Literature DB >> 32128283

Entomopathogenic fungi (Hypocreales: Ophiocordycipitaceae) infecting bark lice (Psocoptera) in Dominican and Baltic amber.

George Poinar1, Fernando E Vega2.   

Abstract

Ophiocordyceps dominicanus Poinar & Vega sp. nov. in Dominican amber and Polycephalomyces baltica Poinar & Vega sp. nov. (Hypocreales: Ophiocordycipitaceae) in Baltic amber are described as entomopathogenic fungi of bark lice (Psocoptera). The specimens possess several features unknown in extant synnematous entomopathogenic fungi such as a tubular dark synnema with a straight, pointed tip bearing spores over the entire surface in O. dominicanus, and a globular yellowish synnema developing on the tip of the host's antenna in P. baltica. These are the only known fossil entomopathogenic fungi of bark lice, making them unique not only for their characters but also in respect to their selection of developmental sites on their bark lice hosts.
© 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  Dominican and Baltic amber; Fossil fungus; Hypocreales; Psocoptera; bark lice

Year:  2019        PMID: 32128283      PMCID: PMC7033690          DOI: 10.1080/21501203.2019.1706657

Source DB:  PubMed          Journal:  Mycology        ISSN: 2150-1203


Introduction

A number of fungi, including some pathogenic on insects and spiders, have conidiophores united into synnemata (large erect reproductive structures bearing compact conidiophores, phialides and conidia) (Kirk et al. 2001). These synnemata can have long stalks arising from the body of their hosts or the stalk can be quite reduced and with the fertile terminal portion sphere-shaped. Some lineages are restricted to just one or a few host species, or even to specific tissues on a host, while others appear to be able to parasitise a range of hosts, even in different orders (Barnett 1958; Kendrick and Carmichael 1973; Poinar and Thomas 1984). The present study describes two new species of fossil fungi of the order Hypocreales and family Ophiocordycipitaceae that formed synnemata on bark lice (Psocoptera) in Dominican and Baltic amber, respectively. These are the only known entomopathogenic fungi of fossil bark lice. Even extant records of infection of bark lice by members of the Hypocreales are limited to one account of a species of Hirsutella infecting a bark louse in Argentina (Toledo et al. 2008).

Materials and methods

The Dominican Republic amber piece containing the infected bark louse measures 12 mm long, 8 mm wide, and 3 mm deep. The specimen originated from mines in the El Mamey Formation (Upper Eocene) in the Cordillera Septentrional of the Dominican Republic. These mines consist of shale-sandstone and rounded pebbles (Eberle et al. 1980) and their age has been estimated at 15–20 Ma (Iturralde-Vinent and MacPhee 1996) and 20–23 Ma (Baroni Urbani and Saunders 1980) based on foraminifera counts, to 30–45 Ma based on coccoliths (Schlee 1990). These are considered minimum dates since they are based on microfossils in the strata containing the amber, which was secondarily deposited in turbiditic sandstones of the Upper Eocene to Lower Miocene Mamey Group (Draper et al. 1994). The location of the amber mines is DD 19.5 N, 70.6 W. Fossiliferous amber from the Baltic region was formed in forests occurring in what have been described either as tropical/subtropical climates or humid warm-temperate climates that covered a large part of northern Europe for some 10 million years during the early Palaeogene (Sadowski et al. 2017). The amber was eroded from the original accumulation and re-deposited in marine sediment layers referred to as the ‘blue earth' layers, in the Samland Peninsula of the Russian Republic (Weitschat and Wichard 2010). Age estimates of amber from this region range from 35 to 55 million years (Larsson 1978; Wolfe et al. 2016). A Nikon SMZ-10 R stereoscopic microscope (Nikon Instruments, Tokyo) and Nikon Optiphot compound microscope (Nikon Instruments, Tokyo) with magnifications up to 800 X were used for observing and photographing the specimens. Photos were stacked using Helicon Focus Pro X64 (HeliconSoft, Kharkiv, Ukraine) to improve clarity and depth of field. Both amber pieces were polished close enough to the surface of the synnemata to observe the spores under oil immersion. The following descriptions are based on features observed in different regions of the synnemata.

Results

Dominican amber specimen

Taxonomy

Kindgom FungiPhylum: AscomycotaOrder: HypocrealesFamily: OphiocordycipitaceaeGenus: Ophiocordyceps Type species: Ophiocordyceps dominicanus Poinar & Vega sp. nov.MycoBank: 830,883Ophiocordyceps dominicanus Poinar & Vega sp. nov. (Figures 1–6).
Figure 1.

Synnema (arrow) of Ophiocordyceps dominicanus sp. nov. attached to the body of a bark louse (Psocoptera: Troctopsocidae) in Dominican amber. Bar = 0.6 mm.

Figure 6.

Detail of conidiophore (C), phialide (P) and conidia (S) of Ophiocordyceps dominicanus sp. nov. in Dominican amber. Bar = 8 µm.

Synnema (arrow) of Ophiocordyceps dominicanus sp. nov. attached to the body of a bark louse (Psocoptera: Troctopsocidae) in Dominican amber. Bar = 0.6 mm. Attachment point (arrow) of the synnema of Ophiocordyceps dominicanus sp. nov. to the body of a bark louse (Psocoptera: Troctopsocidae) in Dominican amber. Bar = 0.3 mm. Surface of synnema covered with spores of Ophiocordyceps dominicanus sp. nov. in Dominican amber. Bar = 12 µm. Chains of conidia of Ophiocordyceps dominicanus sp. nov. arising from surface of synnema in Dominican amber. Bar = 14 µm. Loose spores of Ophiocordyceps dominicanus sp. nov. released from chains in Dominican amber. Bar = 10 µm. Detail of conidiophore (C), phialide (P) and conidia (S) of Ophiocordyceps dominicanus sp. nov. in Dominican amber. Bar = 8 µm.

Diagnosis

Synnema dark, pointed at tip; entire surface covered with unbranched chains of conidia or released conidia; conidiophores micronematous, phialides micronematous, non-diverging; conidia mostly brown or tan, globose, lacking surface ornamentation, formation basipetal.

Description

Synnema simple, 3.5 mm in length, emerging from abdomen of adult bark louse (Psocoptera). Aerial hyphae very rare; entire surface of synnema covered with catenulate or released small, roundish, dark conidia; conidiogenous cells phialiform; conidiophores light coloured, micronematous, length 6–7 µm; phialides light coloured, micronematous, narrow, slender, nondiverging, length, 7–9 µm; conidia globose, one-celled, brown to tan, lacking surface ornamentation or mucus; basocatenate in unbranched spore-chains (with up to 10 spores in a chain), diameter of conidia, 2–3 µm.

Holotype

Holotype No. Sy-1-13A deposited in the Poinar amber collection maintained at Oregon State University.

Host

Adult Troctopsocopsis sp. (length 1.1 mm) (Psocoptera: Troctopsocidae)

Type locality

Amber mine in Altamira faces of the El Mamey Formation in the Cordillera Septentrional of the Dominican Republic. DD latitude and longitude: 19.4, −70.4.

Comments

The Dominican amber specimen is tentatively assigned to the genus Ophiocordyceps at this time, with the realisation that it may be transferred to other genera at a later date, depending on future studies on the Ophiocordycipitaceae. Ophiocordyceps dominicanus is unique among entomopathogenic fungi by possessing a straight, pointed synnema bearing spores over the entire surface, micronematous conidiophores and non-diverging phialides bearing unbranched chains of basipetal, globose, brown or tan conidia lacking surface ornamentation or mucus. Ophiocordyceps dominicanus shares some features with other earlier recorded entomopathogenic fungi in the Cordycipitaceae and Ophiocordycipitaceae. One of these is the genus Gibellula Cav. (Cordycipitaceae). However, species of this genus have the apex of the conidiophores swollen, forming vesicles that produce pro-phialides, which in turn, form flask-shaped phialides bearing elliptical spores. The entire reproductive unit is globose or wedge-shaped. In most other arthropod-infecting genera, the phialides are not borne in heads. These include members of the genera Hymenostilbe Petch (Ophiocordycipitaceae) that produces single, hyaline, elongate conidia on phialides with short lateral branches, and Akanthomyces Leb. (Cordycipitaceae) with light coloured synnemata and hyaline, one-celled, ovate conidia borne on wedge-shaped phialides. The genus Isaria Pers. ex Fr. (Cordycipitaceae) has light coloured synnemata and hyaline, one-celled, clustered, ovoid conidia. The genus Hirsutella Pat. (Ophiocordycipitaceae) has hyaline one-celled mucus-covered conidia borne singly and the phialides are swollen at the base. The genus Pseudogibellula Samson & Evans (Cordycipitaceae) has hyaline conidia borne in globose heads at the tips of conidiophores with enlarged apices (Barnett 1958; Kendrick and Carmichael 1973; Poinar and Thomas 1984). None of the features found in the above-mentioned extant genera match those of the fossil.

Baltic amber specimen

Taxonomy

Kingdom Fungi Phylum: AscomycotaOrder: HypocrealesFamily: OphiocordycipitaceaeGenus: Polycephalomyces Type species: Polycephalomyces baltica Poinar & Vega sp. nov.MycoBank: 830,886Polycephalomyces baltica Poinar & Vega sp. nov. (Figures 7–12).
Figure 7.

Dorsal view of the synnema (arrow) of Polycephalomyces baltica sp. nov. attached to the tip of the left antenna of a bark louse in Baltic amber. Bar = 0.7 mm.

Figure 12.

Detail of synnema of Polycephalomyces baltica sp. nov. showing conidiophores, phialides and catenulate, globose conidia in Baltic amber. Bar = 14 µm.

Dorsal view of the synnema (arrow) of Polycephalomyces baltica sp. nov. attached to the tip of the left antenna of a bark louse in Baltic amber. Bar = 0.7 mm. Lateral view of the synnema (arrow) of Polycephalomyces baltica sp. nov. attached to the tip of the left antenna of a bark louse in Baltic amber. Tip of right antenna was missing. Bar = 0.6 mm. Synnema of Polycephalomyces baltica sp. nov. in Baltic amber showing conidiophores and conidia on left side (between the arrows). Arrowhead shows infected terminal antennomere of host. Bar = 78 µm. Infected terminal antennomere (P) of bark louse host subtending the synnema (S) of Polycephalomyces baltica sp. nov. in Baltic amber. N = uninfected antennomere. Bar = 84 µm. Portion of synnema of Polycephalomyces baltica sp. nov. showing conidiophores bearing developing conidia in Baltic amber. Bar = 20 µm. Detail of synnema of Polycephalomyces baltica sp. nov. showing conidiophores, phialides and catenulate, globose conidia in Baltic amber. Bar = 14 µm. Synnema small, roundish, light, borne at tip of host’s antenna; entire surface of synnema covered with unbranched chains of spores; conidiophores micronematous, phialides flask-shaped, diverging; conidia hyaline, globose, lacking surface ornamentation, with basipetal formation. Synnema simple, small, roundish, 170 µm in length, 142 µm in width, borne at tip of antennomere of bark louse (Psocoptera); aerial hyphae rare; entire surface of synnema covered with developing conidia; conidiogenous cells phialiform; conidiophores light coloured, micronematous, length 5–6 µm; phialides light coloured, micronematous, flask-shaped, non-diverging, length, 3–4 µm; conidia globose, catenulate, one-celled, hyaline, lacking surface ornamentation or mucus; basopetelate in unbranched spore-chains (with up to five spores in a chain), diameter of conidia, 2–3 µm. Holotype No. Sy-1-13B deposited in the Poinar amber collection maintained at Oregon State University. Nymph or short-winged female bark louse (Psocoptera: Troctopsocidae) (length, 1.9 mm). Samland Peninsula of the Baltic Sea in the Kalinin District of the Russian Federation. While the Baltic amber specimen is tentatively assigned to the genus Polycephalomyces, without molecular data, it is not possible to determine its true affiliations within the Ophiocordycipitaceae. Polycephalomyces baltica sp. nov. is unique among entomopathogenic fungi by forming a rounded synnema bearing spores over its entire surface on the tip of the antenna of a bark louse. The shape of the synnema, its age and location on the terminal antennomere of a bark louse plus the nature of the phialides and conidia separate the fossil from other Polycephalomyces species (Kepler et al. 2013; Sanjuan et al. 2015). In earlier arthropod-infecting anamorph genera that form synnemata, such as Hymenostilbe, Isaria, Akanthomyces, Hirsutella, and Pseudogibellula, the combined features of globose, hyaline, catenulate conidia formed in round, hyaline synnemata, parasitising bark lice, as found in Polycephalomyces baltica, are unknown (Barnett 1958; Madelin 1963; Kendrick and Carmichael 1973; Poinar and Thomas 1984).

Discussion

The clavicipitoid fungi consist of three hypocrealean families: Clavicipitaceae sensu stricto, Cordycipitaceae and the Ophiocordycipitaceae. Members of the genus Ophiocordyceps in the Ophiocordycipitaceae include fungi that produce a darkly coloured “rigid, pliant or wiry stipe” and on hosts in soil or rotting wood (Kepler et al. 2013). Such a fungal and host pattern fits that of bark lice that occur on the bark of living or dying trees. The Ophiocordycipitaceae parasitise a diverse clade of arthropods, including Coleoptera, Hemiptera, Hymenoptera and Lepidoptera (Sung et al. 2008; Kepler et al. 2013). The genus Ophiocordyceps sensu Petch, known to contain a diverse assemblage of Neotropical species, is characterised by clavate asci with gradually thickening apices and elongate, fusiform ascospores that do not articulate into part spores (Sanjuan et al. 2015). Species of this genus have been described as both sexual (teleomorph) and asexual (anamorph) species (Kepler et al. 2013; Sanjuan et al. 2015). Polycephalomyces is characterised by superficial perithecia or perithecia immersed in an apical or subapical pulvinate cushion and long asci with ascospores forming many small part-spores of nearly equal length (Kepler et al. 2013). However, the genus has been used for both anamorph and teleomorph forms of some fungal clades (Kepler et al. 2013). The hosts thus far include nymphs of Cicadidae (Hemiptera), Neuroptera and larvae of Coleoptera (Kepler et al. 2013; Sanjuan et al. 2015). The bark louse host could be used as a diagnostic feature of Polycephalomyces baltica. The conidia of Polycephalomyces baltica Poinar & Vega sp. nov. obviously penetrated the wall of the antennal segment to initiate infection. The antennal cell just below the synnema is mostly clear with some hyphal remains (Figure 10) and was probably the site of infection. The earliest fossil record of a synnema-producing entomopathogenic fungus is Paleoophiocordyceps coccophagus (Ophiocordycipitaceae) that was parasitising an Early Cretaceous scale insect in Burmese amber (Upper Albian: 97–105 Mya) (Sung et al. 2008).
Figure 10.

Infected terminal antennomere (P) of bark louse host subtending the synnema (S) of Polycephalomyces baltica sp. nov. in Baltic amber. N = uninfected antennomere. Bar = 84 µm.

Bark lice are known to be infected by representatives of several fungal lineages, including members of the genus Conidiobolus (Ancylistaceae: Entomophthorales) in Switzerland (Keller 2008), by unidentified fungi in Australia (Smithers 1972) and by Pandora (Zygomycota: Entomophthorales) and Hirsutella spp. in Argentina (Toledo et al. 2008, 2013). The records of Hirsutella spp. are the only other reports of members of the Hypocreales attacking these hosts (Toledo et al. 2008, 2013).

Conclusions

These fossils represent the first fossil records of fungal infections of bark lice (Psocoptera). Both the Dominican amber species, Ophiocordyceps dominicanus Poinar & Vega sp. nov. and the Baltic amber species Polycephalomyces baltica Poinar & Vega sp. nov. represent extinct lineages and provide new characters (tubular synnema with a straight, pointed tip bearing spores over the entire surface and globular synnema forming on host’s antenna, respectively) that add to our understanding of the evolution of the entomopathogenic fungal representatives of the Hypocreales.
  5 in total

1.  Five new species of entomopathogenic fungi from the Amazon and evolution of neotropical Ophiocordyceps.

Authors:  Tatiana I Sanjuan; Ana E Franco-Molano; Ryan M Kepler; Joseph W Spatafora; Javier Tabima; Aída M Vasco-Palacios; Silvia Restrepo
Journal:  Fungal Biol       Date:  2015-07-08

2.  The oldest fossil evidence of animal parasitism by fungi supports a Cretaceous diversification of fungal-arthropod symbioses.

Authors:  Gi-Ho Sung; George O Poinar; Joseph W Spatafora
Journal:  Mol Phylogenet Evol       Date:  2008-09-10       Impact factor: 4.286

3.  The phylogenetic placement of hypocrealean insect pathogens in the genus Polycephalomyces: an application of One Fungus One Name.

Authors:  Ryan Kepler; Sayaka Ban; Akira Nakagiri; Joseph Bischoff; Nigel Hywel-Jones; Catherine Alisha Owensby; Joseph W Spatafora
Journal:  Fungal Biol       Date:  2013-07-09

4.  First and southernmost records of Hirsutella (Ascomycota: Hypocreales) and Pandora (Zygomycota: Entomophthorales) species infecting Dermaptera and Psocodea.

Authors:  A V Toledo; R A Humber; C C López Lastra
Journal:  J Invertebr Pathol       Date:  2007-09-14       Impact factor: 2.841

5.  Morphological and molecular characterization of a fungus, Hirsutella sp., isolated from planthoppers and psocids in Argentina.

Authors:  Andrea V Toledo; María E Simurro; Pedro A Balatti
Journal:  J Insect Sci       Date:  2013       Impact factor: 1.857

  5 in total

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