposits (Kerala, India).

The present paper describes a detailed study on the distribution of radionuclides along Chavara – Neendakara placer deposit, a high background radiation area (HBRA) along the Southwest coast of India (Kerala). Judged from our studies using HPGe gamma spectrometric detector, it becomes evident that Uranium (238U), Thorium (232Th) and Potassium (40K) are the major sources for radioactivity prevailing in the area. Our statistical analyses reveal the existence of a high positive correlation between 238U and 232Th, implicating that the levels of these elements are interdependent. Our SEM-EDAX analyses reveal that titanium (Ti) and zircon (Zr) are the major trace elements in the sand samples, followed by aluminum, copper, iron, ruthenium, magnesium, calcium, sulphur and lead. This is first of its kind report on the radiation hazard indices on this placer deposit. The average absorbed dose rates (9795 nGy h−1) computed from the present study is comparable with the top-ranking HBRAs in the world, thus offering the Chavara-Neendakara placer the second position, after Brazil; pertinently, this value is much higher than the World average. The perceptibly high absorbed gamma dose rates, entrained with the high annual external effective dose rates (AEED) and average annual gonadal dose equivalent (AGDE) values existing in this HBRA, encourage us to suggest for a candid assessment of the impact of the background radiation, if any, on the organisms that inhabit along this placer deposit. Future research could effectively address the issue of the possible impact of natural radiation on the biota inhabiting this HBRA.

Cymothoa frontalis, a cymothoid isopod parasitizing the belonid fish Strongylura strongylura from the Malabar Coast (Kerala, India): redescription, description, prevalence and life cycle

BackgroundCymothoa frontalis Milne Edward, 1840 is a very poorly described cymothoid, notwithstanding the previous redescription of the female. Pertinently, to date, the host of C. frontalis has not been identified with adequate precision. Most of the descriptions of cymothoids carried out hitherto were based primarily on females, but practically ignoring other life cycle stages. The present paper redescribes the female and describes other life cycle stages of the species C. frontalis to get better precision in their identification.ResultsThe female phase of C. frontalis is redescribed according to type specimens extant in the NMNH, Paris, and also by the data obtained from live specimens collected during the present study. The general morphology and appendages of various life cycle stages of the species are described. Among 80 fish species from 35 families examined, C. frontalis was recovered only from Strongylura strongylura signifying its oligoxenous host specificity, the prevalence and intensity being 68.65% and 1.9, respectively. Each host fish in more than 85% of the population was infested with a pair of C. frontalis, in three combinations, predominantly with male-female pair (70.9%). C. frontalis exhibited strict site specificity attaching to the buccal cavity of the host fish. The study has also identified three major phases (marsupial, free living and infective) in the life cycle of C. frontalis. The zygotic-staged marsupiumites were developed through five sequential ontogenetic stages. The manca released from the marsupium become infective after a brief period of free swimming life. During the infective phase, C. frontalis completes remaining life cycle stages with successive moulting. Further, six successive stages of the ovigerous females have also been identified.ConclusionsThe present redescription of the female and the description of transitional, male, juvenile and larvae of C. frontalis facilitate precise identification of the species at any stage of the life cycle. Further, the strict host and site specificities of the parasite, as borne out from the present study, and its high degree of prevalence in the host make C. frontalis as an ideal model organism to study the strategies to be adopted for the management of parasites infesting edible fishes.

Mothocya renardi (Bleeker, 1857) (Crustacea: Isopoda: Cymothoidae) parasitising Strongylura leiura (Bleeker) (Belonidae) off the Malabar coast of India: Redescription, occurrence and life-cycle

Mothocya renardi (Bleeker, 1857), a protandrically hermaphroditic cymothoid, parasitising the banded needle fish Strongylura leiura (Bleeker) from the Malabar Coast, India is redescribed and morphological data for different life-cycle stages [male, transitional and ovigerous female, larvae (pre-manca and manca) and juvenile] are provided. Mothocya renardi exhibited strict oligoxenous host specificity by infesting only S. leiura and showed high prevalence levels (reaching up to 92%). The life-cycle of M. renardi comprises three major phases (marsupial phase, free living phase and infestive phase). The marsupial phase comprised one zygotic, three embryonic and two larval stages, all of which remained in the marsupium until the final staged manca is released into the surrounding water. After having led a short free- swimming life, the manca infested the branchial cavity of the host fish, S. leiura. Subsequently it was transformed successively into juvenile, male, transitional and finally functional female through biphasic moult which occurs in between each stage. Based on the presence (or absence) of a brood pouch and/or marsupiumites, six successive stages of the female population were also identified. These data will help precise identification of the female M. renardi irrespective of their stage. The present paper also discusses the host-parasite interactions between S. leiura and M. renardi.

Evaluation of a nested PCR targeting IS6110 of Mycobacterium tuberculosis for detection of the organism in the leukocyte fraction of blood samples

PURPOSE Tuberculosis poses a serious health problem in resource-poor settings such as India. Polymerase chain reaction (PCR) is presently seen as a promising alternative to conventional smear microscopy and culture techniques. Undiagnosed fever is a condition where the aetiology could include tuberculosis in a significant percentage. This paper evaluates a nested PCR (nPCR) using Hotstar Taq for the detection of M. tuberculosis in patients with febrile illness using insertion element, IS6110 as a target. MATERIAL AND METHODS A total of 355 samples (301 HIV status unknown and 54 HIV seropositives) from patients primarily with febrile illness were tested for the presence of M. tuberculosis. Blood culture was done in a commercial automated blood culture system and nPCR in DNA extracts from buffy coat samples. Hotstar Taq polymerase was used to enhance the sensitivity of nPCR and the lower limit of detection was determined by using cloned plasmid. RESULTS Among the patients tested, 2% were positive by automated culture system and 6.8% of patients were positive by nPCR. Majority of the positives were from HIV seropositive individuals. The sensitivity of the nPCR was 100% and the specificity was 95.1%. The lower limit of detection was less than 1 genome copy per microlitre. Among the nPCR positives, patients from rural community were significantly higher than from the peri-urban community. CONCLUSIONS The nPCR had a high sensitivity and specificity on buffy coat samples using Hotstar Taq polymerase in the reaction mix. Thus the technique is a valuable tool in the diagnosis of tuberculosis.

Application of polymerase chain reaction to detect Burkholderia pseudomallei and Brucella species in buffy coat from patients with febrile illness among rural and peri-urban population

Context: Melioidosis and Brucellosis are important endemic infections among people in India, especially in rural settings. Conventional detection techniques have several limitations. Only a few studies exist on the prevalence of Melioidosis and Brucellosis in rural area especially in India. Aim: We sought to evaluate detection of Burkholderia pseudomallei and Brucella spp. among patients presenting febrile illness. Material and Methods: Previously described polymerase chain reaction (PCR) assays for both pathogens were evaluated with Deoxyribonucleic acid extracts of buffy coat samples collected from 301 patients recruited prospectively. Data was not amenable to statistical analysis. Results: The PCR showed specific amplification and no non-specific amplification with heterologous Gram-negative bacilli. The lower limit of detection of the assay for B. pseudomallei was determined to be 1 colony-forming unit /mL and for Brucella it was 1.95 × 103 plasmids per microliter. Blood culture in automated blood culture system was negative for all the samples. This prospective study carried out in southern India for the first time. PCR for Brucella was positive in 1% of the patient samples whereas 0.3% was positive for B. pseudomallei. Conclusion: The finding of Brucella and Burkholderia infections in our populations leads us to suggest that tests for Brucella and B. pseudomallei should also form part of a diagnostic platform for patients with Pyrexia of unknown origin in tropical developing countries.

First record of Glossobius auritus Bovallius 1885 and Glossobius hemiramphi Williams and Williams 1985 (Crustacea: Isopoda: Cymothoidae) parasitizing the marine fishes from Indian Coast

Survey on cymothoids infesting the marine fishes from the Malabar Coast, India recorded two species (Glossobius auritus Bovallius 1885 and Glossobius hemiramphi Williams and Williams 1985), new to India and both appear with new host fish, Cypselurus oligolepis (Bleeker) for G. auritus and Hemiramphus lutkei (Valencinnes) for G. hemiramphi. In the present paper, both species are re-described based on the live and fresh specimens collected from India; Re-description of G. auritus is based on male and female stages, while all the available life cycle stages such as male, transitional, female, juvenile and larvae (manca and premanca) were considered for the re-description of G. hemiramphi. The occurrence, distribution, site specific infestation and fecundity of newly recorded Glossobius spp. are also discussed.

Secretory activity of mandibular organ fluctuates in response to reproductive season of the field crab Paratelphusa sp. (Brachyura; Decapoda): an ultrastructural study

BackgroundMandibular organ (MO) in decapods is suggested to play regulatory role in reproduction, in few species; however, MO is considered to control growth. The present study addresses this question by an ultrastructural study on the MO of the field crab, Paratelphusa sp. Our sampling for consecutive years (2008 to 2012) revealed that Paratelphusa sp. devotes July to October for reproduction, judged by the occurrence of growing ovaries and the berried females. From November to the succeeding June, the females are in a state of reproductive arrest (non-reproductive period); ovaries during this season would appear as white bands with no signs of yolk deposition.ResultsMorphologically, MO of Paratelphusa sp. is positioned posterior to the mandibles and is in close apposition with the distal end of the mandibular apodeme. MO of Paratelphusa sp. exhibited significant levels (t = 8.097, P < 0.0001, N = 10) of season-dependent size variations. Our electron microscopic observations reveal that the MO is highly secretory during the reproductive period, evidenced by the occurrence of sacculated Golgi bodies having dense inclusions, several mitochondria with tubular cristae, and extensive networks of SER and rough endoplasmic reticulum (RER). During the non-reproductive period, however, the MO is least active; RER, the mitochondria, and the Golgi are only sparsely seen. Interestingly, the plasma membrane exhibits a highly convoluted appearance all the way through the non-reproductive period.ConclusionsThe present study reveals that the secretory activity of MO of Paratelphusa sp. is entrained with reproductive activity. The existence of a high correlation between MO secretory activity and ovarian growth implicates the former’s role in reproduction.