KINGDOM OF SAUDI ARABIA

Ministry of Education

TAIBAH UNIVERSTY

A report in Embryology about

Embryonic development in rhinoceros

Prepared by:

Arwa Mohammed Al-Harbi

U.N: 3755129
Section: A

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 Contents
Introduction ............................................................................................... 3

Discussion: ................................................................................................ 4

Ovarian stimulation and transrectal oocyte recovery................................ 4

Sperm selection for ICSI ........................................................................... 6

In vitro oocyte maturation and ICSI and embryo development ............... 8

ES cell line derivation and differentiation .............................................. 10

Embryo development from and Fatu and Suni ....................................... 16

Parentage testing and sex determination ................................................. 17

Karyotype analysis .................................................................................. 18

References ............................................................................................... 19

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Introduction
Conventional approaches toward establishing a self-sustaining
NWR population over the last two decades have been repeatedly
unsuccessful. To date only one study related to ovum pick up and
embryos production in rhinoceros has been reported. There has been no
report of the production of rhinoceros embryo from fertilization to the
pre-implantation stage. Our results suggest that ART might offer an
option for rescuing genes from the NWR, an essential first step in saving
this nearly extinct rhinoceros sub-species. Beyond applying this classical
ART approach, it would be critical to generate artificial gametes. ES
cells are the best source for producing primordial germ cells and also
represent the ―gold standard‖ for assessing artificial gametes derived
from induced pluripotent stem cells (iPSCs).
Scientists today announced they were able to create two embryos
of the rare rhino, raising hopes that new members of the endangered
species could be conceived in the future. The in-vitro creation was made
by a consortium of veterinarians and conservationists from Germany,
Kenya, and the Czech Republic working at the Avantea laboratory in
Cremona, Italy. The embryos are now stored in liquid nitrogen and will
soon be transferred into a surrogate mother.
The news comes just weeks after a team of veterinarians achieved
another milestone by harvesting 10 oocytes from the last two remaining
female northern white rhinos living in Kenya. Najin and Fatu, a mother
and daughter duo, are the only two northern white rhinos left in the
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world and currently live under 24-hour armed guard in Ol Pejeta
Conservancy in Kenya’s central highlands.
Discussion:

Ovarian stimulation and transrectal oocyte recovery

To harvest oocytes from rhinoceros species, we developed
protocols for ovarian stimulation (Supplementary Figure 1) to increase
the number of available follicles, as well as safe procedures for general
anesthesia and for transrectal oocyte recovery1. Based on our
preliminary data and the large body size of WR females (fWR), a
rhinoceros-specific oocyte collection instrument (patent pending) was
developed in order to reach the ovaries through the rectum. This also
required a long double-lumen needle and tubing connected to an
aspiration pump to recover the fluid aspirated from the follicles (Fig. 1).
The donor fSWRs are distributed across different European zoos, and in
each case the collection of oocytes was performed on-site (with the
inherent difficulties of transporting all required materials). All follicles
visible in the ovaries at a size of 1 cm or larger were aspirated using an
ultrasound-guided double lumen 16 Gauge needle, in order to repeatedly
flush them to dislodge the oocyte, as is the procedure in the
horse8 (Fig. 1). A total of 18 OPU procedures were performed (Table 1)
including a post mortem collection from a deceased fNWR for natural
causes related to age (Supplementary figure 2). We recovered 83 oocytes
(26.4%) from the 314 follicles that were punctured (Table 1). Oocytes

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were incubated in holding media for 24–36 h at 22 °C during
transportation to the laboratory in Italy to Cremona by express courier
for subsequent in vitro maturation, fertilization, and embryo culture7,10.
Fig. 1

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 Operational setting of the transrectal oocyte retrieval. a An
anaesthetized white rhinoceros positioned in sternal recumbency during
oocyte collection. One operator guides the OPU instrument inside the
rectum directly to the stimulated ovary. The second operator injects the
needle into the follicles under ultrasound guidance and performs the
aspiration and repeatedly flushing the follicle up to ten times. The third
operator replaces the full sterile 50-ml falcon tubes with an empty one.
The 3D tomographic ultrasound image (b) generated with the portable
3D/4D ultrasound unit Voluson I (GE Healthcare, Solingen, Germany)
shows different slices of the ovarian parenchyma which contain one
central echogenic corpus luteum (white asterisk) and many anechoic
follicles ranging from 4 to 20 mm in diameter. The 3D render mode
ultrasound image (c) shows a virtual cut through the stimulated
rhinoceros ovary. In this section eight different follicles are
visible. d Ten rhinoceros oocytes after transrectal oocyte retrieval. Most
of the oocytes collected had an intact cumulus oocyte complex besides
the fact that the double-lumen aspiration needle used has a length of
950 mm and the vacuum applied was 100 mmHg. Bar 100 µm
Sperm selection for ICSI
Obtaining competent spermatozoa is crucial in the successful
development of embryos, in terms of achieving normal fertilization,
activating the oocyte, and its healthy development to the blastocyst
stage. Good quality semen, fresh or frozen, is available from
mSWR1,2,11,12,13. For mNWR, the situation is more critical. The
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amount of semen is limited, is of poor quality, and has been obtained
from only three bulls. This made ICSI, a routine procedure in horses, the
only option that would likely lead to success14. We obtained samples of
the sperm available from the males and tested their quality by measuring
their ability to sustain pronuclei formation and initiate early cleavage in
pig oocytes following ICSI. We assessed the frozen semen of three
mNWR and five mSWR in this way. After thawing, the mNWR samples
had poor or no motility and led to low rates of fertilization (as
determined by pronuclei formation) and cleavage, in contrast to the
mSWR spermatozoa, although they also exhibited variable motility after
thawing . The results were, however, improved through the introduction
of an electrical activation protocol soon after sperm injection (two DC
pulses of 1.5 kV/cm for 30 µm seconds), a technique used for cell fusion
and activation of oocytes after nuclear transfer in livestock species and
in human-assisted reproduction clinics defined as assisted oocyte
activation (AOA), used in cases of failure to form pronuclei after ICSI
and or to undergo cleavage. This dramatically increased the formation
rate of pronuclei (from 30 to 90% fertilization rate from one mNWR)
and cleavage (from 37 to 67%) in the xenogenic pig oocyte test for two
out of the three bull’s samples tested. Following these results, we
routinely used this protocol when mNWR sperm was used for ICSI. We
also excluded the low-performing mNWR3 sperm sample from our
further work as it would have negatively affected embryo development.

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In vitro oocyte maturation and ICSI and embryo development
Upon reaching the laboratory, oocytes were transferred to
maturation media and incubated at 37.5 °C in 5% CO2 for 36–44 h until
a polar body (PB) was detected. Thirty-two oocytes (38.6%) reached the
metaphase II stage suitable for ICSI. Overall, of 19 oocytes injected with
mSWR1 sperm, six underwent cleavage, and three developed to
blastocysts. Of 13 injected with mNWR, six cleaved and four developed
into blastocysts.The amount of time required for maturation was from 36
to 44 h and the time required to reach morula compaction and
blastulation was 7–9 and 9–12 days, respectively. These periods were
relatively long compared to livestock species that reach the same stages
at day 5 and 8 after fertilization20. Four embryos were used for stem cell
derivation (two SWR × SWR, 051A and 051B and two SWR × NWR,
240A and 240B). Three embryos (one SWR  × SWR, two SWR × NWR)
were cryopreserved for later transfer to recipient females, since the
embryo transfer procedure has yet to be developed and validated in
rhinoceroses. A high proportion of embryos that started cleavage
underwent compaction and blastulation (Fig. 2) and were of high
quality. Most of them had a clearly detectable inner cell mass (ICM).
Fig. 2

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 Embryo development from ICSI to blastocyst stage. a ICSI was
performed on MII oocytes with a Piezo-driven needle, the first polar is
visible at 6 o’clock, a sperm is visible inside the ICSI pipette ready for

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injection. A two-cell embryo 48 h after ICSI (b). Cleaved embryos
developed to the eight cell stage on average 5–6 days after injection (c)
and were at pre-compaction stage on day 5–7 (d). Compacted morulae
were visible on average at day 7–9 (e). The first blastocyst produced was
a pure Southern White Embryo (fSWR5 × mSWR1, day 11 after ICSI)
(f). The zona was removed by pronase digestion and embryo was left to
expand for 2 days. From the isolated ICM of this embryo (g) and its twin
obtained from the same group of oocytes (fSWR5 × mSWR1) two ES
cell lines were derived. Subsequently Hybrid Southern White × Northern
White blastocysts were obtained (h) (fSWR5 × mNWR1, day 9 after
ICSI). One of these hybrid blastocysts (fSWR5 × mNWR2) naturally
hatched from the zona at day 10 (i) and was used for ES cell derivation.
One Southern blastocyst (fSWR4 × mSWR1) and two hybrid blastocysts
(fSWR5 × mNWR2 and fSWR8 × mNWR2 (j)) were frozen with a
standard slow freezing protocol after equilibration in 5% and
subsequently in 10% of glycerol freezing media (fSWR8 × mNWR2
(k, l)). Scale bar corresponds to 100 µm
ES cell line derivation and differentiation
To indirectly assess the quality of such embryos and with the
prospect of deriving germ cells from stem cells, we used four embryos
for stem cell derivation following protocols previously established in
cattle. ES cell lines provide by comparison the best assessment of the
quality of existing rhinoceros iPS cell lines. The two SWR × SWR
embryos plated at day 14 and day 15, exhibited clearly visible, large
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ICMs while the two SWR × NWR embryos plated at day 12 and day 13,
had considerably smaller ICMs. All the embryos were micromanipulated
with fine needles. The mechanically isolated ICMs and trophoblasts
were plated separately on inactivated mouse embryonic fibroblasts
(MEFs) and cultured in medium DMEM-F12 supplemented with serum
replacement and bFGF according to protocols commonly in use for
human ES cell cultures (Fig. 3). When a sufficient number of
undifferentiated cells (characterized by high nucleus/cytoplasm ratios
and large nucleoli in the nucleus, Supplementary Figure 3) were
available, we cryopreserved a proportion of them to secure the lines. We
expanded some for stem cell marker analysis, parentage, and sex
determination and to test their differentiation potential in vitro (Fig. 3).
We also confirmed viability after repeated rounds of cryopreservation
and thawing. From each of the two SWR × SWR female embryos, we
established a cell line based on an expansion of the isolated ICM cells.
However, we were not successful in doing so with SWR  × NWR
embryos due to their lack of a well-formed ICM, probably because they
were plated 2 days earlier, and the fact that their outgrowths were mainly
of trophoblast origin. These exhibited limited proliferation, sufficient
only for a genetic analysis to confirm sex (one male and one female) and
parentage

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Fig. 3

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 Isolation of inner cell mass and derivation/characterization of
embryonic stem cell lines. a Isolated ICM and trophoblast from
rhinoceros embryo after mechanical dissection with insulin needles
(40×); b ICM outgrowth 48 h after plating on feeder cells
(20×). c Representative image of ES colonies 24 h after enzymatic
passaging; d ES colonies ready for the next passaging. Characterization
of undifferentiated ES
colonies: e, i, o OCT4 staining; f, l, p NANOG staining; g, m, q SO
X2 staining; h, n, r SSEA3 staining. Characterization of differentiated
derivatives: s p75 staining of neural crest precursors; t, u Tuj1
and TH staining of neuronal cells; v, z, x GATA4, GATA6,
SOX17 staining of endodermal cells; y, w MYOSIN, NKH2.5,
TNNT2 staining of myocardial cells. Bar 100 µm; j RT-PCR for SOX2,
OCT4, and NANOG in fibroblasts and rESC (n = 1 sample for each cell
line)
The two successfully established cell lines (051A and 051B) had
normal karyotype (Supplementary Figure 7) displaying a typical ES
morphology of tightly packed cells, with a high nucleus/cytoplasm ratio,
exhibiting growth in colonies on top of feeder cells with well-defined
borders. The ES cell phenotype was confirmed by immunocytochemistry
based on the pluripotency markers OCT4, NANOG, SOX2,
and SSEA3 and by real-time PCR (Fig. 3j). OCT4 and SOX2-specific
staining was also confirmed with monoclonal antibody staining

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(Supplementary Figure 4). Negative controls for unspecific binding of
primary or secondary antibodies have been ruled out (Supplementary
Figure 5). To further confirm the nature of true embryonic stem cells,
the two established ES cell lines were induced to differentiate into
neural, mesoderm, and endoderm derivatives. Differentiation towards
the three lineages has been documented with at least three markers per
lineage (Fig. 3). Neural differentiation through the formation of
embryoid bodies and neural rosettes resulted in TuJ1 and Peripherin-
positive cells (Fig. 4). From mesodermal differentiation beating
cardiomyocytes were obtained .Negative controls for unspecific binding
of secondary to undifferentiated cells or primary antibodies to fibroblasts
have been ruled out .
Fig. 4

Bright-field panel of neural differentiation. a Embryoid bodies, 4

days after derivation from proliferating rESC. b Neural
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rosettes. c Proliferating neural precursors with areas of residual radial
cells. d Differentiated neurons. Scale bar corresponds to 100 μm.
Staining for neural differentiation obtained by embryoid body formation
and subsequent induction of differentiation. e Hoechst staining of the
nuclei, f differentiated neurons stained with TUJ1, g Peripherin staining,
and h merge .
Previously housed in a zoo in the Czech Republic, they were
transferred to Kenya in 2009 in the hopes that the climate, natural
habitat, and dietary conditions would provide more favorable breeding
conditions. But those hopes were repeatedly dashed—especially after the
death last year of Sudan, the last male northern white rhino.

AMI VITALE
Egg fertilization and maturation

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 CESARE GALLI AVANTEA
Embryo development from and Fatu and Suni
Here we report the first ever documented generation of blastocyst,
pre-implantation rhinoceros embryos through the application of assisted
reproduction procedures that had never been previously attempted in this
species. Our results suggest that these methods could play a valuable
role in the effort to save rhinoceros populations on the brink of
extinction. We also obtained embryos from SWR oocytes fertilized with
semen of NWR males, clearly indicating the potential of rescuing genes
of the NWR sub-species through intra-specific hybrid breeding.
Moreover, we report the generation of ES cells with all the features of
undifferentiated cells and a high capacity for differentiation in the three
lineages. The next challenges will be to transfer the cryopreserved
embryos into synchronized fSWR surrogate mothers to establish and

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carry a pregnancy to term. In parallel, we plan to harvest oocytes from
the last two remaining fNWR in Kenya. Currently efforts are underway
to achieve the differentiation of rES cells to obtain artificially generated
oocytes from banked somatic cells of several NWR individuals using
iPS technology, as a means of achieving sustainable wide genetic
diversity.
Parentage testing and sex determination
For the two established rESC lines, cells (fSWR × mSWR) at
passage 6–7 cells were pelleted after tryspinization in an eppendorf tube.
For the two hybrid embryos (fSWR × mNWR), outgrowth of trophblast
and differentiated ICM-derived cells were detached from the feeder cells
by short exposure of 5 min to collagenase IV (Gibco) added to the
culture medium at a final concentration of 1 mg/ml. The detached
outgrowths were pooled and transferred to an eppendorf tube with a
minimal volume of media. The eppendorf tube was centrifuged and the
supernatant was discarded, stored at −80 °C, and shipped in dry ice to
the genotyping laboratory. DNA was extracted using peqGold Tissue
DNA Mini Kit following the manufacturer instructions. From the hybrid
embryos, we quantified the total amount of DNA in being 170 ng for
embryos 240A equivalent to 28,000 cells and 285 ng from embryo 240B
equivalent to 47,000 cells. PCR was conducted with the Type-it
Microsatellite PCR Kit (Qiagen) according to manufacturer instructions
but running every marker in a single 12.5 µl reaction. The touchdown
protocol (63–55 °C or 58–50 °C with 2 °C lowering for every of the first
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four cycles) was executed for 25–35 cycles on a peqSTAR universal 96
gradient cycler (Peqlab, Germany). Fragment length analysis was
processed on a 3130xl Genetic Analyzer (Applied Biosystems) with
built in Genotyper software for allele discrimination. Markers, dye
labels, and references are listed in Supplementary Tables 3 and 4. The
analysis of the four samples was performed two times.
Karyotype analysis
The karyotype of the rhinoceros ESCs (between p6 and p16) was
performed by the Laboratory for Human Genetics in Berlin. In brief,
metaphase chromosomes were obtained from rESCs following the
standard protocol for monolayer cultures and by treating the cells for 2 h
with colcemid. Thereafter, the G banding of the mitotic cell was
performed. In total, two passages of the rhinoceros ESCs were screened
and 20 metaphases per passage were analyzed. Afterwards 18
karyograms were generated (standard diagnostic procedure for humans
is to analyze 20 metaphases and to produce 5 karyograms) and no
abnormalities in terms of clonal, structural, or numeric chromosome
aberrations were detected. Chromosomes were identified and numbered
according to previous reports found in Houck et al.31. Karyotypes were
documented with the Axio Imager Z2 from Zeiss 630× and assembled
using the Metafer and Ikaros software from MetaSystems

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References
1. Hikabe, O. et al. Reconstitution in vitro of the entire cycle of the
mouse female germ line. Nature 539, 299–303 (2016).
2. Saragusty, J. et al. Rewinding the process of mammalian
extinction. Zoo Biol. 35, 280–292 (2016).
3. Price, S. & Bininda-Emonds, O. A comprehensive phylogeny of
extant horses, rhinos and tapirs (Perissodactyla) through data
combination. Zoosyst. Evol. 85, 277–292 (2009).
4. https://qz.com/africa/1707103/scientists-make-first-in-vitro-northern-
white-rhino-embryos/

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