Oxyspirura petrowi and Aulonocephalus pennula Infection in Wild Northern Bobwhite Quail in the Rolling Plains Ecoregion, Texas: Possible Evidence of A Die-Off
Received Date: Jul 02, 2017 / Accepted Date: Jul 07, 2017 / Published Date: Jul 10, 2017
We have been monitoring wild Northern bobwhite quail (Colinus virginianus) on a research transect in Mitchell County, Texas. We captured a total of 51 bobwhites in March-May of 2016 and 2017 and examined them for eyeworm (Oxyspirura petrowi) and caecal worm (Aulonocephalus pennula) infections. In March 2017, bobwhites averaged 15 ± 10 eyeworms and 269 ± 90 caecal worms, and by mid-April averages had increased to 18 ± 13 eyeworms and 372 ± 144 caecal worms. These averages were much higher than those observed in March 2016 (11 ± 13 eyeworms and 160 ± 57 caecal worms) and April 2016 (12 ± 12 and 216 ± 56, respectively). We observed a precipitous decline in quail numbers by late April 2017, and average infection had dropped to 7 ± 2 eyeworms and 252 ± 109 caecal worms. The number of trapping sessions needed to capture one bobwhite also increased from 14.26 in 2016 to 36.46 in 2017. These observations warrant further investigation into the effects these helminth parasites may have on bobwhites and their populations within the Rolling Plains.
Keywords: Aulonocephalus pennula; Bobwhite; Cecal worms; Colinus virginianus; Eyeworm; Northern bobwhite; Oxyspirura petrowi; Rolling plains; Texas
Northern bobwhite quail (Colinus virginianus; hereafter, bobwhite) are a well-known game bird in the United States that have been experiencing a steady range-wide decline over the past several decades [1,2]. While this is typically attributed to habitat loss and fragmentation [1,3], bobwhite populations continue to decline even in regions considered to have good quality habitat such as the Rolling Plains ecoregion of Texas [4-6]. This suggests that, at least in some portions of their range, there are other factors affecting bobwhite abundance. Because of their popularity with hunters and economic value to local communities in the Rolling Plains , significant efforts have been made to address other factors affecting bobwhite such as contaminants, disease, pathogens, and parasites. One such effort, known as Operation Idiopathic Decline (OID), found 40% of bobwhites were infected with parasitic eyeworms (Oxyspirura petrowi ) and 73% infected with caecal worms (Aulonocephalus pennula ) in the Rolling Plains, with 90% prevalence for both parasites in some counties [5,8,9].
The eyeworm is found in the orbital cavity and associated tissues of quail [10-12], while the caecal worm is found within the ceca and intestines [13,14]. These parasites are both thought to have an arthropod intermediate host [14,15], and arthropods such as grasshoppers are an important part of the bobwhite diet in the spring and summer . In fact, Kistler et al. identified the plains lubber grasshopper (Brachystola magna ) as a potential intermediate host and documented as many as 90 infective L3 eyeworm larvae in a single lubber . Also, the eyeworm is thought to have pathological consequences due to damage observed in the Harderian gland and cornea of infected quail [18,19]. In addition to this, Dunham et al. reported a lack of digesta found in the caecum of infected quail, which suggests that caecum function may be impaired by caecal worms .
Despite parasites being documented in bobwhite since the 1920s , there have only been sporadic efforts documenting parasites in bobwhite [22-24]. Dunham et al. was the first to report an eyeworm epizootic event and the potential for pathological consequences [12,19]. Further investigation into the impact of parasites on bobwhite in the Rolling Plains is needed when it has been demonstrated that many bobwhite are considered to have a strong infection of both eyeworms (21-40) and caecal worms (101-200) . As helminths have been shown to drive population cycles of another Galliforme, the red grouse (Lagopus lagopus scoticus ) , it is plausible that a similar phenomenon could be occurring in bobwhite in the Rolling Plains. Because of this, the Wildlife Toxicology Laboratory (WTL) at Texas Tech University (TTU) has been involved in a long-term monitoring and research project to document parasitic infection and investigate how these parasites may be affecting bobwhite in the Rolling Plains.
Through extensive research over the last five years, we have been able to monitor parasite burdens in bobwhite within our study area and across the Rolling Plains. These observations provide key insights into factors influencing local bobwhite populations on our study area. Additionally, this permitted us to recognize a precipitous decrease of bobwhite within our study area during April 2017. Here, we will discuss this quail decline and the potential contribution of eyeworm and caecal worm infections to this event by evaluating trap effort and parasite infection from 2016 and 2017.
Materials and Methods
Birds were captured and handled in accordance with Texas Parks and Wildlife research permits SPR-1098-984 and SPR-0715-095. This experiment was approved by Texas Tech University Animal Care and Use Committee under protocols 13066-08 and 16071-08.
The experimental area was on a private ranch in Mitchell County, Texas and was consistent with that used by Dunham et al. .
Quail sampling and parasite assessment
Birds were collected from the same research transect and using the same methods as described in Dunham et al. . Following capture, birds were placed in a cotton cloth bag and weighed using a digital hanging scale. Gender was determined based on the coloration of the head and throat, and the presence or absence of buffed tips on primary wing coverts determined age of the quail [26,27]. Sampling for the present experiment was conducted on a monthly basis during March- May 2016 and March 2017. Because of evidence of strong infection in the March 2017 bobwhites, trapping was adjusted in April 2017 to occur on a bi-weekly basis in order to more closely monitor potentially time-dependent parasite fluctuations within the study area. Midmonth sampling refers to trapping periods that occurred during the 13th-19th, while late month sampling refers to 26th-31st. Eyeworms and caecal worms were extracted in the same manner as described in Dunham et al. 
A trapping session was defined as each time an individual trap was checked for birds. The number of trapping sessions required to capture one bird was used as an index of trapping effort. This was calculated by dividing the total number of trap sessions by the number of birds captured.
All birds collected in March, April, and May 2016 and 2017 were adult bobwhites. In March 2017, 10 birds were collected and required 14 trapping sessions per bird (Table 1); this was only slightly higher than March 2016. By mid-April 2017, 21 trapping sessions were required to collect 5 birds, and by late April 2017, the number of trapping sessions needed to capture one bird had increased to 56. Late April 2017 trapping required 5 times more effort than April 2016 trapping. Trapping the following month was even more difficult with 105 trapping sessions yielding no birds in early May 2017. Our efforts in mid-May 2017 resulted in 4 birds captured and required 61.25 trapping sessions per bird, which was more than double the effort required in May 2016.
|Date||Trapping Sessions||Birds Caught||Average Trapping Sessions/Bird|
Table 1: Quail trapping sessions for March, April, and May 2016-2017
In March 2017, mean abundance for caecal worm infection had increased by over 100 compared to March 2016, and by mid-April 2017 mean abundance had increased by over 150 compared to April 2016. Ranges for caecal worm were also much higher in mid-April 2017 than in April 2016, with 208-572 and 146-334, respectively. Additionally, mean eyeworm abundance in mid-April 2017 was more than 1.5 times higher than eyeworm abundance in April 2016. However, by late April mean abundance for both eyeworms and caecal worms had decreased by 60% and 32%. Mid-May 2017 sampling revealed that infections were increasing for both eyeworms and caecal worms, and again, means abundance was higher for both parasites compared to May 2016.
During 2013, Dunham et al. reported an epizootic of O. petrowi infections in Mitchell County, Texas, speculating that helminths may influence bobwhite declines within the region . After nearly 5 years of continuous monitoring along that same transect, we observed a precipitous drop in bobwhite abundance amidst elevated infections of both eyeworms and caecal worms. In addition to the higher infection levels, collection of bobwhite in March 2017 was more difficult than in 2016 and became progressively more difficult. Furthermore, there were reduced infections in late April which supports Dunham et al. speculation that heavily infected individuals would drop out of the population . Due to the considerable increase in trapping sessions and increased parasite burdens in 2017, we believe that we have witnessed a potential parasite-induced die-off of bobwhites within our study area.
Determining parasite-induced host mortality in the field is very difficult as carcasses are often scavenged in less than 24 hours . For this reason, modeling is often used to demonstrate how parasites may affect wild populations . Dunham et al. estimates of parasite infection levels reflect what is produced by modeling, allowing us to gauge the infection levels on our transect . In March 2016, average caecal worm infections had just reached what Dunham et al. considered a strong infection (101-200), while March 2017 infections were approaching an extreme level (300+) and had exceeded an extreme infection by mid-April . By late April, average caecal worm infection had dropped by nearly 33% and average eyeworm infection had dropped by 60%. This suggests that heavily infected birds were likely eliminated from the population. In addition to the reduction in infection levels, we noted fewer visual observations of quail and a more than two-fold increase in the number of trapping sessions required to capture one quail from mid to late April 2017. Also, late April trapping required five times more effort to capture a single quail than in April 2016, and 105 trapping session in early May yielded 0 quail, which had not been observed in five years of trapping at this location.
With the relative ease of trapping in spring 2016 and local hunters reporting substantial quail populations during winter 2016, we would have expected a stronger quail population in spring 2017. However, the above-average precipitation in late summer 2016  likely facilitated a robust increase in intermediate hosts as Guo et al. and Lenhart et al. observed increases in diversity and survival of arthropods with increased rainfall [31,32]. We believe this facilitated infection going into winter 2016 and lead to the subsequent events during spring 2017. These observations of increased infection following rainfall are similar to those of Dunham et al., who saw higher infection in July and August after heavy rains, followed by reduced infection in September . We likely did not observe this reduced infection due to the parasites entering a state of diapause or arrested development, which are often induced by seasonal variation and diet . Because infection would have occurred going into the fall, changes in bobwhite diet and different seasonal conditions likely provided the environment needed to induce a diapause state in eyeworms and caecal worms [16,34].
Furthermore, this decline in bobwhite prevalence was likely not due to bobwhites leaving transects as bobwhites are not known to have extensive home ranges . We also know that these quail have a high affinity for the areas in which they were trapped based on extensive work on this ranch over several years, and with over 300 radioed birds for tracking, we have data to support our speculation. Haines et al. noted bobwhite ranges in areas that are regularly baited are smaller, and our trap locations are baited regularly . Also, while habitat loss and extreme weather have been cited as causes for bobwhite declines [1,37,38], our study zone has remained stable, and there was no severe weather between early March and late April to adversely affect local quail populations; therefore, habitat loss and weather were not considered to be contributors to this decline. Additionally, we did not encounter mosquitos during trapping in March, April, or May 2017, suggesting avian diseases such as West Nile Virus likely did not contribute to our observed decline as previously postulated . These factors, along with the consistent habitat within our experimental area, suggest that parasites may indeed be responsible for the potential dieoff in April 2017 (Table 2).
|Sample Size||Eyeworm||Caecal Worm|
|%||Mean Abundance||Range||%||Mean Abundance||Range|
|March||10||90||11.3 ± 13.4||0-38||100||159.9 ± 57.1||70-273|
|April||10||80||11.7 ± 11.8||0-30||100||216.0 ± 55.8||146-334|
|May||7||100||16.4 ± 19.5||2-58||100||110.9 ± 53.3||51-208|
|Total||27||90||12.8 ± 14.2||0-58||100||168.0 ± 68.2||51-334|
|March||10||100||15.2 ± 10.1||6-37||100||268.6 ± 90.2||110-454|
|Mid-April||5||100||18.4 ± 12.7||3-34||100||371.8 ± 144.4||208-572|
|Late April||5||100||7.4 ± 2.1||5-10||100||252.4 ±109.0||146-393|
|Mid-May||4||100||26.25 ± 9.8*||17-40||100||259.0 ± 110.7*||101-351|
|Total||24||100||16.1 ± 10.8||3-40||100||285.1 ± 112.1||101-572|
Table 2: Eyeworm (Oxyspirura petrowi ) and caecal worm (Aulonocephalus pennula ) prevalence, mean abundance (± standard deviation), and ranges for March, April, and May of 2016 and 2017. *Approximately 30% of both eyeworms and caecal worms in mid-May were immature worms, suggesting new infection.
In conclusion, we believe that eyeworms and caecal worms are capable of causing parasite-induced die-offs in bobwhites when conditions support extreme infection levels, particularly when compounded with other factors such as predators. This is consistent with previous studies in red grouse (Lagopus lagopus scoticus ) in Scotland, where elevated levels of infection with Trichostrongylus tenuis caused population crashes by increasing grouse vulnerability to predators and reducing fecundity [25,40]. Thus, it is plausible that eyeworms and caecal worms affect bobwhite abundance in the Rolling Plains in a similar manner, and parasites, although previously disregarded as a contributor, may have a substantial effect on bobwhite in the Rolling Plains. Studies on the impacts of multiple parasites are limited and additional studies are needed, particularly since pathological consequences are possible for both eyeworms and caecal worms.
We thank the Rolling Plains Research Foundation and Park Cities Quail for funding this project. We thank the employees of our study site for their continuous hospitality and access to our study ranch. Lastly, we thank the Wildlife Toxicology personnel for their field and laboratory assistance.
- Brennan LA (1991) How can we reverse the northern bobwhite population decline? Wildl Soc Bull 19: 544-555.
- Sauer JR, Link WA, Fallon JE, Pardieck KL, Ziolkowski Jr DJ (2013) The North American breeding bird survey 1966-2011: Summary analysis and species accounts. North American Fauna 79: 1-32.
- Hernández F, Brennan LA, DeMaso SJ, Sands JP, Wester DB (2013) On reversing the northern bobwhite population decline: 20 years later. Wildl Soc Bull 37: 177-188.
- Rollins D (2007) Quails on the Rolling Plains. Brennan LA, Texas Quails: Ecology and Management. Texas A&M University Press, College Station 117-141.
- Bruno A (2014)Survey for Trichomonas gallinae and assessment of helminth parasites in northern bobwhites from the Rolling Plains ecoregion. Thesis. Texas A&M University-Kingsville, USA.
- Texas Parks and Wildlife Department (2016) Annual quail hunting forecast.
- Johnson JL, Rollins D, Reyna KS (2012) What’s A Quail Worth? A Longitudinal Assessment Of Quail Hunter Demographics, Attitudes, And Spending Habits In Texas. Proceedings of the National Quail Symposium 7: 294-299.
- Dunham NR, Peper ST, Downing C, Brake E, Rollins D, et al. (2016) Infection levels of the eyeworm Oxyspirura petrowi and caecal worm Aulonocephalus pennula in the northern bobwhite and scaled quail from the Rolling Plains of Texas. J Helminthol 1-9.
- Dunham NR, Bruno A, Almas S, Rollins D, Fedynich AM, et al. (2016) Eyeworms (Oxyspirura petrowi) in northern bobwhites (Colinus virginianus) from the Rolling Plains ecoregion of Texas and Oklahoma, 2011-13. J Wildl Dis 52: 562--567.
- Saunders GB (1935) Michigan's studies of sharp-tailed grouse. In Transactions of the American Game Conference 21: 342-344.
- Addison EM, Anderson RC (1969) A review of eye worms of the genus Oxyspirura (Nematoda: Spiruroidea). J Wildl Dis 55: 1-58.
- Dunham NR, Soliz LA, Fedynich AM, Rollins D, Kendall RJ (2014) Evidence of an Oxyspirura petrowi epizootic in northern bobwhites (Colinus virginianus), Texas, USA. Journal of Wildlife Diseases 50:552-558.
- Chandler AC (1935) A new genus and species of Subuluriae (Nematodes). Trans Am Microsc Soc 54: 33-35.
- Peterson MJ (2007) Diseases and Parasites of Texas Quails. in L. A. Brennan, editor. Texas Quails: Ecology and management. Texas A&M University Press, College Station 89-114.
- McClure HE (1949) The eyeworm, Oxyspirura petrowi, in Nebraska pheasants.The J Wildl Manag13: 304-307.
- Hernández F, Peterson MJ (2007) Northern Bobwhite Ecology and Life History.Brennan LA, Texas Quails: Ecology and Management. Texas A&M University Press, College Station 40-64.
- Kistler W, Hock S, Hernout B, Brake E, Williams N, et al. (2016) Plains lubber grasshopper (Brachystola magna) as an intermediate host for Oxyspirura petrowi in Northern Bobwhites (Colinus virginianus). Parasitol Open 2: 1-8.
- Bruno A, Fedynich AM, Smith-Herron A, Rollins D (2015) Pathological response of northern bobwhites to Oxyspirura petrowi infections. J Parasitol 101: 364-368.
- Dunham NR, Reed S, Rollins D, Kendall RJ (2016) Oxyspirura petrowi infection leads to pathological consequences in Northern bobwhite (Colinus virginianus). Int J Parasitol Parasites Wildl 5: 273-276.
- Dunham NR, Henry C, Brym M, Rollins D, Helman RG, et al. (2017). Caecal worm, Aulonocephalus pennula, infection in the northern bobwhite quail, Colinus virginianus. Int J Parasitol Parasites Wildl 6: 35-38.
- Stoddard HL (1931) The Bobwhite Quail; Its Habits, Preservation and Increase. illus. Scribner, New York, P 599
- Jackson AS (1969) Quail management handbook for West Texas Rolling Plains. Bulletin Number 48. Texas Parks and Wildlife Department, Austin, USA.
- Davidson WR, Kellogg FE, Doster GL (1980) Seasonal trends of helminth parasites of bobwhite quail. J Wildl Dis 16: 367-375.
- Moore J, Simberloff D (1990) Gastrointestinal helminth communities of bobwhite quail. Ecology 71: 344-359.
- Hudson PJ, Dobson AP, Newborn D (1998) Prevention of population cycles by parasite removal. Science 282: 2256-2258.
- Leopold AS (1945) Sex and age ratios among bobwhite quail in southern Missouri. The Journal of Wildlife Management 9: 30-34.
- Lyons EK, Schroeder MA, Robb LA (2012) Criteria for determining sex and age of birds and mammals. Silvy NJ, The wildlife techniques manual: research. John Hopkins University Press, Baltimore, Maryland, USA, 207-229.
- Wobeser G, Wobeser AG (1992) Carcass disappearance and estimation of mortality in a simulated die-off of small birds.J Wildl Dis28: 548-554.
- Wilber MQ, Weinstein SB, Briggs CJ (2015) Detecting and quantifying parasite-induced host mortality from intensity data: Method comparisons and limitations. Int J Parasitol 46: 59-66.
- National Oceanic and Atmospheric Administration (2017) National Temperature and Precipitation Maps. Available.
- Guo KUN, HAO SG, Sun OJ, Kang LE (2009) Differential responses to warming and increased precipitation among three contrasting grasshopper species. Global Change Biolo 15: 2539-2548.
- Lenhart PA, Eubanks MD, Behmer ST (2015) Water stress in grasslands: dynamic responses of plants and insect herbivores. Oikos 124: 381-390.
- Sommerville RI, Davey KG (2002) Diapause in parasitic nematodes: A review.Cand J Zool80: 1817-1840.
- Korschgen LJ (1948) Late-fall and early-winter food habits of bobwhite quail in Missouri.J Wildl Manag12: 46-57.
- Lehmann VW (1946) Mobility of bobwhite quail in southwestern Texas. The J Wildl Manag 10: 124-136.
- Haines AM, Hernández F, Henke SE, Bingham RL (2004) Effects of road baiting on home range and survival of northern bobwhites in southern Texas.Wildl Soc Bull32: 401-411.
- Bridges AS, Peterson MJ, Silvy NJ, Smeins FE, Ben Wu X (2001) Differential influence of weather on regional quail abundance in Texas. J Wildl Manag 65: 10-18.
- Olsen AC, Brennan LA, Fedynich AM (2016) Helminths and the northern bobwhite population decline: A review. Wildl Soc Bull 40: 388-393.
- Urban KN, Gibson AG, Dabbert CB, Presley SM (2013) Preliminary disease surveillance in west Texas quail (Galliformes: Odontophoridae) populations.J Wildl Dis49: 427-431.
- Hudson PJ, Dobson AP, Newborn D (1992) Do parasites make prey vulnerable to predation? Red grouse and parasites.J Ani Ecol 61: 681-692.
Citation: Henry C, Brym MZ, Kendall RJ (2017) Oxyspirura petrowi and Aulonocephalus pennula Infection in Wild Northern Bobwhite Quail in the Rolling Plains Ecoregion, Texas: Possible Evidence of A Die-Off. Arch Parasitol 1: 109.
Copyright: © 2017 Henry C, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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