Psychrophilic pseudomonas in antarctic freshwater lake at stornes peninsula, larsemann hills over east Antarctica
© Chauhan et al. 2015
Received: 22 January 2015
Accepted: 18 September 2015
Published: 7 October 2015
The Larsemann Hills is an ice-free area of approximately 50 km2, located halfway between the Vestfold Hills and the Amery Ice Shelf on the south-eastern coast of Prydz Bay, Princess Elizabeth Land, East Antarctica (69º30′S, 76º19′58″E). The ice-free area consists of two major peninsulas (Stornes and Broknes), four minor peninsulas, and approximately 130 islands. The Larsemann Hills area contains more than 150 lakes at different Islands and Peninsulas. Nine lake water samples were collected in a gamma sterilized bottles and were kept in an ice pack to prevent any changes in the microbial flora of the samples during the transportation. The water samples were transported to the lab in vertical position maintaining the temperature 1–4 °C with ice pack enveloped conditions. Samples were studied for Psychrophilic bacterial count, Pseudomonas spp., Staphylococcus aureus, Salmonella and Total MPN Coliform per 100 ml. Psychrophillic counts were found in the range of 12 cfu to 1.6 × 102 cfu in all the samples. MPN Coliform per 100 ml was found to be absent in all the samples. No growth and characteristics colonies observed when tested for Salmonella and S.aureus. Pseudomonas sp. was found in ST-2 lake water sample as characteristics colonies (Optimum Growth) were observed on selective media at 22 and 25 °C. Further several biochemical tests were also performed to confirm the presence of this Potential Psychrophilic Pseudomonas sp. for its further application in Science and Technology.
KeywordsPsychrophilic Pseudomonas Antarctic freshwater lake East Antarctica Stornes peninsula
Antarctica has for a long time been viewed as a pristine and isolated environment mostly untouched by human activity. Environmental conditions are generally unfavorable in terrestrial Antarctic environments, with low thermal capacity of the substratum, frequent freeze–thaw and wet-dry cycles, low and transient precipitation, reduced humidity, rapid drainage and limited organic nutrients. Despite the extreme conditions, microorganisms including bacteria, archaea, micro fungi and microalgae, are the dominant life form in the Antarctic ecosystems representing relatively simplified system sensitive to perturbations (Niederberger et al. 2008; Gesheva 2009; Gesheva and Negoita 2012). Psychrophilic and psychrotolerant microorganisms have developed various structural and functional adaptations allowing them to survive in harsh environments. In view of the severe environmental conditions prevailing in Antarctica, it has been argued that the production of extracellular compounds would be a particular advantage in reducing inter-species competition. Thus, it was suggested that Polar Regions may be viewed as a vast untapped reservoir of microorganisms with manifold potential application (Manan et al. 2014). Scientists especially microbiologists throughout the world focusing on cold adopted microorganisms known as Psychrophiles which optimally grow at 15 °C. Cold adopted microorganisms are also reported for the effective bioremediation of oil polluted alpine soils (Margesin 2000). Reddy et al. (2003) and Mountfort et al. (1997) have done the extensive work for the microbial life in the polar environment and have been discovered and described new taxa of Psychrophiles. Several strains of bacteria have been isolated from extreme environments of Antarctica. Gram negative spore-forming, non-spore forming rods, Gram positive cocci were isolated from the snow, ice, and frozen algae of Antarctica (McClean 1918). Temperature-sensitive molecules and enzymes of psychrophiles have applications in pharmaceuticals. The cryoprotectors synthesized by psychrophilic and psychrotolerant microorganisms are used in agriculture, cosmetics, and medicine. Lakes of Antarctica represent a unique ecosystem and not as much considered then lowland lakes mainly because of their remoteness and the short summer open-water period (Bhat et al. 2011).Although they are protected from direct human impact but from last two decades they are largely affected by airborne contaminants, such as acids and nutrients (Rogora et al. 2006), organic pollutants and heavy metals (Carrera et al. 2002). Bharti and Gajananda (2013) reported that even less impact on soft water high altitude lakes might affect significantly the physical and chemical properties to bring changes in species symphony and plenty of the biota and to origin addition of trace substances in higher trophic microorganisms.
The revival of cultivable microorganisms from lakes of Antarctica is not easy; therefore by using rapid and internationally approved method it is possible to understand the diversity, survival, and activity of microorganisms in Antarctic zone. Darling and Siple (1941) isolated 178 strains from the snow, ice, soil and debris of Antarctica. Cultivation and characterization of microorganisms in Antarctic Lakes have also been studied by Zhang et al. 2008. Molecular approach was also adopted for further identification of Antarctic microorganisms. Reddy et al. (2004) evaluated several samples of cyanobacterial mat collected from various water bodies in Antarctica and isolated thirty-one bacteria that belonged to the genus Pseudomonas. All the isolates were found psychrophilic and out of them three novel species of the genus Pseudomonas as Pseudomonas antarctica sp. nov., Pseudomonas meridiana sp. nov. and Pseudomonas proteolytica sp. nov., identified based on Phenotypic and chemotaxonomic characteristics. Richard et al. (2009)studied the microbiology of polar environment and also reported the cultural conditions, nutritional adaptability of Psychrophiles and other novel microorganisms. Present study was designed to identify the microbiological contamination in the lake samples collected during 30th Indian Scientific Expedition to Antarctica. Microbiological Parameters as per the Indian standard of drinking were selected and Emphasis was given to isolate the psychrophilic microorganisms keeping in view the environmental condition of Antarctica.
Method of collection of water samples
Gamma irradiated, clean and sterilized bottles (200 ml capacity) were used for the collection of lake water sample from Antarctica. For dechlorination sodium thiosulphate was added to the clean, dry sampling bottles before gamma sterilization in an amount to provide an approximate concentration of 100 mg/lit in the sample (Chauhan et al. 2015). Aseptic conditions were maintained during the collection of samples. The samples were kept in an ice pack to prevent any changes in the microbial flora of the samples during the transportation. The water samples were transported to the lab in vertical position maintaining the temperature 1–4 °C with ice pack enveloped conditions.
Media, chemical and reagents
All the media were procured form Hi-Media Laboratory, Mumbai, India. Procured dehydrated media were used as per the instructions written on the box and growth promotion test of each media carried out before evaluation of samples. Sodium Chloride, Sodium thiosulphate and other chemicals were of analytical grade.Gram-Stain kit and other reagent procured from Difco Laboratories.
Method for the determination of psychrophilic bacterial count
Serial Dilution Pour plate Method was used for the determination of Psychrophilic Bacterial Count. After proper mixing, collected sample was serially diluted up to 107 dilutions. Diluted sample were further inoculated (1 ml) to each Petri dishes in duplicate. About 15 –20 ml melted media Plate count agar was used for Psychrophilic Bacterial Count as per the guidelines of Indian Standard (IS: 5402-2002, Reaff: 2007). After solidification plates were incubated in an inverted position at 22 °C for 24 h. After incubation the plates were observed for the bacterial colonies with the help of Quebec Colony Counter and then calculated in terms of cfu per ml.
Enumeration of coliform bacteria (MPN Coliform/100 ml)
The most probable number (MPN) technique as per IS1622:1981 was implemented for the enumeration of total coliform. The test procedure included three phases namely presumptive, confirmative and completed phase.
For each water sample; 5 tubes of each 10, 1, and 0.1 ml were used. 10 ml sample was inoculated in double strength Mc Conkey broth media and rest 1 and 0.1 ml was inoculated in single strength Mc Conkey broth media. All the inoculated tubes were incubated at 37 °C for 24–48 h. The test for Coliform is discontinued for further as no growth in all MacConkey broth tubes observed.
Method of detection of Salmonella sp
For the detection of Salmonella. 250 ml water sample was passed through 0.45 micron filter and the filter paper was inoculated in buffer peptone water and then incubated at 37 °C for 24 h. 0.1 ml of above enriched sample was inoculated in 10 ml of Rappaport–Vassiliadis (RV) medium and then incubated at 42 °C for 24 h. Subcultured on the plates of two selective media such as brilliant green agar and bismuth sulphide agar. Plates were observed for characteristic colonies such as pink colonies on brilliant green agar and black metallic sheen colonies with H2S on bismuth sulphide agar plates. Further confirmation through Biochemical and Serological tests was discontinued as no characteristics colonies observed on the plates of selective media (IS: 5887(Part-3) 1999 Reaff.2005).
Method of detection of Staphylococcus aureus
For the detection of Staphylococcus aureus 250 ml water sample was passed through 0.45 micron filter and the filter paper was inoculated in cooked medium and then incubated at 37 °C for 24 h. Subcultured on the Mannitol salt agar and Baird parker agar plates. Plates were observed for characteristic colonies such as yellow colonies on Mannitol salt agar plates and black colonies on Baird parker agar plates. Further confirmation through Biochemical and Serological tests was discontinued as no characteristics colonies observed on the plates of selective media IS: 5887(Partt-2) 1976 Reaff.2005.
Method of detection of Pseudomonas aeruginosa
For the detection of Pseudomonas sp. 250 ml water sample was passed through 0.45 micron filter and the filter paper was inoculated in cetrimide broth and then incubated at 4, 15, 22, 25, 37 °C for 48 h in individual tubes. Subcultured on the plates of cetrimide agar. Plates were observed for characteristic green colonies, optimum growth were observed at 22 and 25 °C. Further confirmation was done by Gram’s staining and Biochemical test as per the guidelines of IS: 13428:2005 (Additional file 1: Table S1).
Results and discussion
With increasing amounts of research taking place it is becoming clear that Antarctica not only profoundly influences us, but that we are globally linked and are having an influence on it too through microbial pollution produced locally and from all over the globe. Most human activity and its associated pollution in Antarctica is highly localized, and waste disposal in the early years was in the form of snow pits, waste dumps, open pit burning, and release of untreated sewage into the oceans. This was the mindset in those times, but has now changed to a more environmentally aware regime. Antarctica is now facing a more serious threat from microbial pollution which began at the time of the industrial revolution. Out of nine samples, only one isolate of Pseudomonas sp. was morphologically and biochemically identified. Presence of this isolate indicates the contamination of fresh water of lake. Coliform organisms, Salmonella and S.aureus were found absent in all the samples which indicate that quality of freshwater of the lake. However, Presence of Gram-negative psychrophylic Pseudomonas isolate specify that there is an urgent need to identify the source of contamination and Hygiene level of Antarctica and residing people. The research outcome also states the requirement of evaluation of Pathogenecity of the isolate and molecular identification for its further use in Science and Technology Globally.
AC and PKB conceived and designed this study. PKB participated in 30th Indian Scientific Expedition to Antarctica and collected the samples. AC and PG analyzed the data. AC wrote and drafted the manuscript. AV and TJ provided their inputs for improving the manuscript quality. All authors read and approved the final manuscript.
The authors are grateful to The Ministry of Earth Sciences (MoES), National Centre for Antarctic and Ocean Research (NCAOR) and SIIR for providing opportunity to carried out the study and participation of Dr. Pawan K. Bharti in 30th Indian Scientific Expedition to Antarctica also want to express their gratitude to leaders and all the expedition members for their continuous support and helps.
The authors declare that they have no competing interests.
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