Detecting Heterobasidion irregulare in Minnesota and Assessment of Indigenous Fungi on Pines

: Heterobasidion irregulare is one of the most problematic forest pathogens in the northern hemisphere, but has only been found relatively recently in the north central United States. Discovered in Wisconsin in 1993, but probably established sometime before that, it quickly spread throughout the state. In November 2014, it was found in southeastern Minnesota. Field surveys were then conducted throughout Minnesota with the focus in the southeast near the initial discovery. To ﬁnd additional infection sites, surveys were conducted with accompanying aerial imagery of red pine ( Pinus resinosa Aiton) stands that were previously thinned. Samples were collected from selected sites with dead and dying trees as well as samples from stumps in recently thinned pine stands. These samples were processed ﬁrst with a nested polymerase chain reaction (PCR) protocol, which was replaced by a real-time PCR assay after its development. No samples tested positive for H. irregulare using these methods and no cultures from isolations were obtained outside the original infection area. Other indigenous fungi were also identiﬁed. The majority were wood decay fungi in the Basidiomycota. A spore collection study was also conducted after ﬁeld surveys. Automated rotary arm spore collectors were used and assayed with an ITS TaqMan real-time PCR assay. Collectors were placed strategically in different areas of Minnesota. A positive control was used in an infected red pine plantation in Wisconsin and this location had the highest number of spores trapped, with 63,776 over a week period. Spores of H. irregulare were detected at several sites in Minnesota, with the highest spore total observed in traps at 413 over a week period. All other locations sampled also had some spores collected except Itasca State Park located in northwestern Minnesota. The weekly deposition of spores ranged from 0 to 1.26 m − 2 h − 1 . Low spore levels occurring in Minnesota indicate that some spores are present, but they are currently being detected in amounts that may not be sufﬁcient for colonization to be successful.


Introduction
The fungal pathogen, Heterobasidion irregulare Garbelotto & Otrosina, is a serious threat to red pine (Pinus resinosa Aiton) and other conifers throughout North America [1]. It is considered one of the most economically damaging forest pathogens in the northern temperate regions of the world. In addition to causing serious economic damage, Heterobasidion root disease (HRD) impacts ecosystem services and can be devastating in urban environments where trees weakened by infection can pose hazards to the general public.
The primary infection is by airborne basidiospores produced by shelf-like basidiocarps [2]. Basidiospores can be disseminated overland to start new infections on recently cut stumps and wounds. The asexual state, Spiniger meineckellus (A.J. Olson) Staplers, produces large numbers of conidiophores and conidia that can form over the surface of exposed infected wood. The role of conidia for infection, however, is not well understood, Additionally, as of December 2020, the Wisconsin Department of Natural Resources reports HRD has been confirmed in 28 counties [15]. Therefore, it was important to establish a Minnesota program to detect this pathogen early to prevent its spread. Since Minnesota is at the leading edge of a potential epidemic, this study was conducted to determine the distribution of H. irregulare in Minnesota through field surveys for diseased trees and spore trapping to detect and calculate the density of basidiospores. In addition, culturing studies from dead/dying trees and stumps were conducted to isolate the pathogen as well as identify other indigenous fungi that were present. Indigenous fungi that were isolated were recorded to help determine what native fungi may be present and influencing any outbreaks since some saprophytic fungi, such as Phlebiopsis gigantea, have previously been shown to control the disease [16][17][18][19].

Field Surveys
Intensified surveys for H. irregulare started in the spring of 2015 ( Figure 1). Surveys focused on red and eastern white pine (Pinus strobus L.) growing areas in southeastern Minnesota, where the first location of H. irregulare had been found and these areas are adjacent to counties in Wisconsin with the disease. Areas in the north and east central regions of Minnesota were also surveyed due to the importance of the pine resource there ( Figure 1). The Minnesota Department of Natural Resources provided aerial maps of multiple survey sites and assisted with the surveys. The aerial maps were created to help navigate at sites and also helped detect large pockets of dead and declining trees. Survey sites chosen were focused on red and white pine stands that were thinned recently and up to 20 years ago. The HRD situation in Wisconsin escalated quickly after it was discovered in 1993. This was due to the lack of a rapid detection method for the disease and a delay in managing the pathogen. The disease is now found in three counties of Wisconsin adjacent to Minnesota. Additionally, as of December 2020, the Wisconsin Department of Natural Resources reports HRD has been confirmed in 28 counties [15]. Therefore, it was important to establish a Minnesota program to detect this pathogen early to prevent its spread. Since Minnesota is at the leading edge of a potential epidemic, this study was conducted to determine the distribution of H. irregulare in Minnesota through field surveys for diseased trees and spore trapping to detect and calculate the density of basidiospores. In addition, culturing studies from dead/dying trees and stumps were conducted to isolate the pathogen as well as identify other indigenous fungi that were present. Indigenous fungi that were isolated were recorded to help determine what native fungi may be present and influencing any outbreaks since some saprophytic fungi, such as Phlebiopsis gigantea, have previously been shown to control the disease [16,17,18,19].

Field Surveys
Intensified surveys for H. irregulare started in the spring of 2015 ( Figure 1). Surveys focused on red and eastern white pine (Pinus strobus L.) growing areas in southeastern Minnesota, where the first location of H. irregulare had been found and these areas are adjacent to counties in Wisconsin with the disease. Areas in the north and east central regions of Minnesota were also surveyed due to the importance of the pine resource there ( Figure 1). The Minnesota Department of Natural Resources provided aerial maps of multiple survey sites and assisted with the surveys. The aerial maps were created to help navigate at sites and also helped detect large pockets of dead and declining trees. Survey sites chosen were focused on red and white pine stands that were thinned recently and up to 20 years ago.  Samples were collected from declining and recently dead trees, stumps, roots, and woody debris. Additionally, basidiocarps resembling H. irregulare were collected. Samples were placed in sterile bags, kept cool during transport, and brought to the University of Minnesota for processing. Genomic DNA was extracted from the majority of wood samples initially with the MO BIO PowerPlant ® Pro DNA Isolation Kit (MO BIO Laboratories, Inc., Carlsbad, CA, USA) and also with the Qiagen DNeasy ® PowerPlant ® Pro Kit (Qiagen, Valencia, CA, USA) following the manufacturer's protocol. A cetyl trimethylammonium bromide (CTAB) DNA extraction protocol [20] was used for basidiocarp samples and for a set of woody samples. The use of this protocol for woody samples was discontinued, however, due to the DNA kits yielding a more pure DNA extract. Initially, samples were processed with conventional PCR using a nested approach that involved the use of two H. irregulare specific primer sets and two successive PCR reactions. PCR amplification for the first round was targeted for the internal transcribed spacer (ITS) region of rDNA with the primer pair ITS1F/4 [21]. PCR amplification reagents included 12.5 µL of 1X GoTaq Green Master Mix (Promega, Madison, WI, USA), 9.5 µL of sterile water, 1 µL of each primer (0.2 µM), 0.5 µL BSA (0.1 mg/µL), and 1 µL of template DNA in a thermocycler with the following parameters: 94 • C for 5 min, 35 cycles of 94 • C for 1 min, 50 • C for 1 min, 72 • C for 1 min, and a final extension step of 5 min at 72 • C. A 1% agarose gel using SYBR green 1 prestain (Life Technologies, Grand Island, NY, USA) and a Dark Reader DR45 transilluminator (Clare Chemical Research, Denver, CO, USA) was used to visualize PCR amplicons. If PCR amplicons were present, then these samples were used in the second round of PCR. For the second round, specific primers for the genus Heterobasidion were used. These primers were Het_4F (CGAATATCGTGCAAGGTTGAAG) and Het_1R (CCACAAGGGTCTCGCTAATG). The primers were developed in our laboratory at the University of Minnesota and were tested to determine amplification efficiency and accuracy for the genus of Heterobasidion. One µL of the ITS1F/4 PCR product was used and diluted 1/50 in sterile water. The same reagents were used as for the first round. Different thermocycler parameters were used: 95 • C for 4 min, 35 cycles of 95 • C for 1 min, 53 • C for 45 s, 72 • C for 1 min, and a final extension step at 72 • C for 5 min. Additionally, positive and negative controls were used in both rounds of PCR. The positive control was DNA of H. irregulare from a culture that originated from the location positive for H. irregulare in Minnesota. The negative control was sterile water and DNA extracted from a wood sample and negative for H. irregulare via PCR and sequencing. PCR amplicons were visualized using the same methods mentioned previously. Sequencing reactions were performed using the forward primer, ITS1F, for PCR amplicons from the first PCR round using an ABI Prism 3730xl DNA sequencer (Applied Biosystems, Foster City, CA, USA). The majority of DNA sequenced was extracted from fungal cultures isolated from samples. A small amount of DNA was sequenced from sporophore and wood samples via a direct DNA extraction. Assembly of consensus sequences was done using Geneious 9.0 [22] and compared to sequences in the GenBank using BLASTn for identification.

qPCR Analysis
A real-time PCR protocol was then developed. A LightCycler 96 real-time PCR system (Roche Applied Science, Penzberg, Germany) was used to carry out the reactions. The reagents consisted of 10 µL of 1× FastStart Essential DNA Probes Master (Roche Applied Science), 1 µL of each primer (0.5 µM) (Hirregulare_4A/G_F435 (CATTCTGAAGACAT-ACGAGGGA) and Hirregulare_R500 (GGTCGGGTTCTTTTGAT)), 2 µL of probe (0.1 µM) (Hannosum_ss_irregulare_T464), 0.5 µL of BSA (0.125 mg/µL), and 0.5 µL of sterile water. A total of 5 µL of DNA was used, which was diluted 1/5 with sterile water; this was to minimize pipetting error. Thus, a total reaction volume of 20 µL. The following parameters were used: preincubation at 98 • C for 90 s and a two-step amplification of 45 cycles, 95 • C for 10 s, 58 • C for 25 s. A synthetic standard of the whole ITS region of H. irregulare synthesized using gBlocks TM by Integrated DNA Technologies (IDT) was used to create the standard curves and a correlation coefficient. The stock of the synthetic standard had a concentration of 1.451 × 10 10 H. irregulare ITS copies/µL. A set of four dilutions were made of the synthetic standard with concentrations of 145,100,000, 14,510,000, 145,100, 14,510, and 145.1 H. irregulare ITS copies/µL. After the reaction, the Ct values were plotted against log H. irregulare ITS copy concentration. The lower limit of detection was determined to be 50 H. irregulare ITS copies.

Culture Methods
Additionally, small segments of wood were cut from samples with aseptic techniques and incubated on culture media. The majority of samples were cultured with a semiselective media for Basidiomycota (BSA). This media was modified from the original recipe and included 15 g of agar, 15 g of malt extract, 2 g of yeast, and 0.06 g of benlate added to 1 L of water and after autoclaving, 0.1 g of streptomycin sulfate and 2 mL of lactic acid was added [23]. Plates were grown at room temperature (~20 • ) and checked often for fungal growth that was then sub-cultured onto new BSA. After cultures were grown out, a cetyl trimethylammonium bromide (CTAB) protocol was used to extract DNA from each isolate as well as basidiocarp samples. The primer pair ITS1F/4 was used for PCR amplification. Amplification, sequencing, and sequence assembly was conducted using the previously mentioned methods used for wood samples.

Spore Surveys
Spore trapping methods followed those used to trap H. irregulare basidiospores in Quebec [24,25]. Two automated rotary arm spore collectors (Aerobiology Research Laboratories, Ottawa, ONT, Canada) were programmed to spin 4 min every 60 min, with rods (1.5 mm × 1.5 mm × 3 cm) placed in the rotary arms that were coated with a 7% silicone-hexane solution. Spore collectors were placed in an open forested setting and moved to different locations after disinfecting with a 10% dilution of bleach, from September to November 2018. The period from late summer to early fall was chosen as the deployment time based on previous research demonstrating that peak deposition is during late summer and fall [5]. The spore collectors were placed at locations previously sampled for H. irregulare and were points of interest due to their proximity to the closest infection site in Wisconsin ( Figure 2). Additionally, spore collectors were placed in Itasca State Park due to the finding of possible Heterobasidion basidiocarps on two separate occasions in the 1970s. Spore collectors were deployed for 7 days at each location except for the Wisconsin location, which had deployment for 8 days and the Itasca locations for 9 days. Rods were then collected and placed in separate 1.5 mL microcentrifuge tubes until processed.
Rods were brought to the University of Minnesota and a DNA extraction was performed on each rod based on that of Lamarche et al. (2016) [26]. One mL of Goof Off Pro Strength Remover (W.M. Barr, Memphis, TN, USA) was added to each tube. The rods were vortexed for 30 s or until the rod was totally dissolved. The tubes were centrifuged for 2 min at 20,000× g and the supernatant was discarded. One mL of Goof Off Pro Strength Remover was used to rinse the spore pellet and then discarded. The tube was then left to dry in a bio-safety cabinet for 1 h. A 3 mm stainless steel bead, 180 µL of buffer ATL, and 1 µL of reagent DX (Qiagen) were added to each tube and placed in a MagNA Lyser (Roche Applied Science, Penzberg, Upper Bavaria, Germany) to lyse the samples for 90 s. Next, 20 µL of Proteinase K was added and was mixed by vortexing for 15 s. The samples were then incubated at 56 • C in a water bath overnight. The following day, DNA extraction was performed using the QIAamp ® DNA Micro Kit (Qiagen) and following the manufacture's protocol.
Real-time PCR was performed to obtain basidiospore counts. A ribosomal ITS TaqMan assay was performed based on that of Lamarche et al. (2016) [26]. The reagents consisted of 5 µL of 1× FastStart Essential DNA Probes Master (Roche Applied Science), 1 µL of each primer (0.5 µM), 1 µL of TaqMan probe (0.1 µM), 1 µL of sterile water, and 2 µL of template DNA for a total reaction volume of 11 µL. The amount of template DNA was 2 µL due to the possible risk of pipetting error. Reactions took place on a LightCycler 96 (Roche Applied Science). Calculations of basidiospore equivalents per rod were calculated by translating Ct values using standard curve equations. A mono-basidiosporal isolate of H. irregulare (#98-008) was used to create the standard curves and a correlation coefficient. The isolate was obtained from the Laurentian Forestry Centre culture collection (Canadian Forest Service, Natural Resources Canada) and originated from a basidiocarp sampled in Lac La Blanche, Quebec, Canada. The isolate was confirmed to have 1-2 nuclei/conidia. The protocol to develop the standard curve equations using the mono-basidiosporal isolate of H. irregulare (#98-008) was based on that of Lamarche et al. (2016) [26]. The standard curve produced had a correlation coefficient (r 2 ) of 0.95. Rods were brought to the University of Minnesota and a DNA extraction was performed on each rod based on that of Lamarche et al. (2016) [26]. One mL of Goof Off Pro Strength Remover (W.M. Barr, Memphis, TN, USA) was added to each tube. The rods were vortexed for 30 s or until the rod was totally dissolved. The tubes were centrifuged for 2 min at 20,000× g and the supernatant was discarded. One mL of Goof Off Pro Strength Remover was used to rinse the spore pellet and then discarded. The tube was then left to dry in a bio-safety cabinet for 1 h. A 3 mm stainless steel bead, 180 µL of buffer ATL, and 1 µL of reagent DX (Qiagen) were added to each tube and placed in a MagNA Lyser (Roche Applied Science, Penzberg, Upper Bavaria, Germany) to lyse the samples for 90 s. Next, 20 µL of Proteinase K was added and was mixed by vortexing for 15 s. The samples were then incubated at 56 °C in a water bath overnight. The following day, DNA extraction was performed using the QIAamp ® DNA Micro Kit (Qiagen) and following the manufacture's protocol.
Real-time PCR was performed to obtain basidiospore counts. A ribosomal ITS TaqMan assay was performed based on that of Lamarche et al. (2016) [26]. The reagents consisted of 5 µL of 1× FastStart Essential DNA Probes Master (Roche Applied Science), 1 µL of each primer (0.5 µM), 1 µL of TaqMan probe (0.1 µM), 1 µL of sterile water, and 2 µL of template DNA for a total reaction volume of 11 µL. The amount of template DNA was 2 µL due to the possible risk of pipetting error. Reactions took place on a LightCycler 96 (Roche Applied Science). Calculations of basidiospore equivalents per rod were calculated by translating Ct values using standard curve equations. A mono-basidiosporal isolate of H. irregulare (#98-008) was used to create the standard curves and a correlation coefficient. The isolate was obtained from the Laurentian Forestry Centre culture collection (Canadian Forest Service, Natural Resources Canada) and originated from a basidiocarp sampled in Lac La Blanche, Quebec, Canada. The isolate was confirmed to  [27]. Furthermore, the total amount of basidiospores that deposit on a 30-cm stump was calculated by using the following formula: total amount of basidiospores m −3 of a site × (stump radius 2 × π). Since the spore collectors were at the Wisconsin site for 8 days, exposure time was a total of 12.27 h and exposure time was 13.8 h at Itasca State Park with spore collectors deployed for 9 days. Calculations were determined for each of the two rods at one location and averaged.

Field Surveys
A total of 949 samples were collected from field survey sites throughout Minnesota (Figure 1). These samples were from dead and dying trees (579), stumps (252), sporophores (87), and downed trees and slash (31). A multitude of different fungi were isolated and subsequently sequenced from collected samples. However, no definitive positive results for H. irregulare were found outside the original H. irregulare infection site. With both conventional PCR and later real-time PCR, H. irregulare was not detected in wood samples. Additionally, isolating from wood did not yield any cultures of H. irregulare except for the original positive location near Minneiska, Minnesota.
The majority of the fungi isolated and sequenced were fungi in the Basidiomycota. A total of 183 pure cultures were obtained and represented 60 different taxa. Cultures of Ascomycota were isolated, but they are not reported here since the focus of this study was on the Basidiomycota and the media primarily used was a semi-selective media for isolating Basidomycota. If the same taxon was isolated from the same substrate, only one was reported. The most commonly isolated basidiomycete was Irpex lacteus (15%). The early colonizer, Phlebiopsis gigantea was the second most common at 14% and Phanerochaete sordida was the third most common (7%). Other fungi isolated included, Coniophora puteana (5%), Armillaria ostoyae (Armillaria solidipes) (4%), Sistotrema brinkmannii (4%), Phaeolus schweinitzii (3%), and Phlebia tremellosa (3%). Of the total isolates (Figure 3), these eight taxa represented 55% of the total Basidiomycota isolates obtained.
The most commonly isolated substrate was from stumps (76), followed by dead and dying trees (69), sporophores (33), and downed trees and slash (5). Additionally, the majority of samples were collected and isolated from red pine (140) followed by white pine (37), and then white spruce (6). White spruce was selected due to Heterobasidion being reportedly found on these species in Itasca State Park and also being reported as a host to H. irregulare in Wisconsin [15].

Spore Surveys
The highest counts of H. irregulare spores (Table 1) were collected at the Wisconsin site with a total of 63,776.07 over a week period. This site was infected with H. irregulare for at least 28 years, at the time of the surveys, and had multiple basidiocarps present throughout the stand. The stand was thinned in both 1990 and 2000, but due to high number of basidiocarps present, the initial infection most likely occurred during the earlier thinning. It is also possible that the spores collected at the Wisconsin site inlcuded conidia, but with multiple basidocarps present, the value most likely represented basidiospores.   Table S1 of Supplementary Materials.

Figure 3.
Basidiomycota taxa isolated from different woody substrates and sporophores throughout Minnesota during surveys for H. irregulare. ** following the taxon name indicates that the best blast match was below 97% similarity. Bar represents number of isolates. GenBank accession numbers for taxa are presented in Table S1 of Supplementary Materials.

Field Surveys
Heterobasidion irregulare was found in Minnesota in November 2014 and other infection sites were expected to be found. However, these studies and field surveys indicated the pathogen is in a very early stage of introduction to Minnesota. No additional basidiocarps were located in the field and no isolates of H. irregulare were obtained from woody samples that were cultured from suspect trees, stumps, and downed conifer wood. Samples collected and processed were of other fungi that colonized the different woody substrates. H. irregulare is known to be a poor competitor and thus needs to colonize stumps early after cutting to become established [4]. H. irregulare can be readily detected from infected trees and stumps via culture methods and qPCR as these methods were successful in detecting it at the original positive location. However, additional sites surveyed were not currently infected and other fungi were present. The discovery of H. irregulare in Minnesota in 2014 leads to the assumption that it was an accidental and isolated introduction or it originated from long distance spore dispersal. As previously noted, the fungus has not been shown to be transported on logging equipment. However, logging equipment could possibly be carrying soil and wood debris from site to site. The asexual stage, Spiniger meineckellus, can survive in the soil for up to 10 months [28], but the exact epidemiological role conidia have is not fully known. However, H. irregulare was notably introduced into Italy, most likely during World War II on transport crates, pallets, and military equipment made of untreated lumber [29]. At this location in Italy it has infected and killed Italian stone pine trees. Thus, it is possible that H. irregulare was introduced on contaminated logging equipment. It could also be possible for infection to occur via long distance dispersal of basidiospores. The closest known infection sites in Wisconsin are approximately 67-68 km away to the first reported site in Minnesota. Previous studies have determined more than 99% of Heterobasidion spores travel within 100 m of a basidiocarp [30]. Studies summarized by Garbelotto and Gonthier (2013) [31] conducted in Fennoscandia, the Alps, and Mediterranean forests found effective spore dispersal that resulted in infection was between 98 and 1255 m. However, in another study spores of Heterobasidion were found to travel very long distances up to 500 km [32]. Therefore, long distance spore dispersal required to reach the Minneiska site from Wisconsin appears possible, but the event may be exceedingly rare.

Basidiomycota Isolated
In addition to Heterobasidion, the culturing of other Basidiomycota was also of interest since saprophytic fungi such as Phlebiopsis gigantea may serve as a biological control. Since Minnesota has escaped HRD for many years, the possibility exists that native saprophytic Basidiomycota may be involved as a naturally occurring biological control. This study provides new information on the early colonizers of pine wood in Minnesota. The majority of Basidiomycota isolated were saprophytic wood decay fungi and only a few known pathogens. The top three species isolated, Irpex lacteus, Phlebiopsis gigantea, and Phanerochaete sordida are common pioneer colonizing wood decay fungi. Armillaria ostoyae (A. solidipes) and Phaeolus schweinitzii were the most prevalent pathogens isolated. Coniophora puteana, a weak pathogen, was also prevalent. These species could have contributed to the decline and mortality of trees that showed evidence of decline in our surveyed sites. Although important, determining the causative agent of dead and declining trees was not the focus of the study, but evidence is provided (Figure 3) for what could be causing the decline and mortality.
Irpex lacteus, the most commonly isolated fungus, is more typically associated with angiosperms. It is known as a cosmopolitan white rot fungus that inhabits dead hardwood trees [33]. In addition to being a white rot fungus in angiosperms, it can also cause a canker-rot. Although rarely associated with gymnosperms, it is interesting how common it occurred in the coniferous forests that were sampled. This study suggests that it is commonly associated with red and white pine in Minnesota. Although not found fruiting in these forests, its presence was revealed with culturing. Further investigation is warranted to examine the role of this fungus and its degradation potential in coniferous forests ecosystems.
The second most common isolated fungus, Phlebiopsis gigantea, is an effective biological control agent used for Heterobasidion root disease worldwide [16][17][18][19]. Its large presence in coniferous forests of Minnesota could result in it functioning as a native biological control against H. irregulare. After trees are cut, it can quickly colonize stumps and thus prevent other fungi from becoming established.
Phanerochaete sordida was also commonly isolated. This fungus can be found worldwide, especially in the northern hemisphere. It is a saprophyte that causes a white rot decay and is noted to be more common on hardwoods and found occasionally on conifers [34]. This is similar to I. lacteus and interesting to find both commonly isolated from gymnosperms. C. puteana is the only brown rot fungus among the other commonly isolated Basidiomycota and is known to cause a root rot. In one study it was found to have infected 4% of the trees sampled [35].
The root rot fungi, Armillaria ostoyae (A. solidipes) and Phaeolus schweinitzii, were also isolated. Armillaria root disease causes significant ecological and economic damage across North America. Different species of Armillaria that occur in Minnesota include A. ostoyae (A. solidipes), A. mellea, A. sinapina, A. gallica, and A. calvescens. In our study, A. ostoyae (A. solidipes) was the most commonly found and it was also the most commonly isolated Armillaria species in a study conducted previously in Minnesota [36]. Additionally, one isolate of A. calvescens and one isolate of A. sinapina was obtained. Another root rot fungus, P. schweinitzii, causes a brown rot in coniferous hosts, but is mostly considered a weak and opportunistic pathogen [28].

Spore Surveys
The infected red pine stand in Wisconsin had the highest number of spores collected at 149.33 m −2 h −1 . The Minneiska site in Minnesota had a total of 1.26 m −2 h −1 basidiospores. This was the highest concentration of basidiospores collected in Minnesota, and is a moderate number of spores. With the eradication of H. irregulare from the Minneiska site, fruiting bodies should not be present, thus the moderate numbers of spores detected are likely depositing from long distance dispersal and not from a local source. However, due to the moderate numbers of spores, it is possible that there is another source besides the closest known infection site in Wisconsin where these spores originated from. At the other locations, spore numbers were moderate to low. All of these sites most likely had spore deposition from long distance dispersal. A previous slightly similar study   [25] in Quebec showed slightly higher numbers of spores being collected. During their 8-week study, spore totals ranged from 0 to 3.48 m −2 h −1 compared to 0 to 1.26 m −2 h −1 for spores collected in Minnesota. The number of basidiospores collected at an infected plantation we studied in Wisconsin was higher than that of   [24] with a highest weekly value of 3.48 m −2 h −1 compared to 149.33 m −2 h −1 in our study. This high number we detected was due to the placement of collectors in a stand with many basidiocarps nearby. Additionally, the automated rotary arm spore collectors used in our study sampled a larger volume of air, 47.8 L/min compared to 21.6 L/min; this could have resulted in a higher number of spores being collected.
Other studies also have reported spore deposition of Heterobasidion species. Edmunds and Driver (1974) [37] used H-shaped Rotorods ® in Douglas-fir forests in Washington to examine dispersion and deposition of H. occidentale. The range of natural spore deposition was 0.0003 to 0.007 spores per cm −2 h −1 . In four different forests in the western Alps, Gonthier et al. (2005) [38] examined spore deposition for H. annosum s.s., H. parviporum, and H. abietinum. The study used a wood-disk exposure method. Maximum spore totals ranged from 169 to 15,550 m −2 h −1 . Spore deposition rates were also examined in three forests of California with means of 298, 61, and 37 m −2 h −1 using the wood-disk exposure method [39]. Also, Kallio (1970) [32] obtained 30,000 spores m −2 h −1 when just 1 m from a basidiocarp. Spore totals in these studies are greater than those we observed. These previous collections were done in infested areas, which would have increased spore deposition. The totals in our study indicate Minnesota is in the very early stages of a potential epidemic.
The majority of previous spore deposition studies used the wood-disk exposure method, which measure differently than those that utilize rotary arm spore collectors. Wood disks measure the amount of infectious basidiospores per m 2 compared to rotary arm spore collectors that measure the number of basidiospores per m 3 [24]. The aerial basidiospore density would likely be more than the number of basidiospores landing on a stump. The number of basidiospores that colonize a stump would then likely be less than the number of basidiospores that germinate on the stump. The highest number of spores recorded in our study for cumulative spores deposited on a 30 cm stump in Minnesota was 0.96. It is expected that low numbers of spores landing on a stump will not colonize due to factors such as competition with other fungi and environmental factors [38]. Also, aerial basidiospore viability was reported to be between 1% and 5% [40].
The number of monokaryotic basidiospores required to initiate an infection on a stump is not yet known. Stump infection was claimed to be rare if the deposition rate was below 100 colonies m −2 h −1 [41]. Moykkynen and Kontiokari (2001) [42] posed that a deposition rate of 10 colonies m −2 h −1 during a harvest event would result in a higher risk of stump infection, with each colony assumed to originate from one viable basidiospore. The study conducted by Gonthier et al. (2005) [38] suggested that a lower number of 5 spores m −2 h −1 , would be needed to cause an infection on a stump. It is important to note that these studies examined the deposition rate of different species of Heterobasidion on different hosts and in different environments, which could affect the deposition rates when applying the findings elsewhere. However, if these deposition rates are compared to the quantity of spores collected in the results reported here, spore numbers in our study are much lower. Yet, it is still of concern that spores are being detected at all. Further investigation examining basidiospore deposition rates of H. irregulare that can initiate infection on red pine in the Great Lakes Region needs to be conducted.
It has been shown that monokaryotic isolates of H. parviporum can cause infection under field conditions when artificially inoculated on a host [43]. However, spore load was found to be low in this study and less than previous thresholds for infection. The number of spores currently being detected may not be sufficient for starting new infec-tions. Additionally, with the spore load being low, single basidiospores are landing and the chance to have two compatible basidiospores grow and fuse is low. Heterokaryons have been suggested as the main colonizers of standing trees as demonstrated from field observations [44]. Thus, monokaryotic basidiospores that can successfully germinate might not be as virulent as heterokaryotic mycelia.
Spore collectors were deployed for a week at a time in our investigations and the number of spores collected might have been higher if deployment was for a longer period of time. Continued monitoring for H. irregulare should be conducted to determine if spore quantities increase with time and thus provide information regarding where to focus more targeted field surveys and management. Spore trapping studies are also important for other forest pathogens, particularly invasive exotic pathogens. Using spore detection networks allows these pathogens to be detected before they can cause environmental and economic damage. Such detection networks are in place for invasive insects, but few are present for invasive pathogens. However, more recent work has used qPCR as well as metagenomics to detect forest invasive pathogens [45,46]. Implementing more spore detection networks in the near future will be paramount to protect our forests. Information gathered from these spore detection networks can provide useful information for forest managers, not just for Heterobasidion, but other invasive forest pathogens as well.

Conclusions
Rigorous field surveys for H. irregulare did not result in any positive samples that were studied using nested PCR, qPCR, and traditional culturing. However, a variety of fungi in the Basidiomycota were isolated. Some of these fungi, such as P. gigantea could be acting as a natural biological control agent by quickly colonizing stumps and preventing H. irregulare from colonizing. Additionally, other basidiomycetes isolated could have promise as biological control agents by possessing different antagonistic properties against H. irregualre. Spore trapping efforts did collect moderate to low numbers of H. irregulare spores, thus helping to confirm that Minnesota is at the precipice of a possible epidemic. Continuing to deploy spore traps would be effective for early detection of H. irregulare and other forest pathogens.