Gurltia paralysans: History
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Subjects: Veterinary Sciences
Contributor:
Lisbeth Rojas-Barón
,
Anja Taubert
,
Carlos Hermosilla
,
Marcelo Gómez
,
Manuel Moroni
,
Pamela Muñoz

Gurltia paralysans is a neglected and re-emerging metastrongyloid angio-neurotropic nematode causing severe chronic meningomyelitis in domestic cats (Felis catus) as well as in free-ranging small wild felids such as kodkods (Leopardus guigna), margays (Leopardus wiedii) and the northern tiger cat (Leopardus triginus) in South America. Within these definitive hosts (DH), adult males and females of G. paralysans parasitize the leptomeningeal veins of the subarachnoid space and/or the meningeal veins of spinal cord parenchyma, inducing vascular alterations.

  • Gurltia paralysans
  • life cycle
  • nematode
  • feline

1. Introduction

Gurltia paralysans is a neglected metastrongyloid nematode (superfamily Metastrongyloidea, family Angiostrongylidae) causing severe chronic meningomyelitis in domestic cats (Felis catus) as well as in free-ranging wild felids of the genus Leopardus in South America. Historically, G. paralysans was first described by Kurt Wolfgang Wolffhügel (1933), a German scientist, naturalist, and parasitologist, who isolated adult nematodes from the vein system of the leptomeninges of 11 domestic cats suffering from chronic pelvic paraparesis within the provinces of Llanquihue and Puerto Varas in Southern Chile [1][2]. The etymology of the genus Gurltia is explained by Wolffhügel’s intention to honour Ernst Friedrich Gurlt (1794–1882), a German veterinary anatomist and teratologist. Wolffhügel (1933) initially described this neurological parasitosis associated with small felines as “paraplejia cruralis parasitaria felis” and placed the nematode species within the genus Hemostrongylus, later renamed Angiostrongylus [1]. One year later, Wolffhügel (1934) published an extended description of its geographic distribution, morphology, pathological findings, and clinical signs and speculated on its transmission and definitive host (DH) spectrum. This author showed the small wild felid species kodkod (Leopardus guigna; Figure 1) to be the main natural DH in Southern Chile and in the border regions of Argentina, locally known as “guiña” or “spotted tiger cat”. In addition, Wolffhügel (1993, 1934) proposed domestic cats as aberrant DH that were first introduced by European settlers into the South American continent and thereafter became exposed to this endemic nematode [3]. More recently, the spectrum of wild felid species acting as DH has increased, nowadays including the margay (Leopardus wiedii) and the northern tiger cat (Leopardus tigrinus) [4]. Additionally, within the genus Leopardus, other small wild felids have also been suggested as potential DH in South America [1][2][3][4][5][6][7]. Alongside the genus Leopardus, larger wild felids of South America, i.e., pumas (Puma concolor concolor), jaguars (Panthera onca), and jaguarondis (Herpailurus yagouaroundi), have also been suggested as potential DH, but this needs further investigation [1][5][7]. In a recent study on free-ranging guiñas in Chile, although no presence of G. paralysans was observed, the isolation of other closely related nematodes such as Angiostrongylus sp., Oslerus sp. and Troglostrongylus sp. was observed, indicating diversity, susceptibility, and the potential risk of lungworm infections in South America [8].
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Figure 1. Distribution of wild guiñas (syn. huiñas, kodkods, spotted tiger cat) in South America. (A) Adult specimen of a guiña (Leopardus guigna) (image reprinted with permission from © Joel Sartore/Photo Ark, 2022). (B) Geographic distribution of guiña in Chile (orange) and Argentina (yellow). (C) Scale representation of an adult guiña.
In vivo, G. paralysans has a marked angio-neurotropism invading the venous system of leptomeninges, specifically the thoracic, lumbar, and sacral spinal cord segments. The distribution of G. paralysans adults within the meningeal veins of the subarachnoid space implies activation of the highly immunoreactive endothelium, as seen for Angiostrongylus vasorum [9], probably resulting in thrombophlebitis with thrombus formation, venous congestion, and meningeal haemorrhages due to endothelium damage, as observed in severe feline gurltiosis [10]. Clinical manifestations can include chronic symmetrical or asymmetrical pelvic limb ataxia, ambulatory paraparesis, uni- or bi-lateral hyperactive patellar reflexes, proprioceptive deficit of pelvic limbs, pelvic limb muscular atrophy, diarrhoea, weight loss, coprostasis, urinary and faecal incontinence, and death [1][2][3][4][5][6] (Table 1). Neurological signs are typically associated with neuroanatomical lesions observed in post mortem examinations and histopathological specimens within the spinal cord [1][10][11][12]. Recently, histological and immunohistochemical characterization of vascular alterations in naturally G. paralysans-infected domestic cats of Chile unveiled suppurative vasculitis, haemorrhages, vascular congestion, and varicosis of not only spinal cord but also cerebrum-, cerebellum- and brain stem-associated veins [13], thereby supporting endothelium-derived pro-inflammatory innate immune reactions.
Table 1. Reported cases of feline gurltiosis including age, geographic location, clinical presentation and diagnosis.
Age Location Number
of Cases		 Clinical Presentation Diagnosis Reference
1–3 y Chile
(Los Ríos/Los Lagos regions)		 3 Paraparesis (ambulatory)
PL ataxia
PL muscle atrophy
Anal/urinary incontinence		 Post mortem
(histopathology)		 [12]
6–8 m Colombia
(Antioquia municipality)		 6 Paraparesis (ambulatory)
PL ataxia
Spinal pain
PL muscle atrophy
Anal/urinary incontinence
Decrease superficial/deep pain in PL		 Post mortem
(histopathology, Myelo)		 [14]
2 y Argentina
(Buenos Aires province)		 1 Paraparesis (non-ambulatory)
PL muscle atrophy
Increase spinal reflexes in PL
Decrease superficial/deep pain in PL		 Post mortem
(histopathology)		 [15]
NA Uruguay
(Fray Bentos)		 2 Paraparesis (ambulatory)
Paraplegia
PL ataxia		 Post mortem
(histopathology)		 [16]
1–3 y Chile 3 Paraparesis (ambulatory)
PL ataxia
PL muscle atrophy
Anal/urinary incontinence
Spinal hyperaesthesia
PL trembling
Increase spinal reflexes in PL
Paraplegia		 Post mortem
(histopathology, specimens extracted from SSE)		 [11]
8 m–10 y Chile 9 Paraparesis (ambulatory)
Paraparesis (non-ambulatory)
Paraplegia
PL ataxia
Increase spinal reflexes in PL
Spinal hyperaesthesia
Anal/urinary incontinence		 Post mortem
(histopathology, specimens extracted from SSE, Myelo, CT, MRI		 [17]
NA Brazil
(Río Grande do Sul)		 4 Paraparesis (ambulatory)
PL muscle atrophy
Vesical atony
Tail atony		 Post mortem
(histopathology)		 [18]
NA Argentina
(Santa Fé)		 3 Paraparesis (ambulatory)
Paraplegia
Decrease spinal reflexes in PL
Decrease superficial pain in PL
Skin lesions in the metatarsal region		 Post mortem
(histopathology)		 [19]
8 m Chile
(Ancud, Los Lagos regions)		 1 Paraparesis (ambulatory)
Anal/urinary incontinence
Tail atony		 Myelo-CT, CSF (mononuclear pleocytosis), post mortem
(histopathology)		 [10]
2 y Spain
(Tenerife)		 1 Uveitis in left eye Specimen extracted from anterior chamber of the eye, PCR [20]
NA Brazil
(Pernambuco)		 11 Paraparesis (ambulatory)
PL ataxia,
PL muscle atrophy
Skin lesions in metatarsal and phalangeal regions		 Post mortem
(histopathology)		 [21]
36 m Chile 10 Paraparesis (ambulatory)
Paraplegia
PL ataxia
Anal/urinary incontinence		 Post mortem
(histopathology), IDEXX (Angio Detect),
specimens extracted from SSE		 [5]
 

2. Hypothetical Life Cycle of Gurltia paralysans (Angiostrongylidae)

Small felids of the genera Felis and Leopardus are considered as DH of G. paralysans, as sexual replication occurs within these carnivorous mammals. As such, intravascular gravid G. paralysans females passing non-embryonated eggs (i.e., those containing 16 blastomeres) within the subarachnoid leptomeningeal veins of spinal cords from domestic cats (F. catus) [12], kodkods (L. guigna) [1][2][3], margays (L. wiedii) and northern tiger cats (L. tigrinus) [4] have been reported. Within Chilean territories, other small wild felids of the genus Leopardus have been discussed as potential DH [1][2][6], such as the Andean cat (Leopardus jacobita) and the Pampas cat (Leopardus colocolo). In semiarid, subtropical and tropical regions of South America, the southern tiger cat (Leopardus guttulus), Geoffroy’s cat (Leopardus geoffroyi) and the ocelot (Leopardus pardalis) might also act as DH [1][2][3][4][22]. Moreover, in South, Central and North America, larger wild felids such as the cougar (P. concolor concolor), the jaguar (P. onca) and the jaguarundi (H. yagouarundi) are proposed as DH, but this needs further clarification [1][7].
Unfortunately, nothing is known on other aspects of the life cycle, such as the mode of DH infection, exogenous larval development in obligate intermediate hosts (IH), endogenous in vivo migration of infective L3, pre-patency, patency and post-patency [5][6][12]. Neither eggs nor first-stage larvae (L1) have been detected in faeces, blood, bronchial lavage and/or other body fluids of naturally G. paralysans-infected domestic cats, northern tiger cats and margays [1][4][22][23].
As reported for other nematodes of the family Angiostrongylidae, terrestrial/aquatic gastropods (snails, semi-slugs and slugs) acting as obligate IH as well as paratenic hosts (PH) have been proposed in the biology of G. paralysans. Therefore, larval development occurring through moults from first-stage larvae (L1) to second-stage larvae (L2) and to the final infective third-stage larvae (L3) (Figure 2) has recently been proposed [1][5][6][7]. The suspected PH in this life cycle, such as crustaceans, amphibians, reptiles, rodents and birds, might become infected after ingesting L3-carrying gastropod IH, as reported for closely related Angiostronglylus species [24][25]. To elucidate the presence of G. paralysans larval stages in obligate gastropod IH, a large-scale epidemiological survey was recently conducted in the southern parts of Chile [26]. In this study, 835 terrestrial gastropods from a previously well-recognized endemic focus surrounding the city of Valdivia, Chile [1][26], were collected, demonstrating that neither PCR, enzymatic digestion nor histological examinations revealed the presence of larvae [1][26]. Collected gastropods included slugs of the families Arionidae, Limacidae and Milacidae as well as snails of the family Helicidae. Nonetheless, neither terrestrial semi-slugs (family Helicarionidae) nor aquatic snails were included in this survey, and thus this needs further investigation [1][7][26].
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Figure 2. Proposed life cycle and migration pathways of Gurltia paralysans. (A) Cranial end of an adult specimen of G. paralysans. (B) Domestic cats (Felis catus) or wild felids (Leopardus spp.) acquire the L3 larvae by ingesting an infected obligate intermediate host (gastropods) or paratenic hosts (lizards, rodents, amphibians, birds or insects). Infective larvae penetrate the stomach and enter the hepatic portal system, and then the caudal vena cava and/or the azygous venous system. From these vein systems, the larvae migrate to the spinal cord via the intervertebral veins and the vertebral venous plexus. The larvae invade the veins of the subarachnoid space of the spinal cord, where they mature and lay eggs. It is still unknown on how domestic cats eliminate the eggs or the first-stage larvae (L1) into the environment, their further development into the L2 and L3 larval stages, or how the obligate intermediate hosts become infected with L1. AV: azygos vein; CV: caudal vena cava; IV: intervertebral veins; H: heart; L: liver; S: stomach; SC: spinal cord; VVP: vertebral venous plexus; L1: first-stage larvae; L2: second-stage larvae; L3: third-stage larvae. The inserted QR code shows a video of a G. paralysans-infected cat with clinical signs of paraparesis.
Proposed infection routes for felid DH are either after consumption of G. paralysans L3-infected gastropod IH or after consumption of L3-infected PH, as initially proposed by Wolffhügel (1934) [3]. As such, in his article, he referred to the colloquial name of feline gurltiosis used by locals, namely “lizard disease”, highlighting the pivotal role of PH in transmission. Alongside lizards, fish, frogs, toads, newts, snakes, turtles, birds, rodents, planarians, crustaceans, insects and myriapods have also been suspected in the life cycle of G. paralysans within South America [1][5][21][26]. Likewise, infective A. cantonensis-L3 larvae liberated from dead or living gastropods can survive outside IH for a short time, forming an important source of infection. The L3 larvae of A. cantonensis can enter new IH through the process known as intermediasis, which might occur in this life cycle as well, thereby extending the survival strategies of G. paralysans. These alternative transmission routes can occur with ease in neotropical South American rainforests, which have the highest biodiversity of protist, invertebrate and vertebrate species in the world [7].
Concerning the endogenous migration of G. paralysans L3 in felid DH in vivo, nothing is known so far. Hypothetically, L3 migration could be through the small intestinal mucosa in order to reach the mesenteric veins and/or lymphatic vessels of the abdominal viscera and thereafter via connections of either the azygos or the caval venous system (CVS) with the thoracic, lumbar or sacral intervertebral veins until they reach the vertebral venous plexus (VVP, Figure 2) [1]. The VVP is in direct communication with the cranial venous system, and because no valves exist in either of them, blood might flow cranially or caudally, depending on blood pressure [1][27]. G. paralysans could take advantage of the absence of valves in the VVP to reach either the spinal subarachnoid space or even the brain [1][12][28]. Similarly, in spinal schistosomiasis in humans, the dissemination of the parasite occurs via the intestinal veins to the VVP [29]. Spinal schistosomiasis usually involves the lower thoracic and lumbosacral spine, probably because the VVP connects the intra-abdominal veins with those of the lower spine [30]. The presence of fertile male and female nematodes, and gravid females passing eggs within the ventral VVP and basivertebral veins located in the vertebral bodies, were isolated during necropsies, confirming the marked angiotropism of G. paralysans in DH [1][12]. Moreover, parasitic localization within the VVP’s venous connections may explain the presence of eggs, L1, pre-adults and adults of G. paralysans in distant places, such as the cerebrum, cerebellum and anterior chamber of the eye of infected cats [1][20][27][31]. Nonetheless and in contrast to all Angiostrongylus species residing within arterial vessels, G. paralysans dwells within venous vessels. Thus, the adaptations of G. paralysans to the VVP’s venous connections might be associated not only with abiotic factors of the venous microenvironment, such as hypoxia and CO2 concentrations, but may also be linked to physical factors (e.g., temperature, blood flow velocity) and even nutrients, among others [1]. It seems indispensable for future investigations on the migratory pathways of G. paralysans to include not only vein tropism but also neuroanatomical localization within the subarachnoid VVP in felids [1]. During the patency period, gravid G. paralysans will then release un-embryonated eggs into the leptomeningeal vein system. Intravascular eggs will develop into L1, and hatching of the L1 will occur within the VVP, as demonstrated previously [1][12]. The free-released L1 will then breach the alveolar walls in order to access the bronchioles, bronchia and trachea, and are most likely expelled via faeces into the environment. Consistently, the life cycles of other closely related angio-neurotropic metastrongyloid genera of cervids (Elaphostrongylus and Parelaphostrongylus) might explain the final localizations of G. paralysans in the subarachnoid leptomeningeal veins of felid spinal cord. Likewise, adults of Elaphostrongylus alces occur in vessels of the epidural space of the vertebral canal and in the skeletal muscles of moose (Alces alces) [32][33]. Similar to G. paralysans, E. alces has obligate gastropod IH, causing neurological disorders in wild moose populations after ingestion of L3-carrying gastropods [32][33]. Earlier researchers suggested that E. alces L3 migrate directly from the gut into the epidural space of the caudal vertebral canal, where development to the adult stages takes place. During endogenous development, E. alces nematodes produce severe inflammation of the epidural tissue and spinal nerves [32]. In line with this, development of Elaphostrongylus rangiferi also takes place only within the brain and spinal cord vessels of reindeer (Rangifer tarandus), with subsequent migration of adult nematodes into the skeletal muscle [34]. In the case of Parelaphostrongylus tenuis, also known as “meningeal worm” or “brain worm”, which typically occurs in wild cervids (Cervidae), adult nematodes mate in the blood vessels of deer heads, and gravid females start releasing eggs into the circulatory system [35]. In fact, the release of eggs or larvae into the circulatory blood system might be linked with the appearance of P. tenuis larvae in the ventral portion of the anterior eye chamber [36], similar to a recent ophthalmic finding in a G. paralysans-infected domestic cat of Tenerife Island, Spain [20].
One of the most peculiar features of some Angiostrongylus species (Angiostrongylidae) is their strong neurotropism within warm-blooded DH or accidental/aberrant hosts (AH). As such, infectious A. cantonensis L3 must migrate through the central nervous system (CNS), where they develop further, reaching the L5 larval stage in the subarachnoidal space within two weeks post infection [37][38]. This part of the life cycle usually does not produce severe signs in DH (e.g., rats); however, infections in AH commonly result in eosinophilic meningitis, with several clinical scenarios [38], as was also the case for G. paralysans-infected domestic cats considered by Wolffhügel (1934) as AH. Clinical manifestations are common between G. paralysans and A. cantonensis due to the signs observed in infected animals resulting in increased intracranial pressure, neural tissue damage, the hosts’ pro-inflammatory response, congestion, thrombosis, thrombophlebitis, varices and thickening of the affected vessels [1][18][37].
 

This entry is adapted from the peer-reviewed paper 10.3390/pathogens11070792

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