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Camelids: new players in the international animal production context

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The Camelidae family comprises the Bactrian camel (Camelus bactrianus), the dromedary camel (Camelus dromedarius), and four species of South American camelids: llama (Lama glama), alpaca (Lama pacos) guanaco (Lama guanicoe), and vicuña (Vicugna vicugna). The main characteristic of these species is their ability to cope with either hard climatic conditions like those found in arid regions (Bactrian and dromedary camels) or high-altitude landscapes like those found in South America (South American camelids). Because of such interesting physiological and adaptive traits, the interest for these animals as livestock species has increased considerably over the last years. In general, the main animal products obtained from these animals are meat, milk, and hair fiber, although they are also used for races and work among other activities. In the near future, climate change will likely decrease agricultural areas for animal production worldwide, particularly in the tropics and subtropics where competition with crops for human consumption is a major problem already. In such conditions, extensive animal production could be limited in some extent to semi-arid rangelands, subjected to periodical draughts and erratic patterns of rainfall, severely affecting conventional livestock production, namely cattle and sheep. In the tropics and subtropics, camelids may become an important protein source for humans. This article aims to review some of the recent literature about the meat, milk, and hair fiber production in the six existing camelid species highlighting their benefits and drawbacks, overall contributing to the development of camelid production in the framework of food security.
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Camelids: new players in the international animal production context
Mousa Zarrin
1
&José L. Riveros
2
&Amir Ahmadpour
1,3
&André M. de Almeida
4
&Gaukhar Konuspayeva
5
&Einar Vargas-
Bello-Pérez
6
&Bernard Faye
7
&Lorenzo E. Hernández-Castellano
8
Received: 30 October 2019 / Accepted: 22 December 2019
#Springer Nature B.V. 2020
Abstract
The Camelidae family comprises the Bactrian camel (Camelus bactrianus), the dromedary camel (Camelus dromedarius), and
four species of South American camelids: llama (Lama glama),alpaca(Lama pacos)guanaco(Lama guanicoe), and vicuña
(Vic ugna vicu gna). The main characteristic of these species is their ability to cope with either hard climatic conditions like those
found in arid regions (Bactrian and dromedary camels) or high-altitude landscapes like those found in South America (South
American camelids). Because of such interesting physiological and adaptive traits, the interest for these animals as livestock
species has increased considerably over the last years. In general, the main animal products obtained from these animals are meat,
milk, and hair fiber, although they are also used for races and work among other activities. In the near future, climate change will
likely decrease agricultural areas for animal production worldwide, particularly in the tropics and subtropics where competition
with crops for human consumption is a major problem already. In such conditions, extensive animal production could be limited
in some extent to semi-arid rangelands, subjected to periodical draughts and erratic patterns of rainfall, severely affecting
conventional livestock production, namely cattle and sheep. In the tropics and subtropics, camelids may become an important
protein source for humans. This article aims to review some of the recent literature about the meat, milk, and hair fiber production
in the six existing camelid species highlighting their benefits and drawbacks, overall contributing to the development of camelid
production in the framework of food security.
Keywords Dromedary camel .Bactrian camel .South American camelids .Meat .Milk .Hair fiber
Introduction
The Camelidae family descends from animals living in North
America during the Eocene period (45 million years ago).
Camelsancestors migrated to South America and across the
Bering Strait into Central Asia, which has resulted in Old
World camels (Bactrian and dromedary camels) and New
World camels (South American camels; SAC). Thus, camel
evolution has been recently addressed using molecular tech-
niques by Manee et al. (2019).
According to Payne and Wilson (1999), camels in central
Asia evolved into the domestic Bactrian camel (Camelus
bactrianus) and wild Bactrian camel (Camelus bactrianus
ferus), being both of them commonly known as two-humped
*Lorenzo E. Hernández-Castellano
lhc@anis.au.dk
1
Department of Animal Sciences, Faculty of Agriculture, Yasouj
University, Yasouj 75918-74831, Iran
2
Departamento de Ciencias Animales, Facultad de Agronomía e
Ingeniería Forestal, Pontificia Universidad Católica de Chile,
7820436 Santiago, Chile
3
Department of Biological Engineering, Utah State University,
Logan, UT 84322, USA
4
Linking Landscape, Environment, Agriculture and Food (LEAF),
Instituto Superior de Agronomia, Universidade de Lisboa,
1349-017 Lisbon, Portugal
5
Department of Biotechnology, Al-Farabi Kazakh National
University, Almaty, Kazakhstan 050040
6
Department of Veterinary and Animal Sciences, Faculty of Health
and Medical Sciences, University of Copenhagen,
1870 Frederiksberg C, Denmark
7
UMR SELMET, CIRAD-ES, Campus International de Baillarguet,
34398 Montpellier cedex, France
8
Department of Animal Science, AU-Foulum, Aarhus University,
Blichers Allé 20, Postboks 50, 8830 Tjele, Denmark
Tropical Animal Health and Production
https://doi.org/10.1007/s11250-019-02197-2
camels. Currently, wild Bactrian camels subsist in secluded
desert areas such as the Gobi Desert in China. Domesticated
Bactrian camels have been reared in several countries in
Central Asia, where they played a primary role in transporting
the goods. Currently, these animals are also used for meat,
milk, and hair fiber production. Domestic Bactrian camels
are distributed from Turkey to Mongolia (Fig. 1). The one-
humped camel or dromedary camel (Camelus dromedarius)
evolved from animals similar to Bactrian camels (Burger et al.
2019). Dromedary camels are essentially domestic, and they
are distributed in Asia and Africa, from East India to Morocco
(Fig. 1). In addition, dromedary camels are distributed in the
Canary Islands (Spain) and Central Australia (Fig. 1).
Dromedaries are used to provide work and transport in addi-
tion to meat, milk, and hair fiber production. Dromedary
camels are also used for races in the Persian Gulf region and
as pack animals in tourist activities in the Canary Islands
(Spain) or Australia.
In South America, guanaco (Lama guanacoe) and vicuña
(Vicugna vicugna) are the two wild SAC species. The estimat-
ed population is about 650,000 and 250,000 animals, respec-
tively (FAOstat 2019). The domestication of guanacos and
vicuñas led to the establishment of the domestic SAC species,
llama (Lama glama) and alpaca (Vicugna pacos), respectively.
According to FAOstat (2019), there are about 5 million llamas
and 4.5 million alpacas in South America. Llamas are used as
pack animals by Andean native communities. In addition,
llamas are also used for meat production. Alpacas are mostly
used for the production of fine fibers. South American camels,
notably alpacas, have been introduced in other countries,
namely Australia and New Zealand where they are used for
fiber production. These animals are very popular as pets and
show animals in Europe, Canada, and the USA.
Camels have very interesting physiological and adaptive
traits (Gerken 2010;Alhidaryetal.2018; Hoter et al. 2019).
Indeed, Bactrian and dromedary camels are particularly well
adapted to arid environments (Wu et al. 2014). Some of these
traits are (a) adipose tissue located in the hump that can be
mobilized in case of food scarcity, (b) long and bushy eye-
lashes to protect eyes from sand and sun daylight, (c)
occludable nostrils to avoid sand entrance and reduce the
amount of water lost during the respiration process, (d)
adapted limbs for sandy conditions, and (e) efficient physio-
logical mechanisms to mitigate heat stress and dehydration.
South American camels have also very interesting physiolog-
ical traits (Wheeler 1995; Vaughan and Tibary 2006; Jiménez
et al. 2010). These include (a) tolerance to hypoxia, which
allows them to live at very high altitudes; (b) soft footpads
adapted to mountain and rocky conditions; (c) thick and iso-
lating hair fiber to protect from cold temperatures; and (d)
specific behavioral traits such as kicking and spitting rumen
fluid as a protection mechanism against predators. In addition,
Bactrian, dromedary, and South American camels have also a
digestive system adapted to consume large amounts of fibrous
and thorny plants (Dehority 2002). As these species have a
three-chamber foregut, they are commonly classified as
pseudoruminants (Dehority 2002).
Despite the important role of Old and New World camels in
the livelihood, food security, and economy of the local com-
munities, these species have never been considered major
players in the international animal production context.
However, changes associated to climate change may modify
this scenario in the near future. The objective of this review is
to describe major features of Old and New World camels as
production animals, particularly in their main productive per-
spectives (i.e., meat, milk, and hair fiber) and to highlight the
Fig. 1 Distribution map of the different camel species (domestic Bactrian camel, wild Bactrian camel, dromedary camel, alpaca, llama, vicuña and
guanaco)
Trop Anim Health Prod
potential and opportunities of using camels in the international
animal production context.
Bactrian camels
Bactrian camels (Camelus bactrianus), also known as double-
humped camels, differ from dromedary camels by the number
of humps and the ecosystem where they are raised (Fig. 2). As
dromedary camels, Bactrian camels are used for meat and
milk production. In addition, Bactrian camels are also used
for hair fiber production. The number of Bactrian camels is
reduced compared with dromedary camels (1 million vs. 34
million animals, respectively; FAOstat 2019). However, in
some countries such as Kazakhstan, the number of Bactrian
camels represents 85% ofthe total camel population (Imamura
et al. 2017). Bactrian camels are raised mainly in Mongolia
(435,000 heads), China (323,000), Kazakhstan (194,000),
Uzbekistan (18,000), and Russia (6400). However, Bactrian
camels are also present in other countries such Kirgizstan,
Tajikistan, Azerbaijan, Iran, Pakistan, India, Turkey, and
Ukraine.
Meat production perspectives
Adult Bactrian camels weight 700800 kg in case of females,
and up to 1250 kg in case of males (Saipolda 2004). In 2017,
about 36,700 tons of Bactrian camel meat was produced, be-
ing China (20,668 tons), Mongolia (7122 tons), Kazakhstan
(6617 tons),Uzbekistan (2120 tons), and Russia (179 tons)the
main leading producers (FAOstat 2019).
Most of the literature regarding meat composition in
Bactrian camels is in Russian (Terentyev 1975), Mongolian
(Indra et al. 2003), Kazakh (Moussaiev et al. 2007), or
Chinese (Zhao et al. 2004). However, recent studies published
in English showed that Bactrian camel meat contains 17.0
21.0% protein, 1.803.80% fat, and 0.901.10% minerals
(Raiymbek et al. 2015;Raiymbeketal.2018). Compared with
other livestock species, meat from Bactrian camels contains
similar protein levels to those from chickens (21.4%), lambs
(20.8%), pigs (20.5%), and veals (20.2%), although meat fat
content in Bactrian camels is lower than those from lambs
(4.40%) and pigs (5.41%) and similar to chickens (3.08%)
and veals (2.87%) (Hernández-Castellano et al. 2013; Cobos
and Díaz 2015).
Regarding the amino acid profile, Bactrian camel meat
contains similar levels of methionine (6.72%); lower concen-
trations of glutamate (6.78%), serine (1.66%), histidine
(3.55%), tyrosine (2.23%), and tryptophan (0.37%); and
higher concentrations of aspartate (12.2%), arginine
(7.48%), proline (13.1%), isoleucine (6.07%), and leucine
(15.3%) compared with dromedary meat (6.78, 7.49, 3.10,
6.09, 5.34, 0.52, 7.93, 5.80, 9.65, 4.91, and 11.7%, respective-
ly) (Raiymbek et al. 2015). Additionally, Bactrian camel meat
contains higher levels of methionine, leucine, and aspartate
compared with other species such as those from beef cattle
(2.20, 8.50, and 8.90%, respectively), lambs (2.40, 7.20, and
8.60%, respectively), and pigs (2.60, 7.60, and 8.80%, respec-
tively) (Ahmad et al. 2018).
Regarding the fatty acid (FA) profile, polyunsaturated fatty
acid (PUFA) levels are lower in Bactrian camel meat (9.60%)
compared with dromedary camel meat (17.7%), while similar
monounsaturated fatty acid (MUFA) levels have been
Fig. 2 Domestic Bactrian camel
(Kazakhstan)
Trop Anim Health Prod
described for Bactrian and dromedary camels (35.4 and
37.9%, respectively) (Raiymbek et al. 2019). Specifically,
Bactrian camel meat contains lower levels of palmitic acid
(26.9%) and palmitoleic acid (3.20%) and higher levels of
myristic (8.60%), oleic (29.8%), and linoleic acid (10.0%)
than dromedary camel meat (29.0, 8.60, 8.10, 26.7, and
7.50%, respectively) (Raiymbek et al. 2019). In addition, cho-
lesterol concentrations in Bactrian camel meat are slightly
higher (0.54 g/kg) than those from dromedary camel meat
(0.49 g/kg). Compared with other livestock species, meat from
Bactrian camels contains higher levels of palmitic acid and
lower levels of oleic acid compared with meat from beef cattle
(25.0 and 36.1%, respectively), lambs (22.2 and 32.7%, re-
spectively), and pigs (23.2 and 32.8%, respectively). Linoleic
acid levels in meat from Bactrian camels are lower than those
from beef cattle and lambs (2.40 and 2.70%, respectively) and
higher than those from pigs (14.2%) (Wood et al. 2004).
Dairy production perspectives
In 2017, Bactrian camels produced about 21,000 tons of milk
(FAOstat 2019). While the Bactrian camel population repre-
sents 2.70% of the total amount of Old World camels world-
wide, milk production from these camels only represents
1.80% of the total milk produced by Old World camels.
Milk yield in Bactrian camels differs among countries. For
instance, Bactrian camels yield about 300 kg (17-month
lactation) in Mongolia (Saipolda 2004), being 2 to 4 kg/day
the highest milk yield in the lactation peak (Indra et al. 2003).
In China, Bactrian camels yield 0.25 to 1.50 kg/day in addi-
tion to the milk consumed by the calf (Zhang et al. 2005),
which represents about 645 kg per lactation (Surong 2019).
Higher milk yields have been recorded in those Bactrian
camels raised in Kazakhstan (8501700 kg; Baimukanov
et al. 2017) and Russia (1827 kg; Indra et al. 2003).
However, milk yield in Bactrian camels is lower than drome-
dary camels. In a recent study, Baimukanov et al. (2017)de-
scribed lower milk yields in Bactrian camels (1270 kg/year)
than dromedary camels (3601 kg/year). Hybridization be-
tween Bactrian and dromedary camels is commonly per-
formed in these countries to increase milk yields from camels
(Faye and Konuspayeva 2012). For instance, Baimukanov
et al. (2017) described how milk production in Bactrian and
dromedary hybrids ranged from 2251 to 2927 kg/year.
Despite low milk yields, consumption of Bactrian camel
milk is prevalent in Central Asia (Accolas et al. 1978;
Konuspayeva and Faye 2011). Regarding the nutritive aspects
of Bactrian camel milk, Faye et al. (2008) showed that
Bactrian camel milk contains 6.67% fat, which is similar to
the fat content in sheep milk from sheep (6.39%) and higher
than the fat content in goat and cow milk (4.47 and 3.26%,
respectively) (Hernández-Castellano et al. 2016). The fatty
acid profile of Bactrian camel milk is characterized by caprylic
(0.53%), lauric (1.24%) myristic (15.4%), iso-heptadecanoic
(0.55%), and oleic (18.8%) acids (Konuspayeva et al. 2008).
Compared with other species, milk from Bactrian camels con-
tains lower caprylic and lauric acids compared with milk from
goats (2.92 and 4.52%, respectively), sheep (1.87 and 3.99%,
respectively), and cows (1.39 and 3.64%, respectively).
However, oleic levels in milk from Bactrian camels are similar
to those found in milk from goats (18.7%) and lower to those
found in milk from sheep and cows (20.2 and 22.4%, respec-
tively) (Markiewicz-Keszycka et al. 2013). Cholesterol con-
centrations in milk from Bactrian camels are higher
(0.37 mg/kg) (Konuspayeva et al. 2008) than in cow milk
(0.81 mg/kg) (Faye 2015). In addition, Faye et al. (2008)
showed that Bactrian camel milk contains high concentrations
of vitamin C (0.18 g/L), calcium (1.30 g/L), and phosphorus
(1.07 g/L).
Hair fiber production perspectives
Besides its use for working (i.e., pulling and carrying heavy
goods) or sportive activities (i.e., races), Bactrian camels are
also reared for hair fiber production, especially in Mongolia
and China (Chapman 1991). Hair fiber from Bactrian camels
is very thin fine (2023 μm), similar to that of merino wool,
and it is considered a high-quality natural fiber. One of the
main Bactrian camel breeds used for hair fiber production is
the Alxa Bactrian camel (China), with a production of hair
fiber about 56 kg in females and up to 12.5 kg in males.
Hair fiber from this breed is characterized by long and strong
fiber and light color (Surong 2019). In recent years, produc-
tion of hair fiber from Bactrian camels has been considerably
increased due to high demand by Europe and North America
(Faye 2015).
Dromedary camels
Dromedary camels (Fig. 3) represent 95% of all Old World
camels (Faraz et al. 2019). Most dromedary camels are dis-
tributed in the Horn of Africa, the Middle East, Pakistan,
India, and the harsh and arid areas of North and West Africa.
Dromedary camels are used for meat, milk, and hair fiber
production as well as for transportation and agriculture labors
(Faraz et al. 2013).
Meat production perspectives
Dromedary camelscapability to use low-quality feeds has
made them one of the main animal protein sources in several
tropical countries (Faraz et al. 2019; Hernández-Castellano
et al. 2019). Based on its importance, several studies have
focused on dromedary camel meat quality and composition
(Kadim et al. 2008; Kadim et al. 2014). Dromedary camel
Trop Anim Health Prod
calves are born with approximately 35 kg BW; however, this
value fluctuates based on breed and region (Kadim et al.
2014). Average daily gain in dromedary camel calves is lower
than dairy calves and limited to 500 g/day. Adult dromedary
camels can weigh up to 650 kg BW (78 years old).
Depending on the slaughtering age, dromedary carcasses can
range from 125 to 400 kg with a carcass dressing ranging from
55 to 70% (Kadim et al. 2014).
Intramuscular fat in meat from dromedary camels ranges
from 5.207.00% (Dawood and Alkanhal 1995; Al-Owaimer
2000; Kadim et al. 2006). However, intramuscular fat content
is affected by animal age, and therefore higher intramuscular
fat percentages are observed in meat from 5- to 8-year-old
dromedary camels (10.5%) than from 1- to 3-year-old drom-
edary camels (4.40%). Dromedary camel meat contains more
PUFA than beef cattle (Dawood and Alkanhal 1995). As
showed by Rawdah et al. (1994), the FA profile in dromedary
camel meat is based 51.5% saturated fatty acids (SFA), 29.9%
MUFA, and 18.6% PUFA. The most abundant fatty acids in
dromedary camel meat are palmitic acid (26.0%), oleic acid
(18.9%), and linoleic acid (12.1%) (Rawdah et al. 1994). In
addition, dromedary camel meat contains lower cholesterol
(0.50 g/kg) than other livestock species such as beef cattle
(0.59 g/kg), sheep (0.71 g/kg), and goat (0.63 g/kg) (El-
Magoli et al. 1973; Kadim et al. 2008; Kadim et al. 2013).
Meat protein content in dromedary camel is similar to beef
cattle (22.7 and 22.5%, respectively; Ahmadpour et al. 2014).
Among the essential amino acids, lysine and leucine are the
most abundant (8.45 and 8.41 g/16 g N, respectively) and
methionine the less abundant (2.41 g/16 g N; Dawood and
Alkanhal 1995).Similarvalueshavebeenreportedforbuffalo
meat (Ziauddin et al. 1994).
Based on these facts, dromedary camel meat is considered
a healthy animal meat source (Schönfeldt and Gibson 2008)
and its consumption might reduce the risk of suffering athero-
sclerosis, obesity, and hypercholesterolemia, and decline the
risk of cancer (Chizzolini et al. 1999).
Dairy production perspectives
Among domestic animals, dromedary camels need to over-
come extreme climate conditions for generation and preserva-
tion of the offspring. Nourishing young calves in harsh cli-
mate conditions characterized by feed and water scarcity has
increased the research interest on camel milk biosynthesis and
composition.
Despite milk production in dromedary camels being low,
this milk is extremely important in arid places, being an ex-
cellent source of proteins for humans living in such areas
(Konuspayeva et al. 2009). Average dromedary milk yield is
not very consistent and rarely exceeds 25 kg/day (Nagy and
Juhasz 2016). The absence of genetic selection, lack of uni-
form milking method, and use of traditional rearing systems
are some of the factors that affect the wide variation among
animals (Wernery et al. 2004; Wernery 2006; Wernery et al.
2006).
Dromedary camels have longer lactation periods than dairy
cows, and they may last up to 24 months (Yagil and Yagil
2000; Wernery 2006). In the last 20 years, milking machines
specifically designed for dromedary camels have caused in-
creased milk yield as well as improved milk hygiene (Wernery
2006; Wernery et al. 2006; Ayadi et al. 2018). Based on a
meta-analysis published by Konuspayeva et al. (2009), drom-
edary camel milk contains on average 3.35% protein, 3.82%
Fig. 3 Dromedary camel (Iran)
Trop Anim Health Prod
fat, 4.46% lactose, 0.79% ash, and 12.5% dry matter.
Interestingly, water content in dromedary camel milk is simi-
lar to human milk (Wernery 2006; Zibaee et al. 2015), and
remains constant under extreme heat-stress conditions
(Wernery 2006;AlhajandAlKanhal2010). However, there
are other factors such as physiological stage, feeding condi-
tions, milk yield, genetic and/or health status that may affect
milk quality and composition in dromedary camels (Musaad
et al. 2013).
Milk proteins are considered one of the main allergens for
humans (Rona et al. 2007; Vargas-Bello-Perez et al. 2019).
For instance, β-casein, β-lactoglobulin, lactoferrin, and im-
munoglobulins from cow milk are common allergens for in-
fants (Khalesi et al. 2017;Matietal.2017). Dromedary camel
milk is characterized by reduced β-caseins content and the
absence of β-lactoglobulin, which contributes to the reduced
allergy in dromedary camel milk consumers (Konuspayeva
et al. 2009). Ehlayel et al. (2011) showed 80% children (6
12 months old) with cow milk allergy showing no allergy to
camel milk.
Regarding fatty acids, dromedary camel milk is character-
ized by reduced short-chain FA and increased long-chain FA
compared with cow milk (Zibaee et al. 2015). Thus, the high
content of PUFA (5.60%) and MUFA (39.9%) in dromedary
camel milk contributes to enhance the positive effects on hu-
man health (Narmuratova et al. 2006; Konuspayeva et al.
2008). The main fatty acids present in dromedary camel milk
are oleic (28.4%), palmitic (21.2%), stearic (13.8%), and
myristic (12.1%), respectively. Dromedary camel milk is also
rich in both lipo- and hydro-soluble vitamins, such as vitamin
A, E, D, B, and C (Kumar et al. 2015; Zibaee et al. 2015). For
instance, dromedary camel milk contains 34.2 mg/L of vita-
min C, being this concentration 3 to 5 times higher than in
milk from dairy cows (Stahl et al. 2006). In addition, drome-
dary camel milk contains higher insulin concentrations
(52.0 U/L) than cow milk (16.3 U/L) (Singh 2001). Based
on this fact, Agrawal et al. (2005) suggested that consumption
of dromedary camel milk could have beneficial effects in pa-
tients suffering diabetes (type II). Besides its nutritional prop-
erties, dromedary camel milk also contains antibacterial and
antiviral enzymes such as lactoferrin, lactoperoxidase, ca-
seins, peptidoglycan recognition protein, N-acetyl-
glucosaminidase, lysozymes, and immunoglobulins (Kumar
et al. 2016).
Hair fiber production perspectives
Hair fiber is another valuable product obtained from drome-
dary camels. Although all other camelids produce higher qual-
ity hair fiber than dromedary camels, hair fiber from drome-
dary camels is highly appreciated by consumers because of its
luster, softness, warmth, and natural color (Sharma and Pant
2013). However, these characteristics are affected by age as
young dromedaries produce thinner and softer hair fiber than
adults. Dromedary camel hair fiber is mainly used for clothes,
veils, carpets, and blankets (Yam and Khomeiri 2015). In ad-
dition to hair fiber, dromedary camels provide long hair, com-
monly used for clothes manufacturing.
South American camelids
South American camelids (SAC) are widely distributed in
South America, being alpacas (Lama pacos; Fig. 4a), llamas
(Lama glama;Fig.4b), and vicuñas (Vicugna vicugna;
Fig. 5a) distributed from Ecuador to northern Argentina and
Chile, while guanacos (Lama guanicoe; Fig. 5b) are found
from southern Peru and Paraguay to Argentina and Chile
(Saeed et al. 2018). In addition, animal production systems
in the Peruvian and Bolivian Altiplano are mostly based on
llamas and alpacas (Fernández-Baca 2005).
South American camels have exceptional physiological
characteristics that allow them to adapt to adverse environ-
ments (Gerken 2010). Due to the adaptability to the environ-
ment, they have been raised as livestock species for meat,
milk, and fiber production.
Meat production perspectives
Meat from llamas and alpacas is one of the major protein
sources for Andean rural communities (Perez et al. 2000).
Llama and alpaca meat is rich in iron and zinc (32.6 and
44.4 mg/kg, respectively) (Polidori et al. 2007). In addition,
meat from llamas and alpacas is low in fat (0.49 and 2.05%,
respectively) and cholesterol (0.51 to 0.56 g/kg, respectively),
especially if compared with meat from other livestock species
(Cristofanelli et al. 2004). Moreover, meat from alpacas con-
tains 51 g SFA/100 g of total intramuscular fat and 2.05 g n3
fatty acids/100 g of total intramuscular fat (Salva et al. 2009).
These facts are particularly attractive for local and internation-
al markets, representing a substantial income for small- and
medium-scale local producers (Mamani-Linares and Gallo
2014). Technological quality parameters such as carcass pH
and temperature, drip loss, thawing loss, expressible juice,
total cooking loss, evaporating cooking loss, and cooking drip
loss in alpaca and llama meat are similar to those reported for
conventional meats (Salva et al. 2009; Mamani-Linares and
Gallo 2014). Several studies performed in Australia have re-
ported that alpaca carcasses have low fat covering which
makes these carcasses susceptible to cold-induced shortening
during processing (Smith et al. 2015). Therefore, these car-
casses are commonly aged up to 10 days and electro stimulat-
ed to improve tenderness.
Interestingly, slaughtering age and gender do not affect
alpaca meat color. Thus, meat from these animals has
unique color characteristics. According to the CIELab
Trop Anim Health Prod
system, alpaca meat has a characteristic color (L* 38.3; a*
11.7 and b* 0.78), which could be used to detect frauds,
especially in markets with meat from multiple species
(Smith et al. 2016). Based on the above-mentioned facts,
SAC meat production has a high growth potential in the
near future (Smith et al. 2019).
One of the main limitations for the production and com-
mercialization of meat from SAC is the presence of macro-
scopic Sarcocystis aucheniae cysts (15 mm cysts), which
leads to carcass refusal by the sanitary authorities and/or de-
valuation of its commercial value (Franco et al. 2018).
Consumption of infected raw or undercooked meat can
Fig. 5 Vicuña (A1 and A2;
Ecuador) and guanaco (B1 and
B2; Chile)
Fig. 4 Alpaca (A1 and A2; Chile)
and llama (B1 and B2; Ecuador)
Trop Anim Health Prod
furthermore cause foodborne illness to the consumers in the
form of gastroenteritis and diarrhea (Franco et al. 2018). This
is therefore an important issue to address in order to increase
the value and importance of this meat in the Andean markets.
Cristofanelli et al. (2004) suggested that improving breed-
ing systems of SAC would be a suitable strategy to stimulate
the economy in the Andean regions. These authors reported
that compared with alpaca, llama has higher BW (46 vs. 63 kg
at 25 months of age, respectively), warm carcass weight (24
vs. 31 kg, respectively), cold carcass weight (23 vs. 30 kg,
respectively), carcass length (71 vs. 130 cm, respectively),
length of hind leg (70 vs. 75 cm, respectively), and length of
front leg (60 vs. 68 cm, respectively). Therefore, llama seems
to be better suited for meat production in the Andean countries
than alpacas. Accordingly, alpaca production systems should
focus on fiber, and then use animals that need to be replaced
for meat production.
Hence, SAC meat production should be promoted at the
local South American markets as an alternative product in
pastoral systems with limited growth potential. This is of par-
ticular importance in high-altitude regions where conventional
livestock species such as cattle or sheep cannot cope so well.
In the rest of the World (excluding Australia), SAC are used as
pets, and consequently, meat consumption from these animals
is not expected to grow significantly in the future.
Dairy production perspectives
Milk yields in SAC are very low compared with dairy cows
(Larico-Medina et al. 2018). However, milk from SAC con-
tains higher protein, fat, and lactose levels than cow milk,
which makes this type of milk very interesting for dairy prod-
ucts manufacturing. Alpaca milk has on average 3.68% fat,
4.53% protein, and 6.00% lactose contents (Chad et al. 2014),
while llama milk has on average 4.70% fat, 4.23% protein,
5.93% lactose contents (Riek and Gerken 2006). Similarly,
vicuña milk contains 4.8% fat, 4.30% protein, and 7.05%
lactose while guanaco milk has 5.50% fat, 5.00% protein,
and 5.44% lactose (Medina et al. 2019).
Regarding fatty acid profile in milk from SAC, Medina
et al. (2019) found that all of them contain less than 1% of
short-chain fatty acids. Within SFA, palmitic acid was the
most abundant (> 25%), followed by stearic acid (> 10%)
and myristic acid (> 10%) in all SAC species. Interestingly,
levels of rumenic acid, also known as conjugated linoleic acid,
in milk from these species range from 1.051.64%. Rumenic
acid is a unique FA that can only be found in both milk and
meat from ruminants. This fatty acid has received particular
attention due to the positive effects on human health (Vargas-
Bello-Perez and Larrain 2017). Despite the studies mentioned
above, data on the nutritional quality of SAC milk is scarce.
Due to its potential as an alternative to cow milk, researchers
should focus on describing the nutritional properties of SAC
milk and its impact on human health (Pauciullo and Erhardt
2015).
Hair fiber production perspectives
In SAC, hair fiber harvesting does not require advanced tech-
nology. This fact makes that fiber production represents one of
the main economic incomes in productive systems with low
primary productivity, such as the Andean highlands and
Patagonia (Lichtenstein and Vila 2003). Domestic SAC, espe-
cially alpacas, have a wide variety of coat colors, which makes
the species valuable for fiber production. Among all possible
colors, white is the most valuable for the industry.
Consequently, current breeding strategies are focused on
selecting those animals producing white fibers (Anello et al.
2019).
Fiber production from SAC is focused on alpacas, with also
some relevant fiber production from Guanacos and Vicuñas.
There are several factors such as age, breed, and fiber color
that affect fiber diameter (higher in darker fleece) (McGregor
and Butler 2004). For instance, llama fiber can be classified as
baby (< 19 μm; 4.60% of the total production), super thin (19
21.9 μm; 43.4% of the total production), thin (2224.9 μm;
35.8% of the total production), medium (2529 μm; 13.6% of
the total production), and thick (> 30 μm; 2.60% of the total
production) in Argentina (Frank et al. 2006). In New Zealand
and Australia, the diameter of alpaca hair fiber ranges from
28.0 to 31.9 μm and from 17.7 to 46.6 μm, respectively
(Wuliji et al. 2000; McGregor and Butler 2004).
The main limitations of fiber production in these species
are the length of the wick and the presence of a double fiber
layer. Consequently, it is necessary to perform a dehairing
fleece processing which causes around 45% production losses
(Frank et al. 2006). This fact requires actions to improve in-
dustrial processing and to optimize harvest and selection of
the fleece to minimize losses due to fiber processing (Frank
et al. 2006).
Concluding remarks
Camelids are among the most adaptable domestic animals.
Indeed, these animals are well adapted to harsh ecosystems
such as the African, Asian, or Australian deserts (dromedary
camels), the central Asian plains and deserts (Bactrian camels)
or the Andean mountains and the Altiplano plateaus (SAC). In
such regions, these animals are essential for the economy and
food security of local populations.
In the near future, climate change might decrease agricul-
tural areas for animal production worldwide. In these condi-
tions, extensive animal production would have to be limited to
some extent to semi-arid rangelands. In such regions, camels
will become an important protein source for humans.
Trop Anim Health Prod
Furthermore, their adaptation traits would lead to more sus-
tainable animal production systems with reduced greenhouse
gas emissions compared with conventional livestock species
and fewer needs for animal production inputs such as infra-
structures, water, and feed supplementation during feed scar-
city periods. In this review, we have focused on the major
aspects related to meat, milk, and fiber production in the four
domestic camel species (i.e., Bactrian camel, dromedary cam-
el, llama, and alpaca) as they will become important players in
the international animal production context.
Acknowledgments Authors acknowledge Mariana Castro (Instituto
Superior de Agronomia, Lisbon University, Portugal) for the graphical
work in Fig. 1, as well as Antonio Morales-delaNuez (Consejo Superior
de Investigaciones Científicas, Spain) for kindly providing pictures in
Figs. 4b1, 4b2, 5a1, and 5a2.
Compliance with ethical standards
Conflict of interest The authors declare that they have no conflict of
interest.
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... In recent years, SAC have been increasingly introduced into North America and Europe [9], including Germany [10]. They are classified into four different species: alpacas (Vicugna pacos), vicuñas (Vicugna vicugna), llamas (Lama glama) and guanacos (Lama guanicoe) [9]. ...
... In recent years, SAC have been increasingly introduced into North America and Europe [9], including Germany [10]. They are classified into four different species: alpacas (Vicugna pacos), vicuñas (Vicugna vicugna), llamas (Lama glama) and guanacos (Lama guanicoe) [9]. The number of SAC in Germany is about 25,000, as estimated by a German breeding organization, the Alpaka Zucht Verband Deutschland [11]. ...
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Background Paratuberculosis, caused by Mycobacterium avium subspecies paratuberculosis (MAP), is a chronic granulomatous enteritis that affects domestic and wild ruminants and camelids. The disease has rarely been reported in alpacas in Germany. This publication describes epidemiologically independent cases of paratuberculosis in two alpacas in Germany. Case presentation Two alpacas, a 26-year-old female zoo animal (case 1) and a 2.5-year-old breeding stallion from a private owner (case 2), presented with progressive emaciation, leading to death (case 2) or euthanasia (case 1) because of deteriorating general condition. In both cases typical granulomatous lesions in the intestinal mucosa and mesenteric lymph nodes were found. In case 2, other lymph nodes were severely enlarged and MAP was detected in the mandibular lymph node, lung, and liver by qPCR. The MAP isolates differed between the alpacas, with two distinct phylogenetic clades (Clade 1 and 8) within Subgroup A of the MAP-C type group and two distinct INMV profiles (INMV 2 and 1) found. These genotypes have been identified in cattle and goats in different regions in Germany. The genotype isolated from case 1 has been detected in goats from the zoo since 2011, indicating transmission between these species. Conclusions MAP can cause severe clinical disease in alpacas of variable age and under different husbandry conditions. Therefore, paratuberculosis should be considered for differential diagnosis in alpacas with emaciation and poor general condition. Although not definitely shown, cross-species infection between ruminant species and camelids is exceedingly likely.
... In the present study, IHC findings revealed that many artiodactyl species, including alpacas, express high levels of APN in their respiratory tracts and intestinal and colonic tissues. Interest in alpaca farming and their popularity as pets or show animals have grown significantly over the past decade [63]. While alpacas are generally raised outdoors at relatively low densities compared to some captive farmed animals, such as American mink or raccoon dogs, species whose confined conditions promote the transmission of respiratory virus infections [64][65][66], alpacas may also be kept in multi-species grazing systems or petting zoos, increasing their exposure to other cloven-hoofed animals and humans. ...
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Aminopeptidase N (APN) is a transmembrane protein that mediates the attachment of the spike protein of several clinically important coronaviruses (CoVs) responsible for respiratory and intestinal diseases in animals and humans. To assess the potential for APN-mediated viral tropism, we characterized APN receptor distribution in the respiratory and intestinal tissues of various artiodactyls (cervids, bovids, camelids and suids) and carnivores (canids, felids, mustelids and phocids) using immunohistochemistry. In the lungs, APN expression was limited to artiodactyls, with strong expression in the bronchiolar epithelium and weaker expression in pneumocytes. Nasal turbinate and tracheal samples, where available, showed stronger APN expression in artiodactyls over carnivores. APN was consistently detected on the microvilli of enterocytes in the small intestine across multiple taxa, while the presence in the colon was more variable. Of the animals examined, pig and alpaca consistently expressed the most abundant APN in the upper and lower respiratory tract. In silico evaluation of APN orthologue sequences from humans, artiodactyls and carnivores identified distinct evolutionary relationships. Further in silico binding predictions for alpaca alphacoronavirus and human coronavirus 229E with cognate and heterologous alpaca and human APN revealed substantial overlapping binding footprints with high conservation of amino acid residues, suggesting an evolutionary divergence and subsequent adaptation of a 229E-like or ancestral virus within a non-human animal host. This combined anatomical and in silico approach enhances understanding of host susceptibility, tissue tropism and viral transmission mechanisms in APN-dependent CoVs and has the potential to inform future strategies for disease modelling, surveillance and control.
... Bactrian or two-humped camels (Camelus bactrianus) are primarily distributed across China, Mongolia, Kazakhstan, Russia, Iran, Afghanistan, and Pakistan (Vyas et al., 2015;Zarrin et al., 2020). Camels have significant economic value due to their ability to adapt to extreme climates (Yagil, 1985). ...
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This study examines the multifaceted role of the two-humped camel ( Camelus bactrianus ) in the livelihoods of Mongolian pastoralists, focusing on its adaptability to extreme climates, economic contributions, and cultural significance. Camels are essential for the production of meat, milk, and wool, which account for 54% of total cash income in certain regions. They also provide essential draft power for transportation, tourism, and sports. The study reveals variations in camel distribution across Mongolia’s natural zones and highlights their resilience in supporting herders under diverse ecological conditions. The reproductive and lactation cycles of camels, adapted to Mongolia’s distinct climate, further highlight their suitability for pastoral systems. This research emphasizes the importance of promoting sustainable camel farming practices through supportive policies and investments to improve pastoral livelihoods and to ensure the preservation of Mongolia’s camel-rearing heritage.
... Bactrian camels (Camelus bactrianus) are among the few large livestock that adapts to the harsh environments of arid and semi-arid regions (Zarrin et al., 2020). Being a precious biological resource, camels can adapt to hostile conditions, such as high temperature, severe cold, drought, food scarcity, and high radiation, better than the other livestock. ...
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Knowledge about the quality of meat obtained from different muscles is crucial for developing high-quality camel meat for commercial use. Metabolomic and proteomic profiles of the longissimus thoracic (LT), semitendinosus (ST), and psoas major (PM) muscles of the bactrian camel, which significantly vary in aspects such as intramuscular fat (IMF) content and shear force, were comprehensively compared to evaluate the impact of these changes on meat quality. Compared with ST and PM muscles, LT muscles had higher IMF content, were more tender, and had a lower shear force. Proteomic analysis unveiled significant differences in metabolic enzymes and binding proteins among different muscles. Based on correlation analysis, 20 key proteins and metabolites closely related to meat quality were screened. Integration of proteomic and metabolomic data highlighted oxidative phosphorylation, TCA cycle, and glycolysis as key distinguishing pathways among different muscles. These results offer effective information for producing high-quality camel meat.
... It was also higher than Chinese Bactrian calves (Zhao et al., 2000). For example, the 6-month DWG was 0.500 kg/day only for Zarrin et al. (2020). ...
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A hybrid camel Tülü (Bactrian male x Dromedary female F1) males are preferred in camel wrestling, which is a culture unique to Anatolia. In this study, changes of live weight (LW), daily weight gain (DWG), and body measurements (BMs) of Tülü calves in the first 6 months of age in a farm in Aydın province, Türkiye, were determined as well as developing equations to estimate LW from body measurements. Tülü calves average birth weight (BW) was 34.7±1.80 kg and reached 175.3±3.38 kg at the age of 6 months with a 0.768±0.03 kg DWG during this time. Although the monthly total weight gains and monthly DWG averages of the calves in the first 6 months were similar, the changes in monthly LW and BMs were statistically significant (P<0.01). Abdominal girth (AG) alone can be used to predict LW in the analysis performed to estimate LW from body measurements by stepwise regression (R²=95.62%). In conclusion, Tülü calves had relatively high growth rate in their first six months of age, and unlike other livestock species, instead of hearth girth (HG), AG that includes the hump can be used to estimate LW of Tülü calves.
... Among the SACs, there are wild species such as the guanaco (Lama guanicoe) and the vicuña (Vicugna vicugna), as well as domesticated ones like the llama (Lama glama) and the alpaca (Vicugna pacos) [2,3]. SACs are an economically significant resource, as they have been bred for meat, milk, and fiber production by Andean communities for centuries [4]. SACs have morphological and physiological adaptations that enable them to inhabit and survive in HAEs characterized by low oxygen availability, rocky substrates, and low temperatures. ...
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South American camelids inhabit high-altitude environments characterized by hypoxia, influencing embryonic, fetal, and placental development. This study examined the term placenta morphology of alpacas (Vicugna pacos, N = 12) and the immunoexpression of antioxidant selenoproteins (SP). We hypothesize that the placenta of alpacas, adapted to high altitudes, has characteristics with other species also adapted to altitude. Placentas were paraffin-embedded, sectioned (3–5 µm), stained with hematoxylin–eosin (H&E), Masson’s trichrome, and picrosirius red, and analyzed via light and polarized light microscopy. The chorion showed simple cuboidal epithelium with binucleated cells, a subepithelial mesenchyme rich in blood capillaries (area: 124.90 ± 9.82 µm²), and type III collagen fibers. The chorionic villi measured 2740.22 ± 132.75 µm. The allantois contained a simple columnar epithelium and mesenchyme with type I collagen fibers. Immunohistochemistry localized SP-N, SP-P, Dio-3, and GPx-3 in the blood capillaries and mesenchymal tissue of the chorion but not in the allantois. These findings were compared to human and sheep placentas from different altitudes due to a lack of camelid data at low levels. The morphological features resembled adaptations to hypoxia observed in other species. This preliminary study suggests a potential role for selenoproteins in hypoxia adaptation, providing a basis for future functional studies.
... Alpaca milk can be used to produce cheese with favorable physicochemical properties and sensory characteristics [144]. The potential of camelids, including alpacas, is noteworthy, as they may become an important source of protein in the face of climate change [145]. ...
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Non-bovine dairy animals, commonly referred to as non-traditional dairy species, include goats, sheep, yaks, buffalo, donkeys, alpacas, llamas, and other less commonly farmed species. These animals have been integral to livestock systems since ancient times, providing milk and other essential products. Despite their historical significance, dairy production from many of these species remains predominantly confined to rural areas in developing countries, where scientific advancements and technical improvements are often limited. As a consequence of this, the scientific literature and technological developments in the processing and characterization of dairy products from these species have lagged behind those for cow's milk. This review aims to compile and analyze existing research on dairy products derived from non-traditional animals, focusing on their molecular characteristics, including proteins (alpha, beta, kappa, and total casein), fats (cholesterol and total fat), lactose, albumin, ash, total solids, and somatic cell count, among others, for each of these species. Additionally, we discuss emerging technologies employed in their processing, encompassing both non-thermal methods (such as high-pressure processing, pulsed electric fields, ultrasound processing, UV-C irradiation, gamma radiation, microfiltration, and cold plasma processing) and thermal methods (such as ohmic heating). This review also explores the specific potential applications and challenges of implementing these technologies. By synthesizing recent findings, we aim to stimulate further research into innovative technologies and strategies that can enhance the quality and yield of non-bovine dairy products. Understanding the unique properties of milk from these species may lead to new opportunities for product development, improved processing methods, and increased commercialization in both developing and developed markets.
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The objective of the present study was to determine the diameter, area, circumference, and blood flow of the corpus luteum (CL) using transrectal ultrasonography in female alpacas with and without the presence of an embryo on Day 9 post‐mating, the time of maternal recognition of pregnancy (MRP). For this purpose, 12 female alpacas with follicles ≥ 7 mm were mated with fertile males and treated with 0.0084 mg of buserelin acetate (Day 0). After that, the females were randomly classified into 2 groups (6 animals/group): (1) CL with embryo and (2) CL without embryo (embryo removed from the uterine horn on Day 9). In both groups, transrectal ultrasonography was performed on Day 2 to determine ovulation, and on Days 5, 7, 9, 11, and 13 to evaluate the CL. The data were analysed using repeated measures ANOVA. The diameter (mm), total area (mm ² ), circumference (mm), and blood flow (%) of the CL were significantly decreased in the CL without embryo group on Days 11 and 13 (6.9 ± 0.6 and 2.9 ± 1.1, 48.3 ± 5.6 and 12.3 ± 4.7, 22.4 ± 1.9 and 7.4 ± 2.5 and 39% and 55%, respectively) compared to the CL with embryo group (12.1 ± 0.9 and 12.1 ± 0.6, 111.1 ± 17.1 and 107.5 ± 8.8, 37.2 ± 2.8 and 37.0 ± 1.7, and 3% and 3%, respectively). In conclusion, the CL characteristics in alpacas with embryo removal changed drastically after Day 9, presenting progressive regression in size and blood flow from Day 11 to 13. These results might indicate that the presence of an embryo on Day 9 is necessary to trigger the signal that prevents luteolysis in this species.
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Old World camels have served humans in cross‐continental caravans, transporting people and goods, connecting different cultures and providing milk, meat, wool and draught since their domestication around 3000–6000 years ago. In a world of modern transport and fast connectivity, these beasts of burden seem to be out‐dated. However, a growing demand for sustainable milk and meat production, especially in countries affected by climate change and increasing desertification, brings dromedaries (Camelus dromedarius) and Bactrian camels (Camelus bactrianus) back onstage and into the focus of animal breeders and scientists. In this review on the molecular genetics of these economically important species we give an overview about the evolutionary history, domestication and dispersal of Old World camels, whereas highlighting the need for conservation of wild two‐humped camels (Camelus ferus) as an evolutionarily unique and highly endangered species. We provide cutting‐edge information on the current molecular resources and on‐going sequencing projects. We cannot emphasise enough the importance of balancing the need for improving camel production traits with maintaining the genetic diversity in two domestic species with specific physiological adaptation to a desert environment.
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Camelus dromedarius has played a pivotal role in both culture and way of life in the Arabian peninsula, particularly in arid regions where other domestic animals cannot be easily domesticated. Although, the mitochondrial genomes have recently been sequenced for several camelid species, wider phylogenetic studies are yet to be performed. The features of conserved gene elements, rapid evolutionary rate, and rare recombination make the mitochondrial genome a useful molecular marker for phylogenetic studies of closely related species. Here we carried out a comparative analysis of previously sequenced mitochondrial genomes of camelids with an emphasis on C. dromedarius, revealing a number of noticeable findings. First, the arrangement of mitochondrial genes in C. dromedarius is similar to those of the other camelids. Second, multiple sequence alignment of intergenic regions shows up to 90% similarity across different kinds of camels, with dromedary camels to reach 99%. Third, we successfully identified the three domains (termination-associated sequence, conserved domain and conserved sequence block) of the control region structure. The phylogenetic tree analysis showed that C. dromedarius mitogenomes were significantly clustered in the same clade with Lama pacos mitogenome. These findings will enhance our understanding of the nucleotide composition and molecular evolution of the mitogenomes of the genus Camelus, and provide more data for comparative mitogenomics in the family Camelidae.
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To cope with the extreme heat stress and drought of the desert, the Arabian camel (Camelus dromedarius) has developed exceptional physiological and biochemical particularities. Previous reports focused mainly on the physiological features of Arabian camel and neglected its cellular and molecular characteristics. Heat shock proteins are suggested to play a key role in the protein homeostasis and thermotolerance. Therefore, we aim by this review to elucidate the implication of camel HSPs in its physiological adaptation to heat stress and compare them with HSPs in related mammalian species. Correlation of these molecules to the adaptive mechanisms in camel is of special importance to expand our understanding of the overall camel physiology and homeostasis.
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The present study is aimed at comparing the fatty acid profiles, cholesterol, and atherogenicity index of Bactrian and dromedary camel meat by using discriminant analysis to identify the more discriminating fatty acids. Six muscles were sampled from nine Bactrian and nine dromedary camels and analyzed for fatty acid parameters and cholesterol content. The mean fatty acid profiles differed in higher proportion between species than between muscles. The main discriminating fatty acids between species (100% well-classed samples) were C15:0, C17:1, C14:1, C20:0, and C18:0. A significant difference was also observed in cholesterol content, with more cholesterol in Bactrian meat (53.6 ± 12.5 mg/100 g) compared to dromedary meat (49.4 ± 11.2 mg/100 g). However, the atherogenicity index was lower in Bactrian meat (1.196 ± 0.148) than in dromedary meat (1.379 ± 0.109). Despite the dietetic interest in camel meat due to its low cholesterol and low-fat content, the high atherogenicity index compared to other red meat appeared as an unfavorable argument.
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The llama (Lama glama) is a fiber‐producing species that presents a wide range of coat colors, among which white is one of the most important for the textile industry. However, there is little information about the molecular mechanisms that control the white phenotype in this species. In domestic mammals, a white coat is usually produced by mutations in the KIT proto‐oncogene receptor tyrosine kinase (KIT) and microphthalmia‐associated transcription factor (MITF) genes. In this work we have sequenced and described the coding regions of KIT and MITF‐M, the melanocyte‐specific isoform, and the two transcriptional variants MITF‐M(−) and MITF‐M(+). Moreover, we studied the expression of these genes in the skin of white and colored llamas. Although no variants were revealed to be associated with white coat color, significant differences between phenotypes were observed in the expression levels of KIT and MITF‐M. Interestingly, white llamas expressed less MITF‐M(+) than did colored ones, which is consistent with a consequent reduction in the synthesis of melanin. Even though our results indicate that downregulation of KIT and MITF‐M expression is involved in white phenotype production in llamas, the causative gene of white coat color remains unknown.
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Dairy cows contribute to 85 % of the total milk produced worldwide. Milk is an important protein source in human diets, providing 32 g protein/L. The most abundant milk proteins are α-lactalbumin, β-lactoglobulin, αs-casein, β-casein, and κ-casein. Besides their nutritional value, milk proteins play a crucial role in milk properties such as solubility, water bonding, heat stability, renneting and foaming, among others. In addition, these proteins are the main source of bioactive components in milk. Due to the wide range of beneficial effects on human health, milk proteins are considered potential ingredients for the production of health-promoting functional foods. Animal genetics and animal nutrition play an important role in the relative proportions of milk proteins and could be used to manipulate the concentration of specific bioactive peptides in milk from ruminants in order to promote beneficial effects on human health. Unfortunately, only few studies in the literature have focused on changes in milk bioactive peptides associated to animal genetics and animal nutrition. The knowledge described in the present review may set the basis for the development of new dairy products with healthy and beneficial properties for humans.
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In the next two decades, the world population will increase significantly; the majority in the developing countries located in the tropics of Africa, Asia, Latin America, and the Caribbean. To feed such a population, it is necessary to increase the availability of food, particularly high-value animal protein foods produced locally, namely meat and dairy products. Dairy production in tropical regions has a lot of growth potential, but also poses a series of problems, particularly as dairy production systems were developed in temperate countries and in most cases are difficult to implement in the tropics. Drawbacks include hot weather and heat stress, the lack of availability of adequate feeds, poor infrastructure, and cold chain and the competition with cheap imports from temperate countries. This position paper reviews the major drawbacks in dairy production for the five major dairy species: cattle, water buffalo, sheep, goat, and camel, as well as the future trends in research and development. It also concerns the major trends in reproduction and production systems and health issues as well as environmental concerns, particularly those related to greenhouse gas emissions. Tropical Animal Health and Production now launches a topical collection on Tropical Dairy Science. We aim to publish interesting and significant papers in tropical dairy science. On behalf of the editorial board of the Tropical Animal Health and Production, we would like to invite all authors working in this field to submit their works on this topic to this topical collection in our journal.
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The longissimus thoracis et lumborum (LL), and adductor femoris (AF) muscles from 39 castrated, 23 (±1) month old huacaya alpacas were used to determine vitamin E content and the impact on lipid oxidation levels. At 24 h post death the LL and AF muscles were removed and sampled for meat quality analysis and subjected to simulated retail display. Vitamin E content of either muscle had no significant impact on colour stability or oxidation traits during retail display. This is thought to be due to the high levels of vitamin E (>5.4 mg/kg) in both muscles. Lipid oxidation levels were 0.2 mg MDA/kg higher in both muscles post retail display. However, overall differences in TBARS levels detected pre and post display were very low (<1.19 mg MDA/kg) and well below sheep threshold values of >3 mg MDA/kg. The mechanism behind why alpaca meat has such high vitamin E levels compared to other species requires further investigation.