Glugea hertwigi Weissenberg, 1911

Common Name: A microsporidian parasite

Synonyms and Other Names:

disease known as microsporidiosis



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Identification: The parasitic spores of G. hertwigi have thick cell walls with rough, wrinkled and loosely folded surfaces. The sporoplasm contains a nucleus and free ribosomes and is surrounded by a plasma membrane. It can be injected into a host cell via a thin polar tube, which is held coiled inside the spore until it is discharged. This tube is surrounded at the base by a polaroplast, or arrangement of membranes or vesicles. In the digestive tracks of host Rainbow Smelt (Osmerus mordax), cysts with up to 200 spores can form (Nakajima and Egusa 1979; Weidner et al. 1984; Scarborough-Bull and Weidner 1985; Pekcan-Hekim et al. 2005).

Spores are 3.5–5.5 μm by 1.5–2.6 μm in size. There is great variation but most populations fall at the larger end of the range. Smaller spores may be a specific variety of this species, proposed to be canadensis (Delisle 1969; Delisle 1972; Scarborough-Bull and Weidner 1985). Cysts range in size from 0.2–5 mm in diameter (Nepszy and Dechtiar 1972; Pekcan-Hekim et al. 2005).


Size: Spores are 3.5–5.5 μm by 1.5–2.6 μm in size. Cysts range in size from 0.2–5 mm in diameter.


Native Range: G. hertwigi was first recorded from smelt in the Baltic Sea and is considered native to Europe (Mills et al. 1993; Pekcan-Hekim et al. 2005).


Map Key
This map only depicts Great Lakes introductions.

 
Great Lakes Nonindigenous Occurrences: The first Great Lakes occurrence of Glugea hertwigi was reported in 1960 from Rainbow Smelt (Osmerus mordax) from Lake Erie at Port Dover and Wheatley, Ontario (Dechtiar 1965b ; see also Chen and Power 1972, Dechtiar 1972a, Dechtiar and Nepszy 1988, Nepszy and Dechtiar 1972, Nepszy et al. 1978, Nsembukya-Katuramu et al. 1981). 


Table 1. Great Lakes region nonindigenous occurrences, the earliest and latest observations in each state/province, and the tally and names of HUCs with observations†. Names and dates are hyperlinked to their relevant specimen records. The list of references for all nonindigenous occurrences of Glugea hertwigi are found here.

State/ProvinceFirst ObservedLast ObservedTotal HUCs with observations†HUCs with observations†
NY196619682Lake Ontario; Salmon-Sandy
OH196019601Lake Erie

Table last updated 5/1/2024

† Populations may not be currently present.


Ecology: Glugea hertwigi typically infects euryhaline smelt species in the genus Osmerus, but it has also been recorded from Pond Smelt (Hypomesus olidus) and some Coregonus spp. (Dykova 1995). In the Great Lakes, Glugea hertwigi has been found only in Rainbow Smelt (Osmerus mordax). G. hertwigi was originally known from marine environments but is now known to thrive in freshwater environments, as well. Infection occurs via spores that enter through water taken in by the fish. Glugea hertwigi infection first occurs in the anterior digestive tract, but cysts can also spread to the posterior digestive tract, liver, pyloric caeca, heart, gonads, fins, and skin (Dechtiar 1965b, Dechtiar 1972a, Nepszy et al. 1978, Putz et al. 1965).

Glugea hertwigi develops in the cytoplasm of host cells. It causes nuclear division without cytokinesis, resulting in one large cell up to 0.5–1 mm in diameter filled with many nuclei. Parasitic spores mature in a central vacuole in the enlarged host cell, undergoing schizogony, or asexual reproduction, many times. Once the spores have finished reproducing, the host cell ruptures and the parasites are eventually released into the water column to be ingested by new hosts. In new hosts, they attach to the digestive tract or other organs. The sporoplasm is then discharged from the spore case at high pressure, entering the host cell. The sporoplasm reorganizes before, during, and after ejection, and the resulting mass is larger than it was inside the spore case. Spore discharge can be triggered by a large change in pH to highly alkaline conditions (Delisle 1972, Scarborough-Bull and Weidner 1985, Wellings et al. 1969).

The number of parasitic cysts in smelt populations typically peak between August and September (Pekcan-Hekim et al. 2005), although die-offs occur in Quebec in both spring and fall (Delisle and Veilleux 1969). Cyst growth may increase with increasing water temperature (Delisle 1969). However, as spores frequently enter both juvenile and adult fish at maximum water temperatures, the largest cysts may not appear until after this time (Pekcan-Hekim et al. 2005). Younger smelt appear more vulnerable to infection, while older smelt may have increased immunity (Pekcan-Hekim et al. 2005).


Means of Introduction: This parasite was introduced to the Great Lakes with its host, O. mordax, which in turn was introduced via stocking and/or dispersal through canal systems (Mills et al. 1993).


Status: Established where recorded.


Great Lakes Impacts:
Summary of species impacts derived from literature review. Click on an icon to find out more...

EnvironmentalSocioeconomicBeneficial



 

There is little or no evidence to support that Glugea hertwigi has significant environmental impacts in the Great Lakes.
Potential:
In the Great Lakes, G. hertwigi exhibits host specificity for Rainbow Smelt (Osmerus mordax) (Muzzall and Whelan 2012), a species which competes with and feeds on several important native and non-native species in the Great Lakes food web. Glugea hertwigi is known to damage the mesentery, intestinal organs, and gonads in Rainbow Smelt. Such parasitism by G. hertwigi can be lethal or non-lethal (Pekcan-Hekim et al. 2005). Infections in the stomach and intestine can cause starvation and intestinal poisoning (Chen and Power 1972, Delisle 1972, Mills et al. 1993, Pekcan-Hekim et al. 2005, Scarborough and Weidner 1979). Die-offs of Rainbow Smelt as a result of G. hertwigi infection have the potential to indirectly cause significant cascading food web effects in the Great Lakes.

Great Lakes native Atlantic Salmon (Salmo salar), Lake Trout (Salvelinus namaycush), and other salmonids are known to prey heavily upon Rainbow Smelt (EPA 2008). Osmerus mordax is believed to have aided the growth of landlocked Atlantic Salmon in Maine (Havey 1973). Die-offs of O. mordax as a result of G. hertwigi could have adverse health effects on Great Lakes salmonids.

While there is no evidence of native coregonid infection in the Great Lakes, G. hertwigi is known to parasitize Coregonus species in northern Russian lakes (Dykova 1995).

There is little or no evidence to support that Glugea hertwigi has significant socio-economic impacts in the Great Lakes.
Potential:
Glugea hertwigi has been implicated in mass mortalities of the introduced Rainbow Smelt (O. mordax) in Lake Erie (Nepszy and Dechtiar 1972, Nepszy et al. 1978) and Lake Ontario (A. Dechtiar, unpublished data). Mortality events are believed to be seasonal and directly related to parasite prevalence (Dechtiar and Nepszy 1988). Glugea hertwigi cysts in ovaries of mature Rainbow Smelt females have also caused greatly reduced egg production (Chen and Power 1972). However, it should be noted that the presence of G. hertwigi in Rainbow Smelt in other dieoff events had no significant effect on fecundity or condition, although it did cause growth to slow somewhat (Nsembukya-Katuramu et al. 1981). While economic impacts of G. hertwigi on the commercial smelt (see Pflieger 1997, Smith 1985) and salmonid (which rely on smelt) fisheries have not been realized, significant impacts could be realized if Rainbow Smelt mortalities were to increase as a result of infection.

Glugea hertwigi poses the largest threat (e.g., high infection rates and mortalities) to Lake Erie Rainbow Smelt populations as compared to any other parasite (Muzzall and Whelan 2012; Nepszy and Dechtiar 1972).

There is little or no evidence to support that Glugea hertwigi has significant beneficial effects in the Great Lakes.

Potential:
Declines in Rainbow Smelt as a result of G. hertwigi infection has the potential to improve resource availability for native Great Lakes species. Several of these scenarios are proposed below.

As Rainbow Smelt preys heavily upon Bloater (Coregonus hoyi), Alewife (Alosa pseudoharegus), Slimy Sculpin (Cottus cognatus), Emerald Shiner (Notropis atherinoides), Burbot (Lota lota), and opossum shrimp (Mysis relicta) (Brandt and Madon 1986, Creaser 1925, O’ Gorman 1974, Stedman and Argyle 1985, Van Oosten 1940), its diet is believed to affect prey population numbers and can be an important component to the total mortality of yearlings (Creaser 1925, O’ Gorman 1974). In turn, commercially valuable native and non-native salmonids rely on several of these prey species. Die-offs of Rainbow Smelt as a result of G. hertwigi may increase prey fish populations, thus increasing feeding opportunities and improving the health and value of the salmonid fisheries. However, such effects have not been realized in the Great Lakes.

Additional potential food web effects include those on Lake Trout (Salvelinus namaycush). Juvenile Lake Trout tend to eat Slimy Sculpin, while adults consume Rainbow smelt (Brandt and Madon 1986). Direct competition for Slimy Sculpin between juvenile Lake Trout and Rainbow Smelt has been observed (Brandt and Madon 1986). Lake Trout may therefore be a keystone predator in the relationship between Rainbow Smelt and Slimy Sculpin (Brandt and Madon 1986). Mortalities in Rainbow Smelt by G. hertwigi could decrease competition and stress in juvenile Lake Trout and could have significant beneficial effects on the Great Lakes food web.

Rainbow Smelt compete with Lake Herring (Coregonus artedii) and Yellow Perch (Perca flavescens) and may be partially responsible for the decline of Great Lakes whitefish (Coregonus spp.) (Becker 1983, Christie 1974, Hrabik et al. 1998, Todd 1986). Increased G. hertwigi infections and die-offs of Rainbow Smelt could lead to a decrease in competition and stress on Lake Herring and Yellow Perch and may increase the commercially valuable whitefish population.

Rainbow Smelt contributed to the extinction of Blue Pike (Sander vitreus glaucus), a subspecies prevalent in the Great Lakes until the 1980s. Rainbow Smelt have also affected imperiled species outside the Great Lakes (EPA 2008). Because of competition between Rainbow Smelt and native species, other imperiled species in the Great Lakes could benefit if Glugea hertwigi limited Osmerus mordax populations.


Management:  

Regulations (pertaining to the Great Lakes)
There are no known regulations for this species.

Note: Check federal, state/provincial, and local regulations for the most up-to-date information.

Control
Biological
There are no known biological control methods for this species.

Physical
There are no known physical control methods for this species.

Chemical
There are no known chemical control methods for this species.

Note: Check state/provincial and local regulations for the most up-to-date information regarding permits for control methods. Follow all label instructions.


References (click for full reference list)


Other Resources:
Author: Kipp, R.M., A.K.Bogdanoff, A. Fusaro and R. Sturtevant


Contributing Agencies:
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Revision Date: 9/13/2019


Citation for this information:
Kipp, R.M., A.K.Bogdanoff, A. Fusaro and R. Sturtevant, 2024, Glugea hertwigi Weissenberg, 1911: U.S. Geological Survey, Nonindigenous Aquatic Species Database, Gainesville, FL, and NOAA Great Lakes Aquatic Nonindigenous Species Information System, Ann Arbor, MI, https://nas.er.usgs.gov/queries/greatLakes/FactSheet.aspx?Species_ID=2368&Potential=N&Type=0&HUCNumber=DGreatLakes, Revision Date: 9/13/2019, Access Date: 5/1/2024

This information is preliminary or provisional and is subject to revision. It is being provided to meet the need for timely best science. The information has not received final approval by the U.S. Geological Survey (USGS) and is provided on the condition that neither the USGS nor the U.S. Government shall be held liable for any damages resulting from the authorized or unauthorized use of the information.