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Citation Information : Journal of Nematology. Volume 50, Issue 2, Pages 91-98, DOI: https://doi.org/10.21307/jofnem-2018-022
License : (PUBLISHER)
Published Online: 03-June-2018
Pasteuria penetrans (Thorne) Sayre & Starr is a Gram-positive, mycelial, endospore forming bacterium that hyper-parasitizes the root-knot nematodes (RKN, Meloidogyne spp.) in natural environments. Endospores attached to the cuticle surface of the second-stage juveniles (J2s) give rise to a germ tube that penetrates the cuticle to form vegetative microcolony, and proliferates throughout the body of the developing nematode (Davies et al., 1988). The first report of an organism resembling Pasteuria was documented by Cobb (1906) from Dorylaimus bulbiferous, but erroneously reported as “perhaps monads.” The taxonomic identification of this bacterium remained obscured for decades until a formal legitimate name, P. penetrans was proposed by Sayre and Starr (1985) using the basis of conserved description of Pasteuria ramosa infecting cladocerans (Metchnikoff, 1888). Extensive and/or serendipitous scientific observations in subsequent periods could identify Pasteuria spp. from many other free living and plant-parasitic nematodes (Sayre et al., 1988, 1991; Kaplan, 1994; Subbotin et al., 1994; Sharma and Davies, 1996; Giblin-Davis et al., 2003; Bishop et al., 2007; Schmidt et al., 2010; Giblin-Davis et al., 2011), but in depth knowledge is still scanty for many of them. Keen inspection of the life stages of the bacterium has revealed the formation of small groups of vegetative sporangia, which subsequently give rise to quartets, doublets, and eventually produce endospores (Chen et al., 1997; Sayre and Starr, 1985). The obligate nature of Pasteuria has become an obvious obstacle for application of traditional classification approaches for the members of the genus and to study the developmental steps of life-cycle (Davies et al., 2011).
Amongst the major emerging gridlocks in present day agriculture, Meloidogyne incognita (Kofoid and White) Chitwood is a widely adapted endoparasitic nematode species inflicting serious yield and quality losses on many different crops (Jones et al., 2013). Biological control, as an alternative to chemotherapeutics, promises to be a good and effective tool to reduce the nematode population density (Hallman et al., 2009; Collange et al., 2011) and P. penetrans is a potent candidate to be used as a biocontrol agent. But, several attempts of in vitro culturing of P. penetrans either by inoculating the spores or vegetative mycelial bodies onto a diverse range of media ended up with disappointment (Williams et al., 1989; Bishop and Ellar, 1991). However, Pasteuria Bioscience, Inc. (now Syngenta Crop Protection, LLC) has commercialized several bionematicides based on in vitro produced Pasteuria endospores as active ingredient. Notable amongst them are, Econem (Pasteuria usage against Belonolaimus longicaudatus), Naviva (Pasteuria sp. -Pr3 against Rotylenchulus reniformis), Clariva (P. nishizawae against Heterodera glycines) and formulations of P. penetrans (Kokalis-Burelle, 2015) (P. penetrans against M. incognita and Meloidogyne arenaria). All these commercial products are based on either clay-based or liquid formulation for seed and/or soil treatment. But, due to proprietary nature of the company research the Pasteuria scientists have no information about the actual technique or media (if any) to grow the endospores in vitro. Although in vitro production of Pasteuria endospores has been claimed by Pasteuria Biosciences Inc. and Gerber and White (2005), the most widely used method of raising the bacterial endospores is accomplished by in vivo techniques, where endospore encumbered juveniles of M. incognita are inoculated onto host plants and culture relies on the tri-trophic interaction in soil-based microcosms (Rao et al., 2012; Davies et al., 2011). Though the bacterium completes its life-cycle inside the developing nematode by ultimately turning the adult female into an endospore sac, concomitant contamination by other soil dwelling bacteria cannot be overruled (Mauchline et al., 2010). However, exploitation of CYG germination pouches (Mega International, St Paul, MN, USA) using adzuki bean (Vigna angularis (Willd.) Ohwi and Ohashi) as a host for RKN has been proposed to provide a clean and contamination free endospore production approach (Atkinson and Harris, 1989; Rao et al., 2012). This soil-free process also facilitates easy diagnosis of bacterial infection inside the developing nematode having methodological swiftness in isolation of the infected females of Meloidogyne sp. from the roots.
Antibiotics are considered as contaminants of environmental concern, often being biologically active and not biodegradable (Kummerer, 2009; Boutin et al., 2013; Gorokhova et al., 2015). However, despite obvious relevance, information on ecotoxicological effects of antibiotics on the naturally coevolved pathogen-hyperparasite system, as occurs in Pasteuria–RKN interaction, is scanty. Post-antibiotic susceptibility of Daphnia to infection by its pathogenic bacterium P. ramosa was examined previously (Zalewski et al., 2011). But, the effect of any antibiotic on the growth and development of P. penetrans is still largely unknown. The present study was aimed to re-investigate the developing stages of P. penetrans using soil-less CYG medium to have a comprehensive depiction of the life-cycle, along with determining the effect of an antibiotic on the establishment of the bacterium species.
A pure culture of an Indian isolate of M. incognita (Kofoid and White) Chitwood race 1 was multiplied on susceptible tomato plant (Solanum lycopersicum L. cv. Pusa ruby) in the glasshouse at ICAR-Indian Agricultural Research Institute, New Delhi, India. Nematode infected roots were washed free of soil, egg masses were hand-picked and kept for hatching in a Petri dish-wire gauze-tissue paper assembly with distilled water (Whitehead and Hemming, 1965). Freshly hatched juveniles (J2s) were used for experimental purpose.
The seeds of adzuki bean were sterilized by submerging in 3.25% sodium hypochlorite solution for 4 min; followed by washing with 70% ethanol for 3 min and then rinsed with double distilled water until traces of ethanol and sodium hypochlorite vanished completely. The seeds continued to be soaked in water for 6 hr and then transferred in Petri dishes containing moist filter paper to germinate at 28°C. Germinated seeds with 2.0 to 2.5 cm radical were transferred into CYG germination pouches and kept in a growth chamber maintained at 28°C, 70% RH and 16:8 hr light:dark photoperiod for proliferation of roots. Pasteuria penetrans (Strain AII-329: Pasteuria collection, ICAR-IARI, New Delhi, India) endospores were produced on adzuki bean with single egg mass culture of M. incognita as described earlier (Rao et al., 2012). Additionally, a seed tray (dimension: 540 mm × 280 mm; hole size: 60 × 30 × 55 mm3 each) was filled with sterilized soil, adzuki bean seeds were sown (one seed per hole) and maintained at growth chamber with aforesaid conditions. The plants, after attaining 6 cm height, were inoculated with endospore encumbered J2s with an inoculum level of 2 J2s/g soil and maintained for 45 days. This soil-based microcosm served as control for the CYG pouch-based system. The plants were supplemented with diluted Hoagland’s solution (1:500 stock solution). Endospore attachment (on J2 cuticle) was pursued by centrifugation method (Hewlett and Dickson, 1993) with a suspension of 2.5 × 106 endospores/ml.
Developing nematodes were collected from the roots at 3 day intervals starting from 4 days after plant inoculation. The roots were teased very gently using a fine pointed needle and forceps under stereozoom binocular to take out the developing females. The dissected-out females were placed in Ringer’s solution on a cavity slide to prevent bursting. The nematode specimens were washed and surface sterilized following standard method (Davies et al., 2011). At each harvesting time, individual females were broken up on a clean glass slide using a cover slip by gentle pressure. On each occasion, 10 females were crushed for microscopic study of bacterial developmental stages. The growth stages of P. penetrans were monitored and photographed using a Zeiss Axiocam M2m compound microscope equipped with differential interference contrast (DIC) optics.
To study the effectiveness of antibiotic treatment on the growth and development of P. penetrans, different concentrations, viz., 50, 100, 200, 500, 1000, and 5000 ppm of streptomycin sulfate was sprayed on the roots in the CYG germination pouches at 7 and 21 days post inoculation. Five replicates were maintained for each concentration with untreated control. Nematode inoculation and maintenance of pouches were pursued as described previously. The pouches were kept for 40 days in a growth chamber with aforesaid conditions for completion of life-cycle of the bacterium. At harvest, each pouch was observed carefully, documenting the occurrence of gelatinous matrix (with or without eggs). Females were then dissected out and individually checked for P. penetrans infection. The percentage of P. penetrans infected females was calculated as [(No. of infected females/(No. of infected females + No. of uninfected females)) × 100] considering each pouch as a replicate.
The developmental stages of P. penetrans inside M. incognita are schematically shown in Fig. 1. Inside the nematode, bacterial growth starts with the formation of germ tube from the endospore, which gives rise to vegetative microcolony within 8 to 10 days post penetration of juveniles. The “cauliflower like” mycelial microcolony then undergoes maturation and subsequent fragmentation. The fragmentation continues through formation of quartets, triplets, doublets, and eventual production of immature endospores at 25 to 28 days post inoculation. The pre-endospores then undergo maturation and ultimately become ellipsoidal cup-shaped when fully developed. Upon crushing the infected females after 38 to 40 days post inoculation, millions of endospores come out from the nematode body. The endospore filled females showed no trace of genital development as compared with the normal female (Fig. 2). The females with Pasteuria inside produced no egg mass, although in some cases very little gelatinous matrix was formed (Fig. 3).
The production of P. penetrans endospores was found to be significantly (P < 0.05) higher in the CYG germination pouches as compared with the soil-based microcosms. Approximately 81.65 ± 5.78 percent infected females were observed in the pouch system, whereas in soil, the infection was recorded to be 60.05 ± 10.94 percent.
The impact of streptomycin sulfate was found variable according to the administered concentrations. Application of 50, 100, and 200 ppm of the antibiotic resulted in 81.44 ± 4.73, 78.60 ± 3.14, and 80.61 ± 5.90 percent infected females respectively, not significantly (P < 0.01) different with the untreated control (81.65±5.78). However, the percent infected females were reduced to 66.34 ± 3.45, 45.92 ± 4.23, and 19.04 ± 5.28 against an exposure dosage of 500, 1000, and 5000 ppm of the antibiotic. Analysis of the data revealed that, higher doses of the antibiotic reduced the establishment of the bacterium (Fcal = 136.37; P < 0.01) (Fig. 4).
The schematic life-cycle of P. penetrans has been studied earlier (Imbriani and Mankau, 1977; Sayre and Wergin, 1977) and majority of the subsequent descriptions are in compliance with them. According to the previous reports, the germ tube develops from the attached endospore giving rise to a “cauliflower like” vegetative mycelial microcolony, eventually forming quartets and then doublets of the developing sporangia (Sayre and Starr, 1989). Finally, endospores are formed due to sporogenesis and proliferate throughout the body of the female nematode turning it into a “spore-filled sac.” A single M. incognita female has been reported to contain ~2000,000 endospores inside its body (Davies et al., 1988). The germination of endospores is triggered by some unknown cue(s) and takes place before the first molt of the J2s inside the root, after establishing the permanent feeding site (Sayre and Wergin, 1977; Davies et al., 1988). Earlier, the life-cycle of Pasteuria was divided into three phases (Williams, 1960) and similar kind of phase division has also been retained later with fair modification (Davies et al., 2011).
In the present study, certain observations were recorded about the life-cycle of P. penetrans infecting M. incognita that were hitherto not depicted. Based on this study, it can be assumed that the newly formed microcolony first undergoes maturation and systematically fragmented before entering sporogenesis. Instead of direct formation of quartets and doublets from the microcolony (through fragmentation), a “star-shaped” structure was found to be formed with many single sporangium attached together. These vegetative bodies may presumably break into smaller fragments or single developing sporangium may detach, ultimately leading to premature endospore development. The formation of “star-shaped” vegetative body between microcolony and quartet and/or “triplet” stage between quartet and doublet has not been reported earlier. Generation of these stages hints for segregation of single sporangium containing endospore at an early stage, and their further progression toward maturation. Crushing of a single developing female at 25 days postinoculation revealed the presence of most of the life stages, starting from the “star-shaped” stage to doublets. The simultaneous occurrence of all these stages together in a single female possibly indicates the asynchrony in germination of the attached endospores. This suggests that the endospores on the J2 nematode cuticle germinate at various time points and proceed toward formation of vegetative microcolony. The genesis of premature endospores was found at around 25 to 28 days after feeding site development by M. incognita, and fully developed ellipsoidal and cup-shaped endospores were formed at 38 to 40 days after nematode invasion. The immature endospores contained a rhomboid exosporium and at maturity became morphologically distinguishable that could be detected through light microscopy. The comparison of sporogenesis in Bacillus and Pasteuria has been overlaid in many earlier publications (Sayre and Starr, 1985; Stragier and Losick, 1996; Chen et al., 1997). Recently it has been suggested that the sporogenesis phenomenon commences in the granular mass composed of aggregated rod-shaped body of Pasteuria (Davies et al., 2011). Similar types of aggregated rod-shaped structures were also seen in the developing nematode body. The rod-shaped bodies have been proposed to grow rapidly leading to the development of aggregated granular masses within the female nematode, directed to exponential growth of P. penetrans (Davies et al., 2011). The whole process of sporulation has been discovered to be unidirectional, committed and controlled by signaling cascades in Bacillus spp. and a similar trend with involvement of cascades have also been detected in Pasteuria spp. (Hoch, 2000; Kojetin et al., 2005). As the formation of endospores progresses, the female reproductive system is completely destroyed and whole body comes out to be full of endospores along with lipid granules.
The use of CYG germination pouches increased the percentage establishment of P. penetrans as compared with the method relied on soil-based microcosm. The higher number of infected females may be a result of assured penetration brought by direct inoculation of endospore encumbered juveniles on roots, which may not be achieved in soil due to uncontrolled infection. Being an obligate parasite, the bacterium cannot be cultured in artificial media and exposure to antibiotic was brought indirectly, i.e., application on germination pouches. Streptomycin sulfate is a systemic aminoglycoside antibiotic and binds irreversibly to bacterial ribosomes inhibiting the protein synthesis (Levin et al., 2000). The bactericide can affect the microbial population even at a concentration of 50 µg/ml (Kogut and Harris, 1969; Yashiro and McManus, 2012). The effect of streptomycin sulfate was found to be concentration dependent on successful establishment of P. penetrans in CYG germination pouches, where higher concentrations (500–5000 ppm) had a negative impact. The observed response of P. penetrans at higher doses may be due to the indirect way of exposure unlike supplementing it directly in the growth media as followed for culturable bacteria. Production of clean and contamination free endospores has been one of the major hindrances so far that affected the basic research on interaction of P. penetrans and M. incognita. Thus, the occasional use of streptomycin sulfate (at low concentration) in CYG germination pouches is advantageous to get clean Pasteuria endospores in high quantity, for any downstream basic research.
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