Real-time PCR reveals endosymbiont titer fluctuations in Metaseiulus occidentalis (Acari: Phytoseiidae) colonies held at different temperatures.
One colony of M. occidentalis was maintained at room-temperature (23-25[degrees]C) and 2 colonies initiated from this line were maintained at 32 and 34[degrees]C for More than 1 year in growth chambers prior to experiments. Female mites (100) were isolated from each colony and their genomic DNA extracted by Puregene and QIAGEN methods (Jeyaprakash & Hoy 2007), and resuspended in 50 [micro]L of sterile water. Four different plasmids carrying endosymbiont 16S rRNA sequences; pAJ233 (Cardinium), pAJ234 (Bacteroidetes), pAJ235 (Wolbachia) and pAJ239 (Enterobacter), were extracted and their yield estimated with a BioPhotometer Plus (Eppendorf AG, Hamburg, Germany). Species-specific primers were designed with Primer 3 software (http:// frodo.wi.mit.edu/primer3/) and a probe was designed with Primer X software (Applied Biosystems, Foster City, CA) from the variable regions for each species (Table 1). Real-time PCR was performed in a 20-[micro]L reaction volume containing genomic DNA from 2 females (1 [micro]L) or serially-diluted plasmid DNA (100 [micro]g to 1 fg) or a no DNA control (1 [micro]L), forward and reverse primers (400 pM), probe (100 pM) and TaqMan master mix (10 [micro] L). Two linked profiles: (1) one cycle of 50[degrees]C for 2 min and 95[degrees]C for 10 min, and (2) 60 cycles consisting of denaturation at 95[degrees]C for 15 s, annealing at 59[degrees]C (Cardinium) or 57[degrees]C (Wolbachia or Enterobacter or Bacteroidetes) for 30 s and extension at 72[degrees]C for 30 s, were used. Each treatment was replicated 3 times. The starting copy number of all plasmid DNA dilutions used in the real-time PCR was obtained with an open-source software (http:/ /molbiol.edu.ru/eng/scripts/h01_07.html). A standard regression curve was generated with the Ctvalue (Number of PCR cycles required for sample fluorescence to reach the threshold level) obtained from all 9 serial plasmid DNA dilutions. The Ct-value obtained from the 2 female mites was then used in the regression analysis to estimate the copy number of bacterial cells present, which was divided by 2 to obtain the copy numbers in a single female.
The titer of Cardinium and Wolbachia was much higher than that of the gut endosymbionts Enterobacter and Bacteroidetes in the room-temperature M. occidentalis COS colony (Table 2). The Cardinium, Wolbachia and Enterobacter titer was reduced, but not eliminated, in both heat-treated colonies. By contrast, Bacteroidetes had a higher titer in the heat-treated colonies, but their density was below detectable levels (1 or 2) in the room-temperature colony, and could not be reliably amplified by real-time PCR (Table 2).
We think that the titer of Wolbachia or Cardinium could play a role in mating compatibility when making crosses between heat-treated (uninfected) females and room-temperature (infected) males. However, it is not clear which endosymbiont actually causes mating incompatibility in the COS colony because this requires generating colonies infected with only Cardinium or Wolbachia. Weeks & Stouthamer (2004) reported that Wolbachia infection in another colony of M. occidentalis is lost when fed a Wolbachia-free two-spotted spider mite diet. During the summer of 2009 we determined, by high-fidelity PCR, that the two-spotted spider mite culture in our greenhouse had inadvertently lost Wolbachia after being heated to 40-42[degrees]C for several months (3-6) due to a maintenance problem and, subsequently, the 23-25, 32 and 34[degrees]C COS colonies that were fed this Wolbachia-free spider mite diet were determined to have lost Wolbachia (data not shown), suggesting that the Wolbachia in these colonies of M. occidentalis was obtained from their spider mite prey.
To determine whether the Wolbachia-free COS colonies reared at 23-25 and 34[degrees]C exhibited incompatibility several inbred lines were generated. They displayed no fluctuation in Cardinium and Enterobacter titers (Table 2). A total of 7 or 8 reciprocal single-pair and control crosses were performed on 3 separate dates. Equal numbers of reciprocal and control crosses were successful and produced unshriveled eggs that subsequently hatched, suggesting that Cardinium is not involved in causing cytoplasmic incompatibility in the COS colony at these titers (Table 2) and that Wolbachia might be involved. It appears that this COS colony is obtaining Wolbachia by feeding on its Wolbachia-infected prey. These results are consistent with earlier data indicating that there are no differences in 16S, ftz and wsp sequences from Wolbachia in the COS and T. urticae colonies (Hoy & Jeyaprakash 2005).
The standard PCR protocol previously used by Johanowicz & Hoy (1996) we now know is not sufficiently sensitive to be certain that endosymbionts truly are lacking (Jeyaprakash & Hoy 2000) and should not be used when comparing heat-treated and room-temperature colonies. Real-time PCR is an efficient tool to quantify endosymbiont titer based on this study and that by Wiwatanaratanabutr & Kittayapong (2009). This research was supported in part by the Davies, Fischer and Eckes Endowment in Biological Control to M. A. Hoy.
Real-time PCR amplification of 16S rRNA sequences from 4 M. occidentalis endosymbionts; Cardinium, Wolbachia, Enterobacter, and Bacteroidetes, provided an estimate of their titer in colonies reared under 3 temperatures. This work also revealed, for the first time, that the Wolbachia and Cardinium titer were reduced in heat-treated COS colonies, but not completely eliminated. However, feeding M. occidentalis colonies the Wolbachia-free two-spotted spider mite diet did eliminate Wolbachia from this predator. No cytoplasmic incompatibility was detected when crosses were made between males reared at room-temperature (23-25[degrees]C) containing Cardinium (and lacking Wolbachia) and females reared at 34[degrees]C containing a much lower titer of Cardinium (and lacking Wolbachia), indicating that Wolbachia may be involved in causing previously observed incompatibilities rather than Cardinium.
HOY, M. A., AND JEYAPRAKASH, A. 2005. Microbial diversity in the predatory mite Metaseiulus occidentalis (Acari: Phytoseiidae) and its prey, Tetranychus urticae (Acari: Tetranychidae). Biol. Control 32: 427-441.
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JOHANOWICZ, D. L., AND HOY, M. A. 1996. Wolbachia in a predator-prey system: 16S ribosomal analysis of two phytoseiids (Acari: Phytoseiidae) and their prey (Acari: Tetranychidae). Ann. Entomol. Soc. America 89: 435-441.
JOHANOWICZ, D. L., AND HOY, M. A. 1998. Experimental induction and termination of non-reciprocal reproductive incompatibilities in a parahaploid mite. En tomol. Expt. Appl. 87: 51-58
WEEKS, A. R., AND STOUTHAMER, R. 2004. Increased fecundity associated with infection by a Cytophagalike intracellular bacterium in the predatory mite, Metaseiulus occidentalis. Proc. R. Soc. London B (Suppl.) 271: S193-S195.
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AYYAMPERUMAL JEYAPRAKASH (1) AND MARJORIE A. HOY
Department of Entomology and Nematology, University of Florida, Gainesville, FL 32611
(1) Presently at Bureau of Entomology, Nematology and Plant Pathology, Florida Department of Agriculture and Consumer Services, Division of Plant Industry, Gainesville, FL 32608
TABLE 1. LIST OF SPECIES-SPECIFIC PRIMERS AND PROBES DESIGNED FOR REAL-TIME PCR. Species Primer and probe sequence Cardinium MoCardRT-F2 5'-GCCGGCGACCGGCGAATG-3' MoCardRT-R1 5'-CGGAGGCTATTCCCCAGTGT-3' MoCardProbe1 6FAM-TGCGTAATGCACATGC-MGBNFQ Wolbachia MoWolRT-F1 5'-GCAACGCGAAAAACCTTACCAC-3' MoWolRT-R1 5'-CCGACCCTATCCCTTCGAAT-3' MoWolProbe 1 6FAM- TCTTGACATGAAAATC-MGBNFQ Bacteroidetes MoBactRT-F1 5'-AGCGGCAGGCCTAATACATG-3' MoBactRT-R1 5'-CTCACCATCTTCGAGCAAGCT-3' MoBactProbe 1 6FAM- AAGTCGGACGGGATC-MGBNFQ Enterobacter MoEnterRT-F1 5'-TGCCAGCAGCCGCGGTAAT-3' MoEnterRT-R1 5'-TTTACGCCCAGTAATTCCGATT-3' MoEnterProbe 1 6FAM- CGGAGGGTGCAAGC-MGBNFQ Species Product size Cardinium 66 bp Wolbachia 65 bp Bacteroidetes 65 bp Enterobacter 59 bp TABLE 2. MEAN NUMBER (S.D.) OF ENDOSYMBIONTS ESTIMATED PER ADULT FEMALE METASEIULUS OCCIDENTALS MAINTAINED AT 3 DIFFERENT TEMPERATURES (1). Rearing Date Colony temperature Cardinium 8/10/09 COS 23-25[degrees]C 26,666 [+ or -] 23 COS 32[degrees]C 127 [+ or -] 16 COS 34[degrees]C 138 [+ or -] 16 9/25/09 COS C10-BaBA 23-25[degrees]C 18,516 [+ or -] 5 inbred lines C10-BA 23-25[degrees]C 19,199 [+ or -] 5 C10-CB 23-25[degrees]C 20,892 [+ or -] 5 F10-FAB 23-25[degrees]C 16,711 [+ or -] 5 F10-BAA 23-25[degrees]C 19,907 [+ or -] 5 F10-IOO 23-25[degrees]C 19,315 [+ or -] 5 Date Colony Wolbachia Enterobacter 8/10/09 COS 13,585 [+ or -] 22 379 [+ or -] 12 COS 68 [+ or -] 15 10 [+ or -] 2 COS 74 [+ or -] 15 15 [+ or -] 2 9/25/09 COS C10-BaBA ND 264 [+ or -] 5 inbred lines C10-BA ND 274 [+ or -] 5 C10-CB ND 295 [+ or -] 5 F10-FAB ND 278 [+ or -] 5 F10-BAA ND 322 [+ or -] 5 F10-IOO ND 329 [+ or -] 5 Date Colony Bacteroidetes 8/10/09 COS BDL COS 543 [+ or -] 12 COS 499 [+ or -] 12 9/25/09 COS C10-BaBA BDL inbred lines C10-BA BDL C10-CB BDL F10-FAB BDL F10-BAA BDL F10-IOO BDL (1) Means were obtained based on 3 reactions per condition. BDL = Below detectable level (1 or 2); COS = Carbaryl-OP-Sulfur resistant; ND = Not detected (0) and had been fed two-spotted spider mite prey lacking Wolbachia.
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|Title Annotation:||Scientific Notes; Polymerase Chain Reaction|
|Author:||Jeyaprakash, Ayyamperumal; Hoy, Marjorie A.|
|Date:||Sep 1, 2010|
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